Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0001816	"[""angiosarcoma"",""hemangiosarcoma""]"	"[{""label"":""KCNN4"",""id"":""3783""},{""label"":""MYC"",""id"":""4609""},{""label"":""PTPRB"",""id"":""5787""},{""label"":""STAT3"",""id"":""6774""}]"	"[""3783"",""4609"",""5787"",""6774""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0001816""}]"
DOID:0002116	"[""pterygium"",""surfer's eye""]"	"[{""label"":""MMP2"",""id"":""4313""},{""label"":""OGG1"",""id"":""4968""}]"	"[""4313"",""4968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0002116""}]"
DOID:0014667	"[""disease of metabolism"",""metabolic disease""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""BAAT"",""id"":""570""},{""label"":""NBN"",""id"":""4683""},{""label"":""SREBF1"",""id"":""6720""},{""label"":""TJP2"",""id"":""9414""}]"	"[""154"",""4683"",""570"",""6720"",""9414""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0014667""}]"
DOID:0014667	"[""disease of metabolism"",""metabolic disease""]"	"[{""label"":""Ptpn11"",""id"":""19247""}]"	"[""19247""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0014667""}]"
DOID:0014667	"[""disease of metabolism"",""metabolic disease""]"	"[{""label"":""Ldh"",""id"":""45880""},{""label"":""Pfk"",""id"":""36060""},{""label"":""PyK"",""id"":""42620""}]"	"[""36060"",""42620"",""45880""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0014667""}]"
DOID:0040085	"[""bacterial sepsis""]"	"[{""label"":""TREM1"",""id"":""54210""}]"	"[""54210""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0040085""}]"
DOID:0040086	"[""Polyomavirus-associated nephropathy"",""PVAN"",""polyomavirus associated nephropathy""]"	"[{""label"":""KIR3DS1"",""id"":""3813""}]"	"[""3813""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0040086""}]"
DOID:0040090	"[""autoimmune gastritis""]"	"[{""label"":""ATP4B"",""id"":""496""}]"	"[""496""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0040090""}]"
DOID:0040091	"[""autoimmune pancreatitis""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0040091""}]"
DOID:0040094	"[""autoimmune glomerulonephritis""]"	"[{""label"":""Fgl2"",""id"":""14190""}]"	"[""14190""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0040094""}]"
DOID:0050012	"[""chikungunya"",""Chikungunya fever""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050012""}]"
DOID:0050073	"[""invasive aspergillosis""]"	"[{""label"":""CYP2C19"",""id"":""1557""},{""label"":""MBL2"",""id"":""4153""},{""label"":""PTX3"",""id"":""5806""},{""label"":""TLR4"",""id"":""7099""}]"	"[""1557"",""4153"",""5806"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050073""}]"
DOID:0050083	"[""Keshan disease""]"	"[{""label"":""GPX1"",""id"":""2876""}]"	"[""2876""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050083""}]"
DOID:0050117	"[""disease by infectious agent"",""infectious disease""]"	"[{""label"":""ERCC5"",""id"":""2073""},{""label"":""MBL2"",""id"":""4153""},{""label"":""SERPIND1"",""id"":""3053""}]"	"[""2073"",""3053"",""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050117""}]"
DOID:0050120	"[""hemophagocytic lymphohistiocytosis"",""haemophagocytic syndrome""]"	"[{""label"":""Elp1"",""id"":""230233""}]"	"[""230233""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050120""}]"
DOID:0050127	"[""sinusitis""]"	"[{""label"":""CFTR"",""id"":""1080""},{""label"":""IL13"",""id"":""3596""},{""label"":""LTA"",""id"":""4049""}]"	"[""1080"",""3596"",""4049""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050127""}]"
DOID:0050144	"[""Kartagener syndrome"",""Kartagener's syndrome""]"	"[{""label"":""DNAH11"",""id"":""8701""},{""label"":""DNAH5"",""id"":""1767""},{""label"":""MBL2"",""id"":""4153""}]"	"[""1767"",""4153"",""8701""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050144""}]"
DOID:0050144	"[""Kartagener syndrome"",""Kartagener's syndrome""]"	"[{""label"":""Dnah11"",""id"":""13411""},{""label"":""Dnah5"",""id"":""110082""},{""label"":""Dnai1"",""id"":""68922""},{""label"":""Drc1"",""id"":""381738""},{""label"":""Slit2"",""id"":""20563""}]"	"[""110082"",""13411"",""20563"",""381738"",""68922""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050144""}]"
DOID:0050152	"[""aspiration pneumonia""]"	"[{""label"":""ACE"",""id"":""1636""}]"	"[""1636""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050152""}]"
DOID:0050156	"[""idiopathic pulmonary fibrosis"",""FIBROCYSTIC PULMONARY DYSPLASIA"",""IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL"",""cryptogenic fibrosing alveolitis""]"	"[{""label"":""BRD4"",""id"":""23476""},{""label"":""EHMT2"",""id"":""10919""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""MUC5B"",""id"":""727897""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SETD2"",""id"":""29072""},{""label"":""SFTPA2"",""id"":""729238""},{""label"":""TERT"",""id"":""7015""}]"	"[""10919"",""23476"",""29072"",""3123"",""5743"",""7015"",""727897"",""729238""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050156""}]"
DOID:0050156	"[""idiopathic pulmonary fibrosis"",""FIBROCYSTIC PULMONARY DYSPLASIA"",""IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL"",""cryptogenic fibrosing alveolitis""]"	"[{""label"":""Fosl2"",""id"":""14284""},{""label"":""Tnf"",""id"":""21926""}]"	"[""14284"",""21926""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050156""}]"
DOID:0050161	"[""lower respiratory tract disease""]"	"[{""label"":""PGRP-LC"",""id"":""39063""},{""label"":""PGRP-LE"",""id"":""32534""}]"	"[""32534"",""39063""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050161""}]"
DOID:0050168	"[""autoimmune polyendocrine syndrome type 2"",""Schmidt syndrome""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3117"",""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050168""}]"
DOID:0050185	"[""erythema multiforme""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050185""}]"
DOID:0050200	"[""Korean hemorrhagic fever""]"	"[{""label"":""Il2ra"",""id"":""25704""}]"	"[""25704""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050200""}]"
DOID:0050211	"[""swine influenza""]"	"[{""label"":""PIK3CG"",""id"":""5294""}]"	"[""5294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050211""}]"
DOID:0050214	"[""Lambert-Eaton myasthenic syndrome"",""Eaton-Lambert syndrome"",""LEMS"",""Lambert-Eaton syndrome""]"	"[{""label"":""CACNA1B"",""id"":""774""},{""label"":""CHRM1"",""id"":""1128""}]"	"[""1128"",""774""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050214""}]"
DOID:0050214	"[""Lambert-Eaton myasthenic syndrome"",""Eaton-Lambert syndrome"",""LEMS"",""Lambert-Eaton syndrome""]"	"[{""label"":""Cacna1a"",""id"":""12286""}]"	"[""12286""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050214""}]"
DOID:0050328	"[""congenital hypothyroidism""]"	"[{""label"":""DUOX2"",""id"":""50506""},{""label"":""PAX8"",""id"":""7849""},{""label"":""SLC5A5"",""id"":""6528""},{""label"":""TPO"",""id"":""7173""}]"	"[""50506"",""6528"",""7173"",""7849""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050328""}]"
DOID:0050328	"[""congenital hypothyroidism""]"	"[{""label"":""Nefl"",""id"":""83613""},{""label"":""Nefm"",""id"":""24588""},{""label"":""Tshr"",""id"":""25360""}]"	"[""24588"",""25360"",""83613""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050328""}]"
DOID:0050328	"[""congenital hypothyroidism""]"	"[{""label"":""Runx2"",""id"":""12393""},{""label"":""Tg"",""id"":""21819""},{""label"":""Tpo"",""id"":""22018""},{""label"":""Trhr"",""id"":""22045""},{""label"":""Tshr"",""id"":""22095""}]"	"[""12393"",""21819"",""22018"",""22045"",""22095""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050328""}]"
DOID:0050331	"[""lacrimoauriculodentodigital syndrome 1"",""LEVY-HOLLISTER SYNDROME"",""Lacrimo-auriculo-dento-digital syndrome 1""]"	"[{""label"":""Fgf10"",""id"":""14165""}]"	"[""14165""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050331""}]"
DOID:0050331	"[""lacrimoauriculodentodigital syndrome 1"",""LEVY-HOLLISTER SYNDROME"",""Lacrimo-auriculo-dento-digital syndrome 1""]"	"[{""label"":""FGFR2"",""id"":""2263""}]"	"[""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050331""}]"
DOID:0050338	"[""primary bacterial infectious disease""]"	"[{""label"":""Duox"",""id"":""33477""},{""label"":""smo"",""id"":""33196""}]"	"[""33196"",""33477""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050338""}]"
DOID:0050419	"[""complement factor I deficiency"",""C3 INACTIVATOR DEFICIENCY"",""COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY""]"	"[{""label"":""CFI"",""id"":""3426""}]"	"[""3426""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050419""}]"
DOID:0050424	"[""familial adenomatous polyposis"",""adenomatous polyposis of the colon""]"	"[{""label"":""HRR25"",""id"":""855897""}]"	"[""855897""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050424""}]"
DOID:0050424	"[""familial adenomatous polyposis"",""adenomatous polyposis of the colon""]"	"[{""label"":""MUTYH"",""id"":""4595""}]"	"[""4595""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050424""}]"
DOID:0050425	"[""restless legs syndrome"",""WED"",""Willis-Ekbom disease"",""Wittmaack-Ekbom syndrome""]"	"[{""label"":""Drd3"",""id"":""13490""}]"	"[""13490""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050425""}]"
DOID:0050425	"[""restless legs syndrome"",""WED"",""Willis-Ekbom disease"",""Wittmaack-Ekbom syndrome""]"	"[{""label"":""TF"",""id"":""7018""}]"	"[""7018""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050425""}]"
DOID:0050426	"[""Stevens-Johnson syndrome""]"	"[{""label"":""HLA-A"",""id"":""3105""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3105"",""3106"",""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050426""}]"
DOID:0050427	"[""xeroderma pigmentosum""]"	"[{""label"":""RAD30"",""id"":""852028""}]"	"[""852028""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050427""}]"
DOID:0050427	"[""xeroderma pigmentosum""]"	"[{""label"":""XPC"",""id"":""7508""}]"	"[""7508""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050427""}]"
DOID:0050430	"[""multiple endocrine neoplasia type 2A"",""MEN2A"",""Sipple syndrome"",""multiple endocrine neoplasia II""]"	"[{""label"":""RET"",""id"":""5979""}]"	"[""5979""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050430""}]"
DOID:0050431	"[""arrhythmogenic right ventricular cardiomyopathy"",""ARVC"",""ARVC cardiomyopathy"",""ARVD"",""arrhythmogenic right ventricular dysplasia"",""arrhythmogenic right ventricular dysplasia/cardiomyopathy"",""right ventricular ACM""]"	"[{""label"":""ACTN2"",""id"":""88""},{""label"":""CDH2"",""id"":""1000""},{""label"":""DES"",""id"":""1674""},{""label"":""DSC2"",""id"":""1824""},{""label"":""DSG2"",""id"":""1829""},{""label"":""DSP"",""id"":""1832""},{""label"":""LMNA"",""id"":""4000""},{""label"":""PKP2"",""id"":""5318""},{""label"":""RYR2"",""id"":""6262""},{""label"":""TGFB3"",""id"":""7043""},{""label"":""TMEM43"",""id"":""79188""}]"	"[""1000"",""1674"",""1824"",""1829"",""1832"",""4000"",""5318"",""6262"",""7043"",""79188"",""88""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050431""}]"
DOID:0050431	"[""arrhythmogenic right ventricular cardiomyopathy"",""ARVC"",""ARVC cardiomyopathy"",""ARVD"",""arrhythmogenic right ventricular dysplasia"",""arrhythmogenic right ventricular dysplasia/cardiomyopathy"",""right ventricular ACM""]"	"[{""label"":""Dsg2"",""id"":""13511""}]"	"[""13511""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050431""}]"
DOID:0050431	"[""arrhythmogenic right ventricular cardiomyopathy"",""ARVC"",""ARVC cardiomyopathy"",""ARVD"",""arrhythmogenic right ventricular dysplasia"",""arrhythmogenic right ventricular dysplasia/cardiomyopathy"",""right ventricular ACM""]"	"[{""label"":""dsc2l"",""id"":""560091""}]"	"[""560091""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050431""}]"
DOID:0050432	"[""Asperger syndrome""]"	"[{""label"":""SLC25A12"",""id"":""8604""}]"	"[""8604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050432""}]"
DOID:0050433	"[""fatal familial insomnia""]"	"[{""label"":""PRNP"",""id"":""5621""}]"	"[""5621""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050433""}]"
DOID:0050433	"[""fatal familial insomnia""]"	"[{""label"":""Prnp"",""id"":""19122""}]"	"[""19122""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050433""}]"
DOID:0050436	"[""mulibrey nanism"",""MUL"",""Mulibrey growth disorder"",""Muscle-Liver-Brain-Eye Nanism"",""PERICARDIAL CONSTRICTION AND GROWTH FAILURE"",""Perheentupa Syndrome""]"	"[{""label"":""Trim37"",""id"":""68729""}]"	"[""68729""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050436""}]"
DOID:0050436	"[""mulibrey nanism"",""MUL"",""Mulibrey growth disorder"",""Muscle-Liver-Brain-Eye Nanism"",""PERICARDIAL CONSTRICTION AND GROWTH FAILURE"",""Perheentupa Syndrome""]"	"[{""label"":""TRIM37"",""id"":""4591""}]"	"[""4591""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050436""}]"
DOID:0050437	"[""Danon disease"",""ANTOPOL DISEASE"",""PSEUDOGLYCOGENOSIS II""]"	"[{""label"":""Lamp2"",""id"":""24944""}]"	"[""24944""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050437""}]"
DOID:0050437	"[""Danon disease"",""ANTOPOL DISEASE"",""PSEUDOGLYCOGENOSIS II""]"	"[{""label"":""LAMP2"",""id"":""3920""}]"	"[""3920""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050437""}]"
DOID:0050437	"[""Danon disease"",""ANTOPOL DISEASE"",""PSEUDOGLYCOGENOSIS II""]"	"[{""label"":""Lamp2"",""id"":""16784""}]"	"[""16784""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050437""}]"
DOID:0050439	"[""Usher syndrome""]"	"[{""label"":""ARSG"",""id"":""22901""},{""label"":""MYO7A"",""id"":""4647""},{""label"":""USH2A"",""id"":""7399""}]"	"[""22901"",""4647"",""7399""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050439""}]"
DOID:0050440	"[""familial partial lipodystrophy"",""Dunnigan Syndrome"",""Koberling-Dunnigan Syndrome""]"	"[{""label"":""Pparg"",""id"":""19016""}]"	"[""19016""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050440""}]"
DOID:0050440	"[""familial partial lipodystrophy"",""Dunnigan Syndrome"",""Koberling-Dunnigan Syndrome""]"	"[{""label"":""ADRA2A"",""id"":""150""},{""label"":""LMNA"",""id"":""4000""}]"	"[""150"",""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050440""}]"
DOID:0050441	"[""mucosulfatidosis"",""Sulfatidosis, Juvenile, Austin Type"",""multiple sulfatase deficiency disease""]"	"[{""label"":""Sumf1"",""id"":""58911""}]"	"[""58911""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050441""}]"
DOID:0050441	"[""mucosulfatidosis"",""Sulfatidosis, Juvenile, Austin Type"",""multiple sulfatase deficiency disease""]"	"[{""label"":""SUMF1"",""id"":""285362""}]"	"[""285362""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00078""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050441""}]"
DOID:0050445	"[""X-linked hypophosphatemic rickets"",""Hypophosphatemia, Vitamin D-Resistant Rickets"",""Vitamin D-Resistant Rickets, X-Linked"",""X-linked dominant hypophosphatemic rickets"",""X-linked hypophosphatemia"",""hypophosphatemic rickets X-linked dominant""]"	"[{""label"":""Phex"",""id"":""18675""}]"	"[""18675""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050445""}]"
DOID:0050445	"[""X-linked hypophosphatemic rickets"",""Hypophosphatemia, Vitamin D-Resistant Rickets"",""Vitamin D-Resistant Rickets, X-Linked"",""X-linked dominant hypophosphatemic rickets"",""X-linked hypophosphatemia"",""hypophosphatemic rickets X-linked dominant""]"	"[{""label"":""PHEX"",""id"":""5251""}]"	"[""5251""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050445""}]"
DOID:0050449	"[""pachyonychia congenita"",""Jackson-Lawler Type Pachyonychia Congenita"",""Jadassohn-Lewandowsky Syndrome"",""PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE"",""Pachyonychia Congenita Type 1""]"	"[{""label"":""KRT17"",""id"":""3872""}]"	"[""3872""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050449""}]"
DOID:0050450	"[""Gitelman syndrome"",""HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA""]"	"[{""label"":""Slc12a3"",""id"":""20497""},{""label"":""Wnk4"",""id"":""69847""}]"	"[""20497"",""69847""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050450""}]"
DOID:0050450	"[""Gitelman syndrome"",""HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA""]"	"[{""label"":""CLCNKB"",""id"":""1188""},{""label"":""SLC12A3"",""id"":""6559""}]"	"[""1188"",""6559""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050450""}]"
DOID:0050452	"[""mevalonic aciduria"",""Mevalonate Kinase Deficiency""]"	"[{""label"":""MVK"",""id"":""4598""}]"	"[""4598""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050452""}]"
DOID:0050453	"[""lissencephaly""]"	"[{""label"":""PAFAH1B1"",""id"":""5048""},{""label"":""POMGNT1"",""id"":""55624""},{""label"":""POMT1"",""id"":""10585""},{""label"":""POMT2"",""id"":""29954""},{""label"":""TUBA1A"",""id"":""7846""}]"	"[""10585"",""29954"",""5048"",""55624"",""7846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050453""}]"
DOID:0050453	"[""lissencephaly""]"	"[{""label"":""Dg"",""id"":""36773""}]"	"[""36773""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050453""}]"
DOID:0050453	"[""lissencephaly""]"	"[{""label"":""Dag1"",""id"":""13138""},{""label"":""Tuba1a"",""id"":""22142""}]"	"[""13138"",""22142""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050453""}]"
DOID:0050454	"[""periventricular nodular heterotopia"",""periventricular heterotopia""]"	"[{""label"":""ARFGEF2"",""id"":""10564""},{""label"":""FLNA"",""id"":""2316""},{""label"":""MAP1B"",""id"":""4131""},{""label"":""NEDD4L"",""id"":""23327""}]"	"[""10564"",""2316"",""23327"",""4131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050454""}]"
DOID:0050456	"[""Buruli ulcer disease"",""Bairnsdale ulcer"",""Daintree ulcer"",""Mossman ulcer"",""Searl ulcer"",""Searle's ulcer""]"	"[{""label"":""SLC11A1"",""id"":""6556""}]"	"[""6556""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050456""}]"
DOID:0050457	"[""Sertoli cell-only syndrome"",""DEL CASTILLO SYNDROME"",""Germinal Cell Aplasia""]"	"[{""label"":""Mast4"",""id"":""328329""}]"	"[""328329""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050457""}]"
DOID:0050458	"[""juvenile myelomonocytic leukemia""]"	"[{""label"":""Flt3"",""id"":""14255""},{""label"":""Kras"",""id"":""16653""},{""label"":""Nf1"",""id"":""18015""},{""label"":""Ptpn11"",""id"":""19247""}]"	"[""14255"",""16653"",""18015"",""19247""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050458""}]"
DOID:0050458	"[""juvenile myelomonocytic leukemia""]"	"[{""label"":""AKAP12"",""id"":""9590""},{""label"":""ARHGAP26"",""id"":""23092""},{""label"":""CBL"",""id"":""867""},{""label"":""CSF2"",""id"":""1437""},{""label"":""JAK3"",""id"":""3718""},{""label"":""NF1"",""id"":""4763""},{""label"":""PTPN11"",""id"":""5781""}]"	"[""1437"",""23092"",""3718"",""4763"",""5781"",""867"",""9590""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050458""}]"
DOID:0050460	"[""Wolf-Hirschhorn syndrome"",""4p deletion syndrome"",""PITT SYNDROME"",""Pitt-Rogers-Danks Syndrome"",""chromosome 4p16.3 deletion syndrome""]"	"[{""label"":""Fgfrl1"",""id"":""116701""}]"	"[""116701""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050460""}]"
DOID:0050461	"[""aspartylglucosaminuria"",""aspartylglucosaminidase deficiency"",""aspartylglycosaminuria"",""glycosylasparaginase deficiency""]"	"[{""label"":""Aga"",""id"":""11593""}]"	"[""11593""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050461""}]"
DOID:0050461	"[""aspartylglucosaminuria"",""aspartylglucosaminidase deficiency"",""aspartylglycosaminuria"",""glycosylasparaginase deficiency""]"	"[{""label"":""AGA"",""id"":""175""}]"	"[""175""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00005""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050461""}]"
DOID:0050462	"[""Antley-Bixler syndrome with disordered steroidogenesis"",""trapezoidocephaly-synostosis syndrome""]"	"[{""label"":""POR"",""id"":""5447""}]"	"[""5447""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050462""}]"
DOID:0050463	"[""campomelic dysplasia"",""Acampomelic Campomelic Dysplasia""]"	"[{""label"":""SOX9"",""id"":""6662""}]"	"[""6662""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050463""}]"
DOID:0050464	"[""Farber lipogranulomatosis"",""Farber disease"",""N-laurylsphingosine deacylase deficiency"",""acid ceramidase deficiency""]"	"[{""label"":""Asah1"",""id"":""11886""}]"	"[""11886""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050464""}]"
DOID:0050464	"[""Farber lipogranulomatosis"",""Farber disease"",""N-laurylsphingosine deacylase deficiency"",""acid ceramidase deficiency""]"	"[{""label"":""ASAH1"",""id"":""427""}]"	"[""427""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00091""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00092""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00093""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00094""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00095""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00096""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050464""}]"
DOID:0050465	"[""Muir-Torre syndrome""]"	"[{""label"":""MLH1"",""id"":""4292""},{""label"":""MSH2"",""id"":""4436""}]"	"[""4292"",""4436""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050465""}]"
DOID:0050466	"[""Loeys-Dietz syndrome""]"	"[{""label"":""Tgfb2"",""id"":""21808""},{""label"":""Tgfbr1"",""id"":""21812""},{""label"":""Tgfbr2"",""id"":""21813""}]"	"[""21808"",""21812"",""21813""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050466""}]"
DOID:0050469	"[""Costello syndrome"",""FCS SYNDROME"",""Faciocutaneoskeletal Syndrome""]"	"[{""label"":""HRAS"",""id"":""3265""}]"	"[""3265""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050469""}]"
DOID:0050470	"[""Donohue syndrome"",""Leprechaunism""]"	"[{""label"":""INSR"",""id"":""3643""}]"	"[""3643""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050470""}]"
DOID:0050471	"[""Carney complex"",""Carney Complex, Type 1"",""Carney Complex, Type 2"",""Carney Syndrome"",""Carney complex variant"",""LAMB Syndrome"",""NAME Syndrome""]"	"[{""label"":""PRKAR1A"",""id"":""5573""}]"	"[""5573""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050471""}]"
DOID:0050473	"[""Alstrom syndrome""]"	"[{""label"":""Alms1"",""id"":""236266""}]"	"[""236266""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050473""}]"
DOID:0050473	"[""Alstrom syndrome""]"	"[{""label"":""ALMS1"",""id"":""7840""}]"	"[""7840""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050473""}]"
DOID:0050474	"[""Netherton syndrome""]"	"[{""label"":""Spink5"",""id"":""72432""}]"	"[""72432""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050474""}]"
DOID:0050475	"[""Weill-Marchesani syndrome"",""GEMSS syndrome"",""Marchesani-Weill Syndrome"",""Mesodermal Dysmorphodystrophy, Congenital"",""Spherophakia Brachymorphia Syndrome"",""congenital mesodermal dystrophy""]"	"[{""label"":""Adamts10"",""id"":""224697""},{""label"":""Fbn1"",""id"":""14118""}]"	"[""14118"",""224697""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050475""}]"
DOID:0050475	"[""Weill-Marchesani syndrome"",""GEMSS syndrome"",""Marchesani-Weill Syndrome"",""Mesodermal Dysmorphodystrophy, Congenital"",""Spherophakia Brachymorphia Syndrome"",""congenital mesodermal dystrophy""]"	"[{""label"":""ADAMTS10"",""id"":""81794""},{""label"":""ADAMTS17"",""id"":""170691""},{""label"":""FBN1"",""id"":""2200""},{""label"":""LTBP2"",""id"":""4053""}]"	"[""170691"",""2200"",""4053"",""81794""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050475""}]"
DOID:0050476	"[""Barth syndrome"",""3-methylglutaconicaciduria type 2"",""3-methylglutaconicaciduria type II"",""MGA Type 2"",""MGA type II""]"	"[{""label"":""Mest"",""id"":""17294""}]"	"[""17294""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050476""}]"
DOID:0050477	"[""Liddle syndrome"",""Liddle's syndrome"",""Pseudoaldosteronism""]"	"[{""label"":""SCNN1A"",""id"":""6337""},{""label"":""SCNN1B"",""id"":""6338""},{""label"":""SCNN1G"",""id"":""6340""}]"	"[""6337"",""6338"",""6340""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050477""}]"
DOID:0050477	"[""Liddle syndrome"",""Liddle's syndrome"",""Pseudoaldosteronism""]"	"[{""label"":""Scnn1b"",""id"":""20277""}]"	"[""20277""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050477""}]"
DOID:0050477	"[""Liddle syndrome"",""Liddle's syndrome"",""Pseudoaldosteronism""]"	"[{""label"":""RSP5"",""id"":""856862""}]"	"[""856862""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050477""}]"
DOID:0050489	"[""multinodular goiter""]"	"[{""label"":""DICER1"",""id"":""23405""}]"	"[""23405""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050489""}]"
DOID:0050523	"[""adult T-cell leukemia/lymphoma"",""ATLL"",""Adult T-cell leukemia/lymphoma (HTLV-1 positive)"",""adult T-cell leukemia""]"	"[{""label"":""FAS"",""id"":""355""},{""label"":""JAK3"",""id"":""3718""},{""label"":""NOTCH1"",""id"":""4851""}]"	"[""355"",""3718"",""4851""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050523""}]"
DOID:0050524	"[""maturity-onset diabetes of the young"",""MODY"",""Mason-type diabetes""]"	"[{""label"":""GLK1"",""id"":""850317""}]"	"[""850317""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050524""}]"
DOID:0050524	"[""maturity-onset diabetes of the young"",""MODY"",""Mason-type diabetes""]"	"[{""label"":""Ins2"",""id"":""16334""},{""label"":""Pdx1"",""id"":""18609""},{""label"":""Tgm2"",""id"":""21817""}]"	"[""16334"",""18609"",""21817""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050524""}]"
DOID:0050524	"[""maturity-onset diabetes of the young"",""MODY"",""Mason-type diabetes""]"	"[{""label"":""HNF1A"",""id"":""6927""}]"	"[""6927""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050524""}]"
DOID:0050534	"[""congenital stationary night blindness"",""congenital essential nyctalopia""]"	"[{""label"":""CACNA1F"",""id"":""778""},{""label"":""GUCY2D"",""id"":""3000""},{""label"":""TRPM1"",""id"":""4308""}]"	"[""3000"",""4308"",""778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050534""}]"
DOID:0050534	"[""congenital stationary night blindness"",""congenital essential nyctalopia""]"	"[{""label"":""Cacna1f"",""id"":""114493""}]"	"[""114493""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050534""}]"
DOID:0050535	"[""exudative vitreoretinopathy"",""FEVR"",""familial exudative vitreoretinopathy""]"	"[{""label"":""Cdh5"",""id"":""12562""},{""label"":""Ctnnb1"",""id"":""12387""},{""label"":""Fzd4"",""id"":""14366""},{""label"":""Lrp5"",""id"":""16973""}]"	"[""12387"",""12562"",""14366"",""16973""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050535""}]"
DOID:0050540	"[""Charcot-Marie-Tooth disease type 3"",""DEJERINE-SOTTAS NEUROPATHY"",""DEJERINE-SOTTAS SYNDROME""]"	"[{""label"":""EGR2"",""id"":""1959""},{""label"":""MPZ"",""id"":""4359""},{""label"":""PMP22"",""id"":""5376""}]"	"[""1959"",""4359"",""5376""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050540""}]"
DOID:0050540	"[""Charcot-Marie-Tooth disease type 3"",""DEJERINE-SOTTAS NEUROPATHY"",""DEJERINE-SOTTAS SYNDROME""]"	"[{""label"":""Mpz"",""id"":""17528""},{""label"":""Pmp22"",""id"":""18858""}]"	"[""17528"",""18858""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050540""}]"
DOID:0050545	"[""visceral heterotaxy"",""heterotaxia"",""situs ambiguus""]"	"[{""label"":""Acvr2b"",""id"":""11481""},{""label"":""Cep290"",""id"":""216274""},{""label"":""Cfc1"",""id"":""12627""},{""label"":""Dnah11"",""id"":""13411""},{""label"":""Dnah5"",""id"":""110082""},{""label"":""Dnai1"",""id"":""68922""},{""label"":""Drc1"",""id"":""381738""},{""label"":""Megf8"",""id"":""269878""},{""label"":""Mmp21"",""id"":""214766""},{""label"":""Pcsk5"",""id"":""18552""},{""label"":""Slit2"",""id"":""20563""},{""label"":""Tmem67"",""id"":""329795""},{""label"":""Zic3"",""id"":""22773""}]"	"[""110082"",""11481"",""12627"",""13411"",""18552"",""20563"",""214766"",""216274"",""22773"",""269878"",""329795"",""381738"",""68922""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050545""}]"
DOID:0050545	"[""visceral heterotaxy"",""heterotaxia"",""situs ambiguus""]"	"[{""label"":""ACVR2B"",""id"":""93""},{""label"":""CFAP53"",""id"":""220136""},{""label"":""CFC1"",""id"":""55997""},{""label"":""CFC1B"",""id"":""653275""},{""label"":""GDF1"",""id"":""2657""},{""label"":""MMP21"",""id"":""118856""},{""label"":""NODAL"",""id"":""4838""},{""label"":""PKD1L1"",""id"":""168507""}]"	"[""118856"",""168507"",""220136"",""2657"",""4838"",""55997"",""653275"",""93""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050545""}]"
DOID:0050546	"[""congenital adrenal insufficiency"",""ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE"",""Adrenal insufficiency, congenital, with 46,XY sex reversal"",""P450scc DEFICIENCY""]"	"[{""label"":""CYP11A1"",""id"":""1583""}]"	"[""1583""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050546""}]"
DOID:0050547	"[""familial medullary thyroid carcinoma"",""THYROID CARCINOMA, FAMILIAL MEDULLARY""]"	"[{""label"":""Prlr"",""id"":""19116""}]"	"[""19116""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050547""}]"
DOID:0050547	"[""familial medullary thyroid carcinoma"",""THYROID CARCINOMA, FAMILIAL MEDULLARY""]"	"[{""label"":""RET"",""id"":""5979""}]"	"[""5979""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050547""}]"
DOID:0050548	"[""hereditary sensory neuropathy"",""familial dysautonomia, type II"",""hereditary sensory and autonomic neuropathy""]"	"[{""label"":""Dst"",""id"":""13518""},{""label"":""Ntrk1"",""id"":""18211""},{""label"":""Scn11a"",""id"":""24046""}]"	"[""13518"",""18211"",""24046""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050548""}]"
DOID:0050548	"[""hereditary sensory neuropathy"",""familial dysautonomia, type II"",""hereditary sensory and autonomic neuropathy""]"	"[{""label"":""DNMT1"",""id"":""1786""},{""label"":""NTRK1"",""id"":""4914""},{""label"":""WNK1"",""id"":""65125""}]"	"[""1786"",""4914"",""65125""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050548""}]"
DOID:0050554	"[""X-linked sideroblastic anemia with ataxia"",""Anemia sideroblastic and spinocerebellar ataxia"",""Anemia, sideroblastic, spinocerebellar ataxia"",""X-linked sideroblastic anaemia and ataxia"",""X-linked sideroblastic anaemia with ataxia"",""X-linked sideroblastic anemia and ataxia""]"	"[{""label"":""ABCB7"",""id"":""22""}]"	"[""22""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050554""}]"
DOID:0050557	"[""congenital muscular dystrophy""]"	"[{""label"":""Col6a3"",""id"":""12835""}]"	"[""12835""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050557""}]"
DOID:0050558	"[""Ullrich congenital muscular dystrophy"",""ULLRICH DISEASE"",""Ullrich scleroatonic muscular dystrophy""]"	"[{""label"":""Col6a1"",""id"":""12833""},{""label"":""Col6a3"",""id"":""12835""}]"	"[""12833"",""12835""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050558""}]"
DOID:0050559	"[""Fukuyama congenital muscular dystrophy""]"	"[{""label"":""Fktn"",""id"":""246179""}]"	"[""246179""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050559""}]"
DOID:0050559	"[""Fukuyama congenital muscular dystrophy""]"	"[{""label"":""FKTN"",""id"":""2218""}]"	"[""2218""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00378""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050559""}]"
DOID:0050560	"[""Walker-Warburg syndrome"",""HARD syndrome"",""cerebroocular dysplasia-muscular dystrophy syndrome""]"	"[{""label"":""b4gat1"",""id"":""101669768""},{""label"":""rxylt1"",""id"":""557187""}]"	"[""101669768"",""557187""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050560""}]"
DOID:0050560	"[""Walker-Warburg syndrome"",""HARD syndrome"",""cerebroocular dysplasia-muscular dystrophy syndrome""]"	"[{""label"":""PMT4"",""id"":""853608""}]"	"[""853608""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050560""}]"
DOID:0050560	"[""Walker-Warburg syndrome"",""HARD syndrome"",""cerebroocular dysplasia-muscular dystrophy syndrome""]"	"[{""label"":""FKRP"",""id"":""79147""},{""label"":""FKTN"",""id"":""2218""},{""label"":""POMGNT1"",""id"":""55624""},{""label"":""POMT1"",""id"":""10585""},{""label"":""POMT2"",""id"":""29954""}]"	"[""10585"",""2218"",""29954"",""55624"",""79147""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00377""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00378""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050560""}]"
DOID:0050560	"[""Walker-Warburg syndrome"",""HARD syndrome"",""cerebroocular dysplasia-muscular dystrophy syndrome""]"	"[{""label"":""rt"",""id"":""39297""},{""label"":""tw"",""id"":""31024""}]"	"[""31024"",""39297""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050560""}]"
DOID:0050560	"[""Walker-Warburg syndrome"",""HARD syndrome"",""cerebroocular dysplasia-muscular dystrophy syndrome""]"	"[{""label"":""Col4a1"",""id"":""12826""},{""label"":""Pomgnt1"",""id"":""68273""}]"	"[""12826"",""68273""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050560""}]"
DOID:0050561	"[""Lennox-Gastaut syndrome"",""Lennox syndrome""]"	"[{""label"":""Dgkd"",""id"":""227333""}]"	"[""227333""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050561""}]"
DOID:0050562	"[""West syndrome""]"	"[{""label"":""MC2R"",""id"":""4158""},{""label"":""STXBP1"",""id"":""6812""}]"	"[""4158"",""6812""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050562""}]"
DOID:0050563	"[""nonsyndromic deafness"",""nonsyndromic hearing loss"",""nonsyndromic hereditary hearing loss""]"	"[{""label"":""USH2A"",""id"":""7399""}]"	"[""7399""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050563""}]"
DOID:0050563	"[""nonsyndromic deafness"",""nonsyndromic hearing loss"",""nonsyndromic hereditary hearing loss""]"	"[{""label"":""Alg10b"",""id"":""380959""},{""label"":""Wfs1"",""id"":""22393""}]"	"[""22393"",""380959""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050563""}]"
DOID:0050565	"[""autosomal recessive nonsyndromic deafness""]"	"[{""label"":""CDH23"",""id"":""64072""},{""label"":""CLRN2"",""id"":""645104""},{""label"":""GPR156"",""id"":""165829""},{""label"":""MINAR2"",""id"":""100127206""},{""label"":""PKHD1L1"",""id"":""93035""},{""label"":""TMTC4"",""id"":""84899""}]"	"[""100127206"",""165829"",""64072"",""645104"",""84899"",""93035""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050565""}]"
DOID:0050567	"[""orofacial cleft""]"	"[{""label"":""ACSS2"",""id"":""55902""},{""label"":""LOXHD1"",""id"":""125336""},{""label"":""MYH9"",""id"":""4627""}]"	"[""125336"",""4627"",""55902""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050567""}]"
DOID:0050569	"[""Seckel syndrome"",""Harper's syndrome"",""Virchow-Seckel dwarfism"",""bird-headed dwarfism"",""microcephalic primordial dwarfism""]"	"[{""label"":""CDK5RAP2"",""id"":""55755""}]"	"[""55755""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050569""}]"
DOID:0050570	"[""congenital disorder of glycosylation type I""]"	"[{""label"":""Pmm2"",""id"":""54128""}]"	"[""54128""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050570""}]"
DOID:0050570	"[""congenital disorder of glycosylation type I""]"	"[{""label"":""dpm1"",""id"":""445202""}]"	"[""445202""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050570""}]"
DOID:0050570	"[""congenital disorder of glycosylation type I""]"	"[{""label"":""Pmm2"",""id"":""39436""}]"	"[""39436""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050570""}]"
DOID:0050570	"[""congenital disorder of glycosylation type I""]"	"[{""label"":""DPM3"",""id"":""54344""}]"	"[""54344""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050570""}]"
DOID:0050570	"[""congenital disorder of glycosylation type I""]"	"[{""label"":""ALG12"",""id"":""855764""},{""label"":""ALG1"",""id"":""852407""},{""label"":""ALG5"",""id"":""855874""},{""label"":""ALG6"",""id"":""854163""},{""label"":""ALG8"",""id"":""854233""},{""label"":""ALG9"",""id"":""855502""},{""label"":""RFT1"",""id"":""852261""}]"	"[""852261"",""852407"",""854163"",""854233"",""855502"",""855764"",""855874""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050570""}]"
DOID:0050571	"[""congenital disorder of glycosylation type II""]"	"[{""label"":""ALG2"",""id"":""85365""},{""label"":""ATP6AP2"",""id"":""10159""},{""label"":""COG3"",""id"":""83548""},{""label"":""EDEM3"",""id"":""80267""},{""label"":""GALNT2"",""id"":""2590""},{""label"":""SLC37A4"",""id"":""2542""}]"	"[""10159"",""2542"",""2590"",""80267"",""83548"",""85365""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00351""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050571""}]"
DOID:0050571	"[""congenital disorder of glycosylation type II""]"	"[{""label"":""nac"",""id"":""40981""}]"	"[""40981""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050571""}]"
DOID:0050572	"[""cone-rod dystrophy"",""cone-rod retinal dystrophy""]"	"[{""label"":""CRB1"",""id"":""23418""}]"	"[""23418""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050572""}]"
DOID:0050572	"[""cone-rod dystrophy"",""cone-rod retinal dystrophy""]"	"[{""label"":""eys"",""id"":""557044""}]"	"[""557044""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050572""}]"
DOID:0050573	"[""2-hydroxyglutaric aciduria""]"	"[{""label"":""L2HGDH"",""id"":""79944""}]"	"[""79944""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050573""}]"
DOID:0050574	"[""L-2-hydroxyglutaric aciduria"",""L-2-HYDROXYGLUTARIC ACIDEMIA""]"	"[{""label"":""L2HGDH"",""id"":""79944""}]"	"[""79944""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050574""}]"
DOID:0050576	"[""Senior-Loken syndrome"",""Loken Senior syndrome"",""renal-retinal syndrome""]"	"[{""label"":""TRAF3IP1"",""id"":""26146""}]"	"[""26146""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050576""}]"
DOID:0050577	"[""cranioectodermal dysplasia"",""Levin syndrome"",""Sensenbrenner syndrome""]"	"[{""label"":""SEC12"",""id"":""855760""}]"	"[""855760""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050577""}]"
DOID:0050578	"[""occult macular dystrophy""]"	"[{""label"":""RP1L1"",""id"":""94137""}]"	"[""94137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050578""}]"
DOID:0050579	"[""glycogen storage disease XV"",""Glycogen storage disease 15"",""Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency"",""glycogen storage disease type XV""]"	"[{""label"":""Gyg1"",""id"":""27357""}]"	"[""27357""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050579""}]"
DOID:0050579	"[""glycogen storage disease XV"",""Glycogen storage disease 15"",""Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency"",""glycogen storage disease type XV""]"	"[{""label"":""GYG1"",""id"":""2992""}]"	"[""2992""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050579""}]"
DOID:0050580	"[""hereditary lymphedema""]"	"[{""label"":""ANGPT2"",""id"":""285""},{""label"":""CALCRL"",""id"":""10203""},{""label"":""CELSR1"",""id"":""9620""},{""label"":""PIEZO1"",""id"":""9780""},{""label"":""THSD1"",""id"":""55901""},{""label"":""TIE1"",""id"":""7075""}]"	"[""10203"",""285"",""55901"",""7075"",""9620"",""9780""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050580""}]"
DOID:0050580	"[""hereditary lymphedema""]"	"[{""label"":""Flt4"",""id"":""14257""},{""label"":""Vegfc"",""id"":""22341""}]"	"[""14257"",""22341""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050580""}]"
DOID:0050581	"[""brachydactyly""]"	"[{""label"":""HOXD13"",""id"":""3239""},{""label"":""SLC26A2"",""id"":""1836""}]"	"[""1836"",""3239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050581""}]"
DOID:0050585	"[""congenital generalized lipodystrophy""]"	"[{""label"":""PCYT1A"",""id"":""5130""}]"	"[""5130""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050585""}]"
DOID:0050587	"[""trichotillomania""]"	"[{""label"":""SLITRK1"",""id"":""114798""}]"	"[""114798""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050587""}]"
DOID:0050588	"[""muscular dystrophy-dystroglycanopathy type B1"",""CMD due to dystroglycanopathy"",""Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1""]"	"[{""label"":""fkrp"",""id"":""571426""}]"	"[""571426""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050588""}]"
DOID:0050588	"[""muscular dystrophy-dystroglycanopathy type B1"",""CMD due to dystroglycanopathy"",""Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1""]"	"[{""label"":""POMT1"",""id"":""10585""}]"	"[""10585""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050588""}]"
DOID:0050588	"[""muscular dystrophy-dystroglycanopathy type B1"",""CMD due to dystroglycanopathy"",""Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1""]"	"[{""label"":""B4gat1"",""id"":""108902""},{""label"":""Fkrp"",""id"":""243853""},{""label"":""Fktn"",""id"":""246179""},{""label"":""Large1"",""id"":""16795""},{""label"":""Pomgnt1"",""id"":""68273""},{""label"":""Pomt1"",""id"":""99011""}]"	"[""108902"",""16795"",""243853"",""246179"",""68273"",""99011""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050588""}]"
DOID:0050589	"[""inflammatory bowel disease""]"	"[{""label"":""Esr2"",""id"":""25149""}]"	"[""25149""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050589""}]"
DOID:0050589	"[""inflammatory bowel disease""]"	"[{""label"":""ADAM17"",""id"":""6868""},{""label"":""AGT"",""id"":""183""},{""label"":""ALPI"",""id"":""248""},{""label"":""ANO6"",""id"":""196527""},{""label"":""B2M"",""id"":""567""},{""label"":""EGFR"",""id"":""1956""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IGFBP3"",""id"":""3486""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""NPSR1"",""id"":""387129""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""TGFB1"",""id"":""7040""}]"	"[""183"",""1956"",""196527"",""248"",""3383"",""3486"",""3557"",""3586"",""387129"",""567"",""6556"",""6868"",""7040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050589""}]"
DOID:0050589	"[""inflammatory bowel disease""]"	"[{""label"":""cora"",""id"":""37205""}]"	"[""37205""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050589""}]"
DOID:0050589	"[""inflammatory bowel disease""]"	"[{""label"":""Cd40lg"",""id"":""21947""},{""label"":""Il10"",""id"":""16153""},{""label"":""Il2"",""id"":""16183""},{""label"":""Il2ra"",""id"":""16184""},{""label"":""St6galnac1"",""id"":""20445""},{""label"":""Stat3"",""id"":""20848""},{""label"":""Tnf"",""id"":""21926""}]"	"[""16153"",""16183"",""16184"",""20445"",""20848"",""21926"",""21947""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050589""}]"
DOID:0050590	"[""severe congenital neutropenia""]"	"[{""label"":""CSF3R"",""id"":""1441""},{""label"":""ELANE"",""id"":""1991""}]"	"[""1441"",""1991""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050590""}]"
DOID:0050591	"[""tooth agenesis"",""familial tooth agenesis"",""hypodontia"",""oligodontia"",""selective tooth agenesis""]"	"[{""label"":""BMP2"",""id"":""650""},{""label"":""BMP4"",""id"":""652""},{""label"":""EDA"",""id"":""1896""},{""label"":""GREM2"",""id"":""64388""},{""label"":""LRP6"",""id"":""4040""},{""label"":""TSPEAR"",""id"":""54084""},{""label"":""WNT10A"",""id"":""80326""},{""label"":""WNT10B"",""id"":""7480""}]"	"[""1896"",""4040"",""54084"",""64388"",""650"",""652"",""7480"",""80326""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050591""}]"
DOID:0050592	"[""asphyxiating thoracic dystrophy"",""Jeune syndrome"",""short-rib thoracic dysplasia with or without polydactyly"",""thoracic pelvic phalangeal dystrophy""]"	"[{""label"":""DYNC2H1"",""id"":""79659""},{""label"":""INTU"",""id"":""27152""},{""label"":""NEK1"",""id"":""4750""}]"	"[""27152"",""4750"",""79659""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050592""}]"
DOID:0050598	"[""extrapulmonary tuberculosis""]"	"[{""label"":""CD209"",""id"":""30835""},{""label"":""CLEC4M"",""id"":""10332""},{""label"":""EREG"",""id"":""2069""}]"	"[""10332"",""2069"",""30835""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050598""}]"
DOID:0050600	"[""ABCD syndrome"",""ABCDS"",""albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness""]"	"[{""label"":""EDNRB"",""id"":""1910""}]"	"[""1910""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050600""}]"
DOID:0050602	"[""triple-A syndrome"",""AAAS"",""Achalasia-Addisonianism-Alacrimia syndrome"",""Allgrove Syndrome""]"	"[{""label"":""AAAS"",""id"":""8086""}]"	"[""8086""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050602""}]"
DOID:0050604	"[""acrocapitofemoral dysplasia""]"	"[{""label"":""IHH"",""id"":""3549""}]"	"[""3549""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050604""}]"
DOID:0050605	"[""acrodermatitis enteropathica""]"	"[{""label"":""SLC39A4"",""id"":""55630""}]"	"[""55630""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050605""}]"
DOID:0050605	"[""acrodermatitis enteropathica""]"	"[{""label"":""Slc39a4"",""id"":""72027""}]"	"[""72027""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050605""}]"
DOID:0050606	"[""acrokeratosis verruciformis"",""Acrokeratosis verruciformis of Hopf"",""Hopf disease""]"	"[{""label"":""ATP2A2"",""id"":""488""}]"	"[""488""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050606""}]"
DOID:0050625	"[""biliary tract benign neoplasm"",""extrahepatic bile duct neoplasm"",""neoplasm of extrahepatic bile ducts"",""tumor of the extrahepatic bile duct""]"	"[{""label"":""ALB"",""id"":""213""},{""label"":""IL4"",""id"":""3565""},{""label"":""MTAP"",""id"":""4507""},{""label"":""MUC1"",""id"":""4582""}]"	"[""213"",""3565"",""4507"",""4582""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050625""}]"
DOID:0050628	"[""advanced sleep phase syndrome"",""familial advanced sleep-phase syndrome""]"	"[{""label"":""HRR25"",""id"":""855897""}]"	"[""855897""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050628""}]"
DOID:0050628	"[""advanced sleep phase syndrome"",""familial advanced sleep-phase syndrome""]"	"[{""label"":""PER2"",""id"":""8864""},{""label"":""PER3"",""id"":""8863""},{""label"":""TIMELESS"",""id"":""8914""}]"	"[""8863"",""8864"",""8914""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050628""}]"
DOID:0050629	"[""Aicardi-Goutieres syndrome"",""AGS"",""Cree encephalitis""]"	"[{""label"":""ADAR"",""id"":""103""},{""label"":""SAMHD1"",""id"":""25939""}]"	"[""103"",""25939""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050629""}]"
DOID:0050629	"[""Aicardi-Goutieres syndrome"",""AGS"",""Cree encephalitis""]"	"[{""label"":""Adar"",""id"":""56417""}]"	"[""56417""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050629""}]"
DOID:0050630	"[""Aland Island eye disease"",""FORSIUS-ERIKSSON TYPE OCULAR ALBINISM"",""Forsius-Eriksson syndrome""]"	"[{""label"":""CACNA1F"",""id"":""778""}]"	"[""778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050630""}]"
DOID:0050632	"[""oculocutaneous albinism""]"	"[{""label"":""Oca2"",""id"":""18431""},{""label"":""Slc45a2"",""id"":""22293""},{""label"":""Tyr"",""id"":""22173""}]"	"[""18431"",""22173"",""22293""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050632""}]"
DOID:0050632	"[""oculocutaneous albinism""]"	"[{""label"":""DCT"",""id"":""1638""},{""label"":""TYR"",""id"":""7299""},{""label"":""TYRP1"",""id"":""7306""}]"	"[""1638"",""7299"",""7306""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050632""}]"
DOID:0050633	"[""ocular albinism 1"",""Albinism ocular 1"",""ocular albinism""]"	"[{""label"":""Gpr143"",""id"":""18241""}]"	"[""18241""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050633""}]"
DOID:0050633	"[""ocular albinism 1"",""Albinism ocular 1"",""ocular albinism""]"	"[{""label"":""GPR143"",""id"":""4935""},{""label"":""TYR"",""id"":""7299""}]"	"[""4935"",""7299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050633""}]"
DOID:0050635	"[""alternating hemiplegia of childhood"",""AHC""]"	"[{""label"":""ATP1A2"",""id"":""477""}]"	"[""477""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050635""}]"
DOID:0050635	"[""alternating hemiplegia of childhood"",""AHC""]"	"[{""label"":""Atp1a3"",""id"":""232975""}]"	"[""232975""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050635""}]"
DOID:0050636	"[""familial visceral amyloidosis"",""AMYLOIDOSIS, FAMILIAL RENAL"",""German type amyloidosis"",""OSTERTAG TYPE AMYLOIDOSIS"",""systemic nonneuropathic amyloidosis""]"	"[{""label"":""FGA"",""id"":""2243""}]"	"[""2243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050636""}]"
DOID:0050637	"[""Finnish type amyloidosis"",""AGel amyloidosis"",""AMYLOIDOSIS, MERETOJA TYPE"",""Lattice corneal dystrophy type II"",""gelsolin amyloidosis""]"	"[{""label"":""GSN"",""id"":""2934""}]"	"[""2934""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050637""}]"
DOID:0050638	"[""transthyretin amyloidosis"",""ATTR amyloidosis"",""ATTRm amyloidosis"",""Amyloidosis, hereditary, transthyretin-related"",""Corino de Andrade's disease"",""Familial transthyretin amyloidosis"",""TTR amyloidosis"",""familial amyloid polyneuropathy"",""paramyloidosis"",""transthyretin-related hereditary amyloidosis""]"	"[{""label"":""Ttr"",""id"":""22139""}]"	"[""22139""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050638""}]"
DOID:0050638	"[""transthyretin amyloidosis"",""ATTR amyloidosis"",""ATTRm amyloidosis"",""Amyloidosis, hereditary, transthyretin-related"",""Corino de Andrade's disease"",""Familial transthyretin amyloidosis"",""TTR amyloidosis"",""familial amyloid polyneuropathy"",""paramyloidosis"",""transthyretin-related hereditary amyloidosis""]"	"[{""label"":""TTR"",""id"":""7276""}]"	"[""7276""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050638""}]"
DOID:0050641	"[""Rh deficiency syndrome""]"	"[{""label"":""RHAG"",""id"":""6005""}]"	"[""6005""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050641""}]"
DOID:0050642	"[""hypochromic microcytic anemia""]"	"[{""label"":""TNF"",""id"":""7124""}]"	"[""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050642""}]"
DOID:0050644	"[""arterial calcification of infancy"",""generalized arterial calcification of infancy"",""idiopathic infantile arterial calcification"",""infantile arteriosclerosis""]"	"[{""label"":""ABCC6"",""id"":""368""},{""label"":""ENPP1"",""id"":""5167""}]"	"[""368"",""5167""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050644""}]"
DOID:0050644	"[""arterial calcification of infancy"",""generalized arterial calcification of infancy"",""idiopathic infantile arterial calcification"",""infantile arteriosclerosis""]"	"[{""label"":""Enpp1"",""id"":""18605""}]"	"[""18605""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050644""}]"
DOID:0050645	"[""arterial tortuosity syndrome""]"	"[{""label"":""EFEMP2"",""id"":""30008""},{""label"":""SLC2A10"",""id"":""81031""}]"	"[""30008"",""81031""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050645""}]"
DOID:0050646	"[""distal arthrogryposis"",""Arthrogryposis Multiplex Congenita""]"	"[{""label"":""ADAMTS15"",""id"":""170689""},{""label"":""MET"",""id"":""4233""}]"	"[""170689"",""4233""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050646""}]"
DOID:0050646	"[""distal arthrogryposis"",""Arthrogryposis Multiplex Congenita""]"	"[{""label"":""Ecel1"",""id"":""13599""},{""label"":""Fbn2"",""id"":""14119""}]"	"[""13599"",""14119""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050646""}]"
DOID:0050647	"[""Arts syndrome"",""ARTS"",""Lethal ataxia with deafness and optic atrophy"",""MRXS18"",""MRXSARTS"",""fatal X-linked ataxia with deafness and loss of vision"",""syndromic X-linked mental retardation 18"",""syndromic X-linked mental retardation Arts type""]"	"[{""label"":""PITX2"",""id"":""5308""},{""label"":""PRPS1"",""id"":""5631""}]"	"[""5308"",""5631""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050647""}]"
DOID:0050648	"[""atelosteogenesis""]"	"[{""label"":""FLNB"",""id"":""2317""},{""label"":""SLC26A2"",""id"":""1836""}]"	"[""1836"",""2317""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00397""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050648""}]"
DOID:0050649	"[""atransferrinemia"",""familial hypotransferrinemia""]"	"[{""label"":""Trf"",""id"":""22041""}]"	"[""22041""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050649""}]"
DOID:0050649	"[""atransferrinemia"",""familial hypotransferrinemia""]"	"[{""label"":""TF"",""id"":""7018""}]"	"[""7018""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050649""}]"
DOID:0050650	"[""familial atrial fibrillation"",""ATFB""]"	"[{""label"":""ABCC9"",""id"":""10060""},{""label"":""KCNE2"",""id"":""9992""},{""label"":""KCNQ1"",""id"":""3784""},{""label"":""NPPA"",""id"":""4878""},{""label"":""NUP155"",""id"":""9631""},{""label"":""SCN1B"",""id"":""6324""},{""label"":""SCN2B"",""id"":""6327""},{""label"":""SCN5A"",""id"":""6331""},{""label"":""ZFHX3"",""id"":""463""}]"	"[""10060"",""3784"",""463"",""4878"",""6324"",""6327"",""6331"",""9631"",""9992""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050650""}]"
DOID:0050651	"[""atrioventricular septal defect"",""AVCD"",""AVSD"",""ECD"",""atrioventricular canal defect"",""endocardial cushion defect""]"	"[{""label"":""CRELD1"",""id"":""78987""},{""label"":""GATA4"",""id"":""2626""}]"	"[""2626"",""78987""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050651""}]"
DOID:0050651	"[""atrioventricular septal defect"",""AVCD"",""AVSD"",""ECD"",""atrioventricular canal defect"",""endocardial cushion defect""]"	"[{""label"":""Bmp4"",""id"":""12159""},{""label"":""Dnah11"",""id"":""13411""},{""label"":""Glyr1"",""id"":""74022""}]"	"[""12159"",""13411"",""74022""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050651""}]"
DOID:0050654	"[""Baller-Gerold syndrome""]"	"[{""label"":""RECQL4"",""id"":""9401""}]"	"[""9401""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050654""}]"
DOID:0050656	"[""pseudo-TORCH syndrome 1"",""BLC-PMG"",""BLCPMG"",""Baraitser-Brett-Piesowicz syndrome"",""Baraitser-Reardon syndrome"",""PTORCH1"",""band-like calcification with simplified gyration and polymicrogyria"",""bilateral band-like calcification with polymicrogyria"",""microcephaly-intracranial calcification-intellectual disability syndrome""]"	"[{""label"":""OCLN"",""id"":""100506658""}]"	"[""100506658""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050656""}]"
DOID:0050657	"[""Bannayan-Riley-Ruvalcaba syndrome"",""Bannayan-Zonana syndrome"",""Cowden syndrome 1"",""Riley-Smith syndrome"",""Ruvalcaba-Myhre-Smith syndrome""]"	"[{""label"":""PTEN"",""id"":""5728""}]"	"[""5728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050657""}]"
DOID:0050659	"[""biotin-responsive basal ganglia disease""]"	"[{""label"":""Slc19a3"",""id"":""80721""}]"	"[""80721""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050659""}]"
DOID:0050659	"[""biotin-responsive basal ganglia disease""]"	"[{""label"":""folt-3"",""id"":""4363081""}]"	"[""4363081""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050659""}]"
DOID:0050659	"[""biotin-responsive basal ganglia disease""]"	"[{""label"":""SLC19A3"",""id"":""80704""}]"	"[""80704""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050659""}]"
DOID:0050660	"[""Beare-Stevenson cutis gyrata syndrome""]"	"[{""label"":""FGFR2"",""id"":""2263""}]"	"[""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050660""}]"
DOID:0050660	"[""Beare-Stevenson cutis gyrata syndrome""]"	"[{""label"":""Fgfr2"",""id"":""14183""}]"	"[""14183""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050660""}]"
DOID:0050661	"[""vitelliform macular dystrophy"",""Best disease"",""Best macular dystrophy"",""juvenile-onset vitelliform macular dystrophy""]"	"[{""label"":""Impg2"",""id"":""224224""}]"	"[""224224""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050661""}]"
DOID:0050661	"[""vitelliform macular dystrophy"",""Best disease"",""Best macular dystrophy"",""juvenile-onset vitelliform macular dystrophy""]"	"[{""label"":""IMPG1"",""id"":""3617""},{""label"":""IMPG2"",""id"":""50939""},{""label"":""PRPH2"",""id"":""5961""}]"	"[""3617"",""50939"",""5961""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050661""}]"
DOID:0050663	"[""Bethlem myopathy"",""benign congenital muscular dystrophy""]"	"[{""label"":""Col6a1"",""id"":""12833""}]"	"[""12833""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050663""}]"
DOID:0050663	"[""Bethlem myopathy"",""benign congenital muscular dystrophy""]"	"[{""label"":""COL12A1"",""id"":""1303""},{""label"":""COL6A1"",""id"":""1291""},{""label"":""COL6A2"",""id"":""1292""},{""label"":""COL6A3"",""id"":""1293""}]"	"[""1291"",""1292"",""1293"",""1303""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050663""}]"
DOID:0050667	"[""alcohol-related neurodevelopmental disorder"",""ARND"",""static encephalopathy""]"	"[{""label"":""mth"",""id"":""38058""}]"	"[""38058""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050667""}]"
DOID:0050671	"[""female breast cancer""]"	"[{""label"":""ATM"",""id"":""472""},{""label"":""CHEK2"",""id"":""11200""},{""label"":""CTCF"",""id"":""10664""},{""label"":""FANCI"",""id"":""55215""},{""label"":""MAST1"",""id"":""22983""},{""label"":""PALB2"",""id"":""79728""},{""label"":""POLH"",""id"":""5429""}]"	"[""10664"",""11200"",""22983"",""472"",""5429"",""55215"",""79728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050671""}]"
DOID:0050675	"[""Birk-Barel syndrome"",""Birk-Barel mental retardation dysmorphism syndrome""]"	"[{""label"":""KCNK9"",""id"":""51305""}]"	"[""51305""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050675""}]"
DOID:0050676	"[""Birt-Hogg-Dube syndrome""]"	"[{""label"":""FLCN"",""id"":""201163""},{""label"":""PRDM10"",""id"":""56980""}]"	"[""201163"",""56980""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050676""}]"
DOID:0050678	"[""Blau syndrome"",""ARTHROCUTANEOUVEAL GRANULOMATOSIS"",""BLAUS"",""Jabs syndrome""]"	"[{""label"":""NOD2"",""id"":""64127""}]"	"[""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050678""}]"
DOID:0050679	"[""blue cone monochromacy""]"	"[{""label"":""Opn1mw"",""id"":""14539""}]"	"[""14539""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050679""}]"
DOID:0050679	"[""blue cone monochromacy""]"	"[{""label"":""OPN1LW"",""id"":""5956""},{""label"":""OPN1MW"",""id"":""2652""}]"	"[""2652"",""5956""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050679""}]"
DOID:0050680	"[""Boomerang dysplasia""]"	"[{""label"":""FLNB"",""id"":""2317""}]"	"[""2317""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050680""}]"
DOID:0050681	"[""Borjeson-Forssman-Lehmann syndrome"",""BFLS"",""BORJ"",""Borjeson syndrome"",""MRXSBFL"",""intellectual deficiency-epilepsy-endocrine disorders syndrome"",""mental retardation, epilepsy, and endocrine disorder"",""syndromic X-linked mental retardation Borjeson-Forssman-Lehmann type""]"	"[{""label"":""PHF6"",""id"":""84295""}]"	"[""84295""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050681""}]"
DOID:0050683	"[""Bothnia retinal dystrophy"",""Vasterbotten dystrophy""]"	"[{""label"":""RLBP1"",""id"":""6017""}]"	"[""6017""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050683""}]"
DOID:0050685	"[""small cell carcinoma"",""Small cell carcinoma - intermediate cell"",""Small cell carcinoma, intermediate cell"",""intermediate cell small cell carcinoma""]"	"[{""label"":""RB1"",""id"":""5925""},{""label"":""TERT"",""id"":""7015""}]"	"[""5925"",""7015""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050685""}]"
DOID:0050686	"[""organ system cancer""]"	"[{""label"":""IL1R2"",""id"":""7850""}]"	"[""7850""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050686""}]"
DOID:0050689	"[""brachydactyly-syndactyly syndrome""]"	"[{""label"":""HOXD13"",""id"":""3239""}]"	"[""3239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050689""}]"
DOID:0050691	"[""branchiooculofacial syndrome""]"	"[{""label"":""TFAP2A"",""id"":""7020""}]"	"[""7020""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050691""}]"
DOID:0050696	"[""fetal alcohol spectrum disorder""]"	"[{""label"":""PER2"",""id"":""8864""},{""label"":""POMC"",""id"":""5443""}]"	"[""5443"",""8864""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050696""}]"
DOID:0050696	"[""fetal alcohol spectrum disorder""]"	"[{""label"":""Drd2"",""id"":""24318""},{""label"":""Grin2b"",""id"":""24410""}]"	"[""24318"",""24410""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050696""}]"
DOID:0050697	"[""chorioamnionitis""]"	"[{""label"":""LTA"",""id"":""4049""},{""label"":""MBL2"",""id"":""4153""},{""label"":""TNF"",""id"":""7124""}]"	"[""4049"",""4153"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050697""}]"
DOID:0050699	"[""Dent disease"",""Dent's disease"",""X-linked hypercalciuric nephrocalcinosis""]"	"[{""label"":""Clcn5"",""id"":""12728""}]"	"[""12728""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050699""}]"
DOID:0050700	"[""cardiomyopathy"",""Cardiomyopathies""]"	"[{""label"":""Casr"",""id"":""24247""},{""label"":""Itga7"",""id"":""81008""}]"	"[""24247"",""81008""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050700""}]"
DOID:0050700	"[""cardiomyopathy"",""Cardiomyopathies""]"	"[{""label"":""Acsl1"",""id"":""14081""},{""label"":""Cxcr4"",""id"":""12767""},{""label"":""Des"",""id"":""13346""},{""label"":""Ifng"",""id"":""15978""},{""label"":""Lrp1"",""id"":""16971""},{""label"":""Ppargc1a"",""id"":""19017""}]"	"[""12767"",""13346"",""14081"",""15978"",""16971"",""19017""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050700""}]"
DOID:0050700	"[""cardiomyopathy"",""Cardiomyopathies""]"	"[{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""DGAT1"",""id"":""8694""},{""label"":""DTNA"",""id"":""1837""},{""label"":""HFE"",""id"":""3077""},{""label"":""JUP"",""id"":""3728""},{""label"":""KLK1"",""id"":""3816""},{""label"":""MLYCD"",""id"":""23417""},{""label"":""MYH7"",""id"":""4625""},{""label"":""NONO"",""id"":""4841""},{""label"":""NOS3"",""id"":""4846""},{""label"":""POMT1"",""id"":""10585""},{""label"":""SLC22A5"",""id"":""6584""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SRF"",""id"":""6722""},{""label"":""TAB2"",""id"":""23118""},{""label"":""TSHR"",""id"":""7253""}]"	"[""10585"",""1837"",""23118"",""23417"",""3077"",""3728"",""3816"",""4625"",""4841"",""4846"",""6584"",""6648"",""6722"",""7253"",""8694"",""9370""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050700""}]"
DOID:0050700	"[""cardiomyopathy"",""Cardiomyopathies""]"	"[{""label"":""CDase"",""id"":""43618""},{""label"":""Egfr"",""id"":""37455""}]"	"[""37455"",""43618""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050700""}]"
DOID:0050704	"[""childhood electroclinical syndrome""]"	"[{""label"":""Cacna1a"",""id"":""12286""}]"	"[""12286""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050704""}]"
DOID:0050709	"[""early infantile epileptic encephalopathy"",""Early Infantile Epileptic Encephalopathy with Burst-Suppression""]"	"[{""label"":""IDH1"",""id"":""855691""},{""label"":""IDH2"",""id"":""854303""}]"	"[""854303"",""855691""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050709""}]"
DOID:0050709	"[""early infantile epileptic encephalopathy"",""Early Infantile Epileptic Encephalopathy with Burst-Suppression""]"	"[{""label"":""Scn8a"",""id"":""20273""}]"	"[""20273""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050709""}]"
DOID:0050711	"[""aceruloplasminemia""]"	"[{""label"":""CP"",""id"":""1356""}]"	"[""1356""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050711""}]"
DOID:0050711	"[""aceruloplasminemia""]"	"[{""label"":""Cp"",""id"":""12870""}]"	"[""12870""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050711""}]"
DOID:0050715	"[""methylmalonic aciduria and homocystinuria type cblC"",""Cobalamin C deficiency"",""MAHCC""]"	"[{""label"":""PRDX1"",""id"":""5052""}]"	"[""5052""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050715""}]"
DOID:0050717	"[""methylmalonic aciduria and homocystinuria type cblF"",""Cobalamin F deficiency"",""MAHCF""]"	"[{""label"":""LMBRD1"",""id"":""55788""}]"	"[""55788""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050717""}]"
DOID:0050719	"[""cerebral folate receptor alpha deficiency"",""Neurodegeneration due to cerebral folate transport deficiency""]"	"[{""label"":""FOLR1"",""id"":""2348""}]"	"[""2348""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050719""}]"
DOID:0050722	"[""PHGDH deficiency"",""PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY""]"	"[{""label"":""PHGDH"",""id"":""26227""}]"	"[""26227""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050722""}]"
DOID:0050723	"[""PSAT deficiency"",""Phosphoserine aminotransferase deficiency""]"	"[{""label"":""PSAT1"",""id"":""29968""}]"	"[""29968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050723""}]"
DOID:0050724	"[""PSPH deficiency"",""PSPHD"",""Phosphoserine phosphatase deficiency""]"	"[{""label"":""PSPH"",""id"":""5723""}]"	"[""5723""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050724""}]"
DOID:0050730	"[""coenzyme Q10 deficiency disease"",""COENZYME Q10 DEFICIENCY, PRIMARY""]"	"[{""label"":""Coq9"",""id"":""67914""}]"	"[""67914""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050730""}]"
DOID:0050731	"[""vitamin B12 deficiency"",""cobalamin deficiency"",""hypocobalaminemia""]"	"[{""label"":""Cd40lg"",""id"":""84349""}]"	"[""84349""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050731""}]"
DOID:0050731	"[""vitamin B12 deficiency"",""cobalamin deficiency"",""hypocobalaminemia""]"	"[{""label"":""FUT2"",""id"":""2524""}]"	"[""2524""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050731""}]"
DOID:0050733	"[""methylmalonic aciduria and homocystinuria type cblG""]"	"[{""label"":""MTR"",""id"":""4548""}]"	"[""4548""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050733""}]"
DOID:0050734	"[""congenital intrinsic factor deficiency"",""hereditary intrinsic factor deficiency""]"	"[{""label"":""CBLIF"",""id"":""2694""}]"	"[""2694""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050734""}]"
DOID:0050741	"[""alcohol dependence"",""alcoholism""]"	"[{""label"":""Slc29a1"",""id"":""63959""}]"	"[""63959""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050741""}]"
DOID:0050741	"[""alcohol dependence"",""alcoholism""]"	"[{""label"":""Bdnf"",""id"":""24225""},{""label"":""Creb1"",""id"":""81646""},{""label"":""Gabbr1"",""id"":""81657""},{""label"":""Gdnf"",""id"":""25453""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Lep"",""id"":""25608""},{""label"":""Mc4r"",""id"":""25635""}]"	"[""24225"",""25453"",""25608"",""25635"",""29595"",""81646"",""81657""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050741""}]"
DOID:0050741	"[""alcohol dependence"",""alcoholism""]"	"[{""label"":""ADH1B"",""id"":""125""},{""label"":""ADH1C"",""id"":""126""},{""label"":""ADH4"",""id"":""127""},{""label"":""ADRA2A"",""id"":""150""},{""label"":""AGO1"",""id"":""26523""},{""label"":""AGO2"",""id"":""27161""},{""label"":""ALDH2"",""id"":""217""},{""label"":""ANGPT1"",""id"":""284""},{""label"":""AR"",""id"":""367""},{""label"":""BMAL1"",""id"":""406""},{""label"":""BPTF"",""id"":""2186""},{""label"":""CCK"",""id"":""885""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CHRNB3"",""id"":""1142""},{""label"":""COMT"",""id"":""1312""},{""label"":""CPE"",""id"":""1363""},{""label"":""CREB1"",""id"":""1385""},{""label"":""DBI"",""id"":""1622""},{""label"":""DRD2"",""id"":""1813""},{""label"":""FMN1"",""id"":""342184""},{""label"":""GABBR1"",""id"":""2550""},{""label"":""GABRA2"",""id"":""2555""},{""label"":""GABRB3"",""id"":""2562""},{""label"":""GABRG2"",""id"":""2566""},{""label"":""GAD1"",""id"":""2571""},{""label"":""GAD2"",""id"":""2572""},{""label"":""GEMIN4"",""id"":""50628""},{""label"":""GRIN2A"",""id"":""2903""},{""label"":""GRM8"",""id"":""2918""},{""label"":""HTR1A"",""id"":""3350""},{""label"":""HTR1B"",""id"":""3351""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""HTR3A"",""id"":""3359""},{""label"":""KCNB2"",""id"":""9312""},{""label"":""LEP"",""id"":""3952""},{""label"":""NCAM1"",""id"":""4684""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""NRXN3"",""id"":""9369""},{""label"":""NTRK2"",""id"":""4915""},{""label"":""OPRD1"",""id"":""4985""},{""label"":""OPRK1"",""id"":""4986""},{""label"":""OPRM1"",""id"":""4988""},{""label"":""PDE4B"",""id"":""5142""},{""label"":""PER2"",""id"":""8864""},{""label"":""POMC"",""id"":""5443""},{""label"":""SLC6A1"",""id"":""6529""},{""label"":""SLC6A2"",""id"":""6530""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""TAS2R16"",""id"":""50833""}]"	"[""1136"",""1142"",""125"",""126"",""127"",""1312"",""1363"",""1385"",""150"",""1622"",""1813"",""217"",""2186"",""2550"",""2555"",""2562"",""2566"",""2571"",""2572"",""26523"",""27161"",""284"",""2903"",""2908"",""2918"",""3350"",""3351"",""3356"",""3359"",""342184"",""367"",""3952"",""406"",""4684"",""4915"",""4985"",""4986"",""4988"",""50628"",""50833"",""5142"",""5443"",""6529"",""6530"",""6532"",""885"",""8864"",""9312"",""9369""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050741""}]"
DOID:0050741	"[""alcohol dependence"",""alcoholism""]"	"[{""label"":""InR"",""id"":""42549""}]"	"[""42549""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050741""}]"
DOID:0050742	"[""nicotine dependence"",""tobacco use disorder""]"	"[{""label"":""Htr2a"",""id"":""29595""},{""label"":""Htr2c"",""id"":""25187""}]"	"[""25187"",""29595""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050742""}]"
DOID:0050742	"[""nicotine dependence"",""tobacco use disorder""]"	"[{""label"":""ADRA2A"",""id"":""150""},{""label"":""APBB1"",""id"":""322""},{""label"":""APC2"",""id"":""10297""},{""label"":""CCK"",""id"":""885""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CHRNA4"",""id"":""1137""},{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CHRNA6"",""id"":""8973""},{""label"":""CHRNB3"",""id"":""1142""},{""label"":""CHRNB4"",""id"":""1143""},{""label"":""COMT"",""id"":""1312""},{""label"":""CYP2B6"",""id"":""1555""},{""label"":""DRD2"",""id"":""1813""},{""label"":""DRD4"",""id"":""1815""},{""label"":""FIGNL1"",""id"":""63979""},{""label"":""GABBR1"",""id"":""2550""},{""label"":""GABBR2"",""id"":""9568""},{""label"":""GALR1"",""id"":""2587""},{""label"":""GRIN2B"",""id"":""2904""},{""label"":""HTR1B"",""id"":""3351""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""HTR3A"",""id"":""3359""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""LCP1"",""id"":""3936""},{""label"":""NCAM1"",""id"":""4684""},{""label"":""NPY1R"",""id"":""4886""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""NRG1"",""id"":""3084""},{""label"":""NRXN3"",""id"":""9369""},{""label"":""NTRK2"",""id"":""4915""},{""label"":""OPRM1"",""id"":""4988""},{""label"":""POMC"",""id"":""5443""},{""label"":""RAPGEF3"",""id"":""10411""},{""label"":""RPTOR"",""id"":""57521""},{""label"":""SLC6A3"",""id"":""6531""},{""label"":""TPH1"",""id"":""7166""}]"	"[""10297"",""10411"",""1136"",""1137"",""1138"",""1142"",""1143"",""1312"",""150"",""1555"",""1813"",""1815"",""2550"",""2587"",""2904"",""2908"",""3084"",""322"",""3351"",""3356"",""3359"",""3557"",""3936"",""4684"",""4886"",""4915"",""4988"",""5443"",""57521"",""63979"",""6531"",""7166"",""885"",""8973"",""9369"",""9568""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050742""}]"
DOID:0050742	"[""nicotine dependence"",""tobacco use disorder""]"	"[{""label"":""acr-15"",""id"":""191602""},{""label"":""acr-16"",""id"":""179235""},{""label"":""dop-2"",""id"":""179347""}]"	"[""179235"",""179347"",""191602""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050742""}]"
DOID:0050744	"[""anaplastic large cell lymphoma""]"	"[{""label"":""IRF4"",""id"":""3662""}]"	"[""3662""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050744""}]"
DOID:0050745	"[""diffuse large B-cell lymphoma"",""DLBCL""]"	"[{""label"":""CARD11"",""id"":""84433""},{""label"":""CD22"",""id"":""933""},{""label"":""CD40"",""id"":""958""},{""label"":""CD79B"",""id"":""974""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""IL21R"",""id"":""50615""},{""label"":""MYD88"",""id"":""4615""}]"	"[""2212"",""4615"",""50615"",""84433"",""933"",""958"",""974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050745""}]"
DOID:0050745	"[""diffuse large B-cell lymphoma"",""DLBCL""]"	"[{""label"":""Trp53"",""id"":""22059""}]"	"[""22059""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050745""}]"
DOID:0050746	"[""mantle cell lymphoma""]"	"[{""label"":""BTK"",""id"":""695""},{""label"":""CCDC50"",""id"":""152137""},{""label"":""CD79B"",""id"":""974""},{""label"":""TNFRSF10A"",""id"":""8797""}]"	"[""152137"",""695"",""8797"",""974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050746""}]"
DOID:0050748	"[""marginal zone lymphoma"",""marginal zone B-cell lymphoma""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3117"",""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050748""}]"
DOID:0050749	"[""peripheral T-cell lymphoma""]"	"[{""label"":""IRF4"",""id"":""3662""}]"	"[""3662""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050749""}]"
DOID:0050752	"[""amyotrophic lateral sclerosis type 8"",""ALS8"",""amyotrophic lateral sclerosis 8""]"	"[{""label"":""VAPB"",""id"":""9217""}]"	"[""9217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050752""}]"
DOID:0050753	"[""cerebellar ataxia""]"	"[{""label"":""L2HGDH"",""id"":""79944""},{""label"":""RPGRIP1L"",""id"":""23322""},{""label"":""SYNE1"",""id"":""23345""}]"	"[""23322"",""23345"",""79944""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050753""}]"
DOID:0050753	"[""cerebellar ataxia""]"	"[{""label"":""Cacna1a"",""id"":""12286""}]"	"[""12286""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050753""}]"
DOID:0050754	"[""ataxia with oculomotor apraxia type 1""]"	"[{""label"":""APTX"",""id"":""54840""}]"	"[""54840""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050754""}]"
DOID:0050755	"[""spinocerebellar ataxia with axonal neuropathy 2"",""AOA2"",""SCAN2"",""SCAR1"",""ataxia with oculomotor apraxia type 2"",""autosomal recessive spinocerebellar ataxia 1"",""autosomal recessive spinocerebellar ataxia with axonal neuropathy 2"",""spinocerebellar ataxia with axonal neuropathy type 2""]"	"[{""label"":""SETX"",""id"":""23064""}]"	"[""23064""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050755""}]"
DOID:0050766	"[""choreaacanthocytosis"",""Levine-Critchley syndrome"",""choreo-acanthocytosis""]"	"[{""label"":""VPS13A"",""id"":""23230""}]"	"[""23230""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050766""}]"
DOID:0050766	"[""choreaacanthocytosis"",""Levine-Critchley syndrome"",""choreo-acanthocytosis""]"	"[{""label"":""Vps13a"",""id"":""271564""}]"	"[""271564""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050766""}]"
DOID:0050768	"[""mitochondrial complex V (ATP synthase) deficiency nuclear type 1"",""MC5DN1""]"	"[{""label"":""ATPAF2"",""id"":""91647""}]"	"[""91647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050768""}]"
DOID:0050770	"[""polycystic liver disease"",""congenital cystic liver disease"",""congenital hepatic cyst"",""fibrocystic liver disease""]"	"[{""label"":""Prkcsh"",""id"":""19089""},{""label"":""Ucp2"",""id"":""22228""}]"	"[""19089"",""22228""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050770""}]"
DOID:0050770	"[""polycystic liver disease"",""congenital cystic liver disease"",""congenital hepatic cyst"",""fibrocystic liver disease""]"	"[{""label"":""GANAB"",""id"":""23193""}]"	"[""23193""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050770""}]"
DOID:0050771	"[""pheochromocytoma"",""phaeochromocytoma""]"	"[{""label"":""HSD17B10"",""id"":""3028""},{""label"":""RET"",""id"":""5979""},{""label"":""SDHB"",""id"":""6390""}]"	"[""3028"",""5979"",""6390""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050771""}]"
DOID:0050771	"[""pheochromocytoma"",""phaeochromocytoma""]"	"[{""label"":""Ret"",""id"":""19713""}]"	"[""19713""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050771""}]"
DOID:0050771	"[""pheochromocytoma"",""phaeochromocytoma""]"	"[{""label"":""Cdkn1b"",""id"":""83571""}]"	"[""83571""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050771""}]"
DOID:0050773	"[""paraganglioma"",""chemodectoma"",""glomus body tumor""]"	"[{""label"":""DLST"",""id"":""1743""},{""label"":""SDHA"",""id"":""6389""},{""label"":""SDHAF2"",""id"":""54949""},{""label"":""SDHB"",""id"":""6390""},{""label"":""SDHC"",""id"":""6391""},{""label"":""SDHD"",""id"":""6392""},{""label"":""SLC25A11"",""id"":""8402""}]"	"[""1743"",""54949"",""6389"",""6390"",""6391"",""6392"",""8402""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050773""}]"
DOID:0050773	"[""paraganglioma"",""chemodectoma"",""glomus body tumor""]"	"[{""label"":""Cdkn1b"",""id"":""83571""}]"	"[""83571""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050773""}]"
DOID:0050774	"[""rapadilino syndrome""]"	"[{""label"":""RECQL4"",""id"":""9401""}]"	"[""9401""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050774""}]"
DOID:0050775	"[""schneckenbecken dysplasia""]"	"[{""label"":""SLC35D1"",""id"":""23169""}]"	"[""23169""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00399""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050775""}]"
DOID:0050776	"[""non-syndromic X-linked intellectual disability"",""non-specific X-linked mental retardation""]"	"[{""label"":""CSTF2"",""id"":""1478""},{""label"":""ZMYM3"",""id"":""9203""}]"	"[""1478"",""9203""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050776""}]"
DOID:0050776	"[""non-syndromic X-linked intellectual disability"",""non-specific X-linked mental retardation""]"	"[{""label"":""TRM732"",""id"":""855301""}]"	"[""855301""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050776""}]"
DOID:0050776	"[""non-syndromic X-linked intellectual disability"",""non-specific X-linked mental retardation""]"	"[{""label"":""Gdi1"",""id"":""14567""},{""label"":""Iqsec2"",""id"":""245666""}]"	"[""14567"",""245666""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050776""}]"
DOID:0050777	"[""Joubert syndrome"",""JBTS""]"	"[{""label"":""ARL3"",""id"":""403""},{""label"":""IFT74"",""id"":""80173""},{""label"":""INPP5E"",""id"":""56623""}]"	"[""403"",""56623"",""80173""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050777""}]"
DOID:0050778	"[""Meckel syndrome"",""Meckel-Gruber syndrome""]"	"[{""label"":""KIF14"",""id"":""9928""},{""label"":""TMEM231"",""id"":""79583""},{""label"":""TXNDC15"",""id"":""79770""}]"	"[""79583"",""79770"",""9928""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050778""}]"
DOID:0050778	"[""Meckel syndrome"",""Meckel-Gruber syndrome""]"	"[{""label"":""Tmem67"",""id"":""329795""}]"	"[""329795""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050778""}]"
DOID:0050782	"[""Zollinger-Ellison syndrome""]"	"[{""label"":""EGF"",""id"":""1950""}]"	"[""1950""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050782""}]"
DOID:0050784	"[""primary progressive multiple sclerosis"",""PPMS"",""Primary-progressive MS""]"	"[{""label"":""ADAMTS14"",""id"":""140766""},{""label"":""GRN"",""id"":""2896""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL4R"",""id"":""3566""}]"	"[""140766"",""2896"",""3119"",""3123"",""3566""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050784""}]"
DOID:0050787	"[""juvenile polyposis syndrome""]"	"[{""label"":""Bmpr1a"",""id"":""12166""},{""label"":""Smad4"",""id"":""17128""}]"	"[""12166"",""17128""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050787""}]"
DOID:0050787	"[""juvenile polyposis syndrome""]"	"[{""label"":""BMPR1A"",""id"":""657""},{""label"":""SMAD4"",""id"":""4089""}]"	"[""4089"",""657""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050787""}]"
DOID:0050787	"[""juvenile polyposis syndrome""]"	"[{""label"":""dpp"",""id"":""33432""}]"	"[""33432""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050787""}]"
DOID:0050788	"[""proximal symphalangism"",""Cushing's symphalangism""]"	"[{""label"":""NOG"",""id"":""9241""}]"	"[""9241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050788""}]"
DOID:0050789	"[""tarsal-carpal coalition syndrome""]"	"[{""label"":""NOG"",""id"":""9241""}]"	"[""9241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050789""}]"
DOID:0050790	"[""fibular hypoplasia and complex brachydactyly"",""Du Pan syndrome"",""acromesomelic dysplasia-2B""]"	"[{""label"":""GDF5"",""id"":""8200""}]"	"[""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050790""}]"
DOID:0050790	"[""fibular hypoplasia and complex brachydactyly"",""Du Pan syndrome"",""acromesomelic dysplasia-2B""]"	"[{""label"":""Gdf5"",""id"":""14563""}]"	"[""14563""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050790""}]"
DOID:0050791	"[""persistent Mullerian duct syndrome"",""persistent Muellerian duct syndrome""]"	"[{""label"":""Amhr2"",""id"":""110542""}]"	"[""110542""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050791""}]"
DOID:0050791	"[""persistent Mullerian duct syndrome"",""persistent Muellerian duct syndrome""]"	"[{""label"":""AMH"",""id"":""268""},{""label"":""AMHR2"",""id"":""269""}]"	"[""268"",""269""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050791""}]"
DOID:0050792	"[""multiple cutaneous and mucosal venous malformations"",""VMCM"",""cutaneomucosal venous malformation"",""mucocutaneous venous malformations""]"	"[{""label"":""TEK"",""id"":""7010""}]"	"[""7010""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050792""}]"
DOID:0050793	"[""short QT syndrome""]"	"[{""label"":""KCNH2"",""id"":""3757""},{""label"":""KCNQ1"",""id"":""3784""}]"	"[""3757"",""3784""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050793""}]"
DOID:0050793	"[""short QT syndrome""]"	"[{""label"":""Kcnh2"",""id"":""16511""}]"	"[""16511""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050793""}]"
DOID:0050794	"[""multiple synostoses syndrome""]"	"[{""label"":""Fgf9"",""id"":""14180""},{""label"":""Gdf5"",""id"":""14563""}]"	"[""14180"",""14563""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050794""}]"
DOID:0050795	"[""cone dystrophy"",""retinal cone dystrophy""]"	"[{""label"":""Yap1"",""id"":""22601""}]"	"[""22601""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050795""}]"
DOID:0050797	"[""peroxisomal acyl-CoA oxidase deficiency"",""Peroxisomal acyl-coenzyme A oxidase""]"	"[{""label"":""ACOX1"",""id"":""51""}]"	"[""51""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050797""}]"
DOID:0050800	"[""cerebral creatine deficiency syndrome 1"",""CEREBRAL CREATINE DEFICIENCY SYNDROME 1"",""SLC6A8 deficiency"",""creatine transporter deficiency""]"	"[{""label"":""Slc6a8"",""id"":""102857""}]"	"[""102857""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050800""}]"
DOID:0050800	"[""cerebral creatine deficiency syndrome 1"",""CEREBRAL CREATINE DEFICIENCY SYNDROME 1"",""SLC6A8 deficiency"",""creatine transporter deficiency""]"	"[{""label"":""SLC6A8"",""id"":""6535""}]"	"[""6535""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050800""}]"
DOID:0050802	"[""Ehlers-Danlos syndrome spondylodysplastic type 2"",""EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2"",""Ehlers-Danlos syndrome progeroid type""]"	"[{""label"":""B3GALT6"",""id"":""126792""}]"	"[""126792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050802""}]"
DOID:0050807	"[""Kahrizi syndrome"",""KHRZ"",""intellectual disability, Kahrizi type"",""intellectual disability-cataract-coloboma-kyphosis syndrome""]"	"[{""label"":""SRD5A3"",""id"":""79644""}]"	"[""79644""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050807""}]"
DOID:0050809	"[""mucopolysaccharidosis IX""]"	"[{""label"":""Hyal1"",""id"":""15586""}]"	"[""15586""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050809""}]"
DOID:0050809	"[""mucopolysaccharidosis IX""]"	"[{""label"":""HYAL1"",""id"":""3373""}]"	"[""3373""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050809""}]"
DOID:0050811	"[""congenital adrenal hyperplasia"",""adrenal hyperplasia 1"",""congenital lipoid adrenal hyperplasia"",""lipoid CAH""]"	"[{""label"":""CYP11A1"",""id"":""1583""},{""label"":""CYP11B1"",""id"":""1584""},{""label"":""CYP17A1"",""id"":""1586""},{""label"":""CYP21A2"",""id"":""1589""},{""label"":""POR"",""id"":""5447""}]"	"[""1583"",""1584"",""1586"",""1589"",""5447""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050811""}]"
DOID:0050812	"[""spondyloepimetaphyseal dysplasia, Pakistani type"",""spondyloepimetaphyseal dysplasia Pakistani type""]"	"[{""label"":""PAPSS2"",""id"":""9060""}]"	"[""9060""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00393""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050812""}]"
DOID:0050813	"[""spondyloepiphyseal dysplasia with congenital joint dislocations"",""CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS"",""CHST3-Related Skeletal Dysplasia"",""Humero-spinal dysostosis with congenital heart disease"",""Kozlowski Celermajer Tink syndrome"",""Omani Type"",""Spondyloepiphyseal Dysplasia"",""humero-spinal dysostosis"",""humerospinal dysostosis""]"	"[{""label"":""CHST3"",""id"":""9469""}]"	"[""9469""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00633""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050813""}]"
DOID:0050814	"[""temtamy preaxial brachydactyly syndrome"",""PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE""]"	"[{""label"":""CHSY1"",""id"":""22856""}]"	"[""22856""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00632""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050814""}]"
DOID:0050816	"[""urofacial syndrome"",""Ochoa syndrome"",""hydronephrosis with peculiar facial expression""]"	"[{""label"":""Hpse2"",""id"":""545291""}]"	"[""545291""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050816""}]"
DOID:0050816	"[""urofacial syndrome"",""Ochoa syndrome"",""hydronephrosis with peculiar facial expression""]"	"[{""label"":""HPSE2"",""id"":""60495""},{""label"":""LRIG2"",""id"":""9860""}]"	"[""60495"",""9860""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050816""}]"
DOID:0050817	"[""Stargardt disease"",""STARGARDT DISEASE 1""]"	"[{""label"":""Abca4"",""id"":""11304""},{""label"":""Elovl4"",""id"":""83603""}]"	"[""11304"",""83603""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050817""}]"
DOID:0050820	"[""atrioventricular block"",""AV block""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050820""}]"
DOID:0050824	"[""sinoatrial node disease"",""SA node"",""sinuatrial node""]"	"[{""label"":""Ank2"",""id"":""109676""}]"	"[""109676""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050824""}]"
DOID:0050827	"[""rheumatic heart disease"",""rheumatic carditis""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3117"",""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050827""}]"
DOID:0050830	"[""peripheral artery disease""]"	"[{""label"":""P2RY12"",""id"":""64805""}]"	"[""64805""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050830""}]"
DOID:0050831	"[""familial encephalopathy with neuroserpin inclusion bodies"",""FENIB""]"	"[{""label"":""SERPINB7"",""id"":""8710""},{""label"":""SERPINI1"",""id"":""5274""}]"	"[""5274"",""8710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050831""}]"
DOID:0050831	"[""familial encephalopathy with neuroserpin inclusion bodies"",""FENIB""]"	"[{""label"":""Serpini1"",""id"":""20713""}]"	"[""20713""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050831""}]"
DOID:0050833	"[""orotic aciduria""]"	"[{""label"":""UMPS"",""id"":""7372""}]"	"[""7372""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050833""}]"
DOID:0050833	"[""orotic aciduria""]"	"[{""label"":""umps-1"",""id"":""176453""}]"	"[""176453""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050833""}]"
DOID:0050834	"[""CHARGE syndrome"",""CHARGE association""]"	"[{""label"":""kis"",""id"":""33185""}]"	"[""33185""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050834""}]"
DOID:0050834	"[""CHARGE syndrome"",""CHARGE association""]"	"[{""label"":""Trp53"",""id"":""22059""}]"	"[""22059""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050834""}]"
DOID:0050834	"[""CHARGE syndrome"",""CHARGE association""]"	"[{""label"":""CHD7"",""id"":""55636""}]"	"[""55636""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050834""}]"
DOID:0050835	"[""generalized dystonia"",""familial dystonia"",""fragments of torsion dystonia""]"	"[{""label"":""Cacna1a"",""id"":""12286""}]"	"[""12286""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050835""}]"
DOID:0050836	"[""focal dystonia""]"	"[{""label"":""Tor1a"",""id"":""30931""}]"	"[""30931""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050836""}]"
DOID:0050840	"[""cervical dystonia"",""spasmodic torticollis""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050840""}]"
DOID:0050848	"[""obstructive sleep apnea"",""obstructive sleep apnea syndrome""]"	"[{""label"":""Adora1"",""id"":""29290""}]"	"[""29290""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050848""}]"
DOID:0050848	"[""obstructive sleep apnea"",""obstructive sleep apnea syndrome""]"	"[{""label"":""Bmp7"",""id"":""12162""}]"	"[""12162""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050848""}]"
DOID:0050848	"[""obstructive sleep apnea"",""obstructive sleep apnea syndrome""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ADRB1"",""id"":""153""},{""label"":""BDNF"",""id"":""627""},{""label"":""EDN1"",""id"":""1906""},{""label"":""EDNRA"",""id"":""1909""},{""label"":""LEPR"",""id"":""3953""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NRG1"",""id"":""3084""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""TNF"",""id"":""7124""}]"	"[""153"",""1636"",""1906"",""1909"",""3084"",""3953"",""4318"",""4846"",""627"",""6532"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050848""}]"
DOID:0050851	"[""glomerulosclerosis""]"	"[{""label"":""HBEGF"",""id"":""1839""},{""label"":""PLA2G7"",""id"":""7941""}]"	"[""1839"",""7941""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050851""}]"
DOID:0050851	"[""glomerulosclerosis""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Agtr2"",""id"":""24182""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Pparg"",""id"":""25664""},{""label"":""Serpine1"",""id"":""24617""}]"	"[""24182"",""24310"",""24617"",""25664"",""81687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050851""}]"
DOID:0050852	"[""limb ischemia""]"	"[{""label"":""Cs"",""id"":""170587""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Vegfa"",""id"":""83785""}]"	"[""170587"",""24600"",""83785""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050852""}]"
DOID:0050852	"[""limb ischemia""]"	"[{""label"":""CSF3"",""id"":""1440""},{""label"":""DLL4"",""id"":""54567""},{""label"":""EPO"",""id"":""2056""},{""label"":""HGF"",""id"":""3082""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PTGIS"",""id"":""5740""}]"	"[""1440"",""2056"",""3082"",""4846"",""54567"",""5740""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050852""}]"
DOID:0050854	"[""Muckle-Wells syndrome"",""MWS"",""neutrophilic urticaria""]"	"[{""label"":""IL1RN"",""id"":""3557""}]"	"[""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050854""}]"
DOID:0050855	"[""renal fibrosis""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Clu"",""id"":""24854""},{""label"":""Ifng"",""id"":""25712""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Tlr4"",""id"":""29260""}]"	"[""24310"",""24536"",""24617"",""24854"",""25712"",""29260""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050855""}]"
DOID:0050855	"[""renal fibrosis""]"	"[{""label"":""CYP2J2"",""id"":""1573""},{""label"":""FCAR"",""id"":""2204""},{""label"":""GFER"",""id"":""2671""},{""label"":""MMP1"",""id"":""4312""}]"	"[""1573"",""2204"",""2671"",""4312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050855""}]"
DOID:0050856	"[""oppositional defiant disorder""]"	"[{""label"":""AR"",""id"":""367""}]"	"[""367""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050856""}]"
DOID:0050857	"[""Perrault syndrome""]"	"[{""label"":""HSD17B4"",""id"":""3295""},{""label"":""LARS2"",""id"":""23395""}]"	"[""23395"",""3295""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050857""}]"
DOID:0050858	"[""Marshall-Smith syndrome""]"	"[{""label"":""NFIX"",""id"":""4784""}]"	"[""4784""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050858""}]"
DOID:0050860	"[""colorectal adenoma""]"	"[{""label"":""CYP24A1"",""id"":""1591""},{""label"":""PTGIS"",""id"":""5740""}]"	"[""1591"",""5740""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050860""}]"
DOID:0050861	"[""colorectal adenocarcinoma""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""CD44"",""id"":""960""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""CYP4F8"",""id"":""11283""},{""label"":""DOK3"",""id"":""79930""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FAM151A"",""id"":""338094""},{""label"":""FGFR2"",""id"":""2263""},{""label"":""FLT3"",""id"":""2322""},{""label"":""IL16"",""id"":""3603""},{""label"":""KCNH1"",""id"":""3756""},{""label"":""KDR"",""id"":""3791""},{""label"":""KMT2B"",""id"":""9757""},{""label"":""NOD2"",""id"":""64127""},{""label"":""PCSK4"",""id"":""54760""},{""label"":""RNASET2"",""id"":""8635""},{""label"":""STAT5B"",""id"":""6777""},{""label"":""TPST1"",""id"":""8460""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""11283"",""1591"",""2146"",""2263"",""2322"",""338094"",""3603"",""3756"",""3791"",""5243"",""54760"",""64127"",""6777"",""7515"",""79930"",""8460"",""8635"",""960"",""9757""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050861""}]"
DOID:0050864	"[""non-arteritic anterior ischemic optic neuropathy"",""non-arteritic anterior ischaemic optic neuropathy"",""nonarteritic anterior ischaemic optic neuropathy"",""nonarteritic anterior ischemic optic neuropathy""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""F5"",""id"":""2153""},{""label"":""GP1BA"",""id"":""2811""},{""label"":""ITGB3"",""id"":""3690""}]"	"[""1636"",""2153"",""2811"",""3690""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050864""}]"
DOID:0050866	"[""oral squamous cell carcinoma"",""mouth squamous cell carcinoma""]"	"[{""label"":""ABL1"",""id"":""25""},{""label"":""BRINP2"",""id"":""57795""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""DAXX"",""id"":""1616""},{""label"":""DDR2"",""id"":""4921""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FAT1"",""id"":""2195""},{""label"":""FGFR3"",""id"":""2261""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""GSK3B"",""id"":""2932""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL2"",""id"":""3558""},{""label"":""TERT"",""id"":""7015""},{""label"":""TP53"",""id"":""7157""},{""label"":""WNT11"",""id"":""7481""}]"	"[""1543"",""1571"",""1591"",""1616"",""2146"",""2195"",""2261"",""2264"",""25"",""2932"",""3558"",""3586"",""4921"",""57795"",""6347"",""7015"",""7157"",""729230"",""7481"",""81037""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050866""}]"
DOID:0050868	"[""hepatocellular adenoma""]"	"[{""label"":""Ptpn11"",""id"":""19247""}]"	"[""19247""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050868""}]"
DOID:0050868	"[""hepatocellular adenoma""]"	"[{""label"":""HNF1A"",""id"":""6927""}]"	"[""6927""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050868""}]"
DOID:0050869	"[""villous adenoma""]"	"[{""label"":""RNF43"",""id"":""54894""}]"	"[""54894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050869""}]"
DOID:0050871	"[""fibroma""]"	"[{""label"":""ANTXR2"",""id"":""118429""}]"	"[""118429""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050871""}]"
DOID:0050873	"[""follicular lymphoma""]"	"[{""label"":""CD40"",""id"":""958""},{""label"":""CD40LG"",""id"":""959""},{""label"":""CD79B"",""id"":""974""},{""label"":""KDSR"",""id"":""2531""}]"	"[""2531"",""958"",""959"",""974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050873""}]"
DOID:0050873	"[""follicular lymphoma""]"	"[{""label"":""BIG1"",""id"":""856501""}]"	"[""856501""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050873""}]"
DOID:0050873	"[""follicular lymphoma""]"	"[{""label"":""Rarres1"",""id"":""109222""}]"	"[""109222""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050873""}]"
DOID:0050879	"[""fragile X-associated tremor/ataxia syndrome"",""FXTAS syndrome""]"	"[{""label"":""FMR1"",""id"":""2332""}]"	"[""2332""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050879""}]"
DOID:0050880	"[""Koolen de Vries syndrome"",""17q21.31 microdeletion syndrome"",""KANSL1-related intellectual disability syndrome"",""KdVS"",""Koolen-De Vries syndrome""]"	"[{""label"":""KANSL1"",""id"":""284058""}]"	"[""284058""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050880""}]"
DOID:0050880	"[""Koolen de Vries syndrome"",""17q21.31 microdeletion syndrome"",""KANSL1-related intellectual disability syndrome"",""KdVS"",""Koolen-De Vries syndrome""]"	"[{""label"":""Kansl1"",""id"":""76719""}]"	"[""76719""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050880""}]"
DOID:0050881	"[""inclusion body myopathy with Paget disease of bone and frontotemporal dementia"",""IBMPFD"",""inclusion body myopathy with Paget's disease of bone and frontotemporal dementia""]"	"[{""label"":""HNRNPA2B1"",""id"":""3181""}]"	"[""3181""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050881""}]"
DOID:0050882	"[""spinocerebellar ataxia type 5""]"	"[{""label"":""SPTBN2"",""id"":""6712""}]"	"[""6712""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050882""}]"
DOID:0050883	"[""infantile cerebellar-retinal degeneration""]"	"[{""label"":""ACO2"",""id"":""50""}]"	"[""50""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050883""}]"
DOID:0050884	"[""triosephosphate isomerase deficiency"",""Triose phosphate-isomerase deficiency""]"	"[{""label"":""Tpi"",""id"":""43582""}]"	"[""43582""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050884""}]"
DOID:0050884	"[""triosephosphate isomerase deficiency"",""Triose phosphate-isomerase deficiency""]"	"[{""label"":""Tpi1"",""id"":""21991""}]"	"[""21991""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050884""}]"
DOID:0050884	"[""triosephosphate isomerase deficiency"",""Triose phosphate-isomerase deficiency""]"	"[{""label"":""TPI1"",""id"":""7167""}]"	"[""7167""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050884""}]"
DOID:0050884	"[""triosephosphate isomerase deficiency"",""Triose phosphate-isomerase deficiency""]"	"[{""label"":""TPI1"",""id"":""851620""}]"	"[""851620""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050884""}]"
DOID:0050886	"[""Troyer syndrome"",""SPG20"",""autosomal recessive spastic paraplegia 20"",""autosomal recessive spastic paraplegia Troyer type"",""autosomal recessive spastic paraplegia type 20"",""childhood-onset spastic paraparesis with distal muscle wasting"",""hereditary spastic paraplegia 20"",""spastic paraplegia 20"",""spastic paraplegia type 20""]"	"[{""label"":""Spart"",""id"":""229285""}]"	"[""229285""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050886""}]"
DOID:0050886	"[""Troyer syndrome"",""SPG20"",""autosomal recessive spastic paraplegia 20"",""autosomal recessive spastic paraplegia Troyer type"",""autosomal recessive spastic paraplegia type 20"",""childhood-onset spastic paraparesis with distal muscle wasting"",""hereditary spastic paraplegia 20"",""spastic paraplegia 20"",""spastic paraplegia type 20""]"	"[{""label"":""SPART"",""id"":""23111""}]"	"[""23111""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050886""}]"
DOID:0050887	"[""Townes-Brocks syndrome""]"	"[{""label"":""DACT1"",""id"":""51339""},{""label"":""SALL1"",""id"":""6299""}]"	"[""51339"",""6299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050887""}]"
DOID:0050888	"[""syndromic intellectual disability""]"	"[{""label"":""mnb"",""id"":""32771""}]"	"[""32771""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050888""}]"
DOID:0050888	"[""syndromic intellectual disability""]"	"[{""label"":""Anapc7"",""id"":""56317""}]"	"[""56317""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050888""}]"
DOID:0050902	"[""medulloblastoma"",""CNS PNET"",""CPNET"",""Medulloblastoma, histologically defined"",""brain medulloblastoma"",""infratentorial primitive neuroectodermal tumor"",""localized primitive neuroectodermal tumor""]"	"[{""label"":""Ifng"",""id"":""15978""},{""label"":""Ptch1"",""id"":""19206""},{""label"":""Smo"",""id"":""319757""}]"	"[""15978"",""19206"",""319757""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050902""}]"
DOID:0050902	"[""medulloblastoma"",""CNS PNET"",""CPNET"",""Medulloblastoma, histologically defined"",""brain medulloblastoma"",""infratentorial primitive neuroectodermal tumor"",""localized primitive neuroectodermal tumor""]"	"[{""label"":""APC"",""id"":""324""},{""label"":""BRCA2"",""id"":""675""},{""label"":""CTNNB1"",""id"":""1499""},{""label"":""ELP1"",""id"":""8518""},{""label"":""GPR161"",""id"":""23432""},{""label"":""PTCH2"",""id"":""8643""},{""label"":""TSC2"",""id"":""7249""}]"	"[""1499"",""23432"",""324"",""675"",""7249"",""8518"",""8643""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050902""}]"
DOID:0050905	"[""inflammatory myofibroblastic tumor""]"	"[{""label"":""RANBP2"",""id"":""5903""}]"	"[""5903""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050905""}]"
DOID:0050908	"[""myelodysplastic syndrome""]"	"[{""label"":""Asxl1"",""id"":""228790""},{""label"":""Atg7"",""id"":""74244""},{""label"":""Bap1"",""id"":""104416""},{""label"":""Egr1"",""id"":""13653""},{""label"":""Npm1"",""id"":""18148""}]"	"[""104416"",""13653"",""18148"",""228790"",""74244""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050908""}]"
DOID:0050908	"[""myelodysplastic syndrome""]"	"[{""label"":""ARPC1B"",""id"":""10095""},{""label"":""ASXL1"",""id"":""171023""},{""label"":""CDKN1B"",""id"":""1027""},{""label"":""CSF3R"",""id"":""1441""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""GATA2"",""id"":""2624""},{""label"":""GNB1"",""id"":""2782""},{""label"":""HFE"",""id"":""3077""},{""label"":""IDH1"",""id"":""3417""},{""label"":""MEFV"",""id"":""4210""},{""label"":""NRAS"",""id"":""4893""},{""label"":""PLCB1"",""id"":""23236""},{""label"":""SF3B1"",""id"":""23451""},{""label"":""SRSF2"",""id"":""6427""},{""label"":""TET2"",""id"":""54790""},{""label"":""TP53"",""id"":""7157""},{""label"":""XRCC1"",""id"":""7515""},{""label"":""ZRSR2"",""id"":""8233""}]"	"[""10095"",""1027"",""1441"",""171023"",""2146"",""2214"",""23236"",""23451"",""2624"",""2782"",""3077"",""3417"",""4210"",""4893"",""54790"",""6427"",""7157"",""7515"",""8233""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050908""}]"
DOID:0050909	"[""extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue"",""MALT lymphoma"",""MALT lymphoma of the dura"",""mucosa-associated lymphoid tissue lymphoma""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""}]"	"[""3117""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050909""}]"
DOID:0050921	"[""pharynx squamous cell carcinoma""]"	"[{""label"":""CLPTM1L"",""id"":""81037""}]"	"[""81037""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050921""}]"
DOID:0050922	"[""gastrointestinal carcinoma""]"	"[{""label"":""NOD2"",""id"":""64127""}]"	"[""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050922""}]"
DOID:0050933	"[""ovarian serous carcinoma""]"	"[{""label"":""MAP2K4"",""id"":""6416""}]"	"[""6416""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050933""}]"
DOID:0050934	"[""ovarian clear cell carcinoma"",""clear-cell ovarian carcinoma""]"	"[{""label"":""ARID1A"",""id"":""8289""}]"	"[""8289""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050934""}]"
DOID:0050941	"[""spastic ataxia 2""]"	"[{""label"":""KIF1C"",""id"":""10749""}]"	"[""10749""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050941""}]"
DOID:0050942	"[""spastic ataxia 3""]"	"[{""label"":""MARS2"",""id"":""92935""}]"	"[""92935""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050942""}]"
DOID:0050946	"[""Charlevoix-Saguenay spastic ataxia""]"	"[{""label"":""SACS"",""id"":""26278""}]"	"[""26278""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050946""}]"
DOID:0050946	"[""Charlevoix-Saguenay spastic ataxia""]"	"[{""label"":""Sacs"",""id"":""50720""}]"	"[""50720""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050946""}]"
DOID:0050947	"[""hereditary hypophosphatemic rickets with hypercalciuria""]"	"[{""label"":""Slc34a1"",""id"":""20505""}]"	"[""20505""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050947""}]"
DOID:0050947	"[""hereditary hypophosphatemic rickets with hypercalciuria""]"	"[{""label"":""SLC34A1"",""id"":""6569""},{""label"":""SLC34A3"",""id"":""142680""}]"	"[""142680"",""6569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050947""}]"
DOID:0050948	"[""autosomal dominant hypophosphatemic rickets""]"	"[{""label"":""FGF23"",""id"":""8074""}]"	"[""8074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050948""}]"
DOID:0050948	"[""autosomal dominant hypophosphatemic rickets""]"	"[{""label"":""Fgf23"",""id"":""64654""}]"	"[""64654""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050948""}]"
DOID:0050949	"[""autosomal recessive hypophosphatemic rickets""]"	"[{""label"":""Dmp1"",""id"":""13406""}]"	"[""13406""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050949""}]"
DOID:0050951	"[""hereditary ataxia""]"	"[{""label"":""Atg5"",""id"":""31666""},{""label"":""cac"",""id"":""32158""}]"	"[""31666"",""32158""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050951""}]"
DOID:0050954	"[""spinocerebellar ataxia type 1""]"	"[{""label"":""Atxn1"",""id"":""20238""}]"	"[""20238""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050954""}]"
DOID:0050954	"[""spinocerebellar ataxia type 1""]"	"[{""label"":""ATXN1"",""id"":""6310""}]"	"[""6310""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050954""}]"
DOID:0050955	"[""spinocerebellar ataxia type 2""]"	"[{""label"":""Atxn2"",""id"":""20239""}]"	"[""20239""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050955""}]"
DOID:0050955	"[""spinocerebellar ataxia type 2""]"	"[{""label"":""ATXN2"",""id"":""6311""}]"	"[""6311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050955""}]"
DOID:0050955	"[""spinocerebellar ataxia type 2""]"	"[{""label"":""Atx2"",""id"":""41883""}]"	"[""41883""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050955""}]"
DOID:0050956	"[""spinocerebellar ataxia type 6""]"	"[{""label"":""CACNA1A"",""id"":""773""}]"	"[""773""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050956""}]"
DOID:0050956	"[""spinocerebellar ataxia type 6""]"	"[{""label"":""Cacna1a"",""id"":""12286""}]"	"[""12286""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050956""}]"
DOID:0050957	"[""spinocerebellar ataxia type 4"",""SCA4""]"	"[{""label"":""ZFHX3"",""id"":""463""}]"	"[""463""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050957""}]"
DOID:0050958	"[""spinocerebellar ataxia type 7""]"	"[{""label"":""ATXN7"",""id"":""6314""}]"	"[""6314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050958""}]"
DOID:0050958	"[""spinocerebellar ataxia type 7""]"	"[{""label"":""Atxn7"",""id"":""246103""}]"	"[""246103""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050958""}]"
DOID:0050961	"[""spinocerebellar ataxia type 11""]"	"[{""label"":""TTBK2"",""id"":""146057""}]"	"[""146057""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050961""}]"
DOID:0050963	"[""spinocerebellar ataxia type 13""]"	"[{""label"":""KCNC3"",""id"":""3748""}]"	"[""3748""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050963""}]"
DOID:0050964	"[""spinocerebellar ataxia type 14""]"	"[{""label"":""Prkcg"",""id"":""18752""}]"	"[""18752""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050964""}]"
DOID:0050965	"[""spinocerebellar ataxia type 15"",""spinocerebellar ataxia type 16""]"	"[{""label"":""ITPR1"",""id"":""3708""}]"	"[""3708""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050965""}]"
DOID:0050967	"[""spinocerebellar ataxia type 17""]"	"[{""label"":""TBP"",""id"":""6908""}]"	"[""6908""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050967""}]"
DOID:0050968	"[""autosomal dominant cerebellar ataxia, deafness and narcolepsy""]"	"[{""label"":""DNMT1"",""id"":""1786""}]"	"[""1786""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050968""}]"
DOID:0050974	"[""spinocerebellar ataxia type 25""]"	"[{""label"":""PNPT1"",""id"":""87178""}]"	"[""87178""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050974""}]"
DOID:0050975	"[""spinocerebellar ataxia type 26""]"	"[{""label"":""EEF2"",""id"":""1938""}]"	"[""1938""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050975""}]"
DOID:0050977	"[""spinocerebellar ataxia type 28""]"	"[{""label"":""Afg3l2"",""id"":""69597""}]"	"[""69597""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050977""}]"
DOID:0050978	"[""spinocerebellar ataxia type 29""]"	"[{""label"":""ITPR1"",""id"":""3708""}]"	"[""3708""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050978""}]"
DOID:0050981	"[""spinocerebellar ataxia type 34""]"	"[{""label"":""ELOVL4"",""id"":""6785""}]"	"[""6785""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050981""}]"
DOID:0050983	"[""spinocerebellar ataxia type 36""]"	"[{""label"":""NOP56"",""id"":""10528""}]"	"[""10528""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050983""}]"
DOID:0050984	"[""spinocerebellar ataxia type 37""]"	"[{""label"":""DAB1"",""id"":""1600""}]"	"[""1600""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050984""}]"
DOID:0050985	"[""spinocerebellar ataxia type 38""]"	"[{""label"":""ELOVL5"",""id"":""60481""}]"	"[""60481""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050985""}]"
DOID:0050986	"[""spinocerebellar ataxia type 40""]"	"[{""label"":""CCDC88C"",""id"":""440193""}]"	"[""440193""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050986""}]"
DOID:0050989	"[""episodic ataxia type 1""]"	"[{""label"":""Kcna1"",""id"":""16485""}]"	"[""16485""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050989""}]"
DOID:0050989	"[""episodic ataxia type 1""]"	"[{""label"":""Kcna1"",""id"":""24520""}]"	"[""24520""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050989""}]"
DOID:0050989	"[""episodic ataxia type 1""]"	"[{""label"":""KCNA1"",""id"":""3736""}]"	"[""3736""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050989""}]"
DOID:0050989	"[""episodic ataxia type 1""]"	"[{""label"":""Sh"",""id"":""32780""}]"	"[""32780""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050989""}]"
DOID:0050990	"[""episodic ataxia type 2""]"	"[{""label"":""Cacna1a"",""id"":""12286""}]"	"[""12286""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050990""}]"
DOID:0050990	"[""episodic ataxia type 2""]"	"[{""label"":""CACNA1A"",""id"":""773""}]"	"[""773""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050990""}]"
DOID:0050994	"[""episodic ataxia type 6""]"	"[{""label"":""SLC1A3"",""id"":""6507""}]"	"[""6507""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050994""}]"
DOID:0050998	"[""nonprogressive cerebellar ataxia with mental retardation""]"	"[{""label"":""CAMTA1"",""id"":""23261""}]"	"[""23261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0050998""}]"
DOID:0060000	"[""infective endocarditis""]"	"[{""label"":""TLR6"",""id"":""10333""}]"	"[""10333""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060000""}]"
DOID:0060001	"[""withdrawal disorder""]"	"[{""label"":""Creb1"",""id"":""81646""},{""label"":""Gria1"",""id"":""50592""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Oprk1"",""id"":""29335""},{""label"":""Ptger3"",""id"":""24929""}]"	"[""24929"",""29335"",""29595"",""50592"",""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060001""}]"
DOID:0060001	"[""withdrawal disorder""]"	"[{""label"":""COMT"",""id"":""1312""},{""label"":""GAD1"",""id"":""2571""},{""label"":""HTR1A"",""id"":""3350""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""KDM4C"",""id"":""23081""},{""label"":""NGF"",""id"":""4803""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""OPRD1"",""id"":""4985""},{""label"":""OPRM1"",""id"":""4988""}]"	"[""1312"",""23081"",""2571"",""2908"",""3350"",""3356"",""4803"",""4985"",""4988""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060001""}]"
DOID:0060009	"[""MHC class I deficiency"",""BLS, TYPE I"",""BLSI"",""HLA CLASS I DEFICIENCY"",""bare lymphocyte syndrome type I""]"	"[{""label"":""TAP1"",""id"":""6890""}]"	"[""6890""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060009""}]"
DOID:0060010	"[""Omenn syndrome"",""combined immunodeficiency with hypereosinophilia""]"	"[{""label"":""DCLRE1C"",""id"":""64421""}]"	"[""64421""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060010""}]"
DOID:0060013	"[""X-linked severe combined immunodeficiency"",""SCID-X1"",""XSCID"",""gamma chain deficiency"",""thymic epithelial hypoplasia""]"	"[{""label"":""IL2RG"",""id"":""3561""}]"	"[""3561""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060013""}]"
DOID:0060019	"[""coronin-1A deficiency""]"	"[{""label"":""CORO1A"",""id"":""11151""}]"	"[""11151""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060019""}]"
DOID:0060020	"[""reticular dysgenesis"",""De Vaal disease""]"	"[{""label"":""AK2"",""id"":""204""}]"	"[""204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060020""}]"
DOID:0060022	"[""CD40 ligand deficiency"",""HIGMX-1"",""X-linked hyper-IgM syndrome""]"	"[{""label"":""CD40LG"",""id"":""959""}]"	"[""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060022""}]"
DOID:0060023	"[""immunodeficiency with hyper IgM type 3"",""CD40 deficiency"",""HIGM3"",""hyper-IgM syndrome due to CD40 deficiency"",""type 3 hyper-IgM immunodeficiency""]"	"[{""label"":""CD40"",""id"":""958""}]"	"[""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060023""}]"
DOID:0060025	"[""immunoglobulin alpha deficiency"",""IgA deficiency"",""gamma-A-globulin deficiency""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""ICOS"",""id"":""29851""}]"	"[""1493"",""29851"",""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060025""}]"
DOID:0060036	"[""intrinsic cardiomyopathy""]"	"[{""label"":""RpS3"",""id"":""42761""}]"	"[""42761""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060036""}]"
DOID:0060036	"[""intrinsic cardiomyopathy""]"	"[{""label"":""Daam1"",""id"":""208846""},{""label"":""Dsg2"",""id"":""13511""}]"	"[""13511"",""208846""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060036""}]"
DOID:0060037	"[""developmental disorder of mental health""]"	"[{""label"":""Lcch3"",""id"":""32554""},{""label"":""PlexB"",""id"":""43766""},{""label"":""Sin3A"",""id"":""36382""},{""label"":""ash1"",""id"":""40133""}]"	"[""32554"",""36382"",""40133"",""43766""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060037""}]"
DOID:0060037	"[""developmental disorder of mental health""]"	"[{""label"":""RUNX3"",""id"":""864""},{""label"":""TACR1"",""id"":""6869""}]"	"[""6869"",""864""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060037""}]"
DOID:0060041	"[""autism spectrum disorder""]"	"[{""label"":""SEC12"",""id"":""855760""}]"	"[""855760""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060041""}]"
DOID:0060041	"[""autism spectrum disorder""]"	"[{""label"":""Arhgap32"",""id"":""330914""},{""label"":""Arhgef10"",""id"":""234094""},{""label"":""Bckdk"",""id"":""12041""},{""label"":""Brinp1"",""id"":""56710""},{""label"":""Cadps2"",""id"":""320405""},{""label"":""Camk2a"",""id"":""12322""},{""label"":""Chd8"",""id"":""67772""},{""label"":""Chrnb2"",""id"":""11444""},{""label"":""Cntnap2"",""id"":""66797""},{""label"":""Ctnnb1"",""id"":""12387""},{""label"":""Dlg4"",""id"":""13385""},{""label"":""Dlgap4"",""id"":""228836""},{""label"":""Ext1"",""id"":""14042""},{""label"":""Gabrb3"",""id"":""14402""},{""label"":""Gprasp2"",""id"":""245607""},{""label"":""Grin1"",""id"":""14810""},{""label"":""Itpr3"",""id"":""16440""},{""label"":""Lrfn2"",""id"":""70530""},{""label"":""Met"",""id"":""17295""},{""label"":""Nbea"",""id"":""26422""},{""label"":""Nlgn1"",""id"":""192167""},{""label"":""Nlgn3"",""id"":""245537""},{""label"":""Nrcam"",""id"":""319504""},{""label"":""Nrp2"",""id"":""18187""},{""label"":""Nrxn1"",""id"":""18189""},{""label"":""Nsf"",""id"":""18195""},{""label"":""Oprm1"",""id"":""18390""},{""label"":""Pak2"",""id"":""224105""},{""label"":""Pdgfrb"",""id"":""18596""},{""label"":""Pianp"",""id"":""319352""},{""label"":""Pogz"",""id"":""229584""},{""label"":""Scn1a"",""id"":""20265""},{""label"":""Scn2a"",""id"":""110876""},{""label"":""Shank2"",""id"":""210274""},{""label"":""Shank3"",""id"":""58234""},{""label"":""Slc6a4"",""id"":""15567""},{""label"":""Slc7a5"",""id"":""20539""},{""label"":""Slc9a9"",""id"":""331004""},{""label"":""Syn1"",""id"":""20964""},{""label"":""Syn2"",""id"":""20965""},{""label"":""Tbr1"",""id"":""21375""},{""label"":""Tcf20"",""id"":""21411""},{""label"":""Tsc1"",""id"":""64930""},{""label"":""Wdfy3"",""id"":""72145""}]"	"[""110876"",""11444"",""12041"",""12322"",""12387"",""13385"",""14042"",""14402"",""14810"",""15567"",""16440"",""17295"",""18187"",""18189"",""18195"",""18390"",""18596"",""192167"",""20265"",""20539"",""20964"",""20965"",""210274"",""21375"",""21411"",""224105"",""228836"",""229584"",""234094"",""245537"",""245607"",""26422"",""319352"",""319504"",""320405"",""330914"",""331004"",""56710"",""58234"",""64930"",""66797"",""67772"",""70530"",""72145""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060041""}]"
DOID:0060041	"[""autism spectrum disorder""]"	"[{""label"":""AVPR1B"",""id"":""553""},{""label"":""BAIAP2"",""id"":""10458""},{""label"":""BCL11A"",""id"":""53335""},{""label"":""CADM2"",""id"":""253559""},{""label"":""CNTNAP2"",""id"":""26047""},{""label"":""COMT"",""id"":""1312""},{""label"":""CYFIP1"",""id"":""23191""},{""label"":""DYRK1A"",""id"":""1859""},{""label"":""FOXP2"",""id"":""93986""},{""label"":""ITGA4"",""id"":""3676""},{""label"":""MAOA"",""id"":""4128""},{""label"":""MBD5"",""id"":""55777""},{""label"":""MBD6"",""id"":""114785""},{""label"":""MMP9"",""id"":""4318""}]"	"[""10458"",""114785"",""1312"",""1859"",""23191"",""253559"",""26047"",""3676"",""4128"",""4318"",""53335"",""553"",""55777"",""93986""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060041""}]"
DOID:0060041	"[""autism spectrum disorder""]"	"[{""label"":""Creb1"",""id"":""81646""},{""label"":""Nlgn3"",""id"":""171297""},{""label"":""Nrxn1"",""id"":""60391""},{""label"":""Shank2"",""id"":""171093""}]"	"[""171093"",""171297"",""60391"",""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060041""}]"
DOID:0060041	"[""autism spectrum disorder""]"	"[{""label"":""DAT"",""id"":""36849""},{""label"":""Dscam1"",""id"":""35652""},{""label"":""LanB2"",""id"":""39118""},{""label"":""Nrx-IV"",""id"":""39387""},{""label"":""ash1"",""id"":""40133""},{""label"":""kis"",""id"":""33185""},{""label"":""sfl"",""id"":""38736""}]"	"[""33185"",""35652"",""36849"",""38736"",""39118"",""39387"",""40133""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060041""}]"
DOID:0060041	"[""autism spectrum disorder""]"	"[{""label"":""mef-2"",""id"":""172732""},{""label"":""nlg-1"",""id"":""181484""}]"	"[""172732"",""181484""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060041""}]"
DOID:0060050	"[""autoimmune disease of blood""]"	"[{""label"":""C1GalTA"",""id"":""34215""}]"	"[""34215""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060050""}]"
DOID:0060058	"[""lymphoma"",""lymphoid cancer""]"	"[{""label"":""CHD4"",""id"":""1108""},{""label"":""MALT1"",""id"":""10892""},{""label"":""PAFAH1B2"",""id"":""5049""},{""label"":""RELA"",""id"":""5970""}]"	"[""10892"",""1108"",""5049"",""5970""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060058""}]"
DOID:0060060	"[""non-Hodgkin lymphoma""]"	"[{""label"":""CD40"",""id"":""958""},{""label"":""CD79B"",""id"":""974""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""GPX1"",""id"":""2876""},{""label"":""KMT2A"",""id"":""4297""},{""label"":""MALT1"",""id"":""10892""},{""label"":""PON1"",""id"":""5444""},{""label"":""PRF1"",""id"":""5551""},{""label"":""TMEM260"",""id"":""54916""}]"	"[""10892"",""1493"",""2212"",""2876"",""4297"",""5444"",""54916"",""5551"",""958"",""974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060060""}]"
DOID:0060060	"[""non-Hodgkin lymphoma""]"	"[{""label"":""Mtss1"",""id"":""211401""},{""label"":""S1pr2"",""id"":""14739""}]"	"[""14739"",""211401""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060060""}]"
DOID:0060062	"[""familial juvenile hyperuricemic nephropathy""]"	"[{""label"":""Umod"",""id"":""22242""}]"	"[""22242""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060062""}]"
DOID:0060062	"[""familial juvenile hyperuricemic nephropathy""]"	"[{""label"":""MUC1"",""id"":""4582""},{""label"":""REN"",""id"":""5972""},{""label"":""UMOD"",""id"":""7369""}]"	"[""4582"",""5972"",""7369""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060062""}]"
DOID:0060071	"[""pre-malignant neoplasm""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Fas"",""id"":""246097""}]"	"[""24310"",""246097""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060071""}]"
DOID:0060072	"[""benign neoplasm""]"	"[{""label"":""scrib"",""id"":""44448""}]"	"[""44448""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060072""}]"
DOID:0060074	"[""ductal carcinoma in situ""]"	"[{""label"":""BRCA2"",""id"":""675""},{""label"":""HOXB13"",""id"":""10481""},{""label"":""NOTCH4"",""id"":""4855""},{""label"":""PAK2"",""id"":""5062""},{""label"":""RELA"",""id"":""5970""},{""label"":""SRC"",""id"":""6714""}]"	"[""10481"",""4855"",""5062"",""5970"",""6714"",""675""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060074""}]"
DOID:0060075	"[""estrogen-receptor positive breast cancer""]"	"[{""label"":""ADAM28"",""id"":""10863""},{""label"":""PIK3CA"",""id"":""5290""}]"	"[""10863"",""5290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060075""}]"
DOID:0060081	"[""triple-receptor negative breast cancer""]"	"[{""label"":""KDM6A"",""id"":""7403""}]"	"[""7403""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060081""}]"
DOID:0060108	"[""brain glioma"",""lower grade glioma""]"	"[{""label"":""PTPRB"",""id"":""5787""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""5787"",""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060108""}]"
DOID:0060108	"[""brain glioma"",""lower grade glioma""]"	"[{""label"":""Fas"",""id"":""246097""},{""label"":""Faslg"",""id"":""25385""}]"	"[""246097"",""25385""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060108""}]"
DOID:0060131	"[""alexithymia""]"	"[{""label"":""SLC6A4"",""id"":""6532""}]"	"[""6532""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060131""}]"
DOID:0060161	"[""Kennedy's disease"",""Kennedy disease"",""SBMA"",""Spinobulbar Muscular Atrophy"",""X-Linked Bulbo-Spinal Atrophy"",""X-linked Spinal and Bulbar Muscular Atrophy"",""spinal bulbar muscular atrophy""]"	"[{""label"":""AR"",""id"":""367""}]"	"[""367""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060161""}]"
DOID:0060162	"[""dentatorubral-pallidoluysian atrophy"",""DRPLA"",""Haw River Syndrome"",""Naito-Oyanagi disease""]"	"[{""label"":""Gug"",""id"":""46156""}]"	"[""46156""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060162""}]"
DOID:0060162	"[""dentatorubral-pallidoluysian atrophy"",""DRPLA"",""Haw River Syndrome"",""Naito-Oyanagi disease""]"	"[{""label"":""ATN1"",""id"":""1822""}]"	"[""1822""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060162""}]"
DOID:0060170	"[""generalized epilepsy with febrile seizures plus"",""GEFS+""]"	"[{""label"":""Gabrg2"",""id"":""14406""},{""label"":""Scn1a"",""id"":""20265""},{""label"":""Scn1b"",""id"":""20266""}]"	"[""14406"",""20265"",""20266""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060170""}]"
DOID:0060170	"[""generalized epilepsy with febrile seizures plus"",""GEFS+""]"	"[{""label"":""SCN1A"",""id"":""6323""},{""label"":""SLC32A1"",""id"":""140679""}]"	"[""140679"",""6323""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060170""}]"
DOID:0060170	"[""generalized epilepsy with febrile seizures plus"",""GEFS+""]"	"[{""label"":""para"",""id"":""32619""}]"	"[""32619""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060170""}]"
DOID:0060173	"[""Timothy syndrome""]"	"[{""label"":""CACNA1C"",""id"":""775""}]"	"[""775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060173""}]"
DOID:0060173	"[""Timothy syndrome""]"	"[{""label"":""Cacna1c"",""id"":""12288""}]"	"[""12288""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060173""}]"
DOID:0060174	"[""GABA aminotransferase deficiency"",""Gamma-amino butyric acid transaminase deficiency"",""gamma-aminobutyric acid transaminase deficiency""]"	"[{""label"":""ABAT"",""id"":""18""}]"	"[""18""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060174""}]"
DOID:0060175	"[""succinic semialdehyde dehydrogenase deficiency"",""4-hydroxybutyric aciduria"",""SSADH"",""gamma-hydroxybutyric aciduria""]"	"[{""label"":""ALDH5A1"",""id"":""7915""}]"	"[""7915""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060175""}]"
DOID:0060178	"[""familial hemiplegic migraine""]"	"[{""label"":""Cacna1a"",""id"":""12286""}]"	"[""12286""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060178""}]"
DOID:0060178	"[""familial hemiplegic migraine""]"	"[{""label"":""Atpalpha"",""id"":""48971""}]"	"[""48971""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060178""}]"
DOID:0060179	"[""Renpenning syndrome"",""Golabi-Ito-Hall syndrome"",""Sutherland-Haan X-linked mental retardation syndrome"",""X-linked intellectual disability due to PQBP1 mutations"",""X-linked intellectual disability, Renpenning type"",""X-linked mental retardation Renpenning type"",""X-linked mental retardation with spastic diplegia"",""syndromic X-linked mental retardation 8""]"	"[{""label"":""PQBP1"",""id"":""10084""}]"	"[""10084""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060179""}]"
DOID:0060180	"[""colitis""]"	"[{""label"":""Cckbr"",""id"":""25706""},{""label"":""Crhr2"",""id"":""64680""},{""label"":""Cxcr2"",""id"":""29385""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Sell"",""id"":""29259""},{""label"":""Tacr2"",""id"":""25007""}]"	"[""25007"",""25706"",""29259"",""29385"",""64680"",""83516""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060180""}]"
DOID:0060180	"[""colitis""]"	"[{""label"":""APOA4"",""id"":""337""},{""label"":""HLA-B"",""id"":""3106""}]"	"[""3106"",""337""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060180""}]"
DOID:0060181	"[""ischemic colitis""]"	"[{""label"":""SERPINE1"",""id"":""5054""}]"	"[""5054""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060181""}]"
DOID:0060186	"[""chemical colitis""]"	"[{""label"":""SERPINA1"",""id"":""5265""}]"	"[""5265""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060186""}]"
DOID:0060189	"[""ileitis"",""Crohn's ileitis""]"	"[{""label"":""SERPINA1"",""id"":""5265""}]"	"[""5265""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060189""}]"
DOID:0060189	"[""ileitis"",""Crohn's ileitis""]"	"[{""label"":""Tlr4"",""id"":""29260""}]"	"[""29260""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060189""}]"
DOID:0060193	"[""amyotrophic lateral sclerosis type 1"",""ALS1"",""amyotrophic lateral sclerosis 1""]"	"[{""label"":""Sncg"",""id"":""20618""},{""label"":""Sod1"",""id"":""20655""},{""label"":""Sod2"",""id"":""20656""},{""label"":""Vegfa"",""id"":""22339""}]"	"[""20618"",""20655"",""20656"",""22339""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060193""}]"
DOID:0060193	"[""amyotrophic lateral sclerosis type 1"",""ALS1"",""amyotrophic lateral sclerosis 1""]"	"[{""label"":""DCTN1"",""id"":""1639""},{""label"":""NEFH"",""id"":""4744""},{""label"":""PRPH"",""id"":""5630""},{""label"":""SOD1"",""id"":""6647""}]"	"[""1639"",""4744"",""5630"",""6647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060193""}]"
DOID:0060196	"[""amyotrophic lateral sclerosis type 4"",""ALS4"",""amyotrophic lateral sclerosis 4"",""amyotrophic lateral sclerosis 4, juvenile"",""dHMN with upper motor neuron signs"",""distal hereditary motor neuropathy with pyramidal features"",""distal hereditary motor neuropathy with upper motor neuron signs""]"	"[{""label"":""Setx"",""id"":""269254""}]"	"[""269254""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060196""}]"
DOID:0060196	"[""amyotrophic lateral sclerosis type 4"",""ALS4"",""amyotrophic lateral sclerosis 4"",""amyotrophic lateral sclerosis 4, juvenile"",""dHMN with upper motor neuron signs"",""distal hereditary motor neuropathy with pyramidal features"",""distal hereditary motor neuropathy with upper motor neuron signs""]"	"[{""label"":""SETX"",""id"":""23064""}]"	"[""23064""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060196""}]"
DOID:0060197	"[""amyotrophic lateral sclerosis type 5"",""ALS5"",""amyotrophic lateral sclerosis 5""]"	"[{""label"":""SPG11"",""id"":""80208""}]"	"[""80208""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060197""}]"
DOID:0060198	"[""amyotrophic lateral sclerosis type 6"",""ALS6"",""amyotrophic lateral sclerosis 6, with or without frontotemporal dementia"",""autosomal recessive amyotrophic lateral sclerosis 6""]"	"[{""label"":""Fus"",""id"":""233908""}]"	"[""233908""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060198""}]"
DOID:0060198	"[""amyotrophic lateral sclerosis type 6"",""ALS6"",""amyotrophic lateral sclerosis 6, with or without frontotemporal dementia"",""autosomal recessive amyotrophic lateral sclerosis 6""]"	"[{""label"":""FUS"",""id"":""2521""}]"	"[""2521""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060198""}]"
DOID:0060201	"[""amyotrophic lateral sclerosis type 10"",""ALS10"",""TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions"",""amyotrophic lateral sclerosis 10"",""amyotrophic lateral sclerosis 10, with or without frontotemporal dementia""]"	"[{""label"":""TARDBP"",""id"":""23435""}]"	"[""23435""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060201""}]"
DOID:0060202	"[""amyotrophic lateral sclerosis type 11"",""ALS11"",""amyotrophic lateral sclerosis 11""]"	"[{""label"":""FIG4"",""id"":""33658""}]"	"[""33658""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060202""}]"
DOID:0060202	"[""amyotrophic lateral sclerosis type 11"",""ALS11"",""amyotrophic lateral sclerosis 11""]"	"[{""label"":""FIG4"",""id"":""855392""}]"	"[""855392""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060202""}]"
DOID:0060202	"[""amyotrophic lateral sclerosis type 11"",""ALS11"",""amyotrophic lateral sclerosis 11""]"	"[{""label"":""FIG4"",""id"":""9896""}]"	"[""9896""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060202""}]"
DOID:0060203	"[""amyotrophic lateral sclerosis type 12"",""ALS12"",""amyotrophic lateral sclerosis 12""]"	"[{""label"":""OPTN"",""id"":""10133""}]"	"[""10133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060203""}]"
DOID:0060205	"[""frontotemporal dementia and/or amyotrophic lateral sclerosis 6"",""ALS14"",""amyotrophic lateral sclerosis 14"",""amyotrophic lateral sclerosis type 14"",""amyotrophic lateral sclerosis, with or without frontotemporal dementia""]"	"[{""label"":""VCP"",""id"":""7415""}]"	"[""7415""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060205""}]"
DOID:0060206	"[""amyotrophic lateral sclerosis type 15"",""ALS15"",""amyotrophic lateral sclerosis 15"",""amyotrophic lateral sclerosis 15, with or without frontotemporal dementia""]"	"[{""label"":""UBQLN2"",""id"":""29978""}]"	"[""29978""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060206""}]"
DOID:0060209	"[""amyotrophic lateral sclerosis type 18"",""ALS18"",""amyotrophic lateral sclerosis 18""]"	"[{""label"":""PFN1"",""id"":""5216""}]"	"[""5216""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060209""}]"
DOID:0060210	"[""amyotrophic lateral sclerosis type 19"",""ALS19"",""amyotrophic lateral sclerosis 19""]"	"[{""label"":""ERBB4"",""id"":""2066""}]"	"[""2066""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060210""}]"
DOID:0060211	"[""amyotrophic lateral sclerosis type 20"",""ALS20"",""amyotrophic lateral sclerosis 20""]"	"[{""label"":""HNRNPA1"",""id"":""3178""}]"	"[""3178""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060211""}]"
DOID:0060212	"[""amyotrophic lateral sclerosis type 21"",""ALS21""]"	"[{""label"":""Matr3"",""id"":""17184""}]"	"[""17184""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060212""}]"
DOID:0060212	"[""amyotrophic lateral sclerosis type 21"",""ALS21""]"	"[{""label"":""MATR3"",""id"":""9782""}]"	"[""9782""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060212""}]"
DOID:0060213	"[""frontotemporal dementia and/or amyotrophic lateral sclerosis 1"",""ALSFTD"",""FTDALS1"",""FTDMND"",""amyotrophic lateral sclerosis and/or frontotemporal dementia"",""frontotemporal dementia and/or motor neuron disease""]"	"[{""label"":""C9orf72"",""id"":""203228""}]"	"[""203228""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060213""}]"
DOID:0060218	"[""CREST syndrome""]"	"[{""label"":""CENPC"",""id"":""1060""},{""label"":""FBN1"",""id"":""2200""}]"	"[""1060"",""2200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060218""}]"
DOID:0060222	"[""Scheie syndrome"",""mucopolysaccharidosis type 1S"",""mucopolysaccharidosis type IS"",""mucopolysaccharidosis type V""]"	"[{""label"":""IDUA"",""id"":""3425""}]"	"[""3425""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00031""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060222""}]"
DOID:0060224	"[""atrial fibrillation"",""A-fib"",""AFib""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGT"",""id"":""183""},{""label"":""ANK2"",""id"":""287""},{""label"":""KCNE1"",""id"":""3753""},{""label"":""KCNE2"",""id"":""9992""},{""label"":""KCNJ5"",""id"":""3762""},{""label"":""KCNQ1"",""id"":""3784""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""VWF"",""id"":""7450""}]"	"[""1636"",""183"",""287"",""3753"",""3762"",""3784"",""4312"",""4314"",""7450"",""9992""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060224""}]"
DOID:0060227	"[""Adams-Oliver syndrome"",""Adams Oliver syndrome""]"	"[{""label"":""Dll4"",""id"":""54485""}]"	"[""54485""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060227""}]"
DOID:0060227	"[""Adams-Oliver syndrome"",""Adams Oliver syndrome""]"	"[{""label"":""ARHGAP31"",""id"":""57514""},{""label"":""DLL4"",""id"":""54567""},{""label"":""DOCK6"",""id"":""57572""},{""label"":""EOGT"",""id"":""285203""},{""label"":""NOTCH1"",""id"":""4851""},{""label"":""RBPJ"",""id"":""3516""}]"	"[""285203"",""3516"",""4851"",""54567"",""57514"",""57572""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060227""}]"
DOID:0060230	"[""basal ganglia calcification"",""Fahr disease""]"	"[{""label"":""Myorg"",""id"":""329828""},{""label"":""Pdgfrb"",""id"":""18596""},{""label"":""Slc20a2"",""id"":""20516""}]"	"[""18596"",""20516"",""329828""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060230""}]"
DOID:0060230	"[""basal ganglia calcification"",""Fahr disease""]"	"[{""label"":""JAM2"",""id"":""58494""},{""label"":""MYORG"",""id"":""57462""},{""label"":""PDGFB"",""id"":""5155""},{""label"":""PDGFRB"",""id"":""5159""},{""label"":""SLC20A2"",""id"":""6575""}]"	"[""5155"",""5159"",""57462"",""58494"",""6575""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060230""}]"
DOID:0060231	"[""Bruck syndrome"",""osteogenesis imperfecta with congenital joint contractures""]"	"[{""label"":""PLOD2"",""id"":""5352""}]"	"[""5352""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00408""}]"
DOID:0060233	"[""cardiofaciocutaneous syndrome"",""CFC syndrome"",""cardio-facial-cutaneous syndrome""]"	"[{""label"":""KRAS"",""id"":""3845""}]"	"[""3845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060233""}]"
DOID:0060233	"[""cardiofaciocutaneous syndrome"",""CFC syndrome"",""cardio-facial-cutaneous syndrome""]"	"[{""label"":""Braf"",""id"":""109880""},{""label"":""Map2k1"",""id"":""26395""}]"	"[""109880"",""26395""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060233""}]"
DOID:0060234	"[""Carpenter syndrome"",""acrocephalopolysyndactyly type II""]"	"[{""label"":""MEGF8"",""id"":""1954""}]"	"[""1954""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060234""}]"
DOID:0060234	"[""Carpenter syndrome"",""acrocephalopolysyndactyly type II""]"	"[{""label"":""Megf8"",""id"":""269878""}]"	"[""269878""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060234""}]"
DOID:0060239	"[""Van der Woude syndrome""]"	"[{""label"":""Grhl3"",""id"":""230824""}]"	"[""230824""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060239""}]"
DOID:0060240	"[""UV-sensitive syndrome""]"	"[{""label"":""ERCC6"",""id"":""2074""}]"	"[""2074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060240""}]"
DOID:0060241	"[""3-M syndrome"",""Le Merrer syndrome"",""Miller-McKusick-Malvaux syndrome"",""Yakut short stature syndrome"",""dolichospondylic dysplasia"",""gloomy face syndrome"",""three M syndrome""]"	"[{""label"":""CUL7"",""id"":""9820""},{""label"":""OBSL1"",""id"":""23363""}]"	"[""23363"",""9820""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060241""}]"
DOID:0060244	"[""specific language impairment""]"	"[{""label"":""CNTNAP2"",""id"":""26047""}]"	"[""26047""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060244""}]"
DOID:0060246	"[""MASA syndrome"",""CRASH syndrome"",""Gareis-Mason syndrome"",""L1 syndrome"",""SPG1"",""X-linked complicated hereditary spastic paraplegia type 1"",""X-linked corpus callosum agenesis"",""X-linked spastic paraplegia 1"",""hereditary spastic paraplegia 1""]"	"[{""label"":""lad-2"",""id"":""177078""},{""label"":""sax-7"",""id"":""177602""}]"	"[""177078"",""177602""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060246""}]"
DOID:0060246	"[""MASA syndrome"",""CRASH syndrome"",""Gareis-Mason syndrome"",""L1 syndrome"",""SPG1"",""X-linked complicated hereditary spastic paraplegia type 1"",""X-linked corpus callosum agenesis"",""X-linked spastic paraplegia 1"",""hereditary spastic paraplegia 1""]"	"[{""label"":""L1cam"",""id"":""16728""}]"	"[""16728""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060246""}]"
DOID:0060246	"[""MASA syndrome"",""CRASH syndrome"",""Gareis-Mason syndrome"",""L1 syndrome"",""SPG1"",""X-linked complicated hereditary spastic paraplegia type 1"",""X-linked corpus callosum agenesis"",""X-linked spastic paraplegia 1"",""hereditary spastic paraplegia 1""]"	"[{""label"":""L1CAM"",""id"":""3897""}]"	"[""3897""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060246""}]"
DOID:0060246	"[""MASA syndrome"",""CRASH syndrome"",""Gareis-Mason syndrome"",""L1 syndrome"",""SPG1"",""X-linked complicated hereditary spastic paraplegia type 1"",""X-linked corpus callosum agenesis"",""X-linked spastic paraplegia 1"",""hereditary spastic paraplegia 1""]"	"[{""label"":""Nrg"",""id"":""31792""}]"	"[""31792""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060246""}]"
DOID:0060248	"[""Simpson-Golabi-Behmel syndrome type 1"",""DGSX Golabi-Rosen syndrome"",""Golabi-Rosen syndrome"",""SGB syndrome"",""Sara Angers syndrome"",""Simpson dysmorphia syndrome"",""X-linked dysplasia gigantism syndrome"",""bulldog syndrome""]"	"[{""label"":""GPC3"",""id"":""2719""}]"	"[""2719""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060248""}]"
DOID:0060248	"[""Simpson-Golabi-Behmel syndrome type 1"",""DGSX Golabi-Rosen syndrome"",""Golabi-Rosen syndrome"",""SGB syndrome"",""Sara Angers syndrome"",""Simpson dysmorphia syndrome"",""X-linked dysplasia gigantism syndrome"",""bulldog syndrome""]"	"[{""label"":""Gpc3"",""id"":""14734""}]"	"[""14734""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060248""}]"
DOID:0060249	"[""scoliosis""]"	"[{""label"":""ELP1"",""id"":""8518""},{""label"":""FBN1"",""id"":""2200""},{""label"":""FBN2"",""id"":""2201""},{""label"":""TPH1"",""id"":""7166""}]"	"[""2200"",""2201"",""7166"",""8518""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060249""}]"
DOID:0060250	"[""idiopathic scoliosis""]"	"[{""label"":""Adgrg6"",""id"":""215798""},{""label"":""Mbtps1"",""id"":""56453""},{""label"":""Ptpn11"",""id"":""19247""}]"	"[""19247"",""215798"",""56453""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060250""}]"
DOID:0060251	"[""sclerosteosis""]"	"[{""label"":""SOST"",""id"":""50964""}]"	"[""50964""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060251""}]"
DOID:0060254	"[""Robinow syndrome"",""Robinow dwarfism"",""acral dysostosis with facial and genital abnormalities"",""fetal face syndrome""]"	"[{""label"":""Wnt5a"",""id"":""22418""}]"	"[""22418""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060254""}]"
DOID:0060256	"[""Dowling-Degos disease"",""dark dot disease"",""reticular pigment anomaly of flexures""]"	"[{""label"":""KRT5"",""id"":""3852""},{""label"":""POFUT1"",""id"":""23509""},{""label"":""POGLUT1"",""id"":""56983""}]"	"[""23509"",""3852"",""56983""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060256""}]"
DOID:0060257	"[""dyschromatosis symmetrica hereditaria"",""reticulate acropigmentation of Dohi""]"	"[{""label"":""ADAR"",""id"":""103""}]"	"[""103""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060257""}]"
DOID:0060258	"[""reticulate acropigmentation of Kitamura"",""RAPK""]"	"[{""label"":""ADAM10"",""id"":""102""}]"	"[""102""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060258""}]"
DOID:0060259	"[""renal-hepatic-pancreatic dysplasia"",""Ivemark's syndrome""]"	"[{""label"":""NPHP3"",""id"":""27031""}]"	"[""27031""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060259""}]"
DOID:0060263	"[""porencephaly""]"	"[{""label"":""COL4A2"",""id"":""1284""}]"	"[""1284""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060263""}]"
DOID:0060263	"[""porencephaly""]"	"[{""label"":""Col4a1"",""id"":""12826""}]"	"[""12826""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060263""}]"
DOID:0060272	"[""pontocerebellar hypoplasia type 3""]"	"[{""label"":""PCLO"",""id"":""27445""}]"	"[""27445""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060272""}]"
DOID:0060275	"[""pontocerebellar hypoplasia type 6""]"	"[{""label"":""RARS2"",""id"":""57038""}]"	"[""57038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060275""}]"
DOID:0060276	"[""pontocerebellar hypoplasia type 7""]"	"[{""label"":""TOE1"",""id"":""114034""}]"	"[""114034""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060276""}]"
DOID:0060278	"[""pontocerebellar hypoplasia type 9""]"	"[{""label"":""AMPD2"",""id"":""271""}]"	"[""271""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060278""}]"
DOID:0060284	"[""paroxysmal nocturnal hemoglobinuria""]"	"[{""label"":""C3"",""id"":""718""},{""label"":""C5"",""id"":""727""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""PIGA"",""id"":""5277""},{""label"":""PIGT"",""id"":""51604""}]"	"[""3117"",""3119"",""51604"",""5277"",""718"",""727""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00414""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060284""}]"
DOID:0060284	"[""paroxysmal nocturnal hemoglobinuria""]"	"[{""label"":""SPT14"",""id"":""855928""}]"	"[""855928""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060284""}]"
DOID:0060285	"[""parietal foramina"",""Caitlin marks"",""enlarged parietal foramina"",""hereditary cranium bifidum""]"	"[{""label"":""ALX4"",""id"":""60529""}]"	"[""60529""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060285""}]"
DOID:0060286	"[""combined oxidative phosphorylation deficiency""]"	"[{""label"":""TEFM"",""id"":""79736""}]"	"[""79736""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060286""}]"
DOID:0060286	"[""combined oxidative phosphorylation deficiency""]"	"[{""label"":""Mto1"",""id"":""68291""}]"	"[""68291""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060286""}]"
DOID:0060287	"[""cornea plana"",""flat cornea""]"	"[{""label"":""Kera"",""id"":""16545""}]"	"[""16545""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060287""}]"
DOID:0060287	"[""cornea plana"",""flat cornea""]"	"[{""label"":""KERA"",""id"":""11081""}]"	"[""11081""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060287""}]"
DOID:0060290	"[""Ohdo syndrome, SBBYS variant"",""Say-Barber-Biesecker-Young-Simpson syndrome"",""blepharophimosis-intellectual disability syndrome, SBBYS type""]"	"[{""label"":""KAT6B"",""id"":""23522""}]"	"[""23522""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060290""}]"
DOID:0060291	"[""oculodentodigital dysplasia"",""ODD syndrome""]"	"[{""label"":""Gja1"",""id"":""14609""}]"	"[""14609""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060291""}]"
DOID:0060292	"[""X-linked chondrodysplasia punctata 1"",""chondrodystrophia calcificans congenita""]"	"[{""label"":""Ebp"",""id"":""13595""}]"	"[""13595""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060292""}]"
DOID:0060292	"[""X-linked chondrodysplasia punctata 1"",""chondrodystrophia calcificans congenita""]"	"[{""label"":""ARSL"",""id"":""415""}]"	"[""415""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060292""}]"
DOID:0060295	"[""complement component 2 deficiency""]"	"[{""label"":""C2"",""id"":""717""}]"	"[""717""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060295""}]"
DOID:0060296	"[""congenital secretory chloride diarrhea 1"",""congenital chloride diarrhea finnish type"",""congenital chloride diarrhoea finnish type"",""congenital chloridorrhea"",""congenital secretory chloride diarrhoea 1""]"	"[{""label"":""SLC26A3"",""id"":""1811""}]"	"[""1811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060296""}]"
DOID:0060296	"[""congenital secretory chloride diarrhea 1"",""congenital chloride diarrhea finnish type"",""congenital chloride diarrhoea finnish type"",""congenital chloridorrhea"",""congenital secretory chloride diarrhoea 1""]"	"[{""label"":""Slc26a3"",""id"":""13487""}]"	"[""13487""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060296""}]"
DOID:0060297	"[""complement component 4a deficiency""]"	"[{""label"":""C4A"",""id"":""720""}]"	"[""720""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060297""}]"
DOID:0060298	"[""complement component 4b deficiency""]"	"[{""label"":""C4B"",""id"":""721""}]"	"[""721""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060298""}]"
DOID:0060299	"[""complement component 6 deficiency""]"	"[{""label"":""C6"",""id"":""729""}]"	"[""729""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060299""}]"
DOID:0060300	"[""complement component 7 deficiency""]"	"[{""label"":""C7"",""id"":""730""}]"	"[""730""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060300""}]"
DOID:0060301	"[""type I complement component 8 deficiency""]"	"[{""label"":""C8A"",""id"":""731""}]"	"[""731""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060301""}]"
DOID:0060302	"[""type II complement component 8 deficiency""]"	"[{""label"":""C8B"",""id"":""732""}]"	"[""732""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060302""}]"
DOID:0060303	"[""complement component 9 deficiency""]"	"[{""label"":""C9"",""id"":""735""}]"	"[""735""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060303""}]"
DOID:0060304	"[""dyschromatosis universalis hereditaria""]"	"[{""label"":""ABCB6"",""id"":""10058""}]"	"[""10058""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060304""}]"
DOID:0060305	"[""megalocornea"",""anterior megalophthalmos"",""congenital anterior megalophthalmia""]"	"[{""label"":""LTBP2"",""id"":""4053""}]"	"[""4053""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060305""}]"
DOID:0060306	"[""Meier-Gorlin syndrome"",""ear-patella-short stature syndrome""]"	"[{""label"":""Bmp5"",""id"":""12160""}]"	"[""12160""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060306""}]"
DOID:0060307	"[""autosomal dominant intellectual developmental disorder"",""autosomal dominant mental retardation"",""autosomal dominant non-syndromic mental retardation""]"	"[{""label"":""AP2M1"",""id"":""1173""},{""label"":""CAMK2G"",""id"":""818""},{""label"":""DIP2B"",""id"":""57609""},{""label"":""GRIA1"",""id"":""2890""},{""label"":""HNRNPC"",""id"":""3183""},{""label"":""KMT2B"",""id"":""9757""},{""label"":""LMAN2L"",""id"":""81562""},{""label"":""MED13"",""id"":""9969""},{""label"":""RFX7"",""id"":""64864""},{""label"":""SET"",""id"":""6418""},{""label"":""SETD2"",""id"":""29072""},{""label"":""SRRM2"",""id"":""23524""},{""label"":""TAF4"",""id"":""6874""},{""label"":""TLK2"",""id"":""11011""},{""label"":""TRIO"",""id"":""7204""},{""label"":""ZNF292"",""id"":""23036""}]"	"[""11011"",""1173"",""23036"",""23524"",""2890"",""29072"",""3183"",""57609"",""6418"",""64864"",""6874"",""7204"",""81562"",""818"",""9757"",""9969""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060307""}]"
DOID:0060308	"[""autosomal recessive intellectual developmental disorder"",""autosomal recessive mental retardation"",""autosomal recessive non-syndromic mental retardation""]"	"[{""label"":""Nrx-IV"",""id"":""39387""}]"	"[""39387""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060308""}]"
DOID:0060308	"[""autosomal recessive intellectual developmental disorder"",""autosomal recessive mental retardation"",""autosomal recessive non-syndromic mental retardation""]"	"[{""label"":""ASCC3"",""id"":""10973""},{""label"":""TPR"",""id"":""7175""}]"	"[""10973"",""7175""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060308""}]"
DOID:0060309	"[""syndromic X-linked intellectual disability"",""syndromic X-linked mental retardation""]"	"[{""label"":""DDX3X"",""id"":""1654""},{""label"":""NKAP"",""id"":""79576""},{""label"":""ZFX"",""id"":""7543""}]"	"[""1654"",""7543"",""79576""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060309""}]"
DOID:0060309	"[""syndromic X-linked intellectual disability"",""syndromic X-linked mental retardation""]"	"[{""label"":""ATP6AP2"",""id"":""41104""}]"	"[""41104""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060309""}]"
DOID:0060316	"[""orofaciodigital syndrome I"",""Papillon-Leage-Psaume syndrome"",""orofaciodigital syndrome 1"",""orofaciodigital syndrome type I""]"	"[{""label"":""Ofd1"",""id"":""237222""}]"	"[""237222""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060316""}]"
DOID:0060318	"[""acute promyelocytic leukemia"",""acute myeloblastic leukaemia type 3"",""acute myeloblastic leukemia type 3"",""acute myeloid leukaemia M3"",""acute myeloid leukemia M3"",""acute promyelocytic leukaemia""]"	"[{""label"":""MYC"",""id"":""4609""}]"	"[""4609""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060318""}]"
DOID:0060319	"[""cardiac arrest"",""cardiopulmonary arrest"",""circulatory arrest""]"	"[{""label"":""Abcc8"",""id"":""25559""}]"	"[""25559""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060319""}]"
DOID:0060326	"[""myelomeningocele""]"	"[{""label"":""SLC2A1"",""id"":""6513""}]"	"[""6513""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060326""}]"
DOID:0060327	"[""omphalocele"",""exomphalos"",""omphalocoele""]"	"[{""label"":""Lrp1"",""id"":""16971""}]"	"[""16971""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060327""}]"
DOID:0060334	"[""transient neonatal diabetes mellitus""]"	"[{""label"":""Abcc8"",""id"":""20927""}]"	"[""20927""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060334""}]"
DOID:0060335	"[""autosomal dominant sideroblastic anemia 4""]"	"[{""label"":""HSPA9"",""id"":""3313""}]"	"[""3313""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060335""}]"
DOID:0060337	"[""CEDNIK syndrome"",""cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome""]"	"[{""label"":""SNAP29"",""id"":""9342""}]"	"[""9342""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060337""}]"
DOID:0060337	"[""CEDNIK syndrome"",""cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome""]"	"[{""label"":""Snap29"",""id"":""67474""}]"	"[""67474""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060337""}]"
DOID:0060340	"[""ciliopathy""]"	"[{""label"":""Spry2"",""id"":""24064""}]"	"[""24064""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060340""}]"
DOID:0060340	"[""ciliopathy""]"	"[{""label"":""pkd2"",""id"":""432387""}]"	"[""432387""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060340""}]"
DOID:0060341	"[""agnathia-otocephaly complex"",""agnathia-holoprosencephaly-situs inversus syndrome"",""dysgnathia complex agnathia-holoprosencephaly"",""holoprosencephaly-agnathia"",""otocephaly""]"	"[{""label"":""Trappc10"",""id"":""216131""}]"	"[""216131""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060341""}]"
DOID:0060342	"[""acromelic frontonasal dysostosis""]"	"[{""label"":""ZSWIM6"",""id"":""57688""}]"	"[""57688""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060342""}]"
DOID:0060348	"[""hypoparathyroidism-retardation-dysmorphism syndrome"",""HRD syndrome"",""Sanjad-Sakati syndrome"",""hypoparathyroidism with short stature, mental retardation and seizures""]"	"[{""label"":""TBCE"",""id"":""6905""}]"	"[""6905""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060348""}]"
DOID:0060349	"[""microcephaly with or without chorioretinopathy, lymphedema, or mental retardation"",""chorioretinal dysplasia-microcephaly-mental retardation syndrome"",""lymphedema and retinal folds with ficrocephaly and microphthalmos"",""lymphedema, microcephaly and chorioretinopathy syndrome"",""microcephaly lymphedema chorioretinal dysplasia"",""microcephaly, lymphedema, chorioretinal dysplasia syndrome""]"	"[{""label"":""KIF11"",""id"":""3832""}]"	"[""3832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060349""}]"
DOID:0060350	"[""adenine phosphoribosyltransferase deficiency"",""2,8-dihydroxyadenine urolithiasis"",""APRT deficiency""]"	"[{""label"":""APRT"",""id"":""353""}]"	"[""353""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060350""}]"
DOID:0060350	"[""adenine phosphoribosyltransferase deficiency"",""2,8-dihydroxyadenine urolithiasis"",""APRT deficiency""]"	"[{""label"":""Aprt"",""id"":""11821""}]"	"[""11821""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060350""}]"
DOID:0060352	"[""Kleefstra syndrome 1"",""9q subtelomeric deletion syndrome"",""9q-syndrome"",""9q34 deletion syndrome""]"	"[{""label"":""EHMT1"",""id"":""79813""}]"	"[""79813""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060352""}]"
DOID:0060352	"[""Kleefstra syndrome 1"",""9q subtelomeric deletion syndrome"",""9q-syndrome"",""9q34 deletion syndrome""]"	"[{""label"":""Ehmt1"",""id"":""77683""}]"	"[""77683""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060352""}]"
DOID:0060354	"[""Stormorken syndrome"",""thrombocytopathy, asplenia and miosis""]"	"[{""label"":""STIM1"",""id"":""6786""}]"	"[""6786""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060354""}]"
DOID:0060354	"[""Stormorken syndrome"",""thrombocytopathy, asplenia and miosis""]"	"[{""label"":""Stim1"",""id"":""20866""}]"	"[""20866""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060354""}]"
DOID:0060355	"[""amyotrophic lateral sclerosis type 22"",""ALS22"",""amyotrohpic lateral sclerosis 22 with or without frontotemporal dementia"",""amyotrophic lateral sclerosis 22""]"	"[{""label"":""TUBA4A"",""id"":""7277""}]"	"[""7277""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060355""}]"
DOID:0060356	"[""Vici syndrome"",""immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum""]"	"[{""label"":""EPG5"",""id"":""57724""}]"	"[""57724""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060356""}]"
DOID:0060358	"[""multiple acyl-CoA dehydrogenase deficiency"",""MAD deficiency"",""MADD"",""electron transfer flavoprotein deficiency"",""electron transfer flavoprotein ubiquinone oxidoreductase deficiency"",""glutaric acidemia type 2"",""glutaric aciduria type 2""]"	"[{""label"":""ETFB"",""id"":""2109""}]"	"[""2109""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060358""}]"
DOID:0060363	"[""glycerol kinase deficiency""]"	"[{""label"":""Gk"",""id"":""14933""}]"	"[""14933""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060363""}]"
DOID:0060363	"[""glycerol kinase deficiency""]"	"[{""label"":""GK"",""id"":""2710""}]"	"[""2710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060363""}]"
DOID:0060363	"[""glycerol kinase deficiency""]"	"[{""label"":""R11F4.1"",""id"":""173747""}]"	"[""173747""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060363""}]"
DOID:0060365	"[""mandibulofacial dysostosis with alopecia"",""MFDA""]"	"[{""label"":""Ednra"",""id"":""13617""}]"	"[""13617""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060365""}]"
DOID:0060365	"[""mandibulofacial dysostosis with alopecia"",""MFDA""]"	"[{""label"":""EDNRA"",""id"":""1909""}]"	"[""1909""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060365""}]"
DOID:0060366	"[""Hennekam syndrome"",""Hennekam lymphangiectasia-lymphedema syndrome"",""lymphedem-lymphangiectasia-intellectual disability syndrome""]"	"[{""label"":""ADAMTS3"",""id"":""9508""},{""label"":""CCBE1"",""id"":""147372""},{""label"":""FAT4"",""id"":""79633""}]"	"[""147372"",""79633"",""9508""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060366""}]"
DOID:0060367	"[""Parkinson's disease 1"",""autosomal dominant Parkinson disease 1"",""autosomal dominant Parkinson's disease 1""]"	"[{""label"":""Snca"",""id"":""20617""}]"	"[""20617""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060367""}]"
DOID:0060367	"[""Parkinson's disease 1"",""autosomal dominant Parkinson disease 1"",""autosomal dominant Parkinson's disease 1""]"	"[{""label"":""SNCA"",""id"":""6622""}]"	"[""6622""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060367""}]"
DOID:0060369	"[""Parkinson's disease 6"",""PARK6"",""autosomal recessive early-onset Parkinson disease 6"",""autosomal recessive early-onset Parkinson's disease 6"",""early-onset Parkinson disease 6""]"	"[{""label"":""PINK1"",""id"":""65018""}]"	"[""65018""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060369""}]"
DOID:0060370	"[""Parkinson's disease 7"",""autosomal recessive early-onset Parkinson disease 7"",""autosomal recessive early-onset Parkinson's disease 7""]"	"[{""label"":""PARK7"",""id"":""11315""}]"	"[""11315""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060370""}]"
DOID:0060370	"[""Parkinson's disease 7"",""autosomal recessive early-onset Parkinson disease 7"",""autosomal recessive early-onset Parkinson's disease 7""]"	"[{""label"":""Park7"",""id"":""57320""}]"	"[""57320""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060370""}]"
DOID:0060371	"[""Parkinson's disease 8"",""autosomal dominant Parkinson disease 8"",""autosomal dominant Parkinson's disease 8""]"	"[{""label"":""LRRK2"",""id"":""120892""}]"	"[""120892""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060371""}]"
DOID:0060372	"[""Parkinson's disease 15"",""Parkinsonian-pyramidal syndrome"",""autosomal recessive early-onset Parkinson disease 15"",""autosomal recessive early-onset Parkinson's disease 15"",""pallidopyramidal syndrome""]"	"[{""label"":""FBXO7"",""id"":""25793""}]"	"[""25793""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060372""}]"
DOID:0060374	"[""orofaciodigital syndrome IV"",""Baraitser-Burn syndrome"",""OFD4""]"	"[{""label"":""TCTN3"",""id"":""26123""}]"	"[""26123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060374""}]"
DOID:0060386	"[""Chilblain lupus""]"	"[{""label"":""SAMHD1"",""id"":""25939""}]"	"[""25939""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060386""}]"
DOID:0060387	"[""chondrodysplasia Blomstrand type"",""Blomstrand lethal chondrodysplasia""]"	"[{""label"":""PTH1R"",""id"":""5745""}]"	"[""5745""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060387""}]"
DOID:0060389	"[""chromosome 10q23 deletion syndrome""]"	"[{""label"":""Bmpr1a"",""id"":""12166""}]"	"[""12166""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060389""}]"
DOID:0060395	"[""chromosome 15q24 deletion syndrome"",""15q24 microdeletion syndrome""]"	"[{""label"":""SIN3A"",""id"":""25942""}]"	"[""25942""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060395""}]"
DOID:0060409	"[""NFIA-related disorder"",""1p31p32 microdeletion syndrome"",""Chromosome 1, Monosomy 1p32"",""brain malformations with or without urinary tract defects"",""chromosome 1p32-p31 deletion syndrome""]"	"[{""label"":""NFIA"",""id"":""4774""}]"	"[""4774""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060409""}]"
DOID:0060410	"[""chromosome 1p36 deletion syndrome"",""1p36 deletion syndrome"",""deletion 1p36"",""monosomy 1p36""]"	"[{""label"":""Casz1"",""id"":""69743""},{""label"":""Kcnab2"",""id"":""16498""}]"	"[""16498"",""69743""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060410""}]"
DOID:0060412	"[""chromosome 1q41-q42 deletion syndrome"",""1q41-q42 microdeletion syndrome"",""1q41q42 microdeletion syndrome""]"	"[{""label"":""Trp53bp2"",""id"":""209456""}]"	"[""209456""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060412""}]"
DOID:0060419	"[""chromosome 3q29 microdeletion syndrome"",""3q subtelomere deletion syndrome"",""3q29 microdeletion syndrome"",""3q29 recurrent deletion"",""3qter deletion""]"	"[{""label"":""CG6836"",""id"":""40070""},{""label"":""Tsf2"",""id"":""39435""}]"	"[""39435"",""40070""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060419""}]"
DOID:0060428	"[""SATB2-associated syndrome"",""2q32-q33 microdeletion syndrome"",""2q32q33 microdeletion syndrome"",""Glass syndrome"",""chromosome 2q32-q33 deletion syndrome"",""monosomy 2q32"",""monosomy 2q32-q33"",""monosomy 2q32q33""]"	"[{""label"":""SATB2"",""id"":""23314""}]"	"[""23314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060428""}]"
DOID:0060438	"[""Cole-Carpenter syndrome""]"	"[{""label"":""P4HB"",""id"":""5034""},{""label"":""SEC24D"",""id"":""9871""}]"	"[""5034"",""9871""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060438""}]"
DOID:0060439	"[""lysinuric protein intolerance"",""LPI"",""dibasic amino aciduria II"",""hyperdibasic aminoaciduria""]"	"[{""label"":""SLC7A7"",""id"":""9056""}]"	"[""9056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060439""}]"
DOID:0060439	"[""lysinuric protein intolerance"",""LPI"",""dibasic amino aciduria II"",""hyperdibasic aminoaciduria""]"	"[{""label"":""Slc7a7"",""id"":""20540""}]"	"[""20540""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060439""}]"
DOID:0060444	"[""granular corneal dystrophy 2"",""CGD2"",""avellino corneal dystrophy"",""combined granular-lattice corneal dystrophy"",""corneal dystrophy, Avellino type"",""granular corneal dystrophy type 2""]"	"[{""label"":""TGFBI"",""id"":""7045""}]"	"[""7045""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060444""}]"
DOID:0060445	"[""congenital stromal corneal dystrophy"",""CSCD"",""congenital hereditary stromal dystrophy""]"	"[{""label"":""Dcn"",""id"":""13179""}]"	"[""13179""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060445""}]"
DOID:0060445	"[""congenital stromal corneal dystrophy"",""CSCD"",""congenital hereditary stromal dystrophy""]"	"[{""label"":""DCN"",""id"":""1634""}]"	"[""1634""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060445""}]"
DOID:0060447	"[""epithelial basement membrane dystrophy"",""Cogan corneal dystrophy"",""EBMD"",""microcystic corneal dystrophy""]"	"[{""label"":""TGFBI"",""id"":""7045""}]"	"[""7045""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060447""}]"
DOID:0060448	"[""Fleck corneal dystrophy"",""FCD"",""Francois-Neetens speckled corneal dystrophy""]"	"[{""label"":""PIKFYVE"",""id"":""200576""}]"	"[""200576""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060448""}]"
DOID:0060449	"[""gelatinous drop-like corneal dystrophy"",""GDCD"",""corneal amyloidosis"",""primary familial amyloidosis of the cornea"",""subepithelial amyloidosis of the cornea""]"	"[{""label"":""TACSTD2"",""id"":""4070""}]"	"[""4070""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060449""}]"
DOID:0060450	"[""Lisch epithelial corneal dystrophy"",""LECD"",""band-shaped and whorled microcystic""]"	"[{""label"":""MCOLN1"",""id"":""57192""}]"	"[""57192""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060450""}]"
DOID:0060453	"[""Reis-Bucklers corneal dystrophy"",""RBCD"",""anterior limiting membrane dystrophy type I"",""corneal dystrophy of Bowman layer type I"",""geographic corneal dystrophy"",""granular corneal dystrophy type III""]"	"[{""label"":""TGFBI"",""id"":""7045""}]"	"[""7045""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060453""}]"
DOID:0060455	"[""Thiel-Behnke corneal dystrophy"",""TBCD"",""Waardenburg-Jonker corneal dystrophy"",""anterior limiting membrane dystrophy type II"",""corneal dystrophy honeycomb-shaped"",""corneal dystrophy of Bowman layer type II""]"	"[{""label"":""TGFBI"",""id"":""7045""}]"	"[""7045""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060455""}]"
DOID:0060462	"[""Desbuquois dysplasia"",""Desbuquois syndrome"",""micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification""]"	"[{""label"":""CANT1"",""id"":""124583""},{""label"":""XYLT1"",""id"":""64131""}]"	"[""124583"",""64131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060462""}]"
DOID:0060462	"[""Desbuquois dysplasia"",""Desbuquois syndrome"",""micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification""]"	"[{""label"":""Cant1"",""id"":""76025""}]"	"[""76025""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060462""}]"
DOID:0060464	"[""Feingold syndrome"",""FGLDS"",""MODED syndrome"",""ODED syndrome"",""digital anomalies with short palpebral fissures and atresia of esophagus or duodenum"",""microcephaly-digital anomalies-normal intelligence syndrome"",""microcephaly-oculo-digito-esophageal-duodenal syndrome"",""oculo-digito-esophageal-duodenal syndrome""]"	"[{""label"":""MYCN"",""id"":""4613""}]"	"[""4613""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060464""}]"
DOID:0060466	"[""gingival fibromatosis"",""hereditary gingival fibromatosis"",""hereditary gingival hyperplasia""]"	"[{""label"":""SOS1"",""id"":""6654""}]"	"[""6654""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060466""}]"
DOID:0060468	"[""Holt-Oram syndrome"",""atrio-digital syndrome"",""atriodigital dysplasia"",""heart-hand syndrome""]"	"[{""label"":""SALL4"",""id"":""57167""}]"	"[""57167""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060468""}]"
DOID:0060469	"[""Miller-Dieker lissencephaly syndrome"",""MDS"",""Miller-Dieker syndrome""]"	"[{""label"":""Mnt"",""id"":""17428""},{""label"":""Ywhae"",""id"":""22627""}]"	"[""17428"",""22627""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060469""}]"
DOID:0060470	"[""salt and pepper syndrome"",""salt \u0026 pepper syndrome"",""salt-and-pepper syndrome""]"	"[{""label"":""ST3GAL5"",""id"":""8869""}]"	"[""8869""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00412""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060470""}]"
DOID:0060473	"[""Kabuki syndrome"",""KMS"",""Kabuki make up syndrome"",""Niikawa-Kuroki syndrome""]"	"[{""label"":""KDM6A"",""id"":""7403""},{""label"":""KMT2D"",""id"":""8085""}]"	"[""7403"",""8085""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060473""}]"
DOID:0060475	"[""myoclonic-atonic epilepsy"",""EEOC"",""childhood onset epileptic encephalopathy""]"	"[{""label"":""SLC6A1"",""id"":""6529""}]"	"[""6529""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060475""}]"
DOID:0060478	"[""Zika fever"",""Zika virus disease""]"	"[{""label"":""STAT2"",""id"":""6773""}]"	"[""6773""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060478""}]"
DOID:0060479	"[""Shwachman-Diamond syndrome"",""Shwachman syndrome"",""Shwachman-Bodian-Diamond syndrome"",""Shwachman-Diamond type metaphyseal dysplasia"",""pancreatic insufficiency and bone marrow dysfunction""]"	"[{""label"":""Serpini2"",""id"":""67931""}]"	"[""67931""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060479""}]"
DOID:0060479	"[""Shwachman-Diamond syndrome"",""Shwachman syndrome"",""Shwachman-Bodian-Diamond syndrome"",""Shwachman-Diamond type metaphyseal dysplasia"",""pancreatic insufficiency and bone marrow dysfunction""]"	"[{""label"":""EFL1"",""id"":""79631""}]"	"[""79631""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060479""}]"
DOID:0060480	"[""left ventricular noncompaction"",""left ventricular hypertrabeculation""]"	"[{""label"":""Chd4"",""id"":""107932""},{""label"":""Slc39a8"",""id"":""67547""},{""label"":""Ywhae"",""id"":""22627""}]"	"[""107932"",""22627"",""67547""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060480""}]"
DOID:0060480	"[""left ventricular noncompaction"",""left ventricular hypertrabeculation""]"	"[{""label"":""DTNA"",""id"":""1837""}]"	"[""1837""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060480""}]"
DOID:0060481	"[""Goldberg-Shprintzen syndrome"",""Goldberg-Shprintzen megacolon syndrome""]"	"[{""label"":""KIFBP"",""id"":""26128""}]"	"[""26128""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060481""}]"
DOID:0060482	"[""oculoauricular syndrome""]"	"[{""label"":""HMX1"",""id"":""3166""}]"	"[""3166""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060482""}]"
DOID:0060485	"[""Mowat-Wilson syndrome"",""Hirschsprung disease mental retardation syndrome"",""microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease""]"	"[{""label"":""Zeb2"",""id"":""24136""}]"	"[""24136""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060485""}]"
DOID:0060486	"[""Perry syndrome"",""parkinsonism with alveolar hypoventilation and mental depression""]"	"[{""label"":""DCTN1"",""id"":""1639""}]"	"[""1639""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060486""}]"
DOID:0060488	"[""Pitt-Hopkins syndrome""]"	"[{""label"":""Tcf4"",""id"":""21413""}]"	"[""21413""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060488""}]"
DOID:0060488	"[""Pitt-Hopkins syndrome""]"	"[{""label"":""TCF4"",""id"":""6925""}]"	"[""6925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060488""}]"
DOID:0060490	"[""Schimke immuno-osseous dysplasia"",""Schimke immunoosseous dysplasia"",""Schimke syndrome"",""immunoosseous dysplasia Schimke type"",""spondyloepiphyseal dysplasia - nephrotic syndrome""]"	"[{""label"":""SMARCAL1"",""id"":""50485""}]"	"[""50485""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060490""}]"
DOID:0060491	"[""SPOAN syndrome"",""spastic paraplegia, optic atropy, and neuropathy"",""spastic paraplegia, optic atropy, and neuropathy syndrome""]"	"[{""label"":""KLC2"",""id"":""64837""}]"	"[""64837""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060491""}]"
DOID:0060496	"[""respiratory allergy"",""airway allergy""]"	"[{""label"":""F2RL1"",""id"":""2150""},{""label"":""IL13"",""id"":""3596""},{""label"":""MBL2"",""id"":""4153""},{""label"":""NOS3"",""id"":""4846""},{""label"":""TLR4"",""id"":""7099""}]"	"[""2150"",""3596"",""4153"",""4846"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060496""}]"
DOID:0060500	"[""drug allergy""]"	"[{""label"":""IL2"",""id"":""3558""}]"	"[""3558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060500""}]"
DOID:0060532	"[""latex allergy""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060532""}]"
DOID:0060536	"[""mitochondrial complex I deficiency"",""isolated NADH-CoQ reductase deficiency"",""isolated NADH-coenzyme Q reductase deficiency"",""isolated NADH-ubiquinone reductase deficiency"",""isolated mitochondrial respiratory chain complex I deficiency""]"	"[{""label"":""NDUFS1"",""id"":""4719""}]"	"[""4719""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060536""}]"
DOID:0060536	"[""mitochondrial complex I deficiency"",""isolated NADH-CoQ reductase deficiency"",""isolated NADH-coenzyme Q reductase deficiency"",""isolated NADH-ubiquinone reductase deficiency"",""isolated mitochondrial respiratory chain complex I deficiency""]"	"[{""label"":""Aifm1"",""id"":""26926""},{""label"":""Ndufs4"",""id"":""17993""}]"	"[""17993"",""26926""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060536""}]"
DOID:0060537	"[""mitochondrial complex II deficiency"",""isolated mitochondrial respiratory chain complex II deficiency"",""isolated succinate-CoQ reductase deficiency"",""isolated succinate-coenzyme Q reductase deficiency"",""isolated succinate-ubiquinone reductase deficiency""]"	"[{""label"":""SDHA"",""id"":""6389""},{""label"":""SDHB"",""id"":""6390""},{""label"":""SDHD"",""id"":""6392""}]"	"[""6389"",""6390"",""6392""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060537""}]"
DOID:0060540	"[""Hermansky-Pudlak syndrome 2""]"	"[{""label"":""AP3B1"",""id"":""8546""}]"	"[""8546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060540""}]"
DOID:0060540	"[""Hermansky-Pudlak syndrome 2""]"	"[{""label"":""Ap3b1"",""id"":""11774""}]"	"[""11774""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060540""}]"
DOID:0060542	"[""Hermansky-Pudlak syndrome 4""]"	"[{""label"":""HPS4"",""id"":""89781""}]"	"[""89781""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060542""}]"
DOID:0060543	"[""Hermansky-Pudlak syndrome 5""]"	"[{""label"":""HPS5"",""id"":""11234""}]"	"[""11234""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060543""}]"
DOID:0060545	"[""Hermansky-Pudlak syndrome 7""]"	"[{""label"":""DTNBP1"",""id"":""84062""}]"	"[""84062""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060545""}]"
DOID:0060546	"[""Hermansky-Pudlak syndrome 8""]"	"[{""label"":""BLOC1S3"",""id"":""388552""}]"	"[""388552""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060546""}]"
DOID:0060549	"[""Barber-Say syndrome""]"	"[{""label"":""TWIST2"",""id"":""117581""}]"	"[""117581""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060549""}]"
DOID:0060550	"[""ablepharon macrostomia syndrome""]"	"[{""label"":""TWIST2"",""id"":""117581""}]"	"[""117581""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060550""}]"
DOID:0060556	"[""Kufor-Rakeb syndrome"",""autosomal recessive Parkinson disease 9"",""autosomal recessive juvenile onset Parkinson disease 9""]"	"[{""label"":""Atp13a2"",""id"":""74772""}]"	"[""74772""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060556""}]"
DOID:0060556	"[""Kufor-Rakeb syndrome"",""autosomal recessive Parkinson disease 9"",""autosomal recessive juvenile onset Parkinson disease 9""]"	"[{""label"":""ATP13A2"",""id"":""23400""}]"	"[""23400""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060556""}]"
DOID:0060558	"[""lethal congenital contracture syndrome""]"	"[{""label"":""VPS1"",""id"":""853870""}]"	"[""853870""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060558""}]"
DOID:0060558	"[""lethal congenital contracture syndrome""]"	"[{""label"":""ADCY6"",""id"":""112""},{""label"":""ADGRG6"",""id"":""57211""},{""label"":""CNTNAP1"",""id"":""8506""},{""label"":""DNM2"",""id"":""1785""},{""label"":""GLDN"",""id"":""342035""},{""label"":""NEK9"",""id"":""91754""}]"	"[""112"",""1785"",""342035"",""57211"",""8506"",""91754""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060558""}]"
DOID:0060559	"[""lethal congenital contracture syndrome 1"",""LCCS1"",""multiple contracture syndrome, Finnish type""]"	"[{""label"":""GLE1"",""id"":""851320""}]"	"[""851320""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060559""}]"
DOID:0060560	"[""lethal congenital contracture syndrome 2"",""LCCS2"",""multiple contracture syndrome, Israeli-Bedouin type""]"	"[{""label"":""ERBB3"",""id"":""2065""}]"	"[""2065""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060560""}]"
DOID:0060563	"[""Char syndrome""]"	"[{""label"":""TFAP2B"",""id"":""7021""}]"	"[""7021""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060563""}]"
DOID:0060563	"[""Char syndrome""]"	"[{""label"":""Tfap2b"",""id"":""21419""}]"	"[""21419""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060563""}]"
DOID:0060564	"[""spinal disease""]"	"[{""label"":""Tsc1"",""id"":""64930""}]"	"[""64930""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060564""}]"
DOID:0060564	"[""spinal disease""]"	"[{""label"":""FLNB"",""id"":""2317""}]"	"[""2317""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060564""}]"
DOID:0060565	"[""Ritscher-Schinzel syndrome"",""CCC dysplasia"",""craniocerebellocardiac dysplasia""]"	"[{""label"":""VPS35L"",""id"":""57020""}]"	"[""57020""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060565""}]"
DOID:0060569	"[""hypertrichotic osteochondrodysplasia Cantu type"",""Cantu syndrome""]"	"[{""label"":""ABCC9"",""id"":""10060""}]"	"[""10060""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060569""}]"
DOID:0060569	"[""hypertrichotic osteochondrodysplasia Cantu type"",""Cantu syndrome""]"	"[{""label"":""Abcc9"",""id"":""20928""}]"	"[""20928""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060569""}]"
DOID:0060571	"[""Ritscher-Schinzel syndrome 1""]"	"[{""label"":""WASHC5"",""id"":""9897""}]"	"[""9897""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060571""}]"
DOID:0060572	"[""Ritscher-Schinzel syndrome 2""]"	"[{""label"":""CCDC22"",""id"":""28952""}]"	"[""28952""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060572""}]"
DOID:0060573	"[""von Willebrand's disease 1"",""VWD type 1"",""VWD1"",""von Willebrand disease type 1"",""von Willebrand disease type I""]"	"[{""label"":""ITGA2"",""id"":""3673""},{""label"":""ITGA2B"",""id"":""3674""},{""label"":""PLAT"",""id"":""5327""},{""label"":""VWF"",""id"":""7450""}]"	"[""3673"",""3674"",""5327"",""7450""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060573""}]"
DOID:0060574	"[""von Willebrand's disease 2"",""VWD type 2"",""VWD2"",""von Willebrand disease type 2"",""von Willebrand disease type II""]"	"[{""label"":""Vwf"",""id"":""22371""}]"	"[""22371""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060574""}]"
DOID:0060574	"[""von Willebrand's disease 2"",""VWD type 2"",""VWD2"",""von Willebrand disease type 2"",""von Willebrand disease type II""]"	"[{""label"":""ITGA2"",""id"":""3673""},{""label"":""VWF"",""id"":""7450""}]"	"[""3673"",""7450""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060574""}]"
DOID:0060575	"[""3MC syndrome 1""]"	"[{""label"":""MASP1"",""id"":""5648""}]"	"[""5648""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060575""}]"
DOID:0060576	"[""3MC syndrome 2""]"	"[{""label"":""COLEC11"",""id"":""78989""}]"	"[""78989""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060576""}]"
DOID:0060577	"[""3MC syndrome 3""]"	"[{""label"":""COLEC10"",""id"":""10584""}]"	"[""10584""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060577""}]"
DOID:0060578	"[""Noonan syndrome 1"",""NS1""]"	"[{""label"":""PTPN11"",""id"":""5781""}]"	"[""5781""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060578""}]"
DOID:0060578	"[""Noonan syndrome 1"",""NS1""]"	"[{""label"":""Ptpn11"",""id"":""19247""}]"	"[""19247""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060578""}]"
DOID:0060581	"[""Noonan syndrome 3"",""NS3""]"	"[{""label"":""Kras"",""id"":""16653""}]"	"[""16653""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060581""}]"
DOID:0060581	"[""Noonan syndrome 3"",""NS3""]"	"[{""label"":""KRAS"",""id"":""3845""}]"	"[""3845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060581""}]"
DOID:0060582	"[""Noonan syndrome 4"",""NS4""]"	"[{""label"":""SOS1"",""id"":""6654""}]"	"[""6654""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060582""}]"
DOID:0060583	"[""Noonan syndrome 5"",""NS5""]"	"[{""label"":""RAF1"",""id"":""5894""}]"	"[""5894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060583""}]"
DOID:0060584	"[""Noonan syndrome 6"",""NS6""]"	"[{""label"":""NRAS"",""id"":""4893""}]"	"[""4893""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060584""}]"
DOID:0060587	"[""Noonan syndrome 9"",""NS9""]"	"[{""label"":""SOS2"",""id"":""6655""}]"	"[""6655""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060587""}]"
DOID:0060589	"[""Yunis-Varon syndrome"",""cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia"",""cleidocranial dysplasia-micrognathia-absent thumbs syndrome""]"	"[{""label"":""FIG4"",""id"":""9896""}]"	"[""9896""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060589""}]"
DOID:0060589	"[""Yunis-Varon syndrome"",""cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia"",""cleidocranial dysplasia-micrognathia-absent thumbs syndrome""]"	"[{""label"":""FIG4"",""id"":""855392""}]"	"[""855392""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060589""}]"
DOID:0060591	"[""WHIM syndrome 1"",""WHIMS"",""warts, hypogammaglobulinemia, infections, and myelokathexis"",""warts-hypogammaglobulinemia-infections-myelokathexis syndrome""]"	"[{""label"":""CXCR4"",""id"":""7852""}]"	"[""7852""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060591""}]"
DOID:0060591	"[""WHIM syndrome 1"",""WHIMS"",""warts, hypogammaglobulinemia, infections, and myelokathexis"",""warts-hypogammaglobulinemia-infections-myelokathexis syndrome""]"	"[{""label"":""Cxcr4"",""id"":""12767""}]"	"[""12767""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060591""}]"
DOID:0060597	"[""atypical chronic myeloid leukemia, BCR-ABL1 negative"",""aCML"",""atypical CML"",""atypical chronic myeloid leukaemia"",""atypical chronic myeloid leukaemia BCR-ABL1 negative"",""atypical chronic myeloid leukemia BCR-ABL1 negative"",""subacute myeloid leukemia""]"	"[{""label"":""FGFR1"",""id"":""2260""}]"	"[""2260""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060597""}]"
DOID:0060599	"[""Nance-Horan syndrome""]"	"[{""label"":""NHS"",""id"":""4810""}]"	"[""4810""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060599""}]"
DOID:0060601	"[""alpha-2-plasmin inhibitor deficiency"",""antiplasmin defiency"",""plasmin inhibitor deficiency""]"	"[{""label"":""Serpinf2"",""id"":""18816""}]"	"[""18816""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060601""}]"
DOID:0060601	"[""alpha-2-plasmin inhibitor deficiency"",""antiplasmin defiency"",""plasmin inhibitor deficiency""]"	"[{""label"":""SERPINF2"",""id"":""5345""}]"	"[""5345""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060601""}]"
DOID:0060602	"[""alpha-methylacyl-CoA racemase deficiency"",""AMACR deficiency""]"	"[{""label"":""AMACR"",""id"":""23600""}]"	"[""23600""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060602""}]"
DOID:0060603	"[""isolated anhidrosis with normal sweat glands"",""Dann-Epstein-Sohar syndrome""]"	"[{""label"":""ITPR2"",""id"":""3709""}]"	"[""3709""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060603""}]"
DOID:0060604	"[""ankyloglossia"",""tongue-tie""]"	"[{""label"":""Lgr5"",""id"":""14160""}]"	"[""14160""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060604""}]"
DOID:0060609	"[""microcephalic osteodysplastic primordial dwarfism type II"",""Majewski osteodysplastic primordial dwarfism type II"",""osteodysplastic primordial dwarfism type II""]"	"[{""label"":""PCNT"",""id"":""5116""}]"	"[""5116""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060609""}]"
DOID:0060610	"[""megacystis-microcolon-intestinal hypoperistalsis syndrome"",""Berdon syndrome"",""Megacystis microcolon intestinal hypoperistalsis syndrome"",""megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH"",""visceral myopathy""]"	"[{""label"":""LMOD1"",""id"":""25802""},{""label"":""MYH11"",""id"":""4629""},{""label"":""MYL9"",""id"":""10398""},{""label"":""MYLK"",""id"":""4638""}]"	"[""10398"",""25802"",""4629"",""4638""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060610""}]"
DOID:0060610	"[""megacystis-microcolon-intestinal hypoperistalsis syndrome"",""Berdon syndrome"",""Megacystis microcolon intestinal hypoperistalsis syndrome"",""megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH"",""visceral myopathy""]"	"[{""label"":""Chrm3"",""id"":""12671""}]"	"[""12671""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060610""}]"
DOID:0060611	"[""abdominal obesity-metabolic syndrome""]"	"[{""label"":""Gucy2c"",""id"":""14917""},{""label"":""Lep"",""id"":""16846""},{""label"":""Neil1"",""id"":""72774""},{""label"":""Pparg"",""id"":""19016""},{""label"":""Prkci"",""id"":""18759""},{""label"":""Slc2a9"",""id"":""117591""}]"	"[""117591"",""14917"",""16846"",""18759"",""19016"",""72774""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060611""}]"
DOID:0060614	"[""ulnar-mammary syndrome"",""Pallister ulnar-mammary syndrome"",""Schinzel syndrome""]"	"[{""label"":""TBX3"",""id"":""6926""}]"	"[""6926""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060614""}]"
DOID:0060614	"[""ulnar-mammary syndrome"",""Pallister ulnar-mammary syndrome"",""Schinzel syndrome""]"	"[{""label"":""Tbx3"",""id"":""21386""}]"	"[""21386""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060614""}]"
DOID:0060639	"[""permanent neonatal diabetes mellitus"",""PDMI"",""PNDM"",""permanent diabetes mellitus of infancy""]"	"[{""label"":""Ins2"",""id"":""16334""},{""label"":""Kcnj11"",""id"":""16514""}]"	"[""16334"",""16514""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060639""}]"
DOID:0060639	"[""permanent neonatal diabetes mellitus"",""PDMI"",""PNDM"",""permanent diabetes mellitus of infancy""]"	"[{""label"":""ABCC8"",""id"":""6833""},{""label"":""GCK"",""id"":""2645""},{""label"":""INS"",""id"":""3630""},{""label"":""KCNJ11"",""id"":""3767""}]"	"[""2645"",""3630"",""3767"",""6833""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060639""}]"
DOID:0060642	"[""recessive dystrophic epidermolysis bullosa"",""RDEB, Hallopeau-Siemens type"",""autosomal recessive dystrophic epidermolysis bullosa generalisata gravis"",""autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type""]"	"[{""label"":""Col7a1"",""id"":""12836""},{""label"":""Grip1"",""id"":""74053""}]"	"[""12836"",""74053""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060642""}]"
DOID:0060643	"[""primary sclerosing cholangitis""]"	"[{""label"":""CFTR"",""id"":""1080""},{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""1080"",""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060643""}]"
DOID:0060643	"[""primary sclerosing cholangitis""]"	"[{""label"":""Abcb4"",""id"":""18670""}]"	"[""18670""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060643""}]"
DOID:0060645	"[""chronic recurrent multifocal osteomyelitis"",""CRMO"",""chronic multifocal osteomyelitis""]"	"[{""label"":""IL1R1"",""id"":""3554""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""LPIN2"",""id"":""9663""}]"	"[""3554"",""3557"",""9663""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060645""}]"
DOID:0060646	"[""congenital chylothorax""]"	"[{""label"":""Itga9"",""id"":""104099""}]"	"[""104099""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060646""}]"
DOID:0060647	"[""fetal encasement syndrome"",""cocoon syndrome""]"	"[{""label"":""CHUK"",""id"":""1147""}]"	"[""1147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060647""}]"
DOID:0060648	"[""anterior segment dysgenesis"",""anterior segment developmental anomaly"",""corneal opacification and other ocular anomalies"",""sclerocornea with other ocular anomalies""]"	"[{""label"":""Tsc1"",""id"":""64930""}]"	"[""64930""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060648""}]"
DOID:0060649	"[""congenital hereditary endothelial dystrophy of cornea"",""CHED""]"	"[{""label"":""Slc4a11"",""id"":""269356""}]"	"[""269356""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060649""}]"
DOID:0060649	"[""congenital hereditary endothelial dystrophy of cornea"",""CHED""]"	"[{""label"":""SLC4A11"",""id"":""83959""}]"	"[""83959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060649""}]"
DOID:0060650	"[""dicarboxylic aminoaciduria"",""glutamate-aspartate transport defect""]"	"[{""label"":""Slc1a1"",""id"":""20510""}]"	"[""20510""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060650""}]"
DOID:0060650	"[""dicarboxylic aminoaciduria"",""glutamate-aspartate transport defect""]"	"[{""label"":""SLC1A1"",""id"":""6505""}]"	"[""6505""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060650""}]"
DOID:0060651	"[""MYH-9 related disease""]"	"[{""label"":""Myh9"",""id"":""17886""}]"	"[""17886""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060651""}]"
DOID:0060651	"[""MYH-9 related disease""]"	"[{""label"":""MYH9"",""id"":""4627""}]"	"[""4627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060651""}]"
DOID:0060652	"[""familial erythrocytosis 1"",""ECYT1"",""autosomal dominant benign erythrocytosis"",""primary familial and congenital polycythemia""]"	"[{""label"":""EPOR"",""id"":""2057""}]"	"[""2057""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060652""}]"
DOID:0060653	"[""lethal congenital contracture syndrome 3"",""Israeli Bedouin type B multiple contracture syndrome""]"	"[{""label"":""PIP5K1C"",""id"":""23396""}]"	"[""23396""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060653""}]"
DOID:0060654	"[""lethal congenital contracture syndrome 4""]"	"[{""label"":""MYBPC1"",""id"":""4604""}]"	"[""4604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060654""}]"
DOID:0060656	"[""autosomal recessive congenital ichthyosis 1"",""ARCI1""]"	"[{""label"":""ABCA12"",""id"":""26154""}]"	"[""26154""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060656""}]"
DOID:0060668	"[""anencephaly""]"	"[{""label"":""Efna5"",""id"":""13640""}]"	"[""13640""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060668""}]"
DOID:0060668	"[""anencephaly""]"	"[{""label"":""NUAK2"",""id"":""81788""},{""label"":""RPGRIP1L"",""id"":""23322""}]"	"[""23322"",""81788""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060668""}]"
DOID:0060669	"[""cerebral cavernous malformation"",""cavernous angiomatous malformations"",""cerebral capillary malformations"",""familial cavernous angioma""]"	"[{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PON1"",""id"":""5444""}]"	"[""5290"",""5444""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060669""}]"
DOID:0060670	"[""cerebral cavernous malformation 2""]"	"[{""label"":""CCM2"",""id"":""83605""}]"	"[""83605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060670""}]"
DOID:0060672	"[""Grn-related frontotemporal lobar degeneration with Tdp43 inclusions""]"	"[{""label"":""Grn"",""id"":""14824""}]"	"[""14824""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060672""}]"
DOID:0060672	"[""Grn-related frontotemporal lobar degeneration with Tdp43 inclusions""]"	"[{""label"":""GRN"",""id"":""2896""}]"	"[""2896""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060672""}]"
DOID:0060673	"[""Peters anomaly""]"	"[{""label"":""CYP1B1"",""id"":""1545""}]"	"[""1545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060673""}]"
DOID:0060674	"[""catecholaminergic polymorphic ventricular tachycardia""]"	"[{""label"":""TRDN"",""id"":""10345""}]"	"[""10345""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060674""}]"
DOID:0060675	"[""catecholaminergic polymorphic ventricular tachycardia 1"",""CVPT1"",""arrhythmogenic right ventricular dysplasia 2""]"	"[{""label"":""Ryr2"",""id"":""20191""}]"	"[""20191""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060675""}]"
DOID:0060675	"[""catecholaminergic polymorphic ventricular tachycardia 1"",""CVPT1"",""arrhythmogenic right ventricular dysplasia 2""]"	"[{""label"":""RYR2"",""id"":""6262""}]"	"[""6262""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060675""}]"
DOID:0060676	"[""catecholaminergic polymorphic ventricular tachycardia 2"",""CVPT2""]"	"[{""label"":""Casq2"",""id"":""12373""}]"	"[""12373""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060676""}]"
DOID:0060676	"[""catecholaminergic polymorphic ventricular tachycardia 2"",""CVPT2""]"	"[{""label"":""CASQ2"",""id"":""845""}]"	"[""845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060676""}]"
DOID:0060679	"[""catecholaminergic polymorphic ventricular tachycardia 5"",""CVPT5""]"	"[{""label"":""TRDN"",""id"":""10345""}]"	"[""10345""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060679""}]"
DOID:0060680	"[""pigment dispersion syndrome"",""glaucoma-related pigment dispersion syndrome"",""pigment-dispersion type glaucoma""]"	"[{""label"":""Col18a1"",""id"":""12822""},{""label"":""Gpnmb"",""id"":""93695""}]"	"[""12822"",""93695""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060680""}]"
DOID:0060681	"[""autosomal dominant nocturnal frontal lobe epilepsy"",""ENFL""]"	"[{""label"":""CHRNB2"",""id"":""1141""}]"	"[""1141""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060681""}]"
DOID:0060682	"[""autosomal dominant nocturnal frontal lobe epilepsy 1"",""ENFL1"",""nocturnal frontal lobe epilepsy 1""]"	"[{""label"":""CHRNA4"",""id"":""1137""}]"	"[""1137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060682""}]"
DOID:0060684	"[""autosomal dominant nocturnal frontal lobe epilepsy 3"",""ENFL3"",""nocturnal frontal lobe epilepsy 3""]"	"[{""label"":""Chrnb2"",""id"":""11444""}]"	"[""11444""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060684""}]"
DOID:0060684	"[""autosomal dominant nocturnal frontal lobe epilepsy 3"",""ENFL3"",""nocturnal frontal lobe epilepsy 3""]"	"[{""label"":""CHRNB2"",""id"":""1141""}]"	"[""1141""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060684""}]"
DOID:0060685	"[""autosomal dominant nocturnal frontal lobe epilepsy 4"",""ENFL4"",""nocturnal frontal lobe epilepsy 4""]"	"[{""label"":""CHRNA2"",""id"":""1135""}]"	"[""1135""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060685""}]"
DOID:0060686	"[""autosomal dominant nocturnal frontal lobe epilepsy 5"",""ENFL5"",""nocturnal frontal lobe epilepsy 5""]"	"[{""label"":""KCNT1"",""id"":""57582""}]"	"[""57582""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060686""}]"
DOID:0060688	"[""arteriovenous malformations of the brain"",""cerebral arteriovenous malformation"",""intracranial arteriovenous malformation""]"	"[{""label"":""Acvrl1"",""id"":""11482""},{""label"":""Eng"",""id"":""13805""},{""label"":""Kras"",""id"":""16653""},{""label"":""Notch4"",""id"":""18132""}]"	"[""11482"",""13805"",""16653"",""18132""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060688""}]"
DOID:0060688	"[""arteriovenous malformations of the brain"",""cerebral arteriovenous malformation"",""intracranial arteriovenous malformation""]"	"[{""label"":""ENG"",""id"":""2022""},{""label"":""IL6"",""id"":""3569""},{""label"":""KRAS"",""id"":""3845""}]"	"[""2022"",""3569"",""3845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060688""}]"
DOID:0060690	"[""autosomal dominant auditory neuropathy 1"",""AUNA1"",""NSDAN"",""nonsyndromic dominant auditory neuropathy""]"	"[{""label"":""DIAPH3"",""id"":""81624""}]"	"[""81624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060690""}]"
DOID:0060691	"[""platelet-type bleeding disorder 16"",""autosomal dominant Glanzmann thrombasthenia"",""autosomal dominant thrombasthenia of Glanzmann and Naegeli""]"	"[{""label"":""Itga2b"",""id"":""16399""},{""label"":""Itgb3"",""id"":""16416""}]"	"[""16399"",""16416""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060691""}]"
DOID:0060691	"[""platelet-type bleeding disorder 16"",""autosomal dominant Glanzmann thrombasthenia"",""autosomal dominant thrombasthenia of Glanzmann and Naegeli""]"	"[{""label"":""ITGA2B"",""id"":""3674""},{""label"":""ITGB3"",""id"":""3690""}]"	"[""3674"",""3690""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060691""}]"
DOID:0060692	"[""platelet-type bleeding disorder 8"",""ADP platelet receptor P2Y12 defect"",""P2Y12 defect""]"	"[{""label"":""P2ry12"",""id"":""70839""}]"	"[""70839""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060692""}]"
DOID:0060692	"[""platelet-type bleeding disorder 8"",""ADP platelet receptor P2Y12 defect"",""P2Y12 defect""]"	"[{""label"":""P2RY12"",""id"":""64805""}]"	"[""64805""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060692""}]"
DOID:0060693	"[""Brunner Syndrome"",""monoamine oxidase A deficiency""]"	"[{""label"":""MAOA"",""id"":""4128""}]"	"[""4128""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060693""}]"
DOID:0060695	"[""hyperekplexia"",""Kok disease"",""congenital stiff man syndrome"",""familial startle disease"",""hereditary hyperekplexia"",""startle disease""]"	"[{""label"":""Glra1"",""id"":""14654""}]"	"[""14654""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060695""}]"
DOID:0060695	"[""hyperekplexia"",""Kok disease"",""congenital stiff man syndrome"",""familial startle disease"",""hereditary hyperekplexia"",""startle disease""]"	"[{""label"":""glra1"",""id"":""30676""}]"	"[""30676""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060695""}]"
DOID:0060696	"[""hyperekplexia 1"",""HKPX1""]"	"[{""label"":""Glra1"",""id"":""14654""}]"	"[""14654""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060696""}]"
DOID:0060696	"[""hyperekplexia 1"",""HKPX1""]"	"[{""label"":""GLRA1"",""id"":""2741""}]"	"[""2741""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060696""}]"
DOID:0060697	"[""hyperekplexia 2"",""HKPX2""]"	"[{""label"":""Glrb"",""id"":""14658""}]"	"[""14658""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060697""}]"
DOID:0060697	"[""hyperekplexia 2"",""HKPX2""]"	"[{""label"":""GLRB"",""id"":""2743""}]"	"[""2743""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060697""}]"
DOID:0060698	"[""hyperekplexia 3"",""HKPX3""]"	"[{""label"":""SLC6A5"",""id"":""9152""}]"	"[""9152""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060698""}]"
DOID:0060700	"[""familial hypocalciuric hypercalcemia 1"",""FHH type 1"",""HHC1"",""familial benign hypercalcemia 1"",""familial hypocalciuric hypercalcemia type I"",""hypocalciuric hypercalcemia type I""]"	"[{""label"":""Casr"",""id"":""12374""}]"	"[""12374""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060700""}]"
DOID:0060700	"[""familial hypocalciuric hypercalcemia 1"",""FHH type 1"",""HHC1"",""familial benign hypercalcemia 1"",""familial hypocalciuric hypercalcemia type I"",""hypocalciuric hypercalcemia type I""]"	"[{""label"":""CASR"",""id"":""846""}]"	"[""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060700""}]"
DOID:0060703	"[""Muenke Syndrome"",""FGFR3-related craniosynostosis""]"	"[{""label"":""FGFR3"",""id"":""2261""}]"	"[""2261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060703""}]"
DOID:0060704	"[""lymphoproliferative syndrome"",""Combined immunodeficiency due to ITK deficiency""]"	"[{""label"":""CD70"",""id"":""970""},{""label"":""FAS"",""id"":""355""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""STAT3"",""id"":""6774""}]"	"[""355"",""3813"",""6556"",""6774"",""970""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060704""}]"
DOID:0060705	"[""X-linked lymphoproliferative syndrome 1"",""XLP1""]"	"[{""label"":""SH2D1A"",""id"":""4068""}]"	"[""4068""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060705""}]"
DOID:0060706	"[""X-linked lymphoproliferative syndrome 2"",""XIAP deficiency"",""XLP2""]"	"[{""label"":""XIAP"",""id"":""331""}]"	"[""331""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060706""}]"
DOID:0060708	"[""lymphoproliferative syndrome 2"",""CD27 deficiency"",""LPFS2""]"	"[{""label"":""CD27"",""id"":""939""}]"	"[""939""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060708""}]"
DOID:0060710	"[""autosomal recessive congenital ichthyosis 2"",""ARCI2"",""BROCQ congenital ichthyosiform erythroderma nonbullous form"",""NCIE1"",""nonbullous congenital ichthyosiform erythroderma 1""]"	"[{""label"":""ALOX12B"",""id"":""242""}]"	"[""242""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060710""}]"
DOID:0060712	"[""autosomal recessive congenital ichthyosis 4A"",""ARCI4A"",""ICR2B"",""ichthyosis congenita IIB"",""lamellar ichthyosis 2""]"	"[{""label"":""ABCA12"",""id"":""26154""}]"	"[""26154""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060712""}]"
DOID:0060713	"[""autosomal recessive congenital ichthyosis 4B"",""ARCI4B"",""harlequin ichthyosis"",""harlequin type ichthyosis congenita"",""harlequin type ichthyosis fetalis""]"	"[{""label"":""ABCA12"",""id"":""26154""}]"	"[""26154""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060713""}]"
DOID:0060713	"[""autosomal recessive congenital ichthyosis 4B"",""ARCI4B"",""harlequin ichthyosis"",""harlequin type ichthyosis congenita"",""harlequin type ichthyosis fetalis""]"	"[{""label"":""Abca12"",""id"":""74591""},{""label"":""Cst6"",""id"":""73720""},{""label"":""Piga"",""id"":""18700""},{""label"":""Prss8"",""id"":""76560""}]"	"[""18700"",""73720"",""74591"",""76560""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060713""}]"
DOID:0060715	"[""autosomal recessive congenital ichthyosis 6"",""ARCI6""]"	"[{""label"":""NIPAL4"",""id"":""348938""}]"	"[""348938""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060715""}]"
DOID:0060717	"[""autosomal recessive congenital ichthyosis 8"",""ARCI8"",""lamellar ichthyosis 4"",""late-onset lamellar ichthyosis""]"	"[{""label"":""LIPN"",""id"":""643418""}]"	"[""643418""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060717""}]"
DOID:0060718	"[""autosomal recessive congenital ichthyosis 9"",""ARCI9""]"	"[{""label"":""CERS3"",""id"":""204219""}]"	"[""204219""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060718""}]"
DOID:0060720	"[""autosomal recessive congenital ichthyosis 11"",""IFAH syndrome"",""IHS"",""autosomal recessive ichthyosis with hypotrichosis"",""hypotrichosis-congenital ichthyosis syndrome"",""ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis"",""ichthyosis-follicular atrophoderma-hypotrichosis syndrome"",""ichthyosis-follicular atrophoderma-hypotrichosis-hypohidrosis syndrome"",""ichthyosis-hypotrichosis syndrome""]"	"[{""label"":""ST14"",""id"":""6768""}]"	"[""6768""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060720""}]"
DOID:0060728	"[""congenital disorder of deglycosylation 1"",""NGLY1-CDDG"",""NGLY1-deficiency"",""congenital disorder of glycosylation type Iv"",""deficiency of N-glycanase 1""]"	"[{""label"":""NGLY1"",""id"":""55768""}]"	"[""55768""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060728""}]"
DOID:0060730	"[""torsion dystonia 1"",""dystonia musculorum deformans""]"	"[{""label"":""ooc-5"",""id"":""174433""}]"	"[""174433""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060730""}]"
DOID:0060730	"[""torsion dystonia 1"",""dystonia musculorum deformans""]"	"[{""label"":""Tor1a"",""id"":""30931""}]"	"[""30931""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060730""}]"
DOID:0060730	"[""torsion dystonia 1"",""dystonia musculorum deformans""]"	"[{""label"":""TOR1A"",""id"":""1861""}]"	"[""1861""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060730""}]"
DOID:0060731	"[""congenital central hypoventilation syndrome"",""CCHS"",""Ondine curse"",""Ondine syndrome"",""central congenital hypoventilation syndrome"",""congenital central alveolar hypoventilation syndrome""]"	"[{""label"":""BDNF"",""id"":""627""}]"	"[""627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060731""}]"
DOID:0060732	"[""chromosome 9p deletion syndrome"",""9p syndrome"",""Alfi syndrome"",""monosomy 9p syndrome""]"	"[{""label"":""Frem1"",""id"":""329872""}]"	"[""329872""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060732""}]"
DOID:0060733	"[""junctional epidermolysis bullosa with pyloric atresia"",""Carmi syndrome"",""JEB-PA"",""epidermolysis bullosa junctionalis with pyloric atresia"",""junctional epidermolysis bullosa-pyloric atresia syndrome""]"	"[{""label"":""ITGA6"",""id"":""3655""},{""label"":""ITGB4"",""id"":""3691""}]"	"[""3655"",""3691""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060733""}]"
DOID:0060733	"[""junctional epidermolysis bullosa with pyloric atresia"",""Carmi syndrome"",""JEB-PA"",""epidermolysis bullosa junctionalis with pyloric atresia"",""junctional epidermolysis bullosa-pyloric atresia syndrome""]"	"[{""label"":""Itgb4"",""id"":""192897""}]"	"[""192897""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060733""}]"
DOID:0060735	"[""epidermolysis bullosa simplex Dowling-Meara type"",""EBS-gen sev"",""EBSDM"",""epidermolysis bullosa herpetiformis Dowling-Meara type"",""epidermolysis bullosa simplex, herpetiformis"",""generalized severe epidermolysis bullosa simplex""]"	"[{""label"":""Krt5"",""id"":""110308""}]"	"[""110308""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060735""}]"
DOID:0060736	"[""epidermolysis bullosa simplex Ogna type"",""EBS-O"",""EBS-Og"",""EBSOG""]"	"[{""label"":""PLEC"",""id"":""5339""}]"	"[""5339""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060736""}]"
DOID:0060736	"[""epidermolysis bullosa simplex Ogna type"",""EBS-O"",""EBS-Og"",""EBSOG""]"	"[{""label"":""Plec"",""id"":""18810""}]"	"[""18810""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060736""}]"
DOID:0060737	"[""junctional epidermolysis bullosa Herlitz type"",""Herlitz type epidermolysis bullosa junctionalis"",""Herlitz-Pearson-type epidermolysis bullosa"",""JEB-H"",""JEB-Herlitz type"",""epidermolysis bullosa letalis"",""junctional epidermolysis bullosa generalisata gravis"",""junctional epidermolysis bullosa, Herlitz-Pearson type""]"	"[{""label"":""Itga6"",""id"":""16403""},{""label"":""Lamb3"",""id"":""16780""},{""label"":""Lamc2"",""id"":""16782""}]"	"[""16403"",""16780"",""16782""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060737""}]"
DOID:0060738	"[""junctional epidermolysis bullosa non-Herlitz type"",""GABEB"",""JEB-nH gen"",""JEN-nH"",""generalized atrophic benign epidermolysis bullosa"",""generalized junctional epidermolysis bullosa, non-Herlitz type"",""junctional epidermolysis bullosa generalisata mitis"",""junctional epidermolysis bullosa, Disentis type""]"	"[{""label"":""Col17a1"",""id"":""12821""},{""label"":""Itgb4"",""id"":""192897""},{""label"":""Lama3"",""id"":""16774""},{""label"":""Lamb3"",""id"":""16780""},{""label"":""Lamc2"",""id"":""16782""}]"	"[""12821"",""16774"",""16780"",""16782"",""192897""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060738""}]"
DOID:0060740	"[""methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency"",""methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency"",""methylmalonic aciduria mut type"",""vitamin B12-unresponsive methylmalonic aciduria""]"	"[{""label"":""MMUT"",""id"":""4594""}]"	"[""4594""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060740""}]"
DOID:0060740	"[""methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency"",""methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency"",""methylmalonic aciduria mut type"",""vitamin B12-unresponsive methylmalonic aciduria""]"	"[{""label"":""Mmut"",""id"":""17850""}]"	"[""17850""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060740""}]"
DOID:0060741	"[""methylmalonic acidemia due to transcobalamin receptor defect"",""methylmalonic acidemia, TCblR type"",""methylmalonic aciduria due to transcobalamin receptor defect""]"	"[{""label"":""Cd320"",""id"":""54219""}]"	"[""54219""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060741""}]"
DOID:0060741	"[""methylmalonic acidemia due to transcobalamin receptor defect"",""methylmalonic acidemia, TCblR type"",""methylmalonic aciduria due to transcobalamin receptor defect""]"	"[{""label"":""CD320"",""id"":""51293""}]"	"[""51293""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060741""}]"
DOID:0060743	"[""methylmalonic acidemia cblB type"",""methylmalonic aciduria cblB type"",""methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type""]"	"[{""label"":""MMAB"",""id"":""326625""}]"	"[""326625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060743""}]"
DOID:0060745	"[""Doyne honeycomb retinal dystrophy"",""DHRD"",""Doyne honeycomb degeneration of retina""]"	"[{""label"":""Efemp1"",""id"":""216616""}]"	"[""216616""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060745""}]"
DOID:0060745	"[""Doyne honeycomb retinal dystrophy"",""DHRD"",""Doyne honeycomb degeneration of retina""]"	"[{""label"":""EFEMP1"",""id"":""2202""}]"	"[""2202""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060745""}]"
DOID:0060746	"[""basal laminar drusen"",""cuticular drusen"",""drusen of bruch membrane"",""early adult-onset grouped drusen""]"	"[{""label"":""CFH"",""id"":""3075""}]"	"[""3075""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060746""}]"
DOID:0060747	"[""Duane-radial ray syndrome"",""DR syndrome"",""Duane anomaly with radial ray abnormalities and deafness"",""Okihiro syndrome"",""acrorenocular syndrome""]"	"[{""label"":""Sall4"",""id"":""99377""}]"	"[""99377""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060747""}]"
DOID:0060747	"[""Duane-radial ray syndrome"",""DR syndrome"",""Duane anomaly with radial ray abnormalities and deafness"",""Okihiro syndrome"",""acrorenocular syndrome""]"	"[{""label"":""SALL4"",""id"":""57167""}]"	"[""57167""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060747""}]"
DOID:0060748	"[""familial temporal lobe epilepsy 1"",""ETL1"",""partial epilepsy with auditory features""]"	"[{""label"":""Lgi1"",""id"":""56839""}]"	"[""56839""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060748""}]"
DOID:0060748	"[""familial temporal lobe epilepsy 1"",""ETL1"",""partial epilepsy with auditory features""]"	"[{""label"":""LGI1"",""id"":""9211""}]"	"[""9211""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060748""}]"
DOID:0060751	"[""familial temporal lobe epilepsy 7"",""ETL7""]"	"[{""label"":""RELN"",""id"":""5649""}]"	"[""5649""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060751""}]"
DOID:0060752	"[""familial temporal lobe epilepsy 5"",""ETL5""]"	"[{""label"":""CPA6"",""id"":""57094""}]"	"[""57094""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060752""}]"
DOID:0060754	"[""familial temporal lobe epilepsy 8"",""ETL8""]"	"[{""label"":""GAL"",""id"":""51083""}]"	"[""51083""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060754""}]"
DOID:0060756	"[""sclerosteosis 1"",""SOST1""]"	"[{""label"":""Sost"",""id"":""74499""}]"	"[""74499""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060756""}]"
DOID:0060756	"[""sclerosteosis 1"",""SOST1""]"	"[{""label"":""SOST"",""id"":""50964""}]"	"[""50964""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060756""}]"
DOID:0060757	"[""sclerosteosis 2"",""SOST2""]"	"[{""label"":""Lrp4"",""id"":""228357""}]"	"[""228357""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060757""}]"
DOID:0060757	"[""sclerosteosis 2"",""SOST2""]"	"[{""label"":""LRP4"",""id"":""4038""}]"	"[""4038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060757""}]"
DOID:0060759	"[""immunodeficiency with hyper IgM type 5"",""HIGM5"",""hyper-IgM syndrome 5"",""hyper-IgM syndrome due to UNG deficiency"",""hyper-IgM syndrome due to uracil N-glycosylase""]"	"[{""label"":""UNG"",""id"":""7374""}]"	"[""7374""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060759""}]"
DOID:0060762	"[""restrictive dermopathy"",""Infantile restrictive dermopathy"",""Lethal tight skin contracture syndrome"",""hyperkeratosis-contracture syndrome"",""lethal restrictive dermopathy"",""tight skin contracture syndrome""]"	"[{""label"":""Fst"",""id"":""14313""}]"	"[""14313""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060762""}]"
DOID:0060764	"[""autosomal recessive Robinow syndrome"",""COVESDEM syndrome"",""RRS"",""costovertebral segmentation defect-mesomelia syndrome""]"	"[{""label"":""Ror2"",""id"":""26564""}]"	"[""26564""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060764""}]"
DOID:0060764	"[""autosomal recessive Robinow syndrome"",""COVESDEM syndrome"",""RRS"",""costovertebral segmentation defect-mesomelia syndrome""]"	"[{""label"":""ROR2"",""id"":""4920""}]"	"[""4920""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060764""}]"
DOID:0060765	"[""autosomal dominant Robinow syndrome 2"",""DRS2""]"	"[{""label"":""DVL1"",""id"":""1855""}]"	"[""1855""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060765""}]"
DOID:0060766	"[""autosomal dominant Robinow syndrome 1"",""DRS1""]"	"[{""label"":""WNT5A"",""id"":""7474""}]"	"[""7474""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060766""}]"
DOID:0060767	"[""autosomal dominant Robinow syndrome 3"",""DRS3""]"	"[{""label"":""DVL3"",""id"":""1857""}]"	"[""1857""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060767""}]"
DOID:0060768	"[""Smith-Magenis syndrome"",""17p11.2 microdeletion syndrome"",""chromosome 17p11.2 deletion syndrome""]"	"[{""label"":""RAI1"",""id"":""10743""}]"	"[""10743""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060768""}]"
DOID:0060768	"[""Smith-Magenis syndrome"",""17p11.2 microdeletion syndrome"",""chromosome 17p11.2 deletion syndrome""]"	"[{""label"":""Rai1"",""id"":""19377""}]"	"[""19377""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060768""}]"
DOID:0060770	"[""dextro-looped transposition of the great arteries"",""D-TGA"",""DTGA1"",""congenitally uncorrected transposition of the great arteries"",""congenitally uncorrected transposition of the great vessels"",""isolated ventriculoarterial discordance"",""ventriculoarterial discordance with atrioventricular concordance""]"	"[{""label"":""Cfc1"",""id"":""12627""},{""label"":""Hspg2"",""id"":""15530""}]"	"[""12627"",""15530""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060770""}]"
DOID:0060770	"[""dextro-looped transposition of the great arteries"",""D-TGA"",""DTGA1"",""congenitally uncorrected transposition of the great arteries"",""congenitally uncorrected transposition of the great vessels"",""isolated ventriculoarterial discordance"",""ventriculoarterial discordance with atrioventricular concordance""]"	"[{""label"":""MED13L"",""id"":""23389""},{""label"":""SLC19A1"",""id"":""6573""}]"	"[""23389"",""6573""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060770""}]"
DOID:0060772	"[""multiple types of congenital heart defects 6"",""DTGA3"",""dextro-looped transposition of the great arteries 3""]"	"[{""label"":""GDF1"",""id"":""2657""}]"	"[""2657""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060772""}]"
DOID:0060773	"[""cleft lip-palate-ectodermal dysplasia syndrome"",""CLPED1"",""Margarita type of ectodermal dysplasia"",""Zlotogora-Zilberman-Tenenbaum syndrome"",""cleft lip/palate-syndactyly-pili torti syndrome"",""syndactyly-ectodermal dysplasia-cleft/lip palate""]"	"[{""label"":""NECTIN1"",""id"":""5818""}]"	"[""5818""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060773""}]"
DOID:0060774	"[""congenital diarrhea""]"	"[{""label"":""ACSL5"",""id"":""51703""},{""label"":""PLVAP"",""id"":""83483""},{""label"":""WNT2B"",""id"":""7482""}]"	"[""51703"",""7482"",""83483""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060774""}]"
DOID:0060776	"[""congenital diarrhea 5 with tufting enteropathy"",""DIAR5"",""congenital diarrhoea 5 with tufting enteropathy"",""congenital familial intractable diarrhea with epithelial or epithelium abnormalities"",""congenital familial intractable diarrhoea with epithelial or epithelium abnormalities"",""congenital tufting enteropathy"",""tufting enteropathy""]"	"[{""label"":""EPCAM"",""id"":""4072""}]"	"[""4072""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060776""}]"
DOID:0060776	"[""congenital diarrhea 5 with tufting enteropathy"",""DIAR5"",""congenital diarrhoea 5 with tufting enteropathy"",""congenital familial intractable diarrhea with epithelial or epithelium abnormalities"",""congenital familial intractable diarrhoea with epithelial or epithelium abnormalities"",""congenital tufting enteropathy"",""tufting enteropathy""]"	"[{""label"":""Epcam"",""id"":""17075""}]"	"[""17075""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060776""}]"
DOID:0060777	"[""congenital secretory sodium diarrhea 8"",""DIAR8""]"	"[{""label"":""SLC9A3"",""id"":""6550""}]"	"[""6550""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060777""}]"
DOID:0060778	"[""congenital diarrhea 7 with exudative enteropathy"",""congenital chronic diarrhea with exudative enteropathy"",""congenital chronic diarrhea with protein-losing enteropathy"",""congenital chronic diarrhoea with exudative enteropathy"",""congenital chronic diarrhoea with protein-losing enteropathy"",""congenital diarrhoea 7 with exudative enteropathy""]"	"[{""label"":""DGAT1"",""id"":""8694""}]"	"[""8694""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060778""}]"
DOID:0060780	"[""congenital diarrhea 6"",""chronic diarrhea due to guanylate cyclase 2C overactivity"",""chronic diarrhoea due to guanylate cyclase 2C overactivity"",""congenital diarrhoea 6""]"	"[{""label"":""GUCY2C"",""id"":""2984""}]"	"[""2984""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060780""}]"
DOID:0060781	"[""congenital secretory sodium diarrhea 3"",""congenital secretory sodium diarrhea 3 syndromic"",""congenital secretory sodium diarrhea 3 with or without other congenital anomalies"",""congenital secretory sodium diarrhoea 3"",""congenital secretory sodium diarrhoea 3 syndromic"",""congenital secretory sodium diarrhoea 3 with or without other congenital anomalies""]"	"[{""label"":""SPINT2"",""id"":""10653""}]"	"[""10653""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060781""}]"
DOID:0060785	"[""typical adult-onset autosomal dominant demyelinating leukodystrophy"",""ADLD"",""adult-onset autosomal dominant leukodystrophy"",""autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease""]"	"[{""label"":""Lmnb1"",""id"":""16906""}]"	"[""16906""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060785""}]"
DOID:0060785	"[""typical adult-onset autosomal dominant demyelinating leukodystrophy"",""ADLD"",""adult-onset autosomal dominant leukodystrophy"",""autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease""]"	"[{""label"":""LMNB1"",""id"":""4001""}]"	"[""4001""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060785""}]"
DOID:0060787	"[""hypomyelinating leukodystrophy 2"",""HLD2"",""PMLD1"",""Pelizaeus-Merzbacher-like disease 1"",""Pelizaeus-Merzbacher-like disease due to GJC2 mutation""]"	"[{""label"":""GJC2"",""id"":""57165""}]"	"[""57165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060787""}]"
DOID:0060788	"[""hypomyelinating leukodystrophy 10"",""HLD10""]"	"[{""label"":""PYCR2"",""id"":""29920""}]"	"[""29920""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060788""}]"
DOID:0060789	"[""hypomyelinating leukodystrophy 4"",""HLD4"",""MitCHAP60 disease"",""Pelizaeus-Merzbacher-like disease due to HSPD1 mutation"",""mitochondrial HSP60 chaperonopathy""]"	"[{""label"":""HSPD1"",""id"":""3329""}]"	"[""3329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060789""}]"
DOID:0060790	"[""hypomyelinating leukodystrophy 3"",""HLD3"",""Pelizaeus-Merzbacher-like disease due to AIMP1 mutation""]"	"[{""label"":""AIMP1"",""id"":""9255""}]"	"[""9255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060790""}]"
DOID:0060793	"[""hypomyelinating leukodystrophy 5"",""HLD5"",""hypomyelination-congenital cataract syndrome""]"	"[{""label"":""HYCC1"",""id"":""84668""}]"	"[""84668""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060793""}]"
DOID:0060794	"[""hypomyelinating leukodystrophy 7"",""HLD7"",""TACH syndrome"",""ataxia-delayed dentition-hypomyelination syndrome; odontoleukodystrophy"",""dentoleukoencephalopathy"",""hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome"",""leukodystrophy with oligodontia"",""leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome"",""tremor-ataxia-central hypomyelination syndrome""]"	"[{""label"":""POLR3A"",""id"":""11128""}]"	"[""11128""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060794""}]"
DOID:0060796	"[""hypomyelinating leukodystrophy 12"",""HLD12""]"	"[{""label"":""VPS11"",""id"":""55823""}]"	"[""55823""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060796""}]"
DOID:0060797	"[""hypomyelinating leukodystrophy 8"",""HLD8""]"	"[{""label"":""POLR3B"",""id"":""55703""}]"	"[""55703""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060797""}]"
DOID:0060798	"[""hypomyelinating leukodystrophy 6"",""H-ABC"",""HABC"",""HLD6"",""hypomyelinating leukodystrophy with atrophy of the basal ganglia and cerebellum"",""hypomyelination with atrophy of basal ganglia and cerebellum""]"	"[{""label"":""Tubb4a"",""id"":""22153""}]"	"[""22153""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060798""}]"
DOID:0060798	"[""hypomyelinating leukodystrophy 6"",""H-ABC"",""HABC"",""HLD6"",""hypomyelinating leukodystrophy with atrophy of the basal ganglia and cerebellum"",""hypomyelination with atrophy of basal ganglia and cerebellum""]"	"[{""label"":""TUBB4A"",""id"":""10382""}]"	"[""10382""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060798""}]"
DOID:0060799	"[""syndromic X-linked intellectual disability Lubs type"",""Lubs X-linked mental retardation syndrome"",""MECP2 duplication syndrome"",""MRXSL"",""X-linked intellectual disability-hypotonia-recurrent Infections syndrome"",""mental retardation, X-linked, syndromic, Lubs type"",""mental retardation, X-linked, with recurrent respiratory infections""]"	"[{""label"":""MECP2"",""id"":""4204""}]"	"[""4204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060799""}]"
DOID:0060801	"[""MEHMO syndrome"",""MRXS20"",""MRXS25"",""X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome"",""mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity"",""syndromic X-linked mental retardation 20"",""syndromic X-linked mental retardation 25""]"	"[{""label"":""EIF2S3"",""id"":""1968""}]"	"[""1968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060801""}]"
DOID:0060805	"[""Prieto syndrome"",""Prieto-Badia-Mulas syndrome"",""X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome""]"	"[{""label"":""WNK3"",""id"":""65267""}]"	"[""65267""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060805""}]"
DOID:0060806	"[""syndromic X-linked intellectual disability Hedera type"",""MRXE"",""MRXSH"",""X-linked mental retardation with epilepsy"",""mental retardation, X-linked, syndromic, Hedera type""]"	"[{""label"":""ARX"",""id"":""170302""},{""label"":""ATP6AP2"",""id"":""10159""}]"	"[""10159"",""170302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060806""}]"
DOID:0060807	"[""syndromic X-linked intellectual disability Najm type"",""MICPCH"",""X-linked intellectual disability-microcephaly-pontocerebellar hypoplasia syndrome"",""mental retardation and microcephaly with pontine and cerebellar hypoplasia""]"	"[{""label"":""HRR25"",""id"":""855897""}]"	"[""855897""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060807""}]"
DOID:0060807	"[""syndromic X-linked intellectual disability Najm type"",""MICPCH"",""X-linked intellectual disability-microcephaly-pontocerebellar hypoplasia syndrome"",""mental retardation and microcephaly with pontine and cerebellar hypoplasia""]"	"[{""label"":""CASK"",""id"":""8573""}]"	"[""8573""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060807""}]"
DOID:0060810	"[""syndromic X-linked intellectual disability type 10"",""HSD10 deficiency, atypical type"",""HSD10 disease, atypical type"",""MRXS10"",""X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome"",""mental retardation, X-linked syndromic 10""]"	"[{""label"":""HSD17B10"",""id"":""3028""}]"	"[""3028""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060810""}]"
DOID:0060811	"[""syndromic X-linked intellectual disability Turner type"",""Brooks-Wisniewski-Brown syndrome"",""MRXST"",""X-linked intellectual disability, Brooks type"",""mental retardation and macrocephaly syndrome"",""mental retardation, X-linked syndromic, Turner type""]"	"[{""label"":""HUWE1"",""id"":""10075""}]"	"[""10075""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060811""}]"
DOID:0060812	"[""syndromic X-linked intellectual disability Siderius type"",""MRXSSD"",""Siderius X-linked mental retardation syndrome"",""Siderius-Hamel syndrome"",""mental retardation syndrome, X-linked, Siderius type""]"	"[{""label"":""PHF8"",""id"":""23133""}]"	"[""23133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060812""}]"
DOID:0060812	"[""syndromic X-linked intellectual disability Siderius type"",""MRXSSD"",""Siderius X-linked mental retardation syndrome"",""Siderius-Hamel syndrome"",""mental retardation syndrome, X-linked, Siderius type""]"	"[{""label"":""Phf8"",""id"":""320595""}]"	"[""320595""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060812""}]"
DOID:0060814	"[""Wilson-Turner syndrome"",""MRXS6"",""WTS"",""X-linked intellectual disability-gynecomastia-obesity syndrome"",""mental retardation, X-linked, syndromic 6"",""mental retardation, X-linked, with gynecomastia and obesity""]"	"[{""label"":""LAS1L"",""id"":""81887""}]"	"[""81887""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060814""}]"
DOID:0060817	"[""syndromic X-linked intellectual disability 34"",""MRXS34"",""MRXSML"",""macrocephaly-intellectual disability-left ventricular non compaction syndrome"",""mental retardation, X-linked, syndromic 34"",""syndromic X-linked mental retardation Mircsof-Langouet type""]"	"[{""label"":""NONO"",""id"":""4841""}]"	"[""4841""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060817""}]"
DOID:0060821	"[""syndromic X-linked intellectual disability 14"",""mental retardation, X-linked, syndromic 14""]"	"[{""label"":""UPF3B"",""id"":""65109""}]"	"[""65109""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060821""}]"
DOID:0060822	"[""syndromic X-linked intellectual disability Cabezas type"",""Cabezas syndrome; syndromic X-linked mental retardation 15"",""MRSS"",""MRXS15"",""MRXSC"",""X-linked mental retardation with short stature"",""X-linked mental retardation with short stature, hypogonadism, and abnormal gait"",""mental retardation, X-linked, syndromic 15"",""mental retardation, X-linked, syndromic 15 (Cabezas type)""]"	"[{""label"":""CUL4B"",""id"":""8450""}]"	"[""8450""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060822""}]"
DOID:0060823	"[""syndromic X-linked intellectual disability 94"",""MRX94"",""MRXS29"",""mental retardation, X-linked 94"",""syndromic X-linked intellectual disability due to GRIA3 anomalies"",""syndromic X-linked mental retardation 29"",""syndromic X-linked mental retardation Wu type""]"	"[{""label"":""GRIA3"",""id"":""2892""}]"	"[""2892""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060823""}]"
DOID:0060825	"[""Christianson syndrome"",""MRXSCH"",""X-linked Angelman-like syndrome"",""X-linked intellectual disability, South African type"",""X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome"",""mental retardation, X-linked syndromic, Christianson type"",""mental retardation, microcephaly, epilepsy, and ataxia syndrome""]"	"[{""label"":""Slc9a6"",""id"":""236794""}]"	"[""236794""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060825""}]"
DOID:0060825	"[""Christianson syndrome"",""MRXSCH"",""X-linked Angelman-like syndrome"",""X-linked intellectual disability, South African type"",""X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome"",""mental retardation, X-linked syndromic, Christianson type"",""mental retardation, microcephaly, epilepsy, and ataxia syndrome""]"	"[{""label"":""SLC9A6"",""id"":""10479""}]"	"[""10479""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060825""}]"
DOID:0060826	"[""syndromic X-linked intellectual disability Shashi type"",""MRXS11"",""SMRXS"",""Shashi X-linked mental retardation syndrome"",""X-linked mental retardation Shashi type"",""mental retardation, X-linked, syndromic 11, Shashi type"",""syndromic X-linked intellectual disability type 11""]"	"[{""label"":""RBMX"",""id"":""27316""}]"	"[""27316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060826""}]"
DOID:0060827	"[""X-linked intellectual disability-psychosis-macroorchidism syndrome"",""Lindsay-Burn syndrome"",""MRXS13"",""PPM-X"",""X-linked mental retardation 79"",""X-linked mental retardation with spasticity"",""mental retardation with psychosis, pyramidal signs, and macroorchidism"",""mental retardation, X-linked, syndromic 13""]"	"[{""label"":""MECP2"",""id"":""4204""}]"	"[""4204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060827""}]"
DOID:0060832	"[""Griscelli syndrome type 1"",""GS1"",""Griscelli syndrome with neurological impairment"",""Griscelli syndrome, cutaneous and neurological type"",""Griscelli-Prunieras syndrome type 1"",""hypopigmentation-neurologic impairment syndrome""]"	"[{""label"":""MYO5A"",""id"":""4644""}]"	"[""4644""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060832""}]"
DOID:0060832	"[""Griscelli syndrome type 1"",""GS1"",""Griscelli syndrome with neurological impairment"",""Griscelli syndrome, cutaneous and neurological type"",""Griscelli-Prunieras syndrome type 1"",""hypopigmentation-neurologic impairment syndrome""]"	"[{""label"":""Myo5a"",""id"":""17918""}]"	"[""17918""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060832""}]"
DOID:0060835	"[""isolated microphthalmia 6"",""MCOP6"",""posterior nonsyndromic microphthalmia""]"	"[{""label"":""Prss56"",""id"":""69453""}]"	"[""69453""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060835""}]"
DOID:0060835	"[""isolated microphthalmia 6"",""MCOP6"",""posterior nonsyndromic microphthalmia""]"	"[{""label"":""PRSS56"",""id"":""646960""}]"	"[""646960""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060835""}]"
DOID:0060836	"[""isolated microphthalmia 4"",""MCOP4""]"	"[{""label"":""GDF6"",""id"":""392255""}]"	"[""392255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060836""}]"
DOID:0060837	"[""isolated microphthalmia 5"",""MCOP5"",""microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome"",""posterior microphthalmia with retinitis pigmentosa, foveoschisis and optic disc drusen""]"	"[{""label"":""MFRP"",""id"":""83552""}]"	"[""83552""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060837""}]"
DOID:0060838	"[""isolated microphthalmia 7"",""MCOP7""]"	"[{""label"":""GDF3"",""id"":""9573""}]"	"[""9573""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060838""}]"
DOID:0060841	"[""isolated microphthalmia 8"",""MCOP8""]"	"[{""label"":""ALDH1A3"",""id"":""220""}]"	"[""220""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060841""}]"
DOID:0060843	"[""hereditary neuropathy with liability to pressure palsies"",""HNPP"",""current pressure-sensitive neuropathy"",""familial recurrent polyneuropathy"",""heterozygous microdeletion 17p11.2p12"",""potato-grubbing palsy"",""tomaculous neuropathy"",""tulip-bulb digger's palsy""]"	"[{""label"":""PMP22"",""id"":""5376""}]"	"[""5376""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060843""}]"
DOID:0060843	"[""hereditary neuropathy with liability to pressure palsies"",""HNPP"",""current pressure-sensitive neuropathy"",""familial recurrent polyneuropathy"",""heterozygous microdeletion 17p11.2p12"",""potato-grubbing palsy"",""tomaculous neuropathy"",""tulip-bulb digger's palsy""]"	"[{""label"":""Pmp22"",""id"":""18858""}]"	"[""18858""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060843""}]"
DOID:0060844	"[""Norrie disease"",""Episkopi blindness"",""Norrie-Warburg disease"",""atrophia bulborum hereditaria""]"	"[{""label"":""Fzd4"",""id"":""14366""}]"	"[""14366""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060844""}]"
DOID:0060848	"[""developmental and epileptic encephalopathy 9"",""DEE9"",""EFMR"",""EIEE9"",""Juberg Hellman syndrome"",""early infantile epileptic encephalopathy 9"",""early infantile female-limited epilecptic encephalopathy"",""female restricted epilepsy with mental retardation""]"	"[{""label"":""PCDH19"",""id"":""57526""}]"	"[""57526""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060848""}]"
DOID:0060849	"[""osteoporosis-pseudoglioma syndrome"",""OPPG"",""ocular form of osteogenesis imperfecta""]"	"[{""label"":""LRP5"",""id"":""4041""}]"	"[""4041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060849""}]"
DOID:0060849	"[""osteoporosis-pseudoglioma syndrome"",""OPPG"",""ocular form of osteogenesis imperfecta""]"	"[{""label"":""Lrp5"",""id"":""16973""}]"	"[""16973""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060849""}]"
DOID:0060850	"[""annular pancreas""]"	"[{""label"":""Gdf1"",""id"":""14559""},{""label"":""Ihh"",""id"":""16147""}]"	"[""14559"",""16147""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060850""}]"
DOID:0060851	"[""pemphigus vulgaris"",""familial pemphigus vulgaris""]"	"[{""label"":""Dsg3"",""id"":""13512""}]"	"[""13512""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060851""}]"
DOID:0060851	"[""pemphigus vulgaris"",""familial pemphigus vulgaris""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060851""}]"
DOID:0060852	"[""Pierson syndrome"",""microcoria-congenital nephrosis syndrome""]"	"[{""label"":""LAMB2"",""id"":""3913""}]"	"[""3913""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060852""}]"
DOID:0060852	"[""Pierson syndrome"",""microcoria-congenital nephrosis syndrome""]"	"[{""label"":""Lamb2"",""id"":""16779""},{""label"":""Tns2"",""id"":""209039""}]"	"[""16779"",""209039""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060852""}]"
DOID:0060853	"[""Potocki-Lupski syndrome"",""17p11.2 microduplication syndrome"",""chromosome 17p11.2 duplication syndrome"",""trisomy 17p11.2""]"	"[{""label"":""Rai1"",""id"":""19377""}]"	"[""19377""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060853""}]"
DOID:0060854	"[""autosomal recessive pseudohypoaldosteronism type 1"",""PHA1B"",""autosomal recessive PHA 1""]"	"[{""label"":""Scnn1b"",""id"":""20277""},{""label"":""Scnn1g"",""id"":""20278""}]"	"[""20277"",""20278""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060854""}]"
DOID:0060855	"[""autosomal dominant pseudohypoaldosteronism type 1"",""PHA1A"",""autosomal dominant PHA 1""]"	"[{""label"":""NR3C2"",""id"":""4306""}]"	"[""4306""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060855""}]"
DOID:0060856	"[""right atrial isomerism"",""Ivemark syndrome"",""asplenia with cardiovascular anomalies""]"	"[{""label"":""Acvr2b"",""id"":""11481""},{""label"":""Cfc1"",""id"":""12627""}]"	"[""11481"",""12627""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060856""}]"
DOID:0060859	"[""salmonellosis"",""Salmonella infection""]"	"[{""label"":""IL12B"",""id"":""3593""}]"	"[""3593""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060859""}]"
DOID:0060861	"[""microphthalmia with limb anomalies"",""MLA"",""OAS"",""Waardenburg anophthalmia syndrome"",""anophthalmia-syndactyly syndrome"",""ophthalmoacromelic syndrome""]"	"[{""label"":""Smoc1"",""id"":""64075""}]"	"[""64075""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060861""}]"
DOID:0060861	"[""microphthalmia with limb anomalies"",""MLA"",""OAS"",""Waardenburg anophthalmia syndrome"",""anophthalmia-syndactyly syndrome"",""ophthalmoacromelic syndrome""]"	"[{""label"":""SMOC1"",""id"":""64093""}]"	"[""64093""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060861""}]"
DOID:0060863	"[""patterned macular dystrophy"",""patterned dystrophy of retinal pigment epithelium""]"	"[{""label"":""PRPH2"",""id"":""5961""}]"	"[""5961""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060863""}]"
DOID:0060864	"[""patterned macular dystrophy 2"",""MDPT2"",""butterfly-shaped pigmentary maculary dystrophy 2""]"	"[{""label"":""CTNNA1"",""id"":""1495""}]"	"[""1495""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060864""}]"
DOID:0060866	"[""patterned macular dystrophy 1"",""MDPT1"",""butterfly-shaped pigmentary maculary dystrophy 1""]"	"[{""label"":""PRPH2"",""id"":""5961""}]"	"[""5961""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060866""}]"
DOID:0060866	"[""patterned macular dystrophy 1"",""MDPT1"",""butterfly-shaped pigmentary maculary dystrophy 1""]"	"[{""label"":""Prph2"",""id"":""19133""}]"	"[""19133""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060866""}]"
DOID:0060867	"[""macrocephaly-autism syndrome"",""macrocephaly-intellectual disability-autism syndrome""]"	"[{""label"":""PTEN"",""id"":""5728""}]"	"[""5728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060867""}]"
DOID:0060868	"[""leukoencephalopathy with vanishing white matter"",""CACH"",""CACH/VWM"",""childhood ataxia with central nervous system hypomyelination"",""vanishing white matter leukodystrophy""]"	"[{""label"":""GCD2"",""id"":""852974""}]"	"[""852974""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060868""}]"
DOID:0060868	"[""leukoencephalopathy with vanishing white matter"",""CACH"",""CACH/VWM"",""childhood ataxia with central nervous system hypomyelination"",""vanishing white matter leukodystrophy""]"	"[{""label"":""Eif2b4"",""id"":""13667""},{""label"":""Eif2b5"",""id"":""224045""}]"	"[""13667"",""224045""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060868""}]"
DOID:0060869	"[""late-onset retinal degeneration"",""LORD"",""autosomal dominant late-onset retinal degeneration""]"	"[{""label"":""C1qtnf5"",""id"":""235312""}]"	"[""235312""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060869""}]"
DOID:0060870	"[""isolated growth hormone deficiency"",""IGHD"",""congenital IGHD"",""congenital isolated GH deficiency"",""congenital isolated growth hormone deficiency"",""familial isolated growth hormone deficiency"",""non-acquired isolated growth hormone deficiency""]"	"[{""label"":""Ghrhr"",""id"":""25321""}]"	"[""25321""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060870""}]"
DOID:0060870	"[""isolated growth hormone deficiency"",""IGHD"",""congenital IGHD"",""congenital isolated GH deficiency"",""congenital isolated growth hormone deficiency"",""familial isolated growth hormone deficiency"",""non-acquired isolated growth hormone deficiency""]"	"[{""label"":""GHR"",""id"":""2690""},{""label"":""GHRHR"",""id"":""2692""}]"	"[""2690"",""2692""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060870""}]"
DOID:0060874	"[""isolated growth hormone deficiency type IB"",""IGHD IB"",""congenital IGHD type IB"",""congenital isolated GH deficiency type IB"",""congenital isolated growth hormone deficiency type IB"",""dwarfism of Sindh""]"	"[{""label"":""GHRHR"",""id"":""2692""}]"	"[""2692""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060874""}]"
DOID:0060875	"[""isolated growth hormone deficiency type III"",""Fleisher syndrome"",""IGHD III"",""X-linked IGHD"",""X-linked agammaglobulinemia and isolated growth hormone deficiency"",""X-linked hypogammaglobulinemia and isolated growth hormone deficiency"",""X-linked isolated growth hormone deficiency"",""congenital IGHD type III"",""congenital isolated GH deficiency type III"",""congenital isolated growth hormone deficiency type III"",""growth hormone deficiency with hypogammaglobulinemia""]"	"[{""label"":""BTK"",""id"":""695""}]"	"[""695""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060875""}]"
DOID:0060877	"[""bullous congenital ichthyosiform erythroderma"",""bullous type ichthyosis"",""ichthyosis bullosa of Siemens"",""superficial epidermolytic ichthyosis""]"	"[{""label"":""Krt2"",""id"":""16681""}]"	"[""16681""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060877""}]"
DOID:0060877	"[""bullous congenital ichthyosiform erythroderma"",""bullous type ichthyosis"",""ichthyosis bullosa of Siemens"",""superficial epidermolytic ichthyosis""]"	"[{""label"":""KRT2"",""id"":""3849""}]"	"[""3849""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060877""}]"
DOID:0060878	"[""hypoparathyroidism-deafness-renal disease syndrome"",""Barakat syndrome"",""HDR syndrome"",""hypoparathyroidism, sensorineural deafness, and renal disease""]"	"[{""label"":""GATA3"",""id"":""2625""}]"	"[""2625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060878""}]"
DOID:0060879	"[""primary hypomagnesemia"",""HOMG"",""primary familial hypomagnesemia""]"	"[{""label"":""EGF"",""id"":""1950""}]"	"[""1950""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060879""}]"
DOID:0060882	"[""renal hypomagnesemia 4"",""HOMG4""]"	"[{""label"":""EGF"",""id"":""1950""}]"	"[""1950""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060882""}]"
DOID:0060883	"[""intestinal hypomagnesemia 1"",""HOMG1"",""hypomagnesemia caused by selective magnesium malabsorption"",""hypomagnesemia intestinal type 1"",""hypomagnesemic tetany"",""intestinal hypomagnesemia with secondary hypocalcemia"",""primary hypomagnesemia with secondary hypocalcemia""]"	"[{""label"":""TRPM6"",""id"":""140803""}]"	"[""140803""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060883""}]"
DOID:0060884	"[""renal hypomagnesemia 6"",""HOMG6""]"	"[{""label"":""CNNM2"",""id"":""54805""}]"	"[""54805""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060884""}]"
DOID:0060887	"[""ossification of the posterior longitudinal ligament of spine"",""OPLL""]"	"[{""label"":""Enpp1"",""id"":""18605""}]"	"[""18605""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060887""}]"
DOID:0060887	"[""ossification of the posterior longitudinal ligament of spine"",""OPLL""]"	"[{""label"":""BMP4"",""id"":""652""},{""label"":""ENPP1"",""id"":""5167""}]"	"[""5167"",""652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060887""}]"
DOID:0060889	"[""prune belly syndrome"",""Eagle-Barret syndrome"",""Obrisnksy syndrome"",""abdominal muscle deficiency syndrome""]"	"[{""label"":""CHRM3"",""id"":""1131""}]"	"[""1131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060889""}]"
DOID:0060892	"[""late onset Parkinson's disease"",""late onset Parkinson disease""]"	"[{""label"":""ADH1C"",""id"":""126""},{""label"":""ATXN2"",""id"":""6311""},{""label"":""ATXN3"",""id"":""4287""},{""label"":""EIF4G1"",""id"":""1981""},{""label"":""GBA1"",""id"":""2629""},{""label"":""HLA-DRA"",""id"":""3122""},{""label"":""MAPT"",""id"":""4137""},{""label"":""PSAP"",""id"":""5660""},{""label"":""TBP"",""id"":""6908""}]"	"[""126"",""1981"",""2629"",""3122"",""4137"",""4287"",""5660"",""6311"",""6908""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060892""}]"
DOID:0060894	"[""early-onset Parkinson's disease"",""Young-onset Parkinson disease"",""early-onset Parkinson disease""]"	"[{""label"":""Psn"",""id"":""40260""}]"	"[""40260""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060894""}]"
DOID:0060895	"[""Parkinson's disease 4"",""autosomal dominant Lewy body Parkinson disease 4"",""autosomal dominant Parkinson disease 4"",""autosomal dominant Parkinson's disease 4""]"	"[{""label"":""SNCA"",""id"":""6622""}]"	"[""6622""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060895""}]"
DOID:0060895	"[""Parkinson's disease 4"",""autosomal dominant Lewy body Parkinson disease 4"",""autosomal dominant Parkinson disease 4"",""autosomal dominant Parkinson's disease 4""]"	"[{""label"":""Snca"",""id"":""20617""}]"	"[""20617""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060895""}]"
DOID:0060896	"[""Parkinson's disease 23"",""autosomal recessive early-onset Parkinson disease 23"",""autosomal recessive early-onset Parkinson's disease 23""]"	"[{""label"":""VPS13C"",""id"":""54832""}]"	"[""54832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060896""}]"
DOID:0060898	"[""Parkinson's disease 20"",""early-onset Parkinson disease 20"",""early-onset Parkinson's disease 20""]"	"[{""label"":""SYNJ1"",""id"":""8867""}]"	"[""8867""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060898""}]"
DOID:0060900	"[""Parkinson's disease 14"",""Dystonia-Parkinsonism Adult-Onset"",""autosomal recessive Parkinson disease 14"",""autosomal recessive Parkinson's disease 14""]"	"[{""label"":""PLA2G6"",""id"":""8398""}]"	"[""8398""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060900""}]"
DOID:0060900	"[""Parkinson's disease 14"",""Dystonia-Parkinsonism Adult-Onset"",""autosomal recessive Parkinson disease 14"",""autosomal recessive Parkinson's disease 14""]"	"[{""label"":""Pla2g6"",""id"":""53357""}]"	"[""53357""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060900""}]"
DOID:0060901	"[""lymphoplasmacytic lymphoma"",""Waldenstroem's macroglobulinemia"",""Waldenstrom Macroglobulinemia"",""lymphoplasmacytic lymphoma with IgM gammopathy""]"	"[{""label"":""CXCR4"",""id"":""7852""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL6"",""id"":""3569""},{""label"":""MYD88"",""id"":""4615""}]"	"[""2214"",""3569"",""3586"",""4615"",""7852""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060901""}]"
DOID:0060902	"[""Norman-Roberts syndrome"",""lissencephaly 2"",""lissencephaly syndrome, Norman-Roberts type""]"	"[{""label"":""RELN"",""id"":""5649""}]"	"[""5649""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060902""}]"
DOID:0060903	"[""thrombosis""]"	"[{""label"":""Ace2"",""id"":""302668""},{""label"":""C5ar1"",""id"":""113959""},{""label"":""Cd40lg"",""id"":""84349""},{""label"":""P2ry12"",""id"":""64803""}]"	"[""113959"",""302668"",""64803"",""84349""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060903""}]"
DOID:0060903	"[""thrombosis""]"	"[{""label"":""F11"",""id"":""2160""},{""label"":""F2"",""id"":""2147""},{""label"":""F5"",""id"":""2153""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FGB"",""id"":""2244""},{""label"":""HRG"",""id"":""3273""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""MMP9"",""id"":""4318""},{""label"":""PROC"",""id"":""5624""},{""label"":""SERPINC1"",""id"":""462""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""VTN"",""id"":""7448""}]"	"[""2147"",""2153"",""2160"",""2212"",""2244"",""3273"",""3673"",""4312"",""4314"",""4318"",""462"",""5054"",""5624"",""7448""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060903""}]"
DOID:0060912	"[""craniosynostosis 7"",""CRS7""]"	"[{""label"":""SMAD6"",""id"":""4091""}]"	"[""4091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060912""}]"
DOID:0060916	"[""proteasome-associated autoinflammatory syndrome 3"",""PRAAS3""]"	"[{""label"":""PSMB4"",""id"":""5692""}]"	"[""5692""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060916""}]"
DOID:0060917	"[""facioscapulohumeral muscular dystrophy 3"",""FSHD3"",""facioscapulohumeral muscular dystrophy type 3""]"	"[{""label"":""LRIF1"",""id"":""55791""}]"	"[""55791""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060917""}]"
DOID:0060929	"[""non-syndromic X-linked intellectual developmental disorder 111"",""XLID111""]"	"[{""label"":""SLITRK2"",""id"":""84631""}]"	"[""84631""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060929""}]"
DOID:0060929	"[""non-syndromic X-linked intellectual developmental disorder 111"",""XLID111""]"	"[{""label"":""Slitrk2"",""id"":""245450""}]"	"[""245450""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060929""}]"
DOID:0060931	"[""developmental dysplasia of the hip 1"",""DDH1""]"	"[{""label"":""GDF5"",""id"":""8200""}]"	"[""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060931""}]"
DOID:0060933	"[""developmental delay, dysmorphic facies, and brain anomalies"",""DEVDFB""]"	"[{""label"":""U2AF2"",""id"":""11338""}]"	"[""11338""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060933""}]"
DOID:0060936	"[""dystonia 28, childhood-onset"",""DYSTONIA 28, CHILDHOOD-ONSET"",""DYT28""]"	"[{""label"":""KMT2B"",""id"":""9757""}]"	"[""9757""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060936""}]"
DOID:0060937	"[""dystonia 30"",""DYT30""]"	"[{""label"":""VPS16"",""id"":""64601""}]"	"[""64601""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060937""}]"
DOID:0060939	"[""dystonia 32"",""DYT32""]"	"[{""label"":""VPS11"",""id"":""55823""}]"	"[""55823""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060939""}]"
DOID:0060940	"[""dystonia 33""]"	"[{""label"":""EIF2AK2"",""id"":""5610""}]"	"[""5610""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060940""}]"
DOID:0060941	"[""interstitial lung disease 1"",""Idiopathic pulmonary fibrosis""]"	"[{""label"":""SFTPA1"",""id"":""653509""}]"	"[""653509""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060941""}]"
DOID:0060942	"[""Ullrich congenital muscular dystrophy 1B""]"	"[{""label"":""COL6A2"",""id"":""1292""}]"	"[""1292""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060942""}]"
DOID:0060943	"[""Ullrich congenital muscular dystrophy 1C""]"	"[{""label"":""COL6A3"",""id"":""1293""}]"	"[""1293""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060943""}]"
DOID:0060944	"[""episodic kinesigenic dyskinesia 3""]"	"[{""label"":""TMEM151A"",""id"":""256472""}]"	"[""256472""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060944""}]"
DOID:0060946	"[""Ullrich congenital muscular dystrophy 1A""]"	"[{""label"":""COL6A1"",""id"":""1291""}]"	"[""1291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060946""}]"
DOID:0060948	"[""Ullrich congenital muscular dystrophy 2""]"	"[{""label"":""COL12A1"",""id"":""1303""}]"	"[""1303""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060948""}]"
DOID:0060949	"[""3-hydroxyisobutryl-CoA hydrolase deficiency"",""HIBCH deficiency"",""Methacrylic aciduria"",""Valine metabolic defect""]"	"[{""label"":""HIBCH"",""id"":""26275""}]"	"[""26275""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060949""}]"
DOID:0060951	"[""polycystic kidney disease 6""]"	"[{""label"":""DNAJB11"",""id"":""51726""}]"	"[""51726""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060951""}]"
DOID:0060952	"[""polycystic kidney disease 7""]"	"[{""label"":""ALG5"",""id"":""29880""}]"	"[""29880""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060952""}]"
DOID:0060953	"[""ZTTK syndrome"",""ZTTK MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDATION SYNDROME"",""Zhu-Tokita-Takenouchi-Kim syndrome""]"	"[{""label"":""SON"",""id"":""6651""}]"	"[""6651""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060953""}]"
DOID:0060956	"[""dystonia 37, early-onset with striatal lesions""]"	"[{""label"":""NUP54"",""id"":""53371""}]"	"[""53371""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060956""}]"
DOID:0060958	"[""orofaciodigital syndrome XIV""]"	"[{""label"":""C2CD3"",""id"":""26005""}]"	"[""26005""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060958""}]"
DOID:0060959	"[""orofaciodigital syndrome II"",""Mohr syndrome"",""Oral-facial-digital syndrome type 2""]"	"[{""label"":""NEK1"",""id"":""4750""}]"	"[""4750""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060959""}]"
DOID:0060965	"[""episodic ataxia type 9""]"	"[{""label"":""SCN2A"",""id"":""6326""}]"	"[""6326""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060965""}]"
DOID:0060969	"[""galactosemia 4"",""GALM deficiency"",""Galactose mutarotase deficiency"",""Galactosemia type 4""]"	"[{""label"":""GALM"",""id"":""130589""}]"	"[""130589""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060969""}]"
DOID:0060970	"[""Cornelia de Lange syndrome 6""]"	"[{""label"":""BRD4"",""id"":""23476""}]"	"[""23476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060970""}]"
DOID:0060971	"[""interstitial lung disease 2""]"	"[{""label"":""MUC5B"",""id"":""727897""},{""label"":""SFTPA2"",""id"":""729238""}]"	"[""727897"",""729238""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060971""}]"
DOID:0060973	"[""WHIM syndrome 2"",""WARTS, HYPOGAMMAGLOBULINEMIA, INFECTIONS, AND MYELOKATHEXIS SYNDROME 2""]"	"[{""label"":""CXCR2"",""id"":""3579""}]"	"[""3579""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060973""}]"
DOID:0060975	"[""polycystic liver disease 2"",""POLYCYSTIC LIVER DISEASE 2 WITH OR WITHOUT KIDNEY CYSTS""]"	"[{""label"":""SEC63"",""id"":""11231""}]"	"[""11231""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060975""}]"
DOID:0060976	"[""polycystic liver disease 3""]"	"[{""label"":""ALG8"",""id"":""79053""}]"	"[""79053""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060976""}]"
DOID:0060977	"[""polycystic liver disease 4""]"	"[{""label"":""LRP5"",""id"":""4041""}]"	"[""4041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060977""}]"
DOID:0060979	"[""Fanconi anemia complementation group S""]"	"[{""label"":""BRCA1"",""id"":""672""}]"	"[""672""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060979""}]"
DOID:0060980	"[""polycystic liver disease 1""]"	"[{""label"":""LRP5"",""id"":""4041""},{""label"":""PRKCSH"",""id"":""5589""}]"	"[""4041"",""5589""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060980""}]"
DOID:0060983	"[""sitosterolemia 2""]"	"[{""label"":""ABCG5"",""id"":""64240""}]"	"[""64240""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060983""}]"
DOID:0060984	"[""digenic dyskeratosis congenita""]"	"[{""label"":""TYMS"",""id"":""7298""}]"	"[""7298""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060984""}]"
DOID:0060985	"[""preaxial polydactyly type IV"",""crossed polydactyly type 1""]"	"[{""label"":""GLI3"",""id"":""2737""}]"	"[""2737""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060985""}]"
DOID:0060986	"[""preaxial polydactyly II"",""polydactyly of a triphalangeal thumb""]"	"[{""label"":""SHH"",""id"":""6469""}]"	"[""6469""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060986""}]"
DOID:0060987	"[""preaxial polydactyly I""]"	"[{""label"":""GLI1"",""id"":""2735""}]"	"[""2735""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060987""}]"
DOID:0060989	"[""short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1"",""SSFSC1""]"	"[{""label"":""BMP2"",""id"":""650""}]"	"[""650""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060989""}]"
DOID:0060990	"[""congenital disorder of deglycosylation 2""]"	"[{""label"":""MAN2C1"",""id"":""4123""}]"	"[""4123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060990""}]"
DOID:0060992	"[""bent bone dysplasia syndrome 1""]"	"[{""label"":""FGFR2"",""id"":""2263""}]"	"[""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060992""}]"
DOID:0060993	"[""bent bone dysplasia syndrome 2""]"	"[{""label"":""LAMA5"",""id"":""3911""}]"	"[""3911""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060993""}]"
DOID:0060994	"[""encephalopathy due to defective mitochondrial and peroxisomal fission 2""]"	"[{""label"":""MFF"",""id"":""56947""}]"	"[""56947""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060994""}]"
DOID:0060997	"[""rhabdoid tumor predisposition syndrome 2"",""RTPS2""]"	"[{""label"":""SMARCA4"",""id"":""6597""}]"	"[""6597""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060997""}]"
DOID:0060998	"[""striatal degeneration 2""]"	"[{""label"":""PDE10A"",""id"":""10846""}]"	"[""10846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060998""}]"
DOID:0060999	"[""mitochondrial trifunctional protein deficiency 2"",""MTPD2""]"	"[{""label"":""HADHB"",""id"":""3032""}]"	"[""3032""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0060999""}]"
DOID:0061001	"[""glycine encephalopathy 2"",""GCE2""]"	"[{""label"":""AMT"",""id"":""275""}]"	"[""275""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0061001""}]"
DOID:0061002	"[""congenital amegakaryocytic thrombocytopenia 2""]"	"[{""label"":""THPO"",""id"":""7066""}]"	"[""7066""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0061002""}]"
DOID:0061003	"[""pancreatic agenesis 1""]"	"[{""label"":""PDX1"",""id"":""3651""}]"	"[""3651""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0061003""}]"
DOID:0070004	"[""myeloid neoplasm""]"	"[{""label"":""CBL"",""id"":""867""},{""label"":""FGFR1"",""id"":""2260""},{""label"":""GPX1"",""id"":""2876""},{""label"":""MECOM"",""id"":""2122""}]"	"[""2122"",""2260"",""2876"",""867""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070004""}]"
DOID:0070005	"[""Seckel syndrome 9"",""SCKL9""]"	"[{""label"":""TRAIP"",""id"":""10293""}]"	"[""10293""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070005""}]"
DOID:0070007	"[""Seckel syndrome 1"",""SCKL1"",""microcephalic primordial dwarfism I""]"	"[{""label"":""ATR"",""id"":""545""}]"	"[""545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070007""}]"
DOID:0070011	"[""Seckel syndrome 7"",""SCKL7""]"	"[{""label"":""NIN"",""id"":""51199""}]"	"[""51199""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070011""}]"
DOID:0070012	"[""Seckel syndrome 5"",""SCKL5""]"	"[{""label"":""CEP152"",""id"":""22995""}]"	"[""22995""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070012""}]"
DOID:0070013	"[""Seckel syndrome 2"",""SCKL2"",""Seckel-type dwarfism 2"",""microcephalic primordial dwarfism 2""]"	"[{""label"":""RBBP8"",""id"":""5932""}]"	"[""5932""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070013""}]"
DOID:0070016	"[""autosomal dominant dyskeratosis congenita 2"",""DKCA2""]"	"[{""label"":""TERT"",""id"":""7015""}]"	"[""7015""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070016""}]"
DOID:0070023	"[""autosomal dominant dyskeratosis congenita 6"",""DKCA6""]"	"[{""label"":""ACD"",""id"":""65057""}]"	"[""65057""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070023""}]"
DOID:0070024	"[""autosomal recessive dyskeratosis congenita 6"",""DKCB6""]"	"[{""label"":""PARN"",""id"":""5073""}]"	"[""5073""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070024""}]"
DOID:0070025	"[""X-linked dyskeratosis congenita"",""DKCX"",""Zinsser-Cole-Engman syndrome""]"	"[{""label"":""DKC1"",""id"":""1736""}]"	"[""1736""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070025""}]"
DOID:0070028	"[""APP-related cerebral amyloid angiopathy"",""Amyloidosis, Cerebroarterial, App-Related"",""Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant"",""Cerebral Amyloid Angiopathy, App-Related, Arctic Variant"",""Cerebral Amyloid Angiopathy, App-Related, Dutch Variant"",""Cerebral Amyloid Angiopathy, App-Related, Flemish Variant"",""Cerebral Amyloid Angiopathy, App-Related, Iowa Variant"",""Cerebral Amyloid Angiopathy, App-Related, Italian Variant"",""HCHWAD""]"	"[{""label"":""APP"",""id"":""351""}]"	"[""351""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070028""}]"
DOID:0070029	"[""ITM2B-related cerebral amyloid angiopathy 1"",""Cerebral Amyloid Angiopathy, British Type"",""FBD"",""Familial British Dementia"",""Presenile Dementia with Spastic Ataxia""]"	"[{""label"":""ITM2B"",""id"":""9445""}]"	"[""9445""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070029""}]"
DOID:0070030	"[""ITM2B-related cerebral amyloid angiopathy 2"",""Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis"",""FDD"",""Familial Danish Dementia"",""HOOE"",""Heredopathia Ophthalmootoencephalica""]"	"[{""label"":""ITM2B"",""id"":""9445""}]"	"[""9445""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070030""}]"
DOID:0070031	"[""autosomal dominant intellectual developmental disorder 1"",""MRD1"",""autosomal dominant mental retardation 1"",""autosomal dominant non-syndromic intellectual disability 1""]"	"[{""label"":""MBD5"",""id"":""55777""}]"	"[""55777""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070031""}]"
DOID:0070033	"[""autosomal dominant intellectual developmental disorder 3"",""MRD3"",""autosomal dominant mental retardation 3"",""autosomal dominant non-syndromic intellectual disability 3""]"	"[{""label"":""CDH15"",""id"":""1013""}]"	"[""1013""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070033""}]"
DOID:0070035	"[""autosomal dominant intellectual developmental disorder 5"",""MRD5"",""autosomal dominant mental retardation 5"",""autosomal dominant non-syndromic intellectual disability 5""]"	"[{""label"":""SYNGAP1"",""id"":""8831""}]"	"[""8831""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070035""}]"
DOID:0070036	"[""autosomal dominant intellectual developmental disorder 6"",""MRD6"",""autosomal dominant mental retardation 6"",""autosomal dominant non-syndromic intellectual disability 6""]"	"[{""label"":""GRIN2B"",""id"":""2904""}]"	"[""2904""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070036""}]"
DOID:0070037	"[""autosomal dominant intellectual developmental disorder 7"",""DYRK1A syndrome"",""MRD7"",""autosomal dominant mental retardation 7"",""autosomal dominant non-syndromic intellectual disability 7""]"	"[{""label"":""DYRK1A"",""id"":""1859""}]"	"[""1859""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070037""}]"
DOID:0070038	"[""autosomal dominant intellectual developmental disorder 8"",""MRD8"",""autosomal dominant mental retardation 8"",""autosomal dominant non-syndromic intellectual disability 8""]"	"[{""label"":""GRIN1"",""id"":""2902""}]"	"[""2902""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070038""}]"
DOID:0070040	"[""autosomal dominant intellectual developmental disorder 10"",""MRD10"",""autosomal dominant mental retardation 10"",""autosomal dominant non-syndromic intellectual disability 10""]"	"[{""label"":""CACNG2"",""id"":""10369""}]"	"[""10369""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070040""}]"
DOID:0070041	"[""autosomal dominant intellectual developmental disorder 11"",""MRD11"",""autosomal dominant mental retardation 11"",""autosomal dominant non-syndromic intellectual disability 11""]"	"[{""label"":""EPB41L1"",""id"":""2036""}]"	"[""2036""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070041""}]"
DOID:0070042	"[""Coffin-Siris syndrome 1"",""CSS1"",""MRD12"",""autosomal dominant mental retardation 12"",""fifth digit syndrome""]"	"[{""label"":""ARID1B"",""id"":""57492""}]"	"[""57492""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070042""}]"
DOID:0070043	"[""autosomal dominant intellectual developmental disorder 13"",""MRD13"",""autosomal dominant mental retardation 13"",""autosomal dominant non-syndromic intellectual disability 13"",""mental retardation, autosomal dominant 13, with neuronal migration defects""]"	"[{""label"":""DYNC1H1"",""id"":""1778""}]"	"[""1778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070043""}]"
DOID:0070044	"[""Coffin-Siris syndrome 2"",""CSS2"",""MRD14"",""autosomal dominant mental retardation 14""]"	"[{""label"":""ARID1A"",""id"":""8289""}]"	"[""8289""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070044""}]"
DOID:0070045	"[""Coffin-Siris syndrome 3"",""CSS3"",""MRD15"",""autosomal dominant mental retardation 15""]"	"[{""label"":""SMARCB1"",""id"":""6598""}]"	"[""6598""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070045""}]"
DOID:0070046	"[""Coffin-Siris syndrome 4"",""CSS4"",""MRD16"",""autosomal dominant mental retardation 16""]"	"[{""label"":""SMARCA4"",""id"":""6597""}]"	"[""6597""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070046""}]"
DOID:0070047	"[""Schuurs-Hoeijmakers Syndrome"",""MRD17"",""SHMS"",""autosomal dominant mental retardation 17""]"	"[{""label"":""PACS1"",""id"":""55690""}]"	"[""55690""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070047""}]"
DOID:0070048	"[""GAND syndrome"",""MRD18"",""autosomal dominant intellectual developmental disorder 18"",""autosomal dominant mental retardation 18"",""autosomal dominant non-syndromic intellectual disability 18""]"	"[{""label"":""Gatad2b"",""id"":""229542""}]"	"[""229542""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070048""}]"
DOID:0070048	"[""GAND syndrome"",""MRD18"",""autosomal dominant intellectual developmental disorder 18"",""autosomal dominant mental retardation 18"",""autosomal dominant non-syndromic intellectual disability 18""]"	"[{""label"":""GATAD2B"",""id"":""57459""}]"	"[""57459""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070048""}]"
DOID:0070049	"[""autosomal dominant intellectual developmental disorder 19"",""MRD19"",""autosomal dominant mental retardation 19"",""autosomal dominant non-syndromic intellectual disability 19""]"	"[{""label"":""CTNNB1"",""id"":""1499""}]"	"[""1499""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070049""}]"
DOID:0070050	"[""neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language"",""MRD20"",""autosomal dominant mental retardation 20"",""mental retardation, autosomal dominant 20""]"	"[{""label"":""MEF2C"",""id"":""4208""}]"	"[""4208""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070050""}]"
DOID:0070051	"[""autosomal dominant intellectual developmental disorder 21"",""MRD21"",""autosomal dominant mental retardation 21"",""autosomal dominant non-syndromic intellectual disability 21""]"	"[{""label"":""CTCF"",""id"":""10664""}]"	"[""10664""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070051""}]"
DOID:0070053	"[""autosomal dominant intellectual developmental disorder 23"",""MRD23"",""autosomal dominant mental retardation 23"",""autosomal dominant non-syndromic intellectual disability 23""]"	"[{""label"":""SETD5"",""id"":""55209""}]"	"[""55209""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070053""}]"
DOID:0070054	"[""Vulto-van Silfout-de Vries syndrome"",""IDDISBAS"",""MRD24"",""VSVS"",""autosomal dominant mental retardation 24"",""autosomal dominant non-syndromic intellectual disability 24"",""intellectual developmental disorder with impaired expressive speech and behavioral abnormalities, with or without seizures""]"	"[{""label"":""DEAF1"",""id"":""10522""}]"	"[""10522""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070054""}]"
DOID:0070055	"[""Xia-Gibbs Syndrome"",""MRD25"",""autosomal dominant mental retardation 25""]"	"[{""label"":""AHDC1"",""id"":""27245""}]"	"[""27245""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070055""}]"
DOID:0070055	"[""Xia-Gibbs Syndrome"",""MRD25"",""autosomal dominant mental retardation 25""]"	"[{""label"":""Ahdc1"",""id"":""230793""}]"	"[""230793""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070055""}]"
DOID:0070056	"[""autosomal dominant intellectual developmental disorder 26"",""MRD26"",""autosomal dominant mental retardation 26"",""autosomal dominant non-syndromic intellectual disability 26""]"	"[{""label"":""AUTS2"",""id"":""26053""}]"	"[""26053""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070056""}]"
DOID:0070058	"[""Helsmoortel-Van Der Aa Syndrome"",""HVDAS"",""MRD28"",""autosomal dominant mental retardation 28""]"	"[{""label"":""ADNP"",""id"":""23394""}]"	"[""23394""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070058""}]"
DOID:0070059	"[""autosomal dominant intellectual developmental disorder 29"",""MRD29"",""autosomal dominant mental retardation 29"",""autosomal dominant non-syndromic intellectual disability 29""]"	"[{""label"":""SETBP1"",""id"":""26040""}]"	"[""26040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070059""}]"
DOID:0070062	"[""Arboleda-Tham syndrome"",""ARTHS"",""MRD32"",""autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome"",""autosomal dominant mental retardation 32"",""autosomal dominant non-syndromic intellectual disability 32""]"	"[{""label"":""KAT6A"",""id"":""7994""}]"	"[""7994""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070062""}]"
DOID:0070063	"[""autosomal dominant intellectual developmental disorder 33"",""MRD33"",""autosomal dominant mental retardation 33"",""autosomal dominant non-syndromic intellectual disability 33""]"	"[{""label"":""DPP6"",""id"":""1804""}]"	"[""1804""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070063""}]"
DOID:0070065	"[""autosomal dominant intellectual developmental disorder 35"",""MRD35"",""autosomal dominant mental retardation 35"",""autosomal dominant non-syndromic intellectual disability 35""]"	"[{""label"":""PPP2R5D"",""id"":""5528""}]"	"[""5528""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070065""}]"
DOID:0070066	"[""autosomal dominant intellectual developmental disorder 36"",""MRD36"",""autosomal dominant mental retardation 36"",""autosomal dominant non-syndromic intellectual disability 36""]"	"[{""label"":""PPP2R1A"",""id"":""5518""}]"	"[""5518""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070066""}]"
DOID:0070067	"[""White-Sutton syndrome"",""MRD37"",""WHSUS"",""autosomal dominant mental retardation 37""]"	"[{""label"":""POGZ"",""id"":""23126""}]"	"[""23126""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070067""}]"
DOID:0070068	"[""autosomal dominant intellectual developmental disorder 38"",""MRD38"",""PRELDS"",""autosomal dominant mental retardation 38"",""autosomal dominant non-syndromic intellectual disability 38"",""psychomotor retardation, epilepsy, and language disability syndrome""]"	"[{""label"":""EEF1A2"",""id"":""1917""}]"	"[""1917""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070068""}]"
DOID:0070068	"[""autosomal dominant intellectual developmental disorder 38"",""MRD38"",""PRELDS"",""autosomal dominant mental retardation 38"",""autosomal dominant non-syndromic intellectual disability 38"",""psychomotor retardation, epilepsy, and language disability syndrome""]"	"[{""label"":""Eef1a2"",""id"":""13628""}]"	"[""13628""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070068""}]"
DOID:0070069	"[""autosomal dominant intellectual developmental disorder 39"",""MRD39"",""autosomal dominant mental retardation 39"",""autosomal dominant non-syndromic intellectual disability 39""]"	"[{""label"":""Myt1l"",""id"":""17933""}]"	"[""17933""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070069""}]"
DOID:0070070	"[""autosomal dominant intellectual developmental disorder 40"",""MRD40"",""autosomal dominant mental retardation 40"",""autosomal dominant non-syndromic intellectual disability 40""]"	"[{""label"":""CHAMP1"",""id"":""283489""}]"	"[""283489""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070070""}]"
DOID:0070072	"[""autosomal dominant intellectual developmental disorder 42"",""MRD42"",""autosomal dominant mental retardation 42"",""autosomal dominant non-syndromic intellectual disability 42""]"	"[{""label"":""GNB1"",""id"":""2782""}]"	"[""2782""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070072""}]"
DOID:0070073	"[""autosomal dominant intellectual developmental disorder 43"",""MRD43"",""autosomal dominant mental retardation 43"",""autosomal dominant non-syndromic intellectual disability 43""]"	"[{""label"":""HIVEP2"",""id"":""3097""}]"	"[""3097""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070073""}]"
DOID:0070074	"[""autosomal dominant intellectual developmental disorder 44"",""MRD44"",""autosomal dominant intellectual developmental disorder 44 with microcephaly"",""autosomal dominant mental retardation 44"",""autosomal dominant non-syndromic intellectual disability 44""]"	"[{""label"":""TRIO"",""id"":""7204""}]"	"[""7204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070074""}]"
DOID:0070082	"[""schizophrenia 6"",""SCZD6""]"	"[{""label"":""NRG1"",""id"":""3084""}]"	"[""3084""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070082""}]"
DOID:0070093	"[""schizophrenia 18"",""Chromosome 7q36.3 Duplication Syndrome, 362-Kb"",""SCZD18""]"	"[{""label"":""SLC1A1"",""id"":""6505""}]"	"[""6505""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070093""}]"
DOID:0070094	"[""oculocutaneous albinism type IA"",""OCA1A"",""Oculocutaneous Albinism, Tyrosinase-Negative""]"	"[{""label"":""TYR"",""id"":""7299""}]"	"[""7299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070094""}]"
DOID:0070095	"[""oculocutaneous albinism type IB"",""Albinism, Yellow Mutant Type"",""OCA1B""]"	"[{""label"":""TYR"",""id"":""7299""}]"	"[""7299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070095""}]"
DOID:0070096	"[""oculocutaneous albinism type II"",""OCA2"",""Oculocutaneous Albinism, Tyrosinase-Positive""]"	"[{""label"":""MC1R"",""id"":""4157""},{""label"":""OCA2"",""id"":""4948""}]"	"[""4157"",""4948""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070096""}]"
DOID:0070097	"[""oculocutaneous albinism type III"",""OCA3"",""Rufous Oculocutaneous Albinism""]"	"[{""label"":""TYRP1"",""id"":""7306""}]"	"[""7306""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070097""}]"
DOID:0070098	"[""oculocutaneous albinism type IV"",""OCA4""]"	"[{""label"":""SLC45A2"",""id"":""51151""}]"	"[""51151""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070098""}]"
DOID:0070111	"[""Niemann-Pick disease type A""]"	"[{""label"":""SMPD1"",""id"":""6609""}]"	"[""6609""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00086""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070111""}]"
DOID:0070112	"[""Niemann-Pick disease type B""]"	"[{""label"":""SMPD1"",""id"":""6609""}]"	"[""6609""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00087""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070112""}]"
DOID:0070113	"[""Niemann-Pick disease type C1"",""NPC1""]"	"[{""label"":""Npc1"",""id"":""18145""}]"	"[""18145""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070113""}]"
DOID:0070113	"[""Niemann-Pick disease type C1"",""NPC1""]"	"[{""label"":""NCR1"",""id"":""856101""}]"	"[""856101""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070113""}]"
DOID:0070113	"[""Niemann-Pick disease type C1"",""NPC1""]"	"[{""label"":""NPC1"",""id"":""4864""}]"	"[""4864""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00089""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070113""}]"
DOID:0070114	"[""Niemann-Pick disease type C2"",""NPC2""]"	"[{""label"":""NPC2"",""id"":""10577""}]"	"[""10577""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00090""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070114""}]"
DOID:0070117	"[""Meckel syndrome 3"",""MKS3"",""Meckel-Gruber syndrome, type 3""]"	"[{""label"":""TMEM67"",""id"":""91147""}]"	"[""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070117""}]"
DOID:0070119	"[""Meckel syndrome 5"",""MKS5"",""Meckel-Gruber syndrome, type 5""]"	"[{""label"":""RPGRIP1L"",""id"":""23322""}]"	"[""23322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070119""}]"
DOID:0070120	"[""Meckel syndrome 6"",""MKS6"",""Meckel-Gruber syndrome, type 6""]"	"[{""label"":""CC2D2A"",""id"":""57545""}]"	"[""57545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070120""}]"
DOID:0070121	"[""Meckel syndrome 7"",""MKS7"",""Meckel-Gruber syndrome, type 7""]"	"[{""label"":""NPHP3"",""id"":""27031""}]"	"[""27031""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070121""}]"
DOID:0070122	"[""Meckel syndrome 8"",""MKS8"",""Meckel-Gruber syndrome, type 8""]"	"[{""label"":""TCTN2"",""id"":""79867""}]"	"[""79867""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070122""}]"
DOID:0070123	"[""congenital nongoitrous hypothyroidism 4"",""CHNG4"",""isolated thyrotropin deficiency""]"	"[{""label"":""TSHB"",""id"":""7252""}]"	"[""7252""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070123""}]"
DOID:0070124	"[""congenital nongoitrous hypothyroidism 2"",""CHNG2"",""congenital hypothyroidism due to thyroid dysgenesis or hypoplasia""]"	"[{""label"":""PAX8"",""id"":""7849""}]"	"[""7849""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070124""}]"
DOID:0070128	"[""congenital nongoitrous hypothyroidism 6"",""CHNG6""]"	"[{""label"":""THRA"",""id"":""7067""}]"	"[""7067""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070128""}]"
DOID:0070129	"[""autosomal recessive cutis laxa type IID"",""ARCL2D""]"	"[{""label"":""ATP6V1A"",""id"":""523""}]"	"[""523""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070129""}]"
DOID:0070130	"[""autosomal dominant cutis laxa 1"",""ADCL1""]"	"[{""label"":""ELN"",""id"":""2006""}]"	"[""2006""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070130""}]"
DOID:0070131	"[""autosomal dominant cutis laxa 3"",""ADCL3""]"	"[{""label"":""ALDH18A1"",""id"":""5832""}]"	"[""5832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070131""}]"
DOID:0070132	"[""autosomal recessive cutis laxa type IIIA"",""ARCL3A"",""De Barsy syndrome A""]"	"[{""label"":""ALDH18A1"",""id"":""5832""}]"	"[""5832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070132""}]"
DOID:0070133	"[""autosomal recessive cutis laxa type IB"",""ARCL1B""]"	"[{""label"":""EFEMP2"",""id"":""30008""}]"	"[""30008""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070133""}]"
DOID:0070134	"[""autosomal recessive cutis laxa type IIA"",""ARCL2A""]"	"[{""label"":""ATP6V0A2"",""id"":""23545""}]"	"[""23545""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00371""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070134""}]"
DOID:0070135	"[""autosomal recessive cutis laxa type IA"",""ARCL1A""]"	"[{""label"":""FBLN5"",""id"":""10516""}]"	"[""10516""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070135""}]"
DOID:0070136	"[""autosomal dominant cutis laxa 2"",""ADCL2""]"	"[{""label"":""FBLN5"",""id"":""10516""}]"	"[""10516""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070136""}]"
DOID:0070137	"[""autosomal recessive cutis laxa type IIB"",""ARCL2, progeroid type"",""ARCL2B""]"	"[{""label"":""PYCR1"",""id"":""5831""}]"	"[""5831""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070137""}]"
DOID:0070138	"[""autosomal recessive cutis laxa type IIIB"",""ARCL3B"",""De Barsy syndrome B""]"	"[{""label"":""PYCR1"",""id"":""5831""}]"	"[""5831""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070138""}]"
DOID:0070139	"[""autosomal recessive cutis laxa type IC"",""ARCL1C"",""autosomal recessive cutis laxa type 1C""]"	"[{""label"":""LTBP4"",""id"":""8425""}]"	"[""8425""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070139""}]"
DOID:0070140	"[""autosomal recessive cutis laxa type IIC""]"	"[{""label"":""ATP6V1E1"",""id"":""529""}]"	"[""529""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070140""}]"
DOID:0070143	"[""autosomal recessive cutis laxa type III"",""De Barsy syndrome"",""cutis laxa-corneal clouding-intellectual disability syndrome""]"	"[{""label"":""ALDH18A1"",""id"":""5832""}]"	"[""5832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070143""}]"
DOID:0070145	"[""hereditary sensory and autonomic neuropathy type 5"",""HSAN5"",""hereditary sensory and autonomic neuropathy type V""]"	"[{""label"":""NGF"",""id"":""4803""}]"	"[""4803""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070145""}]"
DOID:0070146	"[""hereditary sensory neuropathy type 4"",""hereditary sensory neuropathy type IV"",""insensitivity to pain, congenital, with anhidrosis""]"	"[{""label"":""NTRK1"",""id"":""4914""}]"	"[""4914""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070146""}]"
DOID:0070149	"[""hereditary sensory and autonomic neuropathy type 7"",""HSAN7"",""hereditary sensory and autonomic neuropathy type VII""]"	"[{""label"":""SCN11A"",""id"":""11280""}]"	"[""11280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070149""}]"
DOID:0070150	"[""hereditary sensory and autonomic neuropathy type 2B"",""HSAN2B"",""hereditary sensory and autonomic neuropathy type IIB""]"	"[{""label"":""RETREG1"",""id"":""54463""}]"	"[""54463""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070150""}]"
DOID:0070151	"[""hereditary sensory and autonomic neuropathy type 6"",""HSAN6"",""hereditary sensory and autonomic neuropathy type VI""]"	"[{""label"":""DST"",""id"":""667""}]"	"[""667""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070151""}]"
DOID:0070151	"[""hereditary sensory and autonomic neuropathy type 6"",""HSAN6"",""hereditary sensory and autonomic neuropathy type VI""]"	"[{""label"":""Dst"",""id"":""13518""}]"	"[""13518""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070151""}]"
DOID:0070152	"[""hereditary sensory and autonomic neuropathy type 1A"",""HSAN1A"",""hereditary sensory and autonomic neuropathy type IA""]"	"[{""label"":""SPTLC1"",""id"":""10558""}]"	"[""10558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070152""}]"
DOID:0070154	"[""hereditary sensory neuropathy type 1F"",""HSN1F"",""hereditary sensory neuropathy type IF""]"	"[{""label"":""ATL3"",""id"":""25923""}]"	"[""25923""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070154""}]"
DOID:0070155	"[""hereditary sensory and autonomic neuropathy type 2A"",""HSAN2A"",""hereditary sensory and autonomic neuropathy type IIA""]"	"[{""label"":""WNK1"",""id"":""65125""}]"	"[""65125""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070155""}]"
DOID:0070157	"[""hereditary sensory and autonomic neuropathy type 1C"",""HSAN1C"",""hereditary sensory and autonomic neuropathy type IC""]"	"[{""label"":""SPTLC2"",""id"":""9517""}]"	"[""9517""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070157""}]"
DOID:0070158	"[""hereditary sensory neuropathy type 1E"",""HSN1E"",""hereditary sensory neuropathy type IE""]"	"[{""label"":""DNMT1"",""id"":""1786""}]"	"[""1786""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070158""}]"
DOID:0070164	"[""spermatogenic failure 2"",""SPGF2""]"	"[{""label"":""MSH4"",""id"":""4438""}]"	"[""4438""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070164""}]"
DOID:0070165	"[""spermatogenic failure 18"",""SPGF18""]"	"[{""label"":""DNAH1"",""id"":""25981""}]"	"[""25981""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070165""}]"
DOID:0070166	"[""spermatogenic failure 20"",""SPGF20""]"	"[{""label"":""CFAP44"",""id"":""55779""}]"	"[""55779""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070166""}]"
DOID:0070168	"[""spermatogenic failure 3"",""SPGF3""]"	"[{""label"":""SLC26A8"",""id"":""116369""},{""label"":""SRSF6"",""id"":""6431""}]"	"[""116369"",""6431""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070168""}]"
DOID:0070170	"[""spermatogenic failure 19"",""SPGF19""]"	"[{""label"":""CFAP43"",""id"":""80217""}]"	"[""80217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070170""}]"
DOID:0070174	"[""spermatogenic failure 17"",""Male infertility due to oocyte activation failure"",""SPGF17""]"	"[{""label"":""PLCZ1"",""id"":""89869""}]"	"[""89869""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070174""}]"
DOID:0070177	"[""spermatogenic failure 22"",""SPGF22""]"	"[{""label"":""MEIOB"",""id"":""254528""}]"	"[""254528""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070177""}]"
DOID:0070182	"[""spermatogenic failure 13"",""SPGF13""]"	"[{""label"":""TAF4B"",""id"":""6875""}]"	"[""6875""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070182""}]"
DOID:0070187	"[""Y-linked spermatogenic failure 2"",""SPGFY2"",""nonobstructive Y-linked spermatogenic failure""]"	"[{""label"":""USP9Y"",""id"":""8287""}]"	"[""8287""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070187""}]"
DOID:0070195	"[""X-linked chronic granulomatous disease"",""CDGX"",""X-linked chronic cytochrome b-negative granulomatous disease""]"	"[{""label"":""CYBB"",""id"":""1536""}]"	"[""1536""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070195""}]"
DOID:0070197	"[""distal myopathy 1"",""Distal myopathy type 1"",""Gowers disease"",""Laing distal myopathy"",""Laing early-onset distal myopathy"",""MPD1""]"	"[{""label"":""MYH7"",""id"":""4625""}]"	"[""4625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070197""}]"
DOID:0070199	"[""Miyoshi muscular dystrophy 1"",""MMD1"",""Miyoshi myopathy 1""]"	"[{""label"":""DYSF"",""id"":""8291""}]"	"[""8291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070199""}]"
DOID:0070201	"[""Miyoshi muscular dystrophy 3"",""MMD3"",""Miyoshi myopathy 3""]"	"[{""label"":""ANO5"",""id"":""203859""}]"	"[""203859""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070201""}]"
DOID:0070202	"[""familial partial lipodystrophy type 2"",""FPLD2"",""familial lipodystrophy of limbs and lower trunk"",""familial partial lipodystrophy Dunnigan type"",""reverse partial lipodystrophy""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070202""}]"
DOID:0070204	"[""familial partial lipodystrophy type 3"",""FPLD3"",""PPARG-related FPLD"",""PPARG-related familial partial lipodystrophy"",""familial partial lipodystrophy associated with PPARG mutations""]"	"[{""label"":""PPARG"",""id"":""5468""}]"	"[""5468""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070204""}]"
DOID:0070205	"[""familial partial lipodystrophy type 4"",""FPLD4"",""PLIN1-related FPLD"",""PLIN1-related familial partial lipodystrophy"",""familial partial lipodystrophy associated with PLIN1 mutations""]"	"[{""label"":""PLIN1"",""id"":""5346""}]"	"[""5346""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070205""}]"
DOID:0070208	"[""hereditary lymphedema IC"",""LMPH1C""]"	"[{""label"":""GJC2"",""id"":""57165""}]"	"[""57165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070208""}]"
DOID:0070209	"[""hereditary lymphedema ID"",""LMPH1D""]"	"[{""label"":""VEGFC"",""id"":""7424""}]"	"[""7424""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070209""}]"
DOID:0070210	"[""hereditary lymphedema IA"",""LMPH1A""]"	"[{""label"":""FLT4"",""id"":""2324""}]"	"[""2324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070210""}]"
DOID:0070214	"[""familial hyperinsulinemic hypoglycemia 7"",""EIHI"",""HHF7"",""exercise-induced hyperinsulinemic hypoglycemia"",""exercise-induced hyperinsulinism"",""hyperinsulinism due to SLC16A1 deficiency"",""hyperinsulinism due to monocarboxylate transporter 1 deficiency""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070214""}]"
DOID:0070215	"[""familial hyperinsulinemic hypoglycemia 4"",""HHF4"",""hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency"",""hyperinsulinism due to SCHAD deficiency"",""hyperinsulinism due to glutamodehydrogenase deficiency"",""hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency""]"	"[{""label"":""HADH"",""id"":""3033""}]"	"[""3033""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070215""}]"
DOID:0070216	"[""familial hyperinsulinemic hypoglycemia 3"",""HHF3"",""hyperinsulinemic hypoglycemia due to glucokinase deficiency"",""hyperinsulinism due to glucokinase deficiency""]"	"[{""label"":""GCK"",""id"":""2645""}]"	"[""2645""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070216""}]"
DOID:0070216	"[""familial hyperinsulinemic hypoglycemia 3"",""HHF3"",""hyperinsulinemic hypoglycemia due to glucokinase deficiency"",""hyperinsulinism due to glucokinase deficiency""]"	"[{""label"":""Gck"",""id"":""103988""}]"	"[""103988""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070216""}]"
DOID:0070217	"[""familial hyperinsulinemic hypoglycemia 6"",""HHF6"",""HI/HA syndrome"",""hyperinsulinism-hyperammonemia syndrome""]"	"[{""label"":""GLUD1"",""id"":""2746""}]"	"[""2746""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070217""}]"
DOID:0070218	"[""familial hyperinsulinemic hypoglycemia 2"",""Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency"",""HHF2"",""hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia""]"	"[{""label"":""KCNJ11"",""id"":""3767""}]"	"[""3767""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070218""}]"
DOID:0070219	"[""familial hyperinsulinemic hypoglycemia 1"",""HHF1""]"	"[{""label"":""ABCC8"",""id"":""6833""}]"	"[""6833""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070219""}]"
DOID:0070220	"[""familial hyperinsulinemic hypoglycemia 5"",""HHF5"",""hyperinsulinemic hypoglycemia due to INSR deficiency"",""hyperinsulinemic hypoglycemia due to insulin receptor deficiency"",""hyperinsulinism due to INSR deficiency""]"	"[{""label"":""INSR"",""id"":""3643""}]"	"[""3643""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070220""}]"
DOID:0070221	"[""progressive familial intrahepatic cholestasis"",""Byler disease"",""PFIC""]"	"[{""label"":""SEMA7A"",""id"":""8482""},{""label"":""SLC51A"",""id"":""200931""},{""label"":""VPS33B"",""id"":""26276""},{""label"":""ZFYVE19"",""id"":""84936""}]"	"[""200931"",""26276"",""8482"",""84936""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070221""}]"
DOID:0070222	"[""progressive familial intrahepatic cholestasis 2"",""BSEP deficiency"",""PFIC2""]"	"[{""label"":""ABCB11"",""id"":""8647""}]"	"[""8647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070222""}]"
DOID:0070223	"[""progressive familial intrahepatic cholestasis 3"",""MDR3 deficiency"",""PFIC3"",""progressive familial intrahepatic cholestasis with elevated serum gama-glutamyltransferase""]"	"[{""label"":""ABCB4"",""id"":""5244""}]"	"[""5244""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070223""}]"
DOID:0070224	"[""progressive familial intrahepatic cholestasis 4"",""PFIC4"",""TJP2 deficit""]"	"[{""label"":""TJP2"",""id"":""9414""}]"	"[""9414""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070224""}]"
DOID:0070229	"[""intrahepatic cholestasis of pregnancy 3"",""ICP3"",""pregnancy related cholestasis 3""]"	"[{""label"":""ABCB4"",""id"":""5244""}]"	"[""5244""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070229""}]"
DOID:0070232	"[""benign recurrent intrahepatic cholestasis 2"",""BRIC type 2"",""BRIC2""]"	"[{""label"":""ABCB11"",""id"":""8647""}]"	"[""8647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070232""}]"
DOID:0070233	"[""Loeys-Dietz syndrome 4"",""Aneurysm, aortic and cerebral, with arterial tortuosity and skeletal manifestations"",""LDS4""]"	"[{""label"":""TGFB2"",""id"":""7042""}]"	"[""7042""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070233""}]"
DOID:0070234	"[""Loeys-Dietz syndrome 2"",""AAT3"",""LDS2"",""Marfan syndrome type II"",""familial throacic aortic aneurysm 3""]"	"[{""label"":""TGFBR2"",""id"":""7048""}]"	"[""7048""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070234""}]"
DOID:0070235	"[""Loeys-Dietz syndrome 1"",""AAT5"",""Furlong syndrome"",""LDS1"",""familial throacic aortic aneurysm 5""]"	"[{""label"":""TGFBR1"",""id"":""7046""}]"	"[""7046""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070235""}]"
DOID:0070236	"[""Loeys-Dietz syndrome 5"",""LDS5"",""RNHF"",""Reinhoff syndrome""]"	"[{""label"":""TGFB3"",""id"":""7043""}]"	"[""7043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070236""}]"
DOID:0070238	"[""primary coenzyme Q10 deficiency 1"",""COQ10D1"",""CoQ deficiency 1"",""CoQ10 deficiency, primary, 1"",""coenzyme Q deficiency 1"",""ubiquinone deficiency 1""]"	"[{""label"":""COQ2"",""id"":""27235""}]"	"[""27235""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070238""}]"
DOID:0070242	"[""primary coenzyme Q10 deficiency 5"",""COQ10D5"",""coenzyme Q10 deficiency, primary, 5"",""encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome""]"	"[{""label"":""COQ9"",""id"":""57017""}]"	"[""57017""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070242""}]"
DOID:0070243	"[""primary coenzyme Q10 deficiency 6"",""COQ10D6"",""coenzyme Q10 deficiency, primary, 6"",""familial steroid-resistant nephrotic syndrome with sensorineural deafness""]"	"[{""label"":""COQ6"",""id"":""51004""}]"	"[""51004""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070243""}]"
DOID:0070246	"[""X-linked Emery-Dreifuss muscular dystrophy 1"",""EDMD1"",""EMD1"",""Emery-Dreifuss muscular dystrophy 1, X-linked"",""humeroperoneal neuromuscular disease"",""muscular dystrophy, tardive, Dreifuss-Emery type, with contractures"",""scapuloperoneal syndrome, X-linked""]"	"[{""label"":""EMD"",""id"":""2010""}]"	"[""2010""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070246""}]"
DOID:0070247	"[""autosomal dominant Emery-Dreifuss muscular dystrophy 2"",""EDMD2"",""EMD2"",""Emery-Dreifuss muscular dystrophy 2, autosomal dominant"",""Emery-Dreifuss muscular dystrophy, autosomal dominant"",""Hauptmann-Thannhauser muscular dystrophy"",""autosomal dominant limb-girdle muscular dystrophy type 1B"",""muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant"",""scapuloilioperoneal atrophy with cardiopathy""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070247""}]"
DOID:0070248	"[""autosomal recessive Emery-Dreifuss muscular dystrophy 3"",""EDMD3"",""Emery-Dreifuss muscular dystrophy 3, autosomal recessive""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070248""}]"
DOID:0070249	"[""autosomal dominant Emery-Dreifuss muscular dystrophy 4"",""EDMD4"",""Emery-Dreifuss muscular dystrophy 4 with variable features"",""Emery-Dreifuss muscular dystrophy 4, autosomal dominant""]"	"[{""label"":""SYNE1"",""id"":""23345""}]"	"[""23345""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070249""}]"
DOID:0070250	"[""autosomal dominant Emery-Dreifuss muscular dystrophy 5"",""EDMD5"",""Emery-Dreifuss muscular dystrophy 5, autosomal dominant""]"	"[{""label"":""SYNE2"",""id"":""23224""}]"	"[""23224""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070250""}]"
DOID:0070251	"[""X-linked Emery-Dreifuss muscular dystrophy 6"",""EDMD6"",""Emery-Dreifuss muscular dystrophy 6, X-linked"",""XMPMA"",""myopathy, X-linked, with postural muscle atrophy""]"	"[{""label"":""FHL1"",""id"":""2273""}]"	"[""2273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070251""}]"
DOID:0070252	"[""autosomal dominant Emery-Dreifuss muscular dystrophy 7"",""EDMD7"",""Emery-Dreifuss muscular dystrophy 7, autosomal dominant""]"	"[{""label"":""TMEM43"",""id"":""79188""}]"	"[""79188""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070252""}]"
DOID:0070253	"[""congenital disorder of glycosylation type IIa"",""Alkuraya syndrome"",""CDG IIa"",""CDG2A"",""CDGIIa"",""CDGS2"",""carbohydrate-deficient glycoprotein syndrome, type II"",""congenital disorder of glycosylation, type IIa"",""mental retardation, growth retardation, prominent columella, and open mouth""]"	"[{""label"":""MGAT2"",""id"":""4247""}]"	"[""4247""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00358""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070253""}]"
DOID:0070253	"[""congenital disorder of glycosylation type IIa"",""Alkuraya syndrome"",""CDG IIa"",""CDG2A"",""CDGIIa"",""CDGS2"",""carbohydrate-deficient glycoprotein syndrome, type II"",""congenital disorder of glycosylation, type IIa"",""mental retardation, growth retardation, prominent columella, and open mouth""]"	"[{""label"":""Mgat2"",""id"":""217664""}]"	"[""217664""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070253""}]"
DOID:0070254	"[""congenital disorder of glycosylation type IIb"",""CDG IIb"",""CDG2B"",""CDGIIb"",""glucosidase I deficiency""]"	"[{""label"":""MOGS"",""id"":""7841""}]"	"[""7841""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00359""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070254""}]"
DOID:0070255	"[""congenital disorder of glycosylation type IIc"",""CDG IIc"",""CDG2C"",""CDGIIc"",""Rambam-Hasharon syndrome""]"	"[{""label"":""SLC35C1"",""id"":""55343""}]"	"[""55343""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00360""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070255""}]"
DOID:0070256	"[""congenital disorder of glycosylation type IId"",""CDG IId"",""CDG2D"",""CDGIId""]"	"[{""label"":""B4GALT1"",""id"":""2683""}]"	"[""2683""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00361""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070256""}]"
DOID:0070257	"[""congenital disorder of glycosylation type IIe"",""CDG IIe"",""CDG syndrome type IIe"",""CDG2E"",""CDGIIe"",""COG7-CDG"",""Carbohydrate deficient glycoprotein syndrome type IIe""]"	"[{""label"":""COG7"",""id"":""91949""}]"	"[""91949""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00362""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070257""}]"
DOID:0070258	"[""congenital disorder of glycosylation type IIf"",""CDG IIf"",""CDG2F"",""CDGIIf"",""CMP-sialic acid transporter deficiency"",""Carbohydrate deficient glycoprotein syndrome type IIf"",""SLC35A1-CDG""]"	"[{""label"":""SLC35A1"",""id"":""10559""}]"	"[""10559""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00363""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070258""}]"
DOID:0070259	"[""congenital disorder of glycosylation type IIg"",""CDG IIg"",""CDG2G"",""CDGII/COG1 cerebrocostomandibular-like syndrome"",""CDGIIg"",""Carbohydrate deficient glycoprotein syndrome type IIg""]"	"[{""label"":""COG1"",""id"":""9382""}]"	"[""9382""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00364""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070259""}]"
DOID:0070260	"[""congenital disorder of glycosylation type IIh"",""CDG IIh"",""CDG2H"",""CDGIIh"",""COG8-CDG"",""Carbohydrate deficient glycoprotein syndrome type IIh"",""Congenital disorder of glycosylation type 2h""]"	"[{""label"":""COG8"",""id"":""84342""}]"	"[""84342""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00365""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070260""}]"
DOID:0070261	"[""congenital disorder of glycosylation type IIi"",""CDG IIi"",""CDG syndrome type IIi"",""CDG2I"",""CDGIIi"",""COG5-CDG"",""Carbohydrate deficient glycoprotein syndrome type IIi"",""Congenital disorder of glycosylation type 2i""]"	"[{""label"":""COG5"",""id"":""10466""}]"	"[""10466""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00366""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070261""}]"
DOID:0070262	"[""congenital disorder of glycosylation type IIj"",""CDG IIj"",""CDG syndrome type IIj"",""CDG2J"",""CDGIIj"",""COG4-CDG"",""Carbohydrate deficient glycoprotein syndrome type IIj"",""Congenital disorder of glycosylation type 2j""]"	"[{""label"":""COG4"",""id"":""25839""}]"	"[""25839""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00367""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070262""}]"
DOID:0070262	"[""congenital disorder of glycosylation type IIj"",""CDG IIj"",""CDG syndrome type IIj"",""CDG2J"",""CDGIIj"",""COG4-CDG"",""Carbohydrate deficient glycoprotein syndrome type IIj"",""Congenital disorder of glycosylation type 2j""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070262""}]"
DOID:0070263	"[""congenital disorder of glycosylation type IIk"",""CDG IIk"",""CDG syndrome type IIk"",""CDG2K"",""CDGIIk"",""Carbohydrate deficient glycoprotein syndrome type IIk"",""Congenital disorder of glycosylation type 2k"",""TMEM165-CDG""]"	"[{""label"":""TMEM165"",""id"":""55858""}]"	"[""55858""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00626""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070263""}]"
DOID:0070264	"[""congenital disorder of glycosylation type IIl"",""CDG IIl"",""CDG syndrome type IIL"",""CDG2L"",""CDGIIl"",""COG6-CGD"",""Congenital disorder of glycosylation type 2l""]"	"[{""label"":""COG6"",""id"":""57511""}]"	"[""57511""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00627""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070264""}]"
DOID:0070265	"[""congenital disorder of glycosylation type IIm"",""CDG IIm"",""CDGIIm"",""DEE22"",""EIEE22"",""SLC35A2-CDG"",""congenital disorder of glycosylation type 2m"",""developmental and epileptic encephalopathy 22"",""epileptic encephalopathy, early infantile, 22""]"	"[{""label"":""SLC35A2"",""id"":""7355""}]"	"[""7355""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070265""}]"
DOID:0070266	"[""congenital disorder of glycosylation type IIn"",""CDG IIn"",""CDG syndrome type IIn"",""CDG2N"",""CDGIIn"",""Carbohydrate deficient glycoprotein syndrome type IIn"",""Congenital disorder of glycosylation type 2n"",""SLC39A8-CDG""]"	"[{""label"":""SLC39A8"",""id"":""64116""}]"	"[""64116""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070266""}]"
DOID:0070267	"[""congenital disorder of glycosylation type IIo"",""CCDC115-CDG"",""CDG IIo"",""CDG syndrome type IIo"",""CDG2O"",""CDGIIo"",""Carbohydrate deficient glycoprotein syndrome type IIo"",""Congenital disorder of glycosylation type 2o""]"	"[{""label"":""VMA22"",""id"":""84317""}]"	"[""84317""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070267""}]"
DOID:0070268	"[""congenital disorder of glycosylation type IIp"",""CDG IIp"",""CDG syndrome type IIp"",""CDG2P"",""CDGIIp"",""Carbohydrate deficient glycoprotein syndrome type IIp"",""Congenital disorder of glycosylation type 2p"",""TMEM199-CDG""]"	"[{""label"":""VMA12"",""id"":""147007""}]"	"[""147007""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070268""}]"
DOID:0070269	"[""congenital disorder of glycosylation type IIq"",""CDG IIq"",""CDG2Q"",""CDGIIq"",""COG2-CDG"",""COG2-related congenital disorder of glycosylation""]"	"[{""label"":""COG2"",""id"":""22796""}]"	"[""22796""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070269""}]"
DOID:0070270	"[""hereditary nonpolyposis colorectal cancer type 8"",""HNPCC8""]"	"[{""label"":""EPCAM"",""id"":""4072""}]"	"[""4072""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070270""}]"
DOID:0070271	"[""Lynch syndrome 1"",""COCA1"",""FCC1"",""HNPCC1"",""familial nonpolyposis colon cancer type 1"",""hereditary nonpolyposis colorectal cancer type 1""]"	"[{""label"":""MSH2"",""id"":""4436""}]"	"[""4436""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070271""}]"
DOID:0070272	"[""hereditary nonpolyposis colorectal cancer type 5"",""HNPCC5""]"	"[{""label"":""MSH6"",""id"":""2956""}]"	"[""2956""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070272""}]"
DOID:0070273	"[""hereditary nonpolyposis colorectal cancer type 6"",""HNPCC6""]"	"[{""label"":""TGFBR2"",""id"":""7048""}]"	"[""7048""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070273""}]"
DOID:0070274	"[""hereditary nonpolyposis colorectal cancer type 2"",""COCA2"",""FCC2"",""HNPCC2"",""familial nonpolyposis colon cancer type 2""]"	"[{""label"":""MLH1"",""id"":""4292""}]"	"[""4292""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070274""}]"
DOID:0070277	"[""primary autosomal recessive microcephaly 15"",""MCPH15"",""NEDMISBA"",""neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities""]"	"[{""label"":""MFSD2A"",""id"":""84879""}]"	"[""84879""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070277""}]"
DOID:0070279	"[""primary autosomal recessive microcephaly 14"",""MCPH14""]"	"[{""label"":""SASS6"",""id"":""163786""}]"	"[""163786""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070279""}]"
DOID:0070280	"[""primary autosomal recessive microcephaly 5"",""MCPH5""]"	"[{""label"":""ASPM"",""id"":""259266""}]"	"[""259266""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070280""}]"
DOID:0070281	"[""primary autosomal recessive microcephaly 19"",""MCPH19""]"	"[{""label"":""COPB2"",""id"":""9276""}]"	"[""9276""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070281""}]"
DOID:0070282	"[""primary autosomal recessive microcephaly 8"",""MCPH8""]"	"[{""label"":""CEP135"",""id"":""9662""}]"	"[""9662""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070282""}]"
DOID:0070283	"[""primary autosomal recessive microcephaly 13"",""MCPH13""]"	"[{""label"":""CENPE"",""id"":""1062""}]"	"[""1062""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070283""}]"
DOID:0070286	"[""primary autosomal recessive microcephaly 3"",""MCPH3""]"	"[{""label"":""CDK5RAP2"",""id"":""55755""}]"	"[""55755""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070286""}]"
DOID:0070287	"[""primary autosomal recessive microcephaly 11"",""MCPH11""]"	"[{""label"":""PHC1"",""id"":""1911""}]"	"[""1911""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070287""}]"
DOID:0070288	"[""primary autosomal recessive microcephaly 17"",""MCPH17""]"	"[{""label"":""CIT"",""id"":""11113""}]"	"[""11113""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070288""}]"
DOID:0070290	"[""primary autosomal recessive microcephaly 6"",""MCPH6""]"	"[{""label"":""Sas-4"",""id"":""40859""}]"	"[""40859""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070290""}]"
DOID:0070291	"[""primary autosomal recessive microcephaly 4"",""MCPH4""]"	"[{""label"":""KNL1"",""id"":""57082""}]"	"[""57082""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070291""}]"
DOID:0070292	"[""primary autosomal recessive microcephaly 9"",""MCPH9""]"	"[{""label"":""CEP152"",""id"":""22995""}]"	"[""22995""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070292""}]"
DOID:0070293	"[""primary autosomal recessive microcephaly 2 with or without cortical malformations"",""MCPH2""]"	"[{""label"":""WDR62"",""id"":""284403""}]"	"[""284403""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070293""}]"
DOID:0070294	"[""primary autosomal recessive microcephaly 10"",""MCPH10""]"	"[{""label"":""ZNF335"",""id"":""63925""}]"	"[""63925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070294""}]"
DOID:0070295	"[""primary autosomal dominant microcephaly 18"",""MCPH18""]"	"[{""label"":""WDFY3"",""id"":""23001""}]"	"[""23001""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070295""}]"
DOID:0070296	"[""primary autosomal recessive microcephaly"",""MCPH""]"	"[{""label"":""ASPM"",""id"":""259266""},{""label"":""BUB1"",""id"":""699""},{""label"":""KIF14"",""id"":""9928""},{""label"":""KNL1"",""id"":""57082""},{""label"":""LMNB1"",""id"":""4001""},{""label"":""LMNB2"",""id"":""84823""},{""label"":""NCAPD2"",""id"":""9918""},{""label"":""NCAPD3"",""id"":""23310""},{""label"":""PDCD6IP"",""id"":""10015""},{""label"":""TRAPPC14"",""id"":""55262""},{""label"":""WDR62"",""id"":""284403""}]"	"[""10015"",""23310"",""259266"",""284403"",""4001"",""55262"",""57082"",""699"",""84823"",""9918"",""9928""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070296""}]"
DOID:0070297	"[""primary microcephaly"",""true microcephaly""]"	"[{""label"":""CIT"",""id"":""11113""}]"	"[""11113""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070297""}]"
DOID:0070298	"[""multiple epiphyseal dysplasia 2"",""EDM2""]"	"[{""label"":""COL9A2"",""id"":""1298""}]"	"[""1298""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070298""}]"
DOID:0070299	"[""multiple epiphyseal dysplasia 5"",""BHMED"",""EDM5"",""bilateral hereditary microepiphyseal dysplasia"",""multiple epiphyseal dysplasia MATN3-related""]"	"[{""label"":""Matn3"",""id"":""17182""}]"	"[""17182""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070299""}]"
DOID:0070299	"[""multiple epiphyseal dysplasia 5"",""BHMED"",""EDM5"",""bilateral hereditary microepiphyseal dysplasia"",""multiple epiphyseal dysplasia MATN3-related""]"	"[{""label"":""MATN3"",""id"":""4148""}]"	"[""4148""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070299""}]"
DOID:0070300	"[""multiple epiphyseal dysplasia 4"",""EDM4"",""MED4"",""Polyepiphyseal dysplasia type 4"",""multiple epiphyseal dysplasia with bilateral patellae"",""multiple epiphyseal dysplasia with clubfoot"",""rMED""]"	"[{""label"":""SLC26A2"",""id"":""1836""}]"	"[""1836""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00398""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070300""}]"
DOID:0070301	"[""multiple epiphyseal dysplasia 6"",""EDM6""]"	"[{""label"":""COL9A1"",""id"":""1297""}]"	"[""1297""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070301""}]"
DOID:0070302	"[""multiple epiphyseal dysplasia 7"",""EDM7""]"	"[{""label"":""CANT1"",""id"":""124583""}]"	"[""124583""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070302""}]"
DOID:0070303	"[""multiple epiphyseal dysplasia 1"",""EDM1"",""MED1"",""multiple epiphyseal dysplasia COMP-related"",""polyepiphyseal dysplasia type 1""]"	"[{""label"":""COMP"",""id"":""1311""}]"	"[""1311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070303""}]"
DOID:0070304	"[""multiple epiphyseal dysplasia 3"",""EDM3"",""multiple epiphyseal dysplasia 3 with or without myopathy""]"	"[{""label"":""COL9A3"",""id"":""1299""}]"	"[""1299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070304""}]"
DOID:0070307	"[""craniolenticulosutural dysplasia"",""Boyadjiev-Jabs Syndrome"",""cranio-lenticulo-sutural dysplasia, CLSD""]"	"[{""label"":""SEC23A"",""id"":""10484""}]"	"[""10484""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070307""}]"
DOID:0070309	"[""absence epilepsy""]"	"[{""label"":""cacna1aa"",""id"":""562059""}]"	"[""562059""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070309""}]"
DOID:0070311	"[""oligoasthenoteratozoospermia"",""OAT"",""oligoasthenoteratospermia""]"	"[{""label"":""Agfg1"",""id"":""15463""},{""label"":""Spata20"",""id"":""217116""}]"	"[""15463"",""217116""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070311""}]"
DOID:0070316	"[""Miura type epiphyseal chondrodysplasia"",""ECDM"",""tall stature-scoliosis-macrodactyly of the great toes syndrome"",""tall stature-scoliosis-macrodactyly of the halluces syndrome""]"	"[{""label"":""NPR2"",""id"":""4882""}]"	"[""4882""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070316""}]"
DOID:0070330	"[""multiple mitochondrial dysfunctions syndrome"",""fatal multiple mitochondrial dysfunction syndrome""]"	"[{""label"":""GCSH"",""id"":""2653""}]"	"[""2653""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070330""}]"
DOID:0070332	"[""multiple mitochondrial dysfunctions syndrome 6""]"	"[{""label"":""PMPCB"",""id"":""9512""}]"	"[""9512""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070332""}]"
DOID:0070336	"[""arthrogryposis multiplex congenita-6""]"	"[{""label"":""NEB"",""id"":""4703""}]"	"[""4703""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070336""}]"
DOID:0070337	"[""epithelial recurrent erosion dystrophy"",""COL17A1"",""ERED""]"	"[{""label"":""COL17A1"",""id"":""1308""}]"	"[""1308""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070337""}]"
DOID:0070339	"[""cerebellar hyplasia/atrophy, epilepsy, and global developmental delay""]"	"[{""label"":""OXR1"",""id"":""55074""}]"	"[""55074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070339""}]"
DOID:0070340	"[""classic citrullinemia""]"	"[{""label"":""ASS1"",""id"":""445""}]"	"[""445""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070340""}]"
DOID:0070341	"[""neonatal-onset type II citrullinemia"",""neonatal-onset type 2 citrullinemia""]"	"[{""label"":""aralar1"",""id"":""43616""}]"	"[""43616""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070341""}]"
DOID:0070341	"[""neonatal-onset type II citrullinemia"",""neonatal-onset type 2 citrullinemia""]"	"[{""label"":""SLC25A13"",""id"":""10165""}]"	"[""10165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070341""}]"
DOID:0070342	"[""adult-onset type II citrullinemia"",""citrin deficiency""]"	"[{""label"":""SLC25A13"",""id"":""10165""}]"	"[""10165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070342""}]"
DOID:0070343	"[""CSF1R-related brain malformation and osteopetrosis"",""osteoporosis and infantile neuroaxonal dystrophy""]"	"[{""label"":""csf1ra"",""id"":""64274""}]"	"[""64274""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070343""}]"
DOID:0070345	"[""vertebral anomalies and variable endocrine and T-cell dysfunction"",""heterozygotes for TBX2 variants""]"	"[{""label"":""TBX2"",""id"":""6909""}]"	"[""6909""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070345""}]"
DOID:0070346	"[""neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies""]"	"[{""label"":""INTS1"",""id"":""26173""}]"	"[""26173""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070346""}]"
DOID:0070347	"[""encephalopathy due to defective mitochondrial and peroxisomal fission 1""]"	"[{""label"":""DNM1L"",""id"":""10059""}]"	"[""10059""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070347""}]"
DOID:0070351	"[""spinal muscular atrophy with lower extremity predominant 1"",""spinal muscular atrophy with lower extremity predominance 1""]"	"[{""label"":""DYNC1H1"",""id"":""1778""}]"	"[""1778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070351""}]"
DOID:0070352	"[""stress-induced childhood-onset neurodegeneration with variable ataxia and seizures"",""CONDSIAS""]"	"[{""label"":""Parg"",""id"":""31329""}]"	"[""31329""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070352""}]"
DOID:0070352	"[""stress-induced childhood-onset neurodegeneration with variable ataxia and seizures"",""CONDSIAS""]"	"[{""label"":""ADPRS"",""id"":""54936""}]"	"[""54936""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070352""}]"
DOID:0070354	"[""cataract 48"",""CTRCT48""]"	"[{""label"":""DNMBP"",""id"":""23268""}]"	"[""23268""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070354""}]"
DOID:0070355	"[""overactive bladder syndrome"",""OAB"",""overactive bladder"",""urge syndrome"",""urgency-frequency syndrome""]"	"[{""label"":""Bdkrb1"",""id"":""81509""},{""label"":""Ngf"",""id"":""310738""},{""label"":""Trpa1"",""id"":""312896""}]"	"[""310738"",""312896"",""81509""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070355""}]"
DOID:0070355	"[""overactive bladder syndrome"",""OAB"",""overactive bladder"",""urge syndrome"",""urgency-frequency syndrome""]"	"[{""label"":""NGF"",""id"":""4803""}]"	"[""4803""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070355""}]"
DOID:0070356	"[""visual impairment and progressive phthisis bulbi""]"	"[{""label"":""MARK3"",""id"":""4140""}]"	"[""4140""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070356""}]"
DOID:0070365	"[""nevoid basal cell carcinoma syndrome 1"",""basal cell nevus syndrome 1""]"	"[{""label"":""PTCH1"",""id"":""5727""}]"	"[""5727""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070365""}]"
DOID:0070370	"[""restrictive dermopathy 2""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070370""}]"
DOID:0070371	"[""leukoencephalopathy with vanishing white matter 4""]"	"[{""label"":""EIF2B4"",""id"":""8890""}]"	"[""8890""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070371""}]"
DOID:0070372	"[""leukoencephalopathy with vanishing white matter 3""]"	"[{""label"":""EIF2B3"",""id"":""8891""}]"	"[""8891""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070372""}]"
DOID:0070374	"[""leukoencephalopathy with vanishing white matter 1""]"	"[{""label"":""EIF2B1"",""id"":""1967""}]"	"[""1967""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070374""}]"
DOID:0070376	"[""developmental and epileptic encephalopathy 31B"",""DEE31B""]"	"[{""label"":""DNM1"",""id"":""1759""}]"	"[""1759""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070376""}]"
DOID:0070378	"[""developmental and epileptic encephalopathy 109"",""DEE109""]"	"[{""label"":""FZR1"",""id"":""51343""}]"	"[""51343""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070378""}]"
DOID:0070379	"[""developmental and epileptic encephalopathy 6B"",""DEE6B""]"	"[{""label"":""SCN1A"",""id"":""6323""}]"	"[""6323""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070379""}]"
DOID:0070380	"[""developmental and epileptic encephalopathy 85"",""DEE85"",""early infantile epileptic encephalopathy 85""]"	"[{""label"":""SMC1A"",""id"":""8243""}]"	"[""8243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070380""}]"
DOID:0070382	"[""developmental and epileptic encephalopathy 95"",""DEE95"",""early infantile epileptic encephalopathy 95""]"	"[{""label"":""PIGS"",""id"":""94005""}]"	"[""94005""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070382""}]"
DOID:0070383	"[""developmental and epileptic encephalopathy 97"",""DEE97"",""early infantile epileptic encephalopathy 97""]"	"[{""label"":""CELF2"",""id"":""10659""}]"	"[""10659""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070383""}]"
DOID:0070384	"[""developmental and epileptic encephalopathy 98"",""DEE98"",""early infantile epileptic encephalopathy 98""]"	"[{""label"":""ATP1A2"",""id"":""477""}]"	"[""477""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070384""}]"
DOID:0070387	"[""developmental and epileptic encephalopathy 101"",""DEE101"",""early infantile epileptic encephalopathy 101""]"	"[{""label"":""GRIN1"",""id"":""2902""}]"	"[""2902""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070387""}]"
DOID:0070388	"[""developmental and epileptic encephalopathy 102"",""DEE102"",""early infantile epileptic encephalopathy 102""]"	"[{""label"":""SLC38A3"",""id"":""10991""}]"	"[""10991""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070388""}]"
DOID:0070389	"[""developmental and epileptic encephalopathy 103"",""DEE103"",""early infantile epileptic encephalopathy 103""]"	"[{""label"":""KCNC2"",""id"":""3747""}]"	"[""3747""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070389""}]"
DOID:0070390	"[""developmental and epileptic encephalopathy 104"",""DEE104"",""early infantile epileptic encephalopathy 104""]"	"[{""label"":""ATP6V0A1"",""id"":""535""}]"	"[""535""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070390""}]"
DOID:0070391	"[""developmental and epileptic encephalopathy 105"",""DEE105"",""early infantile epileptic encephalopathy 105""]"	"[{""label"":""HID1"",""id"":""283987""}]"	"[""283987""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070391""}]"
DOID:0070394	"[""developmental and epileptic encephalopathy 108"",""DEE108"",""early infantile epileptic encephalopathy 108""]"	"[{""label"":""MAST3"",""id"":""23031""}]"	"[""23031""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070394""}]"
DOID:0070395	"[""developmental and epileptic encephalopathy 110"",""DEE110"",""early infantile epileptic encephalopathy 110""]"	"[{""label"":""CACNA2D1"",""id"":""781""}]"	"[""781""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070395""}]"
DOID:0070396	"[""progressive leukoencephalopathy with ovarian failure""]"	"[{""label"":""AARS2"",""id"":""57505""}]"	"[""57505""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070396""}]"
DOID:0070397	"[""hypomyelinating leukodystrophy 23"",""HLD23""]"	"[{""label"":""RNF220"",""id"":""55182""}]"	"[""55182""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070397""}]"
DOID:0070398	"[""hypomyelinating leukodystrophy 15"",""HLD15""]"	"[{""label"":""EPRS1"",""id"":""2058""}]"	"[""2058""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070398""}]"
DOID:0070399	"[""hypomyelinating leukodystrophy 18"",""HLD18""]"	"[{""label"":""DEGS1"",""id"":""8560""}]"	"[""8560""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070399""}]"
DOID:0070400	"[""hypomyelinating leukodystrophy 19"",""HLD19""]"	"[{""label"":""TMEM63A"",""id"":""9725""}]"	"[""9725""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070400""}]"
DOID:0070403	"[""hypomyelinating leukodystrophy 26"",""HLD26""]"	"[{""label"":""SLC35B2"",""id"":""347734""}]"	"[""347734""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070403""}]"
DOID:0070405	"[""hypomyelinating leukodystrophy 16"",""HLD16""]"	"[{""label"":""TMEM106B"",""id"":""54664""}]"	"[""54664""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070405""}]"
DOID:0070409	"[""autosomal recessive spinocerebellar ataxia 28"",""SCAR28""]"	"[{""label"":""THG1L"",""id"":""54974""}]"	"[""54974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070409""}]"
DOID:0070411	"[""autosomal recessive spinocerebellar ataxia 30"",""SCAR30""]"	"[{""label"":""PITRM1"",""id"":""10531""}]"	"[""10531""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070411""}]"
DOID:0070415	"[""brachycephaly, trichomegaly, and developmental delay"",""BTDD"",""MCINS"",""Macinnes syndrome""]"	"[{""label"":""RPS23"",""id"":""6228""}]"	"[""6228""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070415""}]"
DOID:0070416	"[""Luo-Schoch-Yamamoto syndrome"",""LUSYAM""]"	"[{""label"":""RNF2"",""id"":""6045""}]"	"[""6045""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070416""}]"
DOID:0070417	"[""neurodevelopmental disorder with speech impairment and dysmorphic facies"",""NEDSID""]"	"[{""label"":""SETD1A"",""id"":""9739""}]"	"[""9739""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070417""}]"
DOID:0070418	"[""vertebral hypersegmentation and orofacial anomalies"",""VHO""]"	"[{""label"":""GDF11"",""id"":""10220""}]"	"[""10220""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070418""}]"
DOID:0070420	"[""developmental delay, hypotonia, and impaired language"",""DEDHIL""]"	"[{""label"":""FBXW7"",""id"":""55294""}]"	"[""55294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070420""}]"
DOID:0070422	"[""syndromic X-linked intellectual disability Pilorge type"",""MRXSP""]"	"[{""label"":""GLRA2"",""id"":""2742""}]"	"[""2742""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070422""}]"
DOID:0070423	"[""early onset progressive encephalopathy with brain atrophy and thin corpus callosum"",""PEBAT"",""early-onset progressive encephalopathy with brain atrophy and thin corpus callosum""]"	"[{""label"":""TBCD"",""id"":""6904""}]"	"[""6904""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070423""}]"
DOID:0070425	"[""combined oxidative phosphorylation deficiency 52"",""COXPD52""]"	"[{""label"":""NFS1"",""id"":""9054""}]"	"[""9054""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070425""}]"
DOID:0070430	"[""combined oxidative phosphorylation deficiency 57"",""COXPD57""]"	"[{""label"":""CRLS1"",""id"":""54675""}]"	"[""54675""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070430""}]"
DOID:0070432	"[""hyperphosphatasia with impaired intellectual development syndrome 5"",""GPIBD11"",""HPMRS5"",""glycosylphosphatidylinositol biosynthesis defect 11"",""hyperphosphatasia with mental retardation syndrome 5""]"	"[{""label"":""PIGW"",""id"":""284098""}]"	"[""284098""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070432""}]"
DOID:0070433	"[""hyperphosphatasia with impaired intellectual development syndrome 1"",""GPIBD2"",""HPMRS1"",""glycosylphosphatidylinositol biosynthesis defect 2"",""hyperphosphatasia with mental retardation syndrome 1""]"	"[{""label"":""PIGV"",""id"":""55650""}]"	"[""55650""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00635""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070433""}]"
DOID:0070434	"[""hyperphosphatasia with impaired intellectual development syndrome 2"",""GPIBD6"",""HPMRS2"",""glycosylphosphatidylinositol biosynthesis defect 6"",""hyperphosphatasia with mental retardation syndrome 2""]"	"[{""label"":""PIGO"",""id"":""84720""}]"	"[""84720""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070434""}]"
DOID:0070435	"[""hyperphosphatasia with impaired intellectual development syndrome 3"",""GPIBD8"",""HPMRS3"",""glycosylphosphatidylinositol biosynthesis defect 8"",""hyperphosphatasia with mental retardation syndrome 3""]"	"[{""label"":""PGAP2"",""id"":""27315""}]"	"[""27315""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070435""}]"
DOID:0070436	"[""hyperphosphatasia with impaired intellectual development syndrome 4"",""GPIBD62"",""HPMRS6"",""glycosylphosphatidylinositol biosynthesis defect 62"",""hyperphosphatasia with mental retardation syndrome 6""]"	"[{""label"":""PGAP3"",""id"":""93210""}]"	"[""93210""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070436""}]"
DOID:0070437	"[""hyperphosphatasia with impaired intellectual development syndrome 6"",""GPIBD40"",""HPMRS4"",""glycosylphosphatidylinositol biosynthesis defect 40"",""hyperphosphatasia with mental retardation syndrome 4""]"	"[{""label"":""PIGY"",""id"":""84992""}]"	"[""84992""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070437""}]"
DOID:0070441	"[""retinal macular dystrophy 4"",""MCDR4""]"	"[{""label"":""CLEC3B"",""id"":""7123""}]"	"[""7123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070441""}]"
DOID:0070442	"[""paroxysmal nonkinesigenic dyskinesia 3"",""generalized epilepsy and paroxysmal dyskinesia""]"	"[{""label"":""KCNMA1"",""id"":""3778""}]"	"[""3778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070442""}]"
DOID:0070443	"[""neurodevelopmental disorder with cerebellar atrophy and motor dysfunction""]"	"[{""label"":""GEMIN5"",""id"":""25929""}]"	"[""25929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070443""}]"
DOID:0070444	"[""neurodevelopmental disorder with language delay and seizures""]"	"[{""label"":""TIAM1"",""id"":""7074""}]"	"[""7074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070444""}]"
DOID:0070450	"[""mitochondrial DNA depletion syndrome 19""]"	"[{""label"":""SLC25A10"",""id"":""1468""}]"	"[""1468""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070450""}]"
DOID:0070451	"[""mitochondrial DNA depletion syndrome 20"",""mitochondrial DNA depletion syndrome 20 (MNGIE type)""]"	"[{""label"":""LIG3"",""id"":""3980""}]"	"[""3980""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070451""}]"
DOID:0070453	"[""xanthinuria type II"",""XAN2""]"	"[{""label"":""MOCOS"",""id"":""55034""}]"	"[""55034""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070453""}]"
DOID:0070454	"[""hereditary spastic paraplegia 70"",""SPG70"",""autosomal recessive spastic paraplegia 70""]"	"[{""label"":""MARS1"",""id"":""4141""}]"	"[""4141""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070454""}]"
DOID:0070456	"[""hereditary spastic paraplegia 87"",""SPG87"",""autosomal recessive spastic paraplegia 87""]"	"[{""label"":""TMEM63C"",""id"":""57156""}]"	"[""57156""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070456""}]"
DOID:0070459	"[""hereditary spastic paraplegia 90A"",""SPG90A"",""autosomal dominant spastic paraplegia 90A""]"	"[{""label"":""SPTSSA"",""id"":""171546""}]"	"[""171546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070459""}]"
DOID:0070460	"[""hereditary spastic paraplegia 90B"",""SPG90B"",""autosomal recessive spastic paraplegia 90B""]"	"[{""label"":""SPTSSA"",""id"":""171546""}]"	"[""171546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070460""}]"
DOID:0070461	"[""mitochondrial complex V (ATP synthase) deficiency nuclear type 4A"",""MC5DN4A""]"	"[{""label"":""ATP5F1A"",""id"":""498""}]"	"[""498""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070461""}]"
DOID:0070462	"[""mitochondrial complex V (ATP synthase) deficiency nuclear type 4B"",""MC5DN4B""]"	"[{""label"":""ATP5F1A"",""id"":""498""}]"	"[""498""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070462""}]"
DOID:0070466	"[""carpal tunnel syndrome 1"",""CTS1""]"	"[{""label"":""TTR"",""id"":""7276""}]"	"[""7276""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070466""}]"
DOID:0070467	"[""carpal tunnel syndrome 2"",""CTS2""]"	"[{""label"":""COMP"",""id"":""1311""}]"	"[""1311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070467""}]"
DOID:0070468	"[""Yoon-Bellen neurodevelopmental syndrome"",""YOBELN""]"	"[{""label"":""OGDHL"",""id"":""55753""}]"	"[""55753""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070468""}]"
DOID:0070469	"[""neurodevelopmental disorder with dysmorphic facies and thin corpus callosum"",""NEDDFAC""]"	"[{""label"":""SUPT16H"",""id"":""11198""}]"	"[""11198""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070469""}]"
DOID:0070471	"[""early-onset epilepsy 2"",""EPEO2""]"	"[{""label"":""SETD1A"",""id"":""9739""}]"	"[""9739""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070471""}]"
DOID:0070472	"[""early-onset epilepsy 3"",""EPEO3""]"	"[{""label"":""ATP6V0C"",""id"":""527""}]"	"[""527""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070472""}]"
DOID:0070473	"[""Zaki syndrome""]"	"[{""label"":""WLS"",""id"":""79971""}]"	"[""79971""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070473""}]"
DOID:0070474	"[""childhood-onset neurodegeneration with brain atrophy"",""CONDBA"",""childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder""]"	"[{""label"":""UBTF"",""id"":""7343""}]"	"[""7343""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070474""}]"
DOID:0070478	"[""diphthamide deficiency syndrome 2"",""DEDSSH2"",""developmental delay with short stature, dysmorphic facial features, and sparse hair 2""]"	"[{""label"":""DPH2"",""id"":""1802""}]"	"[""1802""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070478""}]"
DOID:0070480	"[""schwannomatosis 1"",""SMARCB1-related schwannomatosis"",""SWN1""]"	"[{""label"":""SMARCB1"",""id"":""6598""}]"	"[""6598""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070480""}]"
DOID:0070482	"[""spinal neurofibromatosis"",""FNSF"",""SNF"",""familial spinal neurofibromatosis""]"	"[{""label"":""NF1"",""id"":""4763""}]"	"[""4763""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070482""}]"
DOID:0070483	"[""Watson syndrome""]"	"[{""label"":""NF1"",""id"":""4763""}]"	"[""4763""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070483""}]"
DOID:0070484	"[""Legius syndrome"",""LGSS"",""NF1-like syndrome"",""neurofibromatosis type 1-like syndrome""]"	"[{""label"":""SPRED1"",""id"":""161742""}]"	"[""161742""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070484""}]"
DOID:0070485	"[""mitochondrial complex IV deficiency nuclear type 23"",""MC4DN23""]"	"[{""label"":""COX11"",""id"":""1353""}]"	"[""1353""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070485""}]"
DOID:0070486	"[""Parkinson's disease 25"",""PARK25"",""autosomal recessive early-onset Parkinson disease 25 with impaired intellectual development""]"	"[{""label"":""PTPA"",""id"":""5524""}]"	"[""5524""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070486""}]"
DOID:0070489	"[""classic dopamine transporter deficiency syndrome"",""PKDYS1"",""classic DTDS"",""infantile parkinsonism-dystonia 1""]"	"[{""label"":""DAT"",""id"":""36849""}]"	"[""36849""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070489""}]"
DOID:0070489	"[""classic dopamine transporter deficiency syndrome"",""PKDYS1"",""classic DTDS"",""infantile parkinsonism-dystonia 1""]"	"[{""label"":""SLC6A3"",""id"":""6531""}]"	"[""6531""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070489""}]"
DOID:0070490	"[""infantile parkinsonism-dystonia 2"",""Brain dopamine-serotonin vesicular transport disease"",""PKDYS2""]"	"[{""label"":""SLC18A2"",""id"":""6571""}]"	"[""6571""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070490""}]"
DOID:0070491	"[""mitochondrial complex IV deficiency nuclear type 1"",""MC4DN1""]"	"[{""label"":""SURF1"",""id"":""6834""}]"	"[""6834""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070491""}]"
DOID:0070495	"[""mitochondrial complex IV deficiency nuclear type 8"",""MC4DN8""]"	"[{""label"":""TACO1"",""id"":""51204""}]"	"[""51204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070495""}]"
DOID:0070508	"[""metabolic dysfunction and alcohol associated liver disease"",""MetALD"",""metabolic dysfunction and alcohol related liver disease""]"	"[{""label"":""ALDH2"",""id"":""217""},{""label"":""TNF"",""id"":""7124""}]"	"[""217"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070508""}]"
DOID:0070508	"[""metabolic dysfunction and alcohol associated liver disease"",""MetALD"",""metabolic dysfunction and alcohol related liver disease""]"	"[{""label"":""Aldh2"",""id"":""29539""}]"	"[""29539""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070508""}]"
DOID:0070509	"[""Schinzel Giedion syndrome"",""SGS"",""Schinzel-Giedion midface retraction syndrome""]"	"[{""label"":""SETBP1"",""id"":""26040""}]"	"[""26040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070509""}]"
DOID:0070511	"[""polyhydramnios, megalencephaly, and symptomatic epilepsy"",""PMSE"",""PMSE syndrome"",""Pretzel syndrome""]"	"[{""label"":""STRADA"",""id"":""92335""}]"	"[""92335""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070511""}]"
DOID:0070514	"[""neurodevelopmental disorder with dysmorphic facies and distal limb anomalies"",""NEDDFL""]"	"[{""label"":""BPTF"",""id"":""2186""}]"	"[""2186""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070514""}]"
DOID:0070515	"[""chromosome 16p11.2 deletion syndrome, 593-kb"",""Proximal 16p11.2 microdeletion syndrome""]"	"[{""label"":""Atx2"",""id"":""41883""}]"	"[""41883""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070515""}]"
DOID:0070516	"[""Mitchell syndrome""]"	"[{""label"":""ACOX1"",""id"":""51""}]"	"[""51""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070516""}]"
DOID:0070516	"[""Mitchell syndrome""]"	"[{""label"":""ACOX1"",""id"":""37028""}]"	"[""37028""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070516""}]"
DOID:0070517	"[""retinal macular dystrophy 2"",""MCDR2""]"	"[{""label"":""PROM1"",""id"":""8842""}]"	"[""8842""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070517""}]"
DOID:0070519	"[""early-onset vitamin B6-dependent epilepsy 4"",""AASA dehydrogenase deficiency"",""EPEO4"",""PDE-ALDH7A1"",""antiquitin deficiency""]"	"[{""label"":""ALDH7A1"",""id"":""501""}]"	"[""501""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070519""}]"
DOID:0070520	"[""peeling skin syndrome 1"",""PSS1"",""generalized inflammatory peeling skin syndrome"",""inflammatory peeling skin syndrome"",""peeling skin syndrome type B""]"	"[{""label"":""CDSN"",""id"":""1041""}]"	"[""1041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070520""}]"
DOID:0070521	"[""peeling skin syndrome 2"",""PSS2""]"	"[{""label"":""TGM5"",""id"":""9333""}]"	"[""9333""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070521""}]"
DOID:0070525	"[""peeling skin syndrome 6"",""PSS6""]"	"[{""label"":""FLG2"",""id"":""388698""}]"	"[""388698""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070525""}]"
DOID:0070526	"[""PLACK syndrome"",""peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads""]"	"[{""label"":""CAST"",""id"":""831""}]"	"[""831""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070526""}]"
DOID:0070529	"[""Sifrim-Hitz-Weiss syndrome"",""CHD4 Neurodevelopmental Disorder"",""CHD4-related neurodevelopmental disorder"",""CHD4-related neurodevelopmental syndrome"",""SIFRIM-HITZ-WEISS MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDATION SYNDROME"",""SIHIWES""]"	"[{""label"":""CHD4"",""id"":""1108""}]"	"[""1108""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070529""}]"
DOID:0070536	"[""neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures"",""NEDHLSS""]"	"[{""label"":""CACNA1C"",""id"":""775""}]"	"[""775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070536""}]"
DOID:0070537	"[""spastic tetraplegia, thin corpus callosum, and progressive microcephaly"",""SPATCCM""]"	"[{""label"":""Slc1a4"",""id"":""55963""}]"	"[""55963""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070537""}]"
DOID:0070537	"[""spastic tetraplegia, thin corpus callosum, and progressive microcephaly"",""SPATCCM""]"	"[{""label"":""SLC1A4"",""id"":""6509""}]"	"[""6509""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070537""}]"
DOID:0070538	"[""syndromic X-linked intellectual developmental disorder bain type"",""HNRNPH2-RNDD"",""HNRNPH2-related neurodevelopmental disorder"",""MRXSB"",""Mental Retardation, X-linked, Syndrome, Bain Type""]"	"[{""label"":""HNRNPH2"",""id"":""3188""}]"	"[""3188""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070538""}]"
DOID:0070538	"[""syndromic X-linked intellectual developmental disorder bain type"",""HNRNPH2-RNDD"",""HNRNPH2-related neurodevelopmental disorder"",""MRXSB"",""Mental Retardation, X-linked, Syndrome, Bain Type""]"	"[{""label"":""Hnrnph2"",""id"":""56258""}]"	"[""56258""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070538""}]"
DOID:0070539	"[""Halperin-Birk syndrome"",""HLBKS"",""NEDSOSB"",""NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES""]"	"[{""label"":""SEC31A"",""id"":""22872""}]"	"[""22872""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070539""}]"
DOID:0070540	"[""mitochondrial short-chain enoyl-CoA hydratase 1 deficiency"",""ECHS1D""]"	"[{""label"":""ECHS1"",""id"":""1892""}]"	"[""1892""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070540""}]"
DOID:0070541	"[""3-hydroxy-3-methylglutaryl-CoA lyase deficiency"",""3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency"",""HMG-CoA lyase deficiency"",""HMGCL deficiency"",""HMGCLD"",""hydroxymethylglutaric aciduria""]"	"[{""label"":""HMGCL"",""id"":""3155""}]"	"[""3155""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070541""}]"
DOID:0070543	"[""neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities"",""NEDCASB""]"	"[{""label"":""SHMT2"",""id"":""6472""}]"	"[""6472""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070543""}]"
DOID:0070544	"[""congenital glutamine deficiency"",""GLND"",""congenital systemic glutamine synthase deficiency""]"	"[{""label"":""GLUL"",""id"":""2752""}]"	"[""2752""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070544""}]"
DOID:0070545	"[""developmental and epileptic encephalopathy 116"",""DEE116""]"	"[{""label"":""GLUL"",""id"":""2752""}]"	"[""2752""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070545""}]"
DOID:0070546	"[""primary pigmented nodular adrenocortical disease 1"",""PPNAD1""]"	"[{""label"":""PRKAR1A"",""id"":""5573""}]"	"[""5573""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070546""}]"
DOID:0070547	"[""primary pigmented nodular adrenocortical disease 2"",""PPNAD2""]"	"[{""label"":""PDE11A"",""id"":""50940""}]"	"[""50940""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070547""}]"
DOID:0070550	"[""KRT1-related nonepidermolytic palmoplantar keratoderma"",""KRT1-related NEPPK""]"	"[{""label"":""KRT1"",""id"":""3848""}]"	"[""3848""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070550""}]"
DOID:0070551	"[""epidermolytic palmoplantar keratoderma 2"",""EPPK2""]"	"[{""label"":""KRT1"",""id"":""3848""}]"	"[""3848""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070551""}]"
DOID:0070552	"[""epidermolytic palmoplantar keratoderma 1"",""EPPK1""]"	"[{""label"":""KRT9"",""id"":""3857""}]"	"[""3857""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070552""}]"
DOID:0070554	"[""palmoplantar keratoderma and woolly hair"",""PPKWH"",""keratoderma with woolly hair type IV"",""woolly hair-palmoplantar keratoderma syndrome type 4""]"	"[{""label"":""KANK2"",""id"":""25959""}]"	"[""25959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070554""}]"
DOID:0070555	"[""Nagashima-type palmoplantar keratosis"",""NPPK"",""PPKN"",""palmoplantar keratoderma nagashima type""]"	"[{""label"":""SERPINB7"",""id"":""8710""}]"	"[""8710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070555""}]"
DOID:0070556	"[""cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 1"",""CAMRQ syndrome 1"",""CAMRQ1"",""DES-VLDLR"",""VLDLR cerebellar hypoplasia"",""VLDLR-CH"",""VLDLR-associated cerebellar hypoplasia"",""cerebellar ataxia and mental retardation with or without quadrupedal locomotion 1"",""cerebellar ataxia, mental retardation, and disequilibrium syndrome 1"",""cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1"",""cerebellar hypoplasia, VLDLR-associated"",""dysequilibrium syndrome-VLDLR""]"	"[{""label"":""VLDLR"",""id"":""7436""}]"	"[""7436""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070556""}]"
DOID:0070560	"[""glucose transporter type 1 deficiency syndrome"",""GLUT1DS""]"	"[{""label"":""SLC2A1"",""id"":""6513""}]"	"[""6513""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070560""}]"
DOID:0070561	"[""glucose transporter type 1 deficiency syndrome 1"",""De Vivo disease"",""GLUT1 deficiency syndrome 1"",""GLUT1DS1"",""classic GLUT1 deficiency syndrome"",""classic GLUT1-DS"",""classic glucose transporter type 1 deficiency syndrome"",""encephalopathy due to GLUT1 deficiency""]"	"[{""label"":""Slc2a1"",""id"":""20525""}]"	"[""20525""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070561""}]"
DOID:0070561	"[""glucose transporter type 1 deficiency syndrome 1"",""De Vivo disease"",""GLUT1 deficiency syndrome 1"",""GLUT1DS1"",""classic GLUT1 deficiency syndrome"",""classic GLUT1-DS"",""classic glucose transporter type 1 deficiency syndrome"",""encephalopathy due to GLUT1 deficiency""]"	"[{""label"":""SLC2A1"",""id"":""6513""}]"	"[""6513""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070561""}]"
DOID:0070562	"[""Fanconi-Bickel syndrome"",""FBS"",""glycogen storage disease XI"",""glycogenosis type XI"",""glycogenosis, Fanconi type""]"	"[{""label"":""SLC2A2"",""id"":""6514""}]"	"[""6514""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070562""}]"
DOID:0070563	"[""glucose-galactose malabsorption"",""GGM"",""SGLT1 deficiency"",""monosaccharide malabsorption""]"	"[{""label"":""SLC5A1"",""id"":""6523""}]"	"[""6523""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070563""}]"
DOID:0070565	"[""spermatogenic failure 66"",""SPGF66""]"	"[{""label"":""ZPBP"",""id"":""11055""}]"	"[""11055""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070565""}]"
DOID:0070566	"[""spermatogenic failure 67"",""SPGF67""]"	"[{""label"":""CCDC62"",""id"":""84660""}]"	"[""84660""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070566""}]"
DOID:0070567	"[""spermatogenic failure 68"",""SPGF68""]"	"[{""label"":""C2CD6"",""id"":""151254""}]"	"[""151254""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070567""}]"
DOID:0070568	"[""spermatogenic failure 69"",""SPGF69""]"	"[{""label"":""GGN"",""id"":""199720""}]"	"[""199720""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070568""}]"
DOID:0070569	"[""spermatogenic failure 70"",""SPGF70""]"	"[{""label"":""PDHA2"",""id"":""5161""}]"	"[""5161""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070569""}]"
DOID:0070572	"[""spermatogenic failure 73"",""SPGF73""]"	"[{""label"":""MOV10L1"",""id"":""54456""}]"	"[""54456""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070572""}]"
DOID:0070577	"[""spermatogenic failure 78"",""SPGF78""]"	"[{""label"":""IQCN"",""id"":""80726""}]"	"[""80726""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070577""}]"
DOID:0070578	"[""spermatogenic failure 79"",""SPGF79""]"	"[{""label"":""KCNU1"",""id"":""157855""}]"	"[""157855""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070578""}]"
DOID:0070579	"[""spermatogenic failure 80"",""SPGF80""]"	"[{""label"":""DRC1"",""id"":""92749""}]"	"[""92749""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070579""}]"
DOID:0070580	"[""spermatogenic failure 81"",""SPGF81""]"	"[{""label"":""TEKT3"",""id"":""64518""}]"	"[""64518""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070580""}]"
DOID:0070583	"[""spermatogenic failure 84"",""SPGF84""]"	"[{""label"":""CFAP61"",""id"":""26074""}]"	"[""26074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070583""}]"
DOID:0070584	"[""spermatogenic failure 85"",""SPGF85""]"	"[{""label"":""SPACA1"",""id"":""81833""}]"	"[""81833""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070584""}]"
DOID:0070586	"[""spermatogenic failure 87"",""SPGF87""]"	"[{""label"":""ACR"",""id"":""49""}]"	"[""49""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070586""}]"
DOID:0070587	"[""spermatogenic failure 88"",""SPGF88""]"	"[{""label"":""KASH5"",""id"":""147872""}]"	"[""147872""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070587""}]"
DOID:0070588	"[""spermatogenic failure 89"",""SPGF89""]"	"[{""label"":""AK9"",""id"":""221264""}]"	"[""221264""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070588""}]"
DOID:0070595	"[""X-linked spermatogenic failure 4"",""SPGFX4""]"	"[{""label"":""GCNA"",""id"":""93953""}]"	"[""93953""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070595""}]"
DOID:0070597	"[""X-linked spermatogenic failure 6"",""SPGFX6""]"	"[{""label"":""USP26"",""id"":""83844""}]"	"[""83844""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070597""}]"
DOID:0070599	"[""X-linked spermatogenic failure 8"",""SPGFX8""]"	"[{""label"":""CYLC1"",""id"":""1538""}]"	"[""1538""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070599""}]"
DOID:0070600	"[""intellectual disability and myopathy syndrome"",""ABCC9-related intellectual disability and myopathy"",""AIMS"",""IDMYS""]"	"[{""label"":""ABCC9"",""id"":""10060""}]"	"[""10060""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070600""}]"
DOID:0070601	"[""autosomal dominant nonsyndromic deafness 37"",""DFNA37"",""autosomal dominant deafness 37""]"	"[{""label"":""COL11A1"",""id"":""1301""}]"	"[""1301""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070601""}]"
DOID:0070602	"[""autosomal dominant nonsyndromic deafness 80"",""DFNA80"",""autosomal dominant deafness 80""]"	"[{""label"":""GREB1L"",""id"":""80000""}]"	"[""80000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070602""}]"
DOID:0070605	"[""autosomal dominant nonsyndromic deafness 85"",""DFNA85"",""autosomal dominant deafness 85""]"	"[{""label"":""USP48"",""id"":""84196""}]"	"[""84196""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070605""}]"
DOID:0070606	"[""autosomal dominant nonsyndromic deafness 87"",""DFNA87"",""autosomal dominant deafness 87""]"	"[{""label"":""PI4KB"",""id"":""5298""}]"	"[""5298""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070606""}]"
DOID:0070609	"[""autosomal dominant nonsyndromic deafness 83"",""DFNA83"",""autosomal dominant deafness 83""]"	"[{""label"":""MAP1B"",""id"":""4131""}]"	"[""4131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070609""}]"
DOID:0070610	"[""autosomal dominant nonsyndromic deafness 86"",""DFNA86"",""autosomal dominant deafness 86""]"	"[{""label"":""THOC1"",""id"":""9984""}]"	"[""9984""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070610""}]"
DOID:0070611	"[""autosomal dominant nonsyndromic deafness 88"",""DFNA88"",""autosomal dominant deafness 88""]"	"[{""label"":""EPHA10"",""id"":""284656""}]"	"[""284656""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070611""}]"
DOID:0070613	"[""familial renal glucosuria"",""FRG"",""SGLT2 deficiency"",""familial renal glycosuria"",""hereditary renal glycosuria""]"	"[{""label"":""SLC5A2"",""id"":""6524""}]"	"[""6524""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070613""}]"
DOID:0070615	"[""autoinflammation, antibody deficiency, and immune dysregulation syndrome"",""APLAID"",""autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation""]"	"[{""label"":""PLCG2"",""id"":""5336""}]"	"[""5336""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070615""}]"
DOID:0070616	"[""glycine encephalopathy 1"",""GCE1""]"	"[{""label"":""GLDC"",""id"":""2731""}]"	"[""2731""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070616""}]"
DOID:0070618	"[""rhabdoid tumor predisposition syndrome 1"",""RTPS1""]"	"[{""label"":""SMARCB1"",""id"":""6598""}]"	"[""6598""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070618""}]"
DOID:0070619	"[""mitochondrial trifunctional protein deficiency 1"",""MTPD1""]"	"[{""label"":""HADHA"",""id"":""3030""}]"	"[""3030""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0070619""}]"
DOID:0080000	"[""muscular disease""]"	"[{""label"":""CLU"",""id"":""1191""},{""label"":""CPT2"",""id"":""1376""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""ITGA7"",""id"":""3679""},{""label"":""LPL"",""id"":""4023""}]"	"[""1191"",""1376"",""3156"",""3679"",""4023""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080000""}]"
DOID:0080001	"[""bone disease""]"	"[{""label"":""Npr3"",""id"":""18162""}]"	"[""18162""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080001""}]"
DOID:0080001	"[""bone disease""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080001""}]"
DOID:0080005	"[""bone remodeling disease""]"	"[{""label"":""Idh2"",""id"":""269951""}]"	"[""269951""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080005""}]"
DOID:0080006	"[""bone development disease""]"	"[{""label"":""Npr2"",""id"":""230103""}]"	"[""230103""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080006""}]"
DOID:0080006	"[""bone development disease""]"	"[{""label"":""FLNB"",""id"":""2317""},{""label"":""TNFRSF11A"",""id"":""8792""}]"	"[""2317"",""8792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080006""}]"
DOID:0080010	"[""bone structure disease""]"	"[{""label"":""Postn"",""id"":""50706""},{""label"":""Qrfpr"",""id"":""229214""}]"	"[""229214"",""50706""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080010""}]"
DOID:0080015	"[""physical disorder"",""congenital disorder""]"	"[{""label"":""Bmp4"",""id"":""12159""}]"	"[""12159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080015""}]"
DOID:0080016	"[""spina bifida""]"	"[{""label"":""APEX1"",""id"":""328""},{""label"":""GLI2"",""id"":""2736""},{""label"":""MTHFD1"",""id"":""4522""},{""label"":""MTR"",""id"":""4548""}]"	"[""2736"",""328"",""4522"",""4548""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080016""}]"
DOID:0080019	"[""metaphyseal dysplasia"",""Bakwin-Krida syndrome"",""Pyle's disease"",""Pyle-Cohn syndrome""]"	"[{""label"":""SFRP4"",""id"":""6424""}]"	"[""6424""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080019""}]"
DOID:0080020	"[""Jansen's metaphyseal chondrodysplasia"",""Jansen Disease"",""Jansen Metaphyseal Dysostosis"",""Jansen metaphyseal chondrodysplasia"",""Murk Jansen Type Metaphyseal Chondrodysplasia""]"	"[{""label"":""PTH1R"",""id"":""5745""}]"	"[""5745""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080020""}]"
DOID:0080021	"[""Schmid metaphyseal chondrodysplasia"",""Japanese type spondylometaphyseal dysplasia"",""Schmid type metaphyseal dysplasia""]"	"[{""label"":""COL10A1"",""id"":""1300""}]"	"[""1300""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080021""}]"
DOID:0080026	"[""otospondylomegaepiphyseal dysplasia, autosomal recessive"",""CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS"",""NANCE-INSLEY SYNDROME"",""NANCE-SWEENEY CHONDRODYSPLASIA"",""OSMEDB""]"	"[{""label"":""COL11A2"",""id"":""1302""}]"	"[""1302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080026""}]"
DOID:0080026	"[""otospondylomegaepiphyseal dysplasia, autosomal recessive"",""CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS"",""NANCE-INSLEY SYNDROME"",""NANCE-SWEENEY CHONDRODYSPLASIA"",""OSMEDB""]"	"[{""label"":""Col11a2"",""id"":""12815""}]"	"[""12815""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080026""}]"
DOID:0080027	"[""spondyloepimetaphyseal dysplasia""]"	"[{""label"":""Col2a1"",""id"":""12824""}]"	"[""12824""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080027""}]"
DOID:0080028	"[""spondyloepimetaphyseal dysplasia, Strudwick type""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080028""}]"
DOID:0080030	"[""spondyloepimetaphyseal dysplasia, Missouri type""]"	"[{""label"":""MMP13"",""id"":""4322""}]"	"[""4322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080030""}]"
DOID:0080036	"[""SOST-related sclerosing bone dysplasia"",""van Buchem disease""]"	"[{""label"":""Sost"",""id"":""74499""}]"	"[""74499""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080036""}]"
DOID:0080037	"[""Worth syndrome"",""Worth's syndrome"",""autosomal dominant endosteal hyperostosis"",""autosomal dominant osteosclerosis"",""benign form of Worth hyperostosis corticalis generalisata with torus platinus""]"	"[{""label"":""LRP5"",""id"":""4041""}]"	"[""4041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080037""}]"
DOID:0080038	"[""pycnodysostosis""]"	"[{""label"":""CTSK"",""id"":""1513""}]"	"[""1513""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080038""}]"
DOID:0080041	"[""hypochondroplasia""]"	"[{""label"":""FGFR3"",""id"":""2261""}]"	"[""2261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080041""}]"
DOID:0080042	"[""autosomal recessive spinocerebellar ataxia 18"",""SCAR18""]"	"[{""label"":""GRID2"",""id"":""2895""}]"	"[""2895""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080042""}]"
DOID:0080042	"[""autosomal recessive spinocerebellar ataxia 18"",""SCAR18""]"	"[{""label"":""Grid2"",""id"":""14804""}]"	"[""14804""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080042""}]"
DOID:0080044	"[""hypochondrogenesis""]"	"[{""label"":""Col2a1"",""id"":""12824""}]"	"[""12824""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080044""}]"
DOID:0080045	"[""Kniest dysplasia""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080045""}]"
DOID:0080046	"[""Stickler syndrome""]"	"[{""label"":""Col11a1"",""id"":""12814""},{""label"":""Col11a2"",""id"":""12815""}]"	"[""12814"",""12815""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080046""}]"
DOID:0080046	"[""Stickler syndrome""]"	"[{""label"":""COL2A1"",""id"":""1280""},{""label"":""COL9A1"",""id"":""1297""},{""label"":""COL9A2"",""id"":""1298""},{""label"":""COL9A3"",""id"":""1299""}]"	"[""1280"",""1297"",""1298"",""1299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080046""}]"
DOID:0080047	"[""pseudoachondroplasia"",""SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC"",""pseudoachondroplastic dysplasia""]"	"[{""label"":""COMP"",""id"":""1311""}]"	"[""1311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080047""}]"
DOID:0080047	"[""pseudoachondroplasia"",""SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC"",""pseudoachondroplastic dysplasia""]"	"[{""label"":""Comp"",""id"":""12845""}]"	"[""12845""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080047""}]"
DOID:0080050	"[""acromesomelic dysplasia, Maroteaux type"",""acromesomelic dysplasia-1""]"	"[{""label"":""Npr2"",""id"":""230103""}]"	"[""230103""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080050""}]"
DOID:0080050	"[""acromesomelic dysplasia, Maroteaux type"",""acromesomelic dysplasia-1""]"	"[{""label"":""NPR2"",""id"":""4882""}]"	"[""4882""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080050""}]"
DOID:0080051	"[""acromesomelic dysplasia, Hunter-Thompson type"",""acromesomelic dwarfism"",""acromesomelic dysplasia-2C""]"	"[{""label"":""Gdf5"",""id"":""14563""}]"	"[""14563""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080051""}]"
DOID:0080051	"[""acromesomelic dysplasia, Hunter-Thompson type"",""acromesomelic dwarfism"",""acromesomelic dysplasia-2C""]"	"[{""label"":""GDF5"",""id"":""8200""}]"	"[""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080051""}]"
DOID:0080052	"[""acromesomelic dysplasia, Grebe type"",""acromesomelic dysplasia-2A"",""grebe chondrodysplasia""]"	"[{""label"":""GDF5"",""id"":""8200""}]"	"[""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080052""}]"
DOID:0080052	"[""acromesomelic dysplasia, Grebe type"",""acromesomelic dysplasia-2A"",""grebe chondrodysplasia""]"	"[{""label"":""Gdf5"",""id"":""14563""}]"	"[""14563""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080052""}]"
DOID:0080053	"[""pseudohypoparathyroidism type 1A"",""Albright hereditary osteodystrophy"",""Albright's hereditary osteodystrophy"",""PHP Ia""]"	"[{""label"":""Gnas"",""id"":""14683""}]"	"[""14683""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080053""}]"
DOID:0080053	"[""pseudohypoparathyroidism type 1A"",""Albright hereditary osteodystrophy"",""Albright's hereditary osteodystrophy"",""PHP Ia""]"	"[{""label"":""GNAS"",""id"":""2778""}]"	"[""2778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080053""}]"
DOID:0080054	"[""achondrogenesis type IA"",""achondrogenesis Houston-Harris type""]"	"[{""label"":""TRIP11"",""id"":""9321""}]"	"[""9321""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080054""}]"
DOID:0080055	"[""achondrogenesis type IB"",""achondrogenesis Fraccaro type""]"	"[{""label"":""SLC26A2"",""id"":""1836""}]"	"[""1836""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00396""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080055""}]"
DOID:0080056	"[""achondrogenesis type II""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080056""}]"
DOID:0080056	"[""achondrogenesis type II""]"	"[{""label"":""Col2a1"",""id"":""12824""}]"	"[""12824""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080056""}]"
DOID:0080058	"[""autosomal recessive spinocerebellar ataxia 14"",""SCAR14""]"	"[{""label"":""SPTBN2"",""id"":""6712""}]"	"[""6712""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080058""}]"
DOID:0080059	"[""autosomal recessive spinocerebellar ataxia 7"",""SCAR7""]"	"[{""label"":""TPP1"",""id"":""1200""}]"	"[""1200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080059""}]"
DOID:0080061	"[""autosomal recessive spinocerebellar ataxia 2"",""SCAR2""]"	"[{""label"":""PMPCA"",""id"":""23203""}]"	"[""23203""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080061""}]"
DOID:0080062	"[""autosomal recessive spinocerebellar ataxia 13"",""SCAR13""]"	"[{""label"":""GRM1"",""id"":""2911""}]"	"[""2911""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080062""}]"
DOID:0080062	"[""autosomal recessive spinocerebellar ataxia 13"",""SCAR13""]"	"[{""label"":""Grm1"",""id"":""14816""}]"	"[""14816""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080062""}]"
DOID:0080065	"[""autosomal recessive spinocerebellar ataxia 19"",""Lichtenstein-Knorr syndrome"",""SCAR19""]"	"[{""label"":""SLC9A1"",""id"":""6548""}]"	"[""6548""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080065""}]"
DOID:0080066	"[""autosomal recessive spinocerebellar ataxia 20"",""SCAR20""]"	"[{""label"":""MDM1"",""id"":""854867""}]"	"[""854867""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080066""}]"
DOID:0080070	"[""mucolipidosis II alpha/beta"",""I-cell disease"",""inclusion-cell disease"",""mucolipidosis II""]"	"[{""label"":""Gnptab"",""id"":""432486""}]"	"[""432486""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080070""}]"
DOID:0080070	"[""mucolipidosis II alpha/beta"",""I-cell disease"",""inclusion-cell disease"",""mucolipidosis II""]"	"[{""label"":""GNPTAB"",""id"":""79158""}]"	"[""79158""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00025""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080070""}]"
DOID:0080070	"[""mucolipidosis II alpha/beta"",""I-cell disease"",""inclusion-cell disease"",""mucolipidosis II""]"	"[{""label"":""gnptab"",""id"":""553365""}]"	"[""553365""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080070""}]"
DOID:0080071	"[""mucolipidosis III alpha/beta"",""mucolipidosis III"",""pseudo-Hurler polydystrophy""]"	"[{""label"":""GNPTAB"",""id"":""79158""}]"	"[""79158""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00026""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080071""}]"
DOID:0080072	"[""intestinal pseudo-obstruction"",""Chronic intestinal pseudo-obstruction"",""neuronal intestinal dysplasia""]"	"[{""label"":""Nup35"",""id"":""69482""},{""label"":""Spry2"",""id"":""24064""}]"	"[""24064"",""69482""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080072""}]"
DOID:0080074	"[""neural tube defect""]"	"[{""label"":""CBS"",""id"":""875""},{""label"":""FUZ"",""id"":""80199""},{""label"":""MTHFD1"",""id"":""4522""},{""label"":""MTHFD1L"",""id"":""25902""},{""label"":""TBXT"",""id"":""6862""}]"	"[""25902"",""4522"",""6862"",""80199"",""875""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080074""}]"
DOID:0080074	"[""neural tube defect""]"	"[{""label"":""Lrp6"",""id"":""16974""}]"	"[""16974""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080074""}]"
DOID:0080075	"[""Neu-Laxova syndrome 2""]"	"[{""label"":""PSAT1"",""id"":""29968""}]"	"[""29968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080075""}]"
DOID:0080076	"[""Neu-Laxova syndrome 1""]"	"[{""label"":""PHGDH"",""id"":""26227""}]"	"[""26227""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080076""}]"
DOID:0080077	"[""hypophosphatemic nephrolithiasis/osteoporosis 1""]"	"[{""label"":""SLC34A1"",""id"":""6569""}]"	"[""6569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080077""}]"
DOID:0080079	"[""nonsyndromic congenital nail disorder 1"",""nonsyndromic congenital nail disorder 10"",""twenty-nail dystrophy""]"	"[{""label"":""FZD6"",""id"":""8323""}]"	"[""8323""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080079""}]"
DOID:0080081	"[""nonsyndromic congenital nail disorder 3""]"	"[{""label"":""PLCD1"",""id"":""5333""}]"	"[""5333""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080081""}]"
DOID:0080082	"[""nonsyndromic congenital nail disorder 4"",""HYPONYCHIA CONGENITA"",""anonychia congenita""]"	"[{""label"":""RSPO4"",""id"":""343637""}]"	"[""343637""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080082""}]"
DOID:0080086	"[""nonsyndromic congenital nail disorder 8"",""isolated toenail dystrophy""]"	"[{""label"":""COL7A1"",""id"":""1294""}]"	"[""1294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080086""}]"
DOID:0080089	"[""tubular aggregate myopathy 1""]"	"[{""label"":""Stim1"",""id"":""20866""}]"	"[""20866""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080089""}]"
DOID:0080089	"[""tubular aggregate myopathy 1""]"	"[{""label"":""STIM1"",""id"":""6786""}]"	"[""6786""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080089""}]"
DOID:0080090	"[""reducing body myopathy 1A""]"	"[{""label"":""FHL1"",""id"":""2273""}]"	"[""2273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080090""}]"
DOID:0080092	"[""myofibrillar myopathy 1"",""autosomal recessive limb-girdle muscular dystrophy type 2R"",""desminopathy""]"	"[{""label"":""DES"",""id"":""1674""}]"	"[""1674""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080092""}]"
DOID:0080092	"[""myofibrillar myopathy 1"",""autosomal recessive limb-girdle muscular dystrophy type 2R"",""desminopathy""]"	"[{""label"":""Des"",""id"":""13346""},{""label"":""Ldb3"",""id"":""24131""}]"	"[""13346"",""24131""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080092""}]"
DOID:0080093	"[""myofibrillar myopathy 2"",""alpha-b crystallinopathy""]"	"[{""label"":""Cryab"",""id"":""12955""}]"	"[""12955""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080093""}]"
DOID:0080093	"[""myofibrillar myopathy 2"",""alpha-b crystallinopathy""]"	"[{""label"":""CRYAB"",""id"":""1410""}]"	"[""1410""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080093""}]"
DOID:0080095	"[""myofibrillar myopathy 4"",""zaspopathy""]"	"[{""label"":""LDB3"",""id"":""11155""}]"	"[""11155""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080095""}]"
DOID:0080095	"[""myofibrillar myopathy 4"",""zaspopathy""]"	"[{""label"":""Zasp52"",""id"":""36740""}]"	"[""36740""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080095""}]"
DOID:0080096	"[""myofibrillar myopathy 5"",""filaminopathy""]"	"[{""label"":""Flnc"",""id"":""68794""}]"	"[""68794""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080096""}]"
DOID:0080096	"[""myofibrillar myopathy 5"",""filaminopathy""]"	"[{""label"":""FLNC"",""id"":""2318""}]"	"[""2318""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080096""}]"
DOID:0080097	"[""myofibrillar myopathy 6""]"	"[{""label"":""BAG3"",""id"":""9531""}]"	"[""9531""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080097""}]"
DOID:0080101	"[""Compton-North congenital myopathy"",""congenital myopathy 12""]"	"[{""label"":""Cntn1"",""id"":""12805""}]"	"[""12805""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080101""}]"
DOID:0080101	"[""Compton-North congenital myopathy"",""congenital myopathy 12""]"	"[{""label"":""CNTN1"",""id"":""1272""}]"	"[""1272""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080101""}]"
DOID:0080105	"[""microcephaly and chorioretinopathy 1""]"	"[{""label"":""TUBGCP6"",""id"":""85378""}]"	"[""85378""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080105""}]"
DOID:0080107	"[""microcephaly and chorioretinopathy 3""]"	"[{""label"":""TUBGCP4"",""id"":""27229""}]"	"[""27229""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080107""}]"
DOID:0080108	"[""myoglobinuria""]"	"[{""label"":""PGAM2"",""id"":""5224""}]"	"[""5224""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080108""}]"
DOID:0080109	"[""infantile myofibromatosis"",""lipofibromatosis""]"	"[{""label"":""Pdgfrb"",""id"":""18596""}]"	"[""18596""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080109""}]"
DOID:0080109	"[""infantile myofibromatosis"",""lipofibromatosis""]"	"[{""label"":""NOTCH3"",""id"":""4854""},{""label"":""PDGFRB"",""id"":""5159""}]"	"[""4854"",""5159""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080109""}]"
DOID:0080110	"[""contractures, pterygia, and spondylocarpotarsal fusion syndrome"",""multiple pterygium syndrome""]"	"[{""label"":""CHRNG"",""id"":""1146""}]"	"[""1146""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080110""}]"
DOID:0080114	"[""mitochondrial complex III deficiency nuclear type 5""]"	"[{""label"":""UQCRC2"",""id"":""7385""}]"	"[""7385""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080114""}]"
DOID:0080118	"[""mitochondrial complex III deficiency nuclear type 9""]"	"[{""label"":""UQCC3"",""id"":""790955""}]"	"[""790955""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080118""}]"
DOID:0080119	"[""mitochondrial DNA depletion syndrome 1"",""mitochondrial DNA depletion syndrome 1 (MNGIE type)"",""mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related""]"	"[{""label"":""TYMP"",""id"":""1890""}]"	"[""1890""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080119""}]"
DOID:0080124	"[""mitochondrial DNA depletion syndrome 5"",""succinate-CoA ligase deficiency""]"	"[{""label"":""SUCLA2"",""id"":""8803""}]"	"[""8803""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080124""}]"
DOID:0080124	"[""mitochondrial DNA depletion syndrome 5"",""succinate-CoA ligase deficiency""]"	"[{""label"":""Sucla2"",""id"":""20916""}]"	"[""20916""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080124""}]"
DOID:0080128	"[""mitochondrial DNA depletion syndrome 9"",""fatal infantile lactic acidosis""]"	"[{""label"":""SUCLG1"",""id"":""8802""}]"	"[""8802""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080128""}]"
DOID:0080131	"[""mitochondrial DNA depletion syndrome 13"",""FBXL4 deficiency"",""FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome"",""mitochondrial DNA depletion syndrome 13, encephalomyopathic type""]"	"[{""label"":""FBXL4"",""id"":""26235""}]"	"[""26235""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080131""}]"
DOID:0080132	"[""Sengers syndrome"",""mitochondrial DNA depletion syndrome 10"",""mitochondrial DNA depletion syndrome 10 (cardiomyopathic type)""]"	"[{""label"":""AGK"",""id"":""55750""}]"	"[""55750""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080132""}]"
DOID:0080133	"[""multiple mitochondrial dysfunctions syndrome 1"",""NFU1 deficiency""]"	"[{""label"":""NFU1"",""id"":""27247""}]"	"[""27247""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080133""}]"
DOID:0080135	"[""multiple mitochondrial dysfunctions syndrome 3"",""IBA57 deficiency""]"	"[{""label"":""IBA57"",""id"":""200205""}]"	"[""200205""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080135""}]"
DOID:0080136	"[""multiple mitochondrial dysfunctions syndrome 4""]"	"[{""label"":""ISCA2"",""id"":""122961""}]"	"[""122961""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080136""}]"
DOID:0080137	"[""multiple endocrine neoplasia type 4"",""Multiple Endocrine Neoplasia, Type IV""]"	"[{""label"":""CDKN1B"",""id"":""1027""}]"	"[""1027""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080137""}]"
DOID:0080138	"[""multiple congenital anomalies-hypotonia-seizures syndrome 1""]"	"[{""label"":""PIGN"",""id"":""23556""}]"	"[""23556""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00636""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080138""}]"
DOID:0080139	"[""multiple congenital anomalies-hypotonia-seizures syndrome 2"",""developmental and epileptic encephalopathy 20"",""early infantile epileptic encephalopathy 20"",""glycosylphosphatidylinositol biosynthesis defect 4""]"	"[{""label"":""PIGA"",""id"":""5277""}]"	"[""5277""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080139""}]"
DOID:0080139	"[""multiple congenital anomalies-hypotonia-seizures syndrome 2"",""developmental and epileptic encephalopathy 20"",""early infantile epileptic encephalopathy 20"",""glycosylphosphatidylinositol biosynthesis defect 4""]"	"[{""label"":""PIG-A"",""id"":""37020""}]"	"[""37020""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080139""}]"
DOID:0080140	"[""multiple congenital anomalies-hypotonia-seizures syndrome 3"",""M syndrome"",""light fixation seizure syndrome""]"	"[{""label"":""PIGT"",""id"":""51604""}]"	"[""51604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080140""}]"
DOID:0080141	"[""mosaic variegated aneuploidy syndrome 1""]"	"[{""label"":""BUB1B"",""id"":""701""}]"	"[""701""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080141""}]"
DOID:0080142	"[""mosaic variegated aneuploidy syndrome 2""]"	"[{""label"":""CEP57"",""id"":""9702""}]"	"[""9702""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080142""}]"
DOID:0080143	"[""congenital fibrosis of the extraocular muscles""]"	"[{""label"":""Kif21a"",""id"":""16564""},{""label"":""Tubb3"",""id"":""22152""}]"	"[""16564"",""22152""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080143""}]"
DOID:0080153	"[""medium chain acyl-CoA dehydrogenase deficiency""]"	"[{""label"":""ACADM"",""id"":""34""}]"	"[""34""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080153""}]"
DOID:0080153	"[""medium chain acyl-CoA dehydrogenase deficiency""]"	"[{""label"":""Acadm"",""id"":""11364""}]"	"[""11364""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080153""}]"
DOID:0080154	"[""short chain acyl-CoA dehydrogenase deficiency""]"	"[{""label"":""ACADS"",""id"":""35""}]"	"[""35""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080154""}]"
DOID:0080154	"[""short chain acyl-CoA dehydrogenase deficiency""]"	"[{""label"":""Acads"",""id"":""11409""}]"	"[""11409""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080154""}]"
DOID:0080155	"[""very long chain acyl-CoA dehydrogenase deficiency"",""VLCAD deficiency""]"	"[{""label"":""Acadvl"",""id"":""11370""}]"	"[""11370""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080155""}]"
DOID:0080155	"[""very long chain acyl-CoA dehydrogenase deficiency"",""VLCAD deficiency""]"	"[{""label"":""ACADVL"",""id"":""37""}]"	"[""37""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080155""}]"
DOID:0080156	"[""X-linked adrenal hypoplasia congenita"",""congenital adrenal hypoplasia""]"	"[{""label"":""NR0B1"",""id"":""190""}]"	"[""190""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080156""}]"
DOID:0080158	"[""herpes simplex virus keratitis"",""dendritic keratitis""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""IL1RN"",""id"":""3557""}]"	"[""348"",""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080158""}]"
DOID:0080159	"[""Cryptococcal meningitis""]"	"[{""label"":""MBL2"",""id"":""4153""}]"	"[""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080159""}]"
DOID:0080160	"[""Cytomegalovirus retinitis"",""CMV retinitis""]"	"[{""label"":""HLA-B"",""id"":""3106""}]"	"[""3106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080160""}]"
DOID:0080162	"[""lupus nephritis""]"	"[{""label"":""AGER"",""id"":""177""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CD40LG"",""id"":""959""},{""label"":""CFH"",""id"":""3075""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IFNG"",""id"":""3458""},{""label"":""ITGAM"",""id"":""3684""},{""label"":""KLKB1"",""id"":""3818""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MPO"",""id"":""4353""},{""label"":""PDCD1"",""id"":""5133""},{""label"":""SNRPE"",""id"":""6635""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""1493"",""177"",""2212"",""2214"",""3075"",""3117"",""3123"",""3458"",""3684"",""3818"",""4153"",""4353"",""5133"",""54106"",""6347"",""6635"",""7133"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080162""}]"
DOID:0080163	"[""otulipenia"",""autoinflammation, panniculitis and dermatosis syndrome"",""otulin-related autoinflammatory syndrome""]"	"[{""label"":""OTULIN"",""id"":""90268""}]"	"[""90268""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080163""}]"
DOID:0080170	"[""normophosphatemic familial tumoral calcinosis""]"	"[{""label"":""SAMD9"",""id"":""54809""}]"	"[""54809""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080170""}]"
DOID:0080171	"[""esophageal atresia/tracheoesophageal fistula"",""esophageal atresia and/or tracheoesophageal fistula"",""tracheoesophageal fistula with or without esohageal atresia""]"	"[{""label"":""Nog"",""id"":""18121""}]"	"[""18121""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080171""}]"
DOID:0080176	"[""meningococcal meningitis""]"	"[{""label"":""CD46"",""id"":""4179""},{""label"":""NOD2"",""id"":""64127""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""}]"	"[""4179"",""64127"",""7097"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080176""}]"
DOID:0080177	"[""hepatic veno-occlusive disease"",""veno-occlusive disease""]"	"[{""label"":""HFE"",""id"":""3077""}]"	"[""3077""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080177""}]"
DOID:0080179	"[""haemophilus meningitis""]"	"[{""label"":""FCGR2A"",""id"":""2212""}]"	"[""2212""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080179""}]"
DOID:0080181	"[""PHARC syndrome"",""polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract""]"	"[{""label"":""abhd12"",""id"":""767657""}]"	"[""767657""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080181""}]"
DOID:0080181	"[""PHARC syndrome"",""polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract""]"	"[{""label"":""Abhd12"",""id"":""76192""}]"	"[""76192""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080181""}]"
DOID:0080181	"[""PHARC syndrome"",""polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract""]"	"[{""label"":""ABHD12"",""id"":""26090""}]"	"[""26090""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080181""}]"
DOID:0080187	"[""chronic neutrophilic leukemia""]"	"[{""label"":""CSF3R"",""id"":""1441""}]"	"[""1441""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080187""}]"
DOID:0080188	"[""chronic myelomonocytic leukemia""]"	"[{""label"":""ASXL1"",""id"":""171023""},{""label"":""CSF3R"",""id"":""1441""},{""label"":""EZH2"",""id"":""2146""},{""label"":""TET2"",""id"":""54790""}]"	"[""1441"",""171023"",""2146"",""54790""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080188""}]"
DOID:0080188	"[""chronic myelomonocytic leukemia""]"	"[{""label"":""Kdm6a"",""id"":""22289""}]"	"[""22289""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080188""}]"
DOID:0080191	"[""PTEN hamartoma tumor syndrome""]"	"[{""label"":""PTEN"",""id"":""5728""}]"	"[""5728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080191""}]"
DOID:0080195	"[""Marinesco-Sjogren syndrome"",""Garland-Moorhouse syndrome"",""Marinesco-Garland syndrome"",""Oligophrenic cerebellolenticular degeneration"",""hereditary oligophrenic cerebello-lental degeneration""]"	"[{""label"":""SIL1"",""id"":""854126""}]"	"[""854126""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080195""}]"
DOID:0080196	"[""mandibulofacial dysostosis, Guion-Almeida type"",""MFDM syndrome"",""mandibulofacial dysostosis with microcephaly"",""mandibulofacial dysostosis-microcephaly syndrome""]"	"[{""label"":""EFTUD2"",""id"":""9343""}]"	"[""9343""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080196""}]"
DOID:0080197	"[""congenital muscular dystrophy with cataracts and intellectual disability""]"	"[{""label"":""INPP5K"",""id"":""51763""}]"	"[""51763""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080197""}]"
DOID:0080199	"[""colorectal carcinoma""]"	"[{""label"":""Cd59b"",""id"":""25407""}]"	"[""25407""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080199""}]"
DOID:0080199	"[""colorectal carcinoma""]"	"[{""label"":""AKAP12"",""id"":""9590""},{""label"":""ANTXR1"",""id"":""84168""},{""label"":""BMI1"",""id"":""648""},{""label"":""CD59"",""id"":""966""},{""label"":""EFNB2"",""id"":""1948""},{""label"":""ERCC6"",""id"":""2074""},{""label"":""MAPK14"",""id"":""1432""},{""label"":""MBD4"",""id"":""8930""},{""label"":""MSH6"",""id"":""2956""},{""label"":""MYD88"",""id"":""4615""},{""label"":""NCOA2"",""id"":""10499""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PTPRB"",""id"":""5787""},{""label"":""RAC1"",""id"":""5879""},{""label"":""STRAP"",""id"":""11171""},{""label"":""TP53"",""id"":""7157""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10499"",""11171"",""1432"",""1948"",""2074"",""2956"",""4615"",""5290"",""5787"",""5879"",""648"",""7157"",""7515"",""84168"",""8930"",""9590"",""966""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080199""}]"
DOID:0080201	"[""Peters plus syndrome"",""Krause-Kivlin syndrome"",""Peters anomaly-short limb dwarfism syndrome"",""Peters-plus syndrome""]"	"[{""label"":""B3GLCT"",""id"":""145173""}]"	"[""145173""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00404""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080201""}]"
DOID:0080201	"[""Peters plus syndrome"",""Krause-Kivlin syndrome"",""Peters anomaly-short limb dwarfism syndrome"",""Peters-plus syndrome""]"	"[{""label"":""B3glct"",""id"":""381694""}]"	"[""381694""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080201""}]"
DOID:0080202	"[""adenoid cystic carcinoma""]"	"[{""label"":""ATR"",""id"":""545""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""KMT2C"",""id"":""58508""},{""label"":""NTRK3"",""id"":""4916""},{""label"":""XRN2"",""id"":""22803""}]"	"[""22803"",""4916"",""545"",""58508"",""7403""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080202""}]"
DOID:0080204	"[""renal hypoplasia""]"	"[{""label"":""RET"",""id"":""5979""}]"	"[""5979""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080204""}]"
DOID:0080205	"[""CAKUT"",""Congenital anomalies of the kidney and urinary tract"",""Renal or urinary tract malformation""]"	"[{""label"":""Lifr"",""id"":""16880""}]"	"[""16880""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080205""}]"
DOID:0080205	"[""CAKUT"",""Congenital anomalies of the kidney and urinary tract"",""Renal or urinary tract malformation""]"	"[{""label"":""BMP4"",""id"":""652""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""NRIP1"",""id"":""8204""}]"	"[""3304"",""652"",""8204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080205""}]"
DOID:0080206	"[""CAKUT1"",""Congenital anomalies of the kidney and urinary tract 1""]"	"[{""label"":""DSTYK"",""id"":""25778""}]"	"[""25778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080206""}]"
DOID:0080207	"[""CAKUT2"",""Congenital anomalies of the kidney and urinary tract 2""]"	"[{""label"":""BMP4"",""id"":""652""}]"	"[""652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080207""}]"
DOID:0080208	"[""metabolic dysfunction-associated steatotic liver disease"",""MAFLD"",""MASLD"",""NAFLD"",""metabolic dysfunction-associated fatty liver disease"",""metabolic dysfunction-related steatotic liver disease"",""metabolic-associated fatty liver disease"",""non-alcoholic fatty liver disease"",""nonalcoholic fatty liver disease""]"	"[{""label"":""ABCC2"",""id"":""1244""},{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""ADRB3"",""id"":""155""},{""label"":""AKT1"",""id"":""207""},{""label"":""ALDH2"",""id"":""217""},{""label"":""CCR2"",""id"":""729230""},{""label"":""DGAT2"",""id"":""84649""},{""label"":""HFE"",""id"":""3077""},{""label"":""IL6"",""id"":""3569""},{""label"":""LEPR"",""id"":""3953""},{""label"":""PNPLA3"",""id"":""80339""},{""label"":""PPARGC1A"",""id"":""10891""},{""label"":""SAMM50"",""id"":""25813""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TG"",""id"":""7038""}]"	"[""10891"",""1244"",""155"",""207"",""217"",""25813"",""3077"",""3569"",""3953"",""6648"",""7038"",""729230"",""80339"",""84649"",""9370""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080208""}]"
DOID:0080208	"[""metabolic dysfunction-associated steatotic liver disease"",""MAFLD"",""MASLD"",""NAFLD"",""metabolic dysfunction-associated fatty liver disease"",""metabolic dysfunction-related steatotic liver disease"",""metabolic-associated fatty liver disease"",""non-alcoholic fatty liver disease"",""nonalcoholic fatty liver disease""]"	"[{""label"":""Lep"",""id"":""16846""},{""label"":""Lepr"",""id"":""16847""},{""label"":""Pnpla3"",""id"":""116939""},{""label"":""Sidt2"",""id"":""214597""}]"	"[""116939"",""16846"",""16847"",""214597""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080208""}]"
DOID:0080208	"[""metabolic dysfunction-associated steatotic liver disease"",""MAFLD"",""MASLD"",""NAFLD"",""metabolic dysfunction-associated fatty liver disease"",""metabolic dysfunction-related steatotic liver disease"",""metabolic-associated fatty liver disease"",""non-alcoholic fatty liver disease"",""nonalcoholic fatty liver disease""]"	"[{""label"":""Actb"",""id"":""81822""},{""label"":""Atp5f1a"",""id"":""65262""},{""label"":""Col1a1"",""id"":""29393""},{""label"":""Lpl"",""id"":""24539""},{""label"":""Nfe2l2"",""id"":""83619""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Ucp2"",""id"":""54315""}]"	"[""24539"",""29393"",""54315"",""65262"",""81822"",""83516"",""83619""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080208""}]"
DOID:0080209	"[""sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay"",""SIFD""]"	"[{""label"":""TRNT1"",""id"":""51095""}]"	"[""51095""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080209""}]"
DOID:0080212	"[""polycystic kidney disease 4"",""pkd3"",""polycystic kidney and hepatic disease 1"",""polycystic kidney disease 4 with or without hepatic disease"",""polycystic kidney disease, autosomal recessive"",""polycystic kidney disease, infantile, type i""]"	"[{""label"":""Pkhd1"",""id"":""241035""}]"	"[""241035""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080212""}]"
DOID:0080212	"[""polycystic kidney disease 4"",""pkd3"",""polycystic kidney and hepatic disease 1"",""polycystic kidney disease 4 with or without hepatic disease"",""polycystic kidney disease, autosomal recessive"",""polycystic kidney disease, infantile, type i""]"	"[{""label"":""PKHD1"",""id"":""5314""}]"	"[""5314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080212""}]"
DOID:0080217	"[""lysosomal acid lipase deficiency"",""LAL deficiency"",""LAL-D""]"	"[{""label"":""LIPA"",""id"":""3988""}]"	"[""3988""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00100""}]"
DOID:0080217	"[""lysosomal acid lipase deficiency"",""LAL deficiency"",""LAL-D""]"	"[{""label"":""Lipa"",""id"":""16889""}]"	"[""16889""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080217""}]"
DOID:0080218	"[""primary spontaneous pneumothorax""]"	"[{""label"":""FLCN"",""id"":""201163""}]"	"[""201163""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080218""}]"
DOID:0080219	"[""dystransthyretinemic hyperthyroxinemia""]"	"[{""label"":""TTR"",""id"":""7276""}]"	"[""7276""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080219""}]"
DOID:0080222	"[""pseudohypoparathyroidism type 1B"",""PHP Ib""]"	"[{""label"":""GNAS"",""id"":""2778""}]"	"[""2778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080222""}]"
DOID:0080224	"[""autosomal dominant dystrophic epidermolysis bullosa""]"	"[{""label"":""COL7A1"",""id"":""1294""}]"	"[""1294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080224""}]"
DOID:0080226	"[""autosomal dominant intellectual developmental disorder 56"",""autosomal dominant intellectual developmental disorder-56"",""autosomal dominant mental retardation 56""]"	"[{""label"":""CLTC"",""id"":""1213""}]"	"[""1213""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080226""}]"
DOID:0080227	"[""autosomal dominant intellectual developmental disorder 55"",""autosomal dominant intellectual developmental disorder-55 with seizures"",""autosomal dominant mental retardation 55""]"	"[{""label"":""NUS1"",""id"":""116150""}]"	"[""116150""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080227""}]"
DOID:0080228	"[""autosomal dominant intellectual developmental disorder 53"",""autosomal dominant mental retardation 53""]"	"[{""label"":""CAMK2A"",""id"":""815""}]"	"[""815""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080228""}]"
DOID:0080230	"[""autosomal dominant intellectual developmental disorder 54"",""autosomal dominant mental retardation 54""]"	"[{""label"":""CAMK2B"",""id"":""816""}]"	"[""816""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080230""}]"
DOID:0080231	"[""autosomal dominant intellectual developmental disorder 52"",""autosomal dominant mental retardation 52""]"	"[{""label"":""ASH1L"",""id"":""55870""}]"	"[""55870""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080231""}]"
DOID:0080232	"[""autosomal dominant intellectual developmental disorder 51"",""autosomal dominant mental retardation 51""]"	"[{""label"":""KMT5B"",""id"":""51111""}]"	"[""51111""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080232""}]"
DOID:0080233	"[""autosomal dominant intellectual developmental disorder 50"",""autosomal dominant intellectual developmental disorder-50 with behavioral abnormalities"",""autosomal dominant mental retardation 50""]"	"[{""label"":""NAA15"",""id"":""80155""}]"	"[""80155""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080233""}]"
DOID:0080234	"[""Clark-Baraitser syndrome"",""Baraitser syndrome"",""CLABARS"",""autosomal dominant intellectual disability 49"",""autosomal dominant mental retardation 49""]"	"[{""label"":""TRIP12"",""id"":""9320""}]"	"[""9320""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080234""}]"
DOID:0080235	"[""autosomal dominant intellectual developmental disorder 48"",""autosomal dominant mental retardation 48""]"	"[{""label"":""RAC1"",""id"":""5879""}]"	"[""5879""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080235""}]"
DOID:0080236	"[""autosomal dominant intellectual developmental disorder 45"",""autosomal dominant mental retardation 45""]"	"[{""label"":""CIC"",""id"":""23152""}]"	"[""23152""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080236""}]"
DOID:0080237	"[""autosomal dominant intellectual developmental disorder 46"",""autosomal dominant mental retardation 46""]"	"[{""label"":""KCNQ5"",""id"":""56479""}]"	"[""56479""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080237""}]"
DOID:0080238	"[""autosomal dominant intellectual developmental disorder 47"",""autosomal dominant mental retardation 47""]"	"[{""label"":""STAG1"",""id"":""10274""}]"	"[""10274""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080238""}]"
DOID:0080239	"[""autosomal recessive intellectual developmental disorder 61"",""Alwadei syndrome"",""autosomal recessive intellectual developmental disorder-61"",""autosomal recessive mental retardation 61""]"	"[{""label"":""RUSC2"",""id"":""9853""}]"	"[""9853""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080239""}]"
DOID:0080240	"[""non-syndromic X-linked intellectual disability 106"",""MRX106"",""X-linked mental retardation 106""]"	"[{""label"":""sxc"",""id"":""35486""}]"	"[""35486""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080240""}]"
DOID:0080240	"[""non-syndromic X-linked intellectual disability 106"",""MRX106"",""X-linked mental retardation 106""]"	"[{""label"":""OGT"",""id"":""8473""}]"	"[""8473""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080240""}]"
DOID:0080242	"[""syndromic X-linked mental retardation Hough type""]"	"[{""label"":""CNKSR2"",""id"":""22866""}]"	"[""22866""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080242""}]"
DOID:0080244	"[""Galloway-Mowat syndrome 2""]"	"[{""label"":""LAGE3"",""id"":""8270""}]"	"[""8270""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080244""}]"
DOID:0080245	"[""Galloway-Mowat syndrome 3""]"	"[{""label"":""OSGEP"",""id"":""55644""}]"	"[""55644""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080245""}]"
DOID:0080250	"[""erythrokeratodermia variabilis et progressiva 4""]"	"[{""label"":""KDSR"",""id"":""2531""}]"	"[""2531""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080250""}]"
DOID:0080253	"[""Meckel syndrome 13""]"	"[{""label"":""TMEM107"",""id"":""84314""}]"	"[""84314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080253""}]"
DOID:0080254	"[""orofaciodigital syndrome XVI""]"	"[{""label"":""TMEM107"",""id"":""84314""}]"	"[""84314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080254""}]"
DOID:0080257	"[""autosomal recessive congenital ichthyosis 13""]"	"[{""label"":""SDR9C7"",""id"":""121214""}]"	"[""121214""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080257""}]"
DOID:0080258	"[""autosomal recessive congenital ichthyosis 14""]"	"[{""label"":""SULT2B1"",""id"":""6820""}]"	"[""6820""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080258""}]"
DOID:0080260	"[""autosomal recessive spinocerebellar ataxia 26"",""SCAR26""]"	"[{""label"":""XRCC1"",""id"":""7515""}]"	"[""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080260""}]"
DOID:0080261	"[""autosomal recessive nonsyndromic deafness 106""]"	"[{""label"":""EPS8L2"",""id"":""64787""}]"	"[""64787""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080261""}]"
DOID:0080263	"[""autosomal recessive nonsyndromic deafness 108""]"	"[{""label"":""ROR1"",""id"":""4919""}]"	"[""4919""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080263""}]"
DOID:0080264	"[""exudative vitreoretinopathy 7"",""EVR7""]"	"[{""label"":""CTNNB1"",""id"":""1499""}]"	"[""1499""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080264""}]"
DOID:0080265	"[""nephrotic syndrome type 14""]"	"[{""label"":""SGPL1"",""id"":""8879""}]"	"[""8879""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080265""}]"
DOID:0080266	"[""primary ciliary dyskinesia 37""]"	"[{""label"":""DNAH1"",""id"":""25981""}]"	"[""25981""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080266""}]"
DOID:0080267	"[""autosomal dominant nonsyndromic deafness 71""]"	"[{""label"":""DMXL2"",""id"":""23312""}]"	"[""23312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080267""}]"
DOID:0080268	"[""autosomal dominant nonsyndromic deafness 72""]"	"[{""label"":""SLC44A4"",""id"":""80736""}]"	"[""80736""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080268""}]"
DOID:0080272	"[""nephrotic syndrome type 16""]"	"[{""label"":""KANK2"",""id"":""25959""}]"	"[""25959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080272""}]"
DOID:0080280	"[""gingival fibromatosis 5""]"	"[{""label"":""REST"",""id"":""5978""}]"	"[""5978""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080280""}]"
DOID:0080281	"[""schizophrenia 19""]"	"[{""label"":""RBM12"",""id"":""10137""}]"	"[""10137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080281""}]"
DOID:0080282	"[""developmental and epileptic encephalopathy 56"",""DEE56"",""early infantile epileptic encephalopathy 56""]"	"[{""label"":""YWHAG"",""id"":""7532""}]"	"[""7532""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080282""}]"
DOID:0080283	"[""developmental and epileptic encephalopathy 55"",""DEE55"",""GPIBD14"",""early infantile epileptic encephalopathy 55"",""glycosylphosphatidylinositol biosynthesis defect 14""]"	"[{""label"":""PIGP"",""id"":""51227""}]"	"[""51227""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080283""}]"
DOID:0080284	"[""developmental and epileptic encephalopathy 57"",""DEE57"",""early infantile epileptic encephalopathy 57""]"	"[{""label"":""KCNT2"",""id"":""343450""}]"	"[""343450""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080284""}]"
DOID:0080285	"[""developmental and epileptic encephalopathy 58"",""DEE58"",""early infantile epileptic encephalopathy 58""]"	"[{""label"":""NTRK2"",""id"":""4915""}]"	"[""4915""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080285""}]"
DOID:0080286	"[""spinocerebellar ataxia 44""]"	"[{""label"":""GRM1"",""id"":""2911""}]"	"[""2911""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080286""}]"
DOID:0080287	"[""spinocerebellar ataxia 45""]"	"[{""label"":""FAT2"",""id"":""2196""}]"	"[""2196""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080287""}]"
DOID:0080288	"[""spinocerebellar ataxia 46""]"	"[{""label"":""PLD3"",""id"":""23646""}]"	"[""23646""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080288""}]"
DOID:0080289	"[""orofaciodigital syndrome XVII""]"	"[{""label"":""INTU"",""id"":""27152""}]"	"[""27152""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080289""}]"
DOID:0080290	"[""familial erythrocytosis 5"",""ECYT5""]"	"[{""label"":""EPO"",""id"":""2056""}]"	"[""2056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080290""}]"
DOID:0080291	"[""developmental and epileptic encephalopathy 59"",""DEE59"",""early infantile epileptic encephalopathy 59""]"	"[{""label"":""GABBR2"",""id"":""9568""}]"	"[""9568""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080291""}]"
DOID:0080294	"[""Charcot-Marie-Tooth disease dominant intermediate G""]"	"[{""label"":""NEFL"",""id"":""4747""}]"	"[""4747""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080294""}]"
DOID:0080297	"[""Coffin-Siris syndrome 6""]"	"[{""label"":""ARID2"",""id"":""196528""}]"	"[""196528""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080297""}]"
DOID:0080299	"[""partial lipodystrophy""]"	"[{""label"":""LMNB2"",""id"":""84823""}]"	"[""84823""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080299""}]"
DOID:0080301	"[""atypical hemolytic-uremic syndrome""]"	"[{""label"":""C3"",""id"":""718""},{""label"":""CD46"",""id"":""4179""},{""label"":""CFB"",""id"":""629""},{""label"":""CFH"",""id"":""3075""},{""label"":""CFHR1"",""id"":""3078""},{""label"":""CFHR3"",""id"":""10878""},{""label"":""CFI"",""id"":""3426""},{""label"":""THBD"",""id"":""7056""}]"	"[""10878"",""3075"",""3078"",""3426"",""4179"",""629"",""7056"",""718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080301""}]"
DOID:0080301	"[""atypical hemolytic-uremic syndrome""]"	"[{""label"":""Cfh"",""id"":""12628""}]"	"[""12628""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080301""}]"
DOID:0080308	"[""myofibrillar myopathy 8""]"	"[{""label"":""PYROXD1"",""id"":""79912""}]"	"[""79912""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080308""}]"
DOID:0080309	"[""fatal infantile hypertonic myofibrillar myopathy""]"	"[{""label"":""CRYAB"",""id"":""1410""}]"	"[""1410""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080309""}]"
DOID:0080311	"[""X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance""]"	"[{""label"":""OPHN1"",""id"":""4983""}]"	"[""4983""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080311""}]"
DOID:0080312	"[""neurodevelopmental disorder with midbrain and hindbrain malformations"",""NEDMHM""]"	"[{""label"":""Arhgef2"",""id"":""16800""}]"	"[""16800""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080312""}]"
DOID:0080312	"[""neurodevelopmental disorder with midbrain and hindbrain malformations"",""NEDMHM""]"	"[{""label"":""ARHGEF2"",""id"":""9181""}]"	"[""9181""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080312""}]"
DOID:0080313	"[""cleft palate-lateral synechia syndrome"",""CPLS syndrome"",""syngnathia""]"	"[{""label"":""Bmp4"",""id"":""12159""}]"	"[""12159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080313""}]"
DOID:0080315	"[""megalencephalic leukoencephalopathy with subcortical cysts"",""megalencephalic leukodystrophy megalencephaly-cystic leukodystorphy syndrome"",""vacuolating megalencephalic leukoencephalopathy with subcortical cysts""]"	"[{""label"":""AQP4"",""id"":""361""},{""label"":""GPRC5B"",""id"":""51704""}]"	"[""361"",""51704""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080315""}]"
DOID:0080315	"[""megalencephalic leukoencephalopathy with subcortical cysts"",""megalencephalic leukodystrophy megalencephaly-cystic leukodystorphy syndrome"",""vacuolating megalencephalic leukoencephalopathy with subcortical cysts""]"	"[{""label"":""Hepacam"",""id"":""72927""}]"	"[""72927""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080315""}]"
DOID:0080317	"[""megalencephalic leukoencephalopathy with subcortical cysts 2B"",""megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation""]"	"[{""label"":""HEPACAM"",""id"":""220296""}]"	"[""220296""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080317""}]"
DOID:0080318	"[""megalencephalic leukoencephalopathy with subcortical cysts 2A""]"	"[{""label"":""HEPACAM"",""id"":""220296""}]"	"[""220296""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080318""}]"
DOID:0080319	"[""X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia"",""XMEN""]"	"[{""label"":""MAGT1"",""id"":""84061""}]"	"[""84061""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080319""}]"
DOID:0080322	"[""polycystic kidney disease""]"	"[{""label"":""GANAB"",""id"":""23193""},{""label"":""PKD2"",""id"":""5311""}]"	"[""23193"",""5311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080322""}]"
DOID:0080322	"[""polycystic kidney disease""]"	"[{""label"":""pkd2"",""id"":""432387""}]"	"[""432387""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080322""}]"
DOID:0080322	"[""polycystic kidney disease""]"	"[{""label"":""Agt"",""id"":""24179""},{""label"":""Pparg"",""id"":""25664""},{""label"":""Ptgs2"",""id"":""29527""}]"	"[""24179"",""25664"",""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080322""}]"
DOID:0080322	"[""polycystic kidney disease""]"	"[{""label"":""Kif3a"",""id"":""16568""},{""label"":""Ptma"",""id"":""19231""},{""label"":""Xylt2"",""id"":""217119""}]"	"[""16568"",""19231"",""217119""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080322""}]"
DOID:0080324	"[""tuberous sclerosis 1""]"	"[{""label"":""TSC1"",""id"":""7248""}]"	"[""7248""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080324""}]"
DOID:0080325	"[""tuberous sclerosis 2""]"	"[{""label"":""IFNG"",""id"":""3458""},{""label"":""TSC2"",""id"":""7249""}]"	"[""3458"",""7249""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080325""}]"
DOID:0080326	"[""familial hypertrophic cardiomyopathy""]"	"[{""label"":""ALPK3"",""id"":""57538""},{""label"":""CORIN"",""id"":""10699""},{""label"":""FHOD3"",""id"":""80206""},{""label"":""MYBPC3"",""id"":""4607""},{""label"":""MYL9"",""id"":""10398""}]"	"[""10398"",""10699"",""4607"",""57538"",""80206""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080326""}]"
DOID:0080328	"[""Culler-Jones syndrome""]"	"[{""label"":""GLI2"",""id"":""2736""}]"	"[""2736""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080328""}]"
DOID:0080329	"[""cold-induced sweating syndrome 1""]"	"[{""label"":""CRLF1"",""id"":""9244""}]"	"[""9244""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080329""}]"
DOID:0080330	"[""cold-induced sweating syndrome 2""]"	"[{""label"":""CLCF1"",""id"":""23529""}]"	"[""23529""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080330""}]"
DOID:0080331	"[""cold-induced sweating syndrome 3""]"	"[{""label"":""KLHL7"",""id"":""55975""}]"	"[""55975""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080331""}]"
DOID:0080333	"[""aortic valve disease 1""]"	"[{""label"":""NOTCH1"",""id"":""4851""}]"	"[""4851""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080333""}]"
DOID:0080334	"[""aortic valve disease 2""]"	"[{""label"":""FTO"",""id"":""79068""},{""label"":""SMAD6"",""id"":""4091""}]"	"[""4091"",""79068""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080334""}]"
DOID:0080336	"[""mitochondrial DNA depletion syndrome 14""]"	"[{""label"":""OPA1"",""id"":""4976""}]"	"[""4976""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080336""}]"
DOID:0080337	"[""mitochondrial DNA depletion syndrome 15""]"	"[{""label"":""TFAM"",""id"":""7019""}]"	"[""7019""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080337""}]"
DOID:0080339	"[""familial erythrocytosis 4"",""ECYT4""]"	"[{""label"":""EPAS1"",""id"":""2034""}]"	"[""2034""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080339""}]"
DOID:0080345	"[""blepharocheilodontic syndrome 1""]"	"[{""label"":""CDH1"",""id"":""999""}]"	"[""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080345""}]"
DOID:0080346	"[""blepharocheilodontic syndrome 2""]"	"[{""label"":""CTNND1"",""id"":""1500""}]"	"[""1500""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080346""}]"
DOID:0080348	"[""Alzheimer's disease 1"",""Alzheimer's disease 1, early onset""]"	"[{""label"":""Appl"",""id"":""31002""}]"	"[""31002""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080348""}]"
DOID:0080348	"[""Alzheimer's disease 1"",""Alzheimer's disease 1, early onset""]"	"[{""label"":""APP"",""id"":""351""},{""label"":""MPO"",""id"":""4353""},{""label"":""PLAU"",""id"":""5328""}]"	"[""351"",""4353"",""5328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080348""}]"
DOID:0080349	"[""developmental and epileptic encephalopathy 39"",""AGC1 deficiency"",""early infantile epileptic encephalopathy 39"",""epileptic encephalopathy with global cerebral demyelination""]"	"[{""label"":""SLC25A12"",""id"":""8604""}]"	"[""8604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080349""}]"
DOID:0080350	"[""retinitis pigmentosa 77""]"	"[{""label"":""Reep6"",""id"":""70335""}]"	"[""70335""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080350""}]"
DOID:0080351	"[""CLOVES syndrome"",""congenital lipomatous overgrowth, vascular malformations, and epidermal nevi""]"	"[{""label"":""Pik3ca"",""id"":""18706""}]"	"[""18706""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080351""}]"
DOID:0080351	"[""CLOVES syndrome"",""congenital lipomatous overgrowth, vascular malformations, and epidermal nevi""]"	"[{""label"":""PIK3CA"",""id"":""5290""}]"	"[""5290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080351""}]"
DOID:0080352	"[""X-linked chondrodysplasia punctata 2"",""Conradi-Hunermann Syndrome"",""Happle syndrome""]"	"[{""label"":""EBP"",""id"":""10682""}]"	"[""10682""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080352""}]"
DOID:0080353	"[""X-linked recessive hypophosphatemic rickets""]"	"[{""label"":""CLCN5"",""id"":""1184""}]"	"[""1184""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080353""}]"
DOID:0080354	"[""Phelan-McDermid syndrome"",""22q13.3 deletion syndrome"",""monosomy 22q13 syndrome""]"	"[{""label"":""Shank3"",""id"":""58234""},{""label"":""Tcf20"",""id"":""21411""}]"	"[""21411"",""58234""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080354""}]"
DOID:0080365	"[""endometrial hyperplasia""]"	"[{""label"":""KRAS"",""id"":""3845""}]"	"[""3845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080365""}]"
DOID:0080376	"[""trichorhinophalangeal syndrome type III"",""trichorhinophalangeal syndrome type 3""]"	"[{""label"":""TRPS1"",""id"":""7227""}]"	"[""7227""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080376""}]"
DOID:0080379	"[""nephrotic syndrome type 2"",""steroid-resistant autosomal recessive nephrotic syndrome""]"	"[{""label"":""NPHS2"",""id"":""7827""},{""label"":""PLA2G7"",""id"":""7941""},{""label"":""PLCE1"",""id"":""51196""},{""label"":""TRPC6"",""id"":""7225""}]"	"[""51196"",""7225"",""7827"",""7941""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080379""}]"
DOID:0080380	"[""nephrotic syndrome type 5"",""nephrotic syndrome type 5, with or without ocular abnormalities""]"	"[{""label"":""LAMB2"",""id"":""3913""}]"	"[""3913""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080380""}]"
DOID:0080381	"[""nephrotic syndrome type 13""]"	"[{""label"":""NUP205"",""id"":""23165""}]"	"[""23165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080381""}]"
DOID:0080382	"[""nephrotic syndrome type 3"",""early onset nephrotic syndrome type 3""]"	"[{""label"":""PLCE1"",""id"":""51196""}]"	"[""51196""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080382""}]"
DOID:0080384	"[""nephrotic syndrome type 6""]"	"[{""label"":""PTPRO"",""id"":""5800""}]"	"[""5800""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080384""}]"
DOID:0080385	"[""nephrotic syndrome type 11""]"	"[{""label"":""NUP107"",""id"":""57122""}]"	"[""57122""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080385""}]"
DOID:0080386	"[""nephrotic syndrome type 10""]"	"[{""label"":""EMP2"",""id"":""2013""}]"	"[""2013""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080386""}]"
DOID:0080387	"[""nephrotic syndrome type 12""]"	"[{""label"":""NUP93"",""id"":""9688""}]"	"[""9688""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080387""}]"
DOID:0080388	"[""nephrotic syndrome type 7"",""Ig-mediated MPGN"",""Ig-mediated membranoproliferative glomerulonephritis"",""Immunoglobulin-mediated MPGN"",""immunoglobulin-mediated membranoproliferative glomerulonephritis"",""nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis""]"	"[{""label"":""DGKE"",""id"":""8526""}]"	"[""8526""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080388""}]"
DOID:0080390	"[""nephrotic syndrome type 1"",""Finnish congenital nephrosis""]"	"[{""label"":""NPHS1"",""id"":""4868""}]"	"[""4868""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080390""}]"
DOID:0080393	"[""nephrotic syndrome type 18""]"	"[{""label"":""NUP133"",""id"":""55746""}]"	"[""55746""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080393""}]"
DOID:0080394	"[""nephrotic syndrome type 19""]"	"[{""label"":""NUP160"",""id"":""23279""}]"	"[""23279""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080394""}]"
DOID:0080403	"[""orofacial cleft 10"",""nonsyndromic cleft lip with or without cleft palate 10""]"	"[{""label"":""SUMO1"",""id"":""7341""}]"	"[""7341""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080403""}]"
DOID:0080404	"[""orofacial cleft 11"",""nonsyndromic cleft lip with or without cleft palate 11""]"	"[{""label"":""BMP4"",""id"":""652""}]"	"[""652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080404""}]"
DOID:0080409	"[""familial adenomatous polyposis 1"",""adenocarcinoma in adenomatous polyposis coli""]"	"[{""label"":""APC"",""id"":""324""}]"	"[""324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080409""}]"
DOID:0080410	"[""familial adenomatous polyposis 2"",""MUTYH-associated polyposis"",""MUTYH-related attenuated FAP"",""MUTYH-related attenuated familial adenomatous polyposis"",""MUTYH-related attenuated familial polyposis coli""]"	"[{""label"":""MUTYH"",""id"":""4595""}]"	"[""4595""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080410""}]"
DOID:0080411	"[""familial adenomatous polyposis 3""]"	"[{""label"":""NTHL1"",""id"":""4913""}]"	"[""4913""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080411""}]"
DOID:0080413	"[""developmental and epileptic encephalopathy 18"",""DEE18"",""early infantile epileptic encephalopathy 18""]"	"[{""label"":""SZT2"",""id"":""23334""}]"	"[""23334""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080413""}]"
DOID:0080414	"[""developmental and epileptic encephalopathy 15"",""DEE15"",""early infantile epileptic encephalopathy 15""]"	"[{""label"":""ST3GAL3"",""id"":""6487""}]"	"[""6487""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080414""}]"
DOID:0080415	"[""developmental and epileptic encephalopathy 23"",""DEE23"",""Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome"",""Epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome"",""early infantile epileptic encephalopathy 23""]"	"[{""label"":""DOCK7"",""id"":""85440""}]"	"[""85440""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080415""}]"
DOID:0080416	"[""developmental and epileptic encephalopathy 32"",""DEE32"",""early infantile epileptic encephalopathy 32""]"	"[{""label"":""KCNA2"",""id"":""3737""}]"	"[""3737""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080416""}]"
DOID:0080417	"[""developmental and epileptic encephalopathy 38"",""DEE38"",""early infantile epileptic encephalopathy 38""]"	"[{""label"":""ARV1"",""id"":""850943""}]"	"[""850943""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080417""}]"
DOID:0080418	"[""developmental and epileptic encephalopathy 54"",""DEE54"",""early infantile epileptic encephalopathy 54""]"	"[{""label"":""HNRNPU"",""id"":""3192""}]"	"[""3192""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080418""}]"
DOID:0080418	"[""developmental and epileptic encephalopathy 54"",""DEE54"",""early infantile epileptic encephalopathy 54""]"	"[{""label"":""Hnrnpu"",""id"":""51810""}]"	"[""51810""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080418""}]"
DOID:0080419	"[""developmental and epileptic encephalopathy 50"",""CDG syndrome type Iz"",""CDG-Iz"",""Carbohydrate deficient glycoprotein syndrome type Iz"",""Congenital disorder of glycosylation type 1z"",""DEE50"",""early infantile epileptic encephalopathy 50""]"	"[{""label"":""CAD"",""id"":""790""}]"	"[""790""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080419""}]"
DOID:0080420	"[""developmental and epileptic encephalopathy 62"",""DEE62"",""early infantile epileptic encephalopathy 62""]"	"[{""label"":""SCN3A"",""id"":""6328""}]"	"[""6328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080420""}]"
DOID:0080421	"[""developmental and epileptic encephalopathy 11"",""DEE11"",""early infantile epileptic encephalopathy 11""]"	"[{""label"":""SCN2A"",""id"":""6326""}]"	"[""6326""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080421""}]"
DOID:0080422	"[""Dravet syndrome"",""DEE6"",""DEE6A"",""developmental and epileptic encephalopathy 6"",""developmental and epileptic encephalopathy 6A"",""early infantile epileptic encephalopathy 6"",""severe myoclonic epilepsy of infancy""]"	"[{""label"":""SCN1A"",""id"":""6323""}]"	"[""6323""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080422""}]"
DOID:0080422	"[""Dravet syndrome"",""DEE6"",""DEE6A"",""developmental and epileptic encephalopathy 6"",""developmental and epileptic encephalopathy 6A"",""early infantile epileptic encephalopathy 6"",""severe myoclonic epilepsy of infancy""]"	"[{""label"":""Scn1a"",""id"":""20265""}]"	"[""20265""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080422""}]"
DOID:0080422	"[""Dravet syndrome"",""DEE6"",""DEE6A"",""developmental and epileptic encephalopathy 6"",""developmental and epileptic encephalopathy 6A"",""early infantile epileptic encephalopathy 6"",""severe myoclonic epilepsy of infancy""]"	"[{""label"":""para"",""id"":""32619""}]"	"[""32619""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080422""}]"
DOID:0080428	"[""developmental and epileptic encephalopathy 45"",""DEE45"",""early infantile epileptic encephalopathy 45""]"	"[{""label"":""GABRB1"",""id"":""2560""}]"	"[""2560""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080428""}]"
DOID:0080429	"[""developmental and epileptic encephalopathy 24"",""DEE24"",""early infantile epileptic encephalopathy 24""]"	"[{""label"":""HCN1"",""id"":""348980""}]"	"[""348980""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080429""}]"
DOID:0080430	"[""developmental and epileptic encephalopathy 65"",""DEE65"",""early infantile epileptic encephalopathy 65""]"	"[{""label"":""CYFIP2"",""id"":""26999""}]"	"[""26999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080430""}]"
DOID:0080431	"[""developmental and epileptic encephalopathy 19"",""DEE19"",""early infantile epileptic encephalopathy 19""]"	"[{""label"":""GABRA1"",""id"":""2554""}]"	"[""2554""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080431""}]"
DOID:0080432	"[""developmental and epileptic encephalopathy 60"",""DEE60"",""early infantile epileptic encephalopathy 60""]"	"[{""label"":""CNPY3"",""id"":""10695""}]"	"[""10695""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080432""}]"
DOID:0080433	"[""developmental and epileptic encephalopathy 51"",""DEE51"",""early infantile epileptic encephalopathy 51""]"	"[{""label"":""MDH2"",""id"":""4191""}]"	"[""4191""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080433""}]"
DOID:0080433	"[""developmental and epileptic encephalopathy 51"",""DEE51"",""early infantile epileptic encephalopathy 51""]"	"[{""label"":""MDH1"",""id"":""853777""}]"	"[""853777""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080433""}]"
DOID:0080434	"[""developmental and epileptic encephalopathy 61"",""DEE61"",""early infantile epileptic encephalopathy 61""]"	"[{""label"":""ADAM22"",""id"":""53616""}]"	"[""53616""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080434""}]"
DOID:0080436	"[""developmental and epileptic encephalopathy 4"",""DEE4"",""early infantile epileptic encephalopathy 4""]"	"[{""label"":""STXBP1"",""id"":""6812""}]"	"[""6812""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080436""}]"
DOID:0080437	"[""developmental and epileptic encephalopathy 31A"",""DEE31"",""DEE31A"",""developmental and epileptic encephalopathy 31"",""early infantile epileptic encephalopathy 31""]"	"[{""label"":""DNM1"",""id"":""1759""}]"	"[""1759""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080437""}]"
DOID:0080438	"[""developmental and epileptic encephalopathy 5"",""DEE5"",""early infantile epileptic encephalopathy 5""]"	"[{""label"":""SPTAN1"",""id"":""6709""}]"	"[""6709""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080438""}]"
DOID:0080439	"[""developmental and epileptic encephalopathy 14"",""DEE14"",""early infantile epileptic encephalopathy 14""]"	"[{""label"":""KCNT1"",""id"":""57582""}]"	"[""57582""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080439""}]"
DOID:0080439	"[""developmental and epileptic encephalopathy 14"",""DEE14"",""early infantile epileptic encephalopathy 14""]"	"[{""label"":""Kcnt1"",""id"":""227632""}]"	"[""227632""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080439""}]"
DOID:0080441	"[""developmental and epileptic encephalopathy 49"",""DEE49"",""early infantile epileptic encephalopathy 49""]"	"[{""label"":""DENND5A"",""id"":""23258""}]"	"[""23258""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080441""}]"
DOID:0080442	"[""developmental and epileptic encephalopathy 41"",""DEE41"",""early infantile epileptic encephalopathy 41""]"	"[{""label"":""SLC1A2"",""id"":""6506""}]"	"[""6506""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080442""}]"
DOID:0080443	"[""developmental and epileptic encephalopathy 21"",""DEE21"",""early infantile epileptic encephalopathy 21""]"	"[{""label"":""NECAP1"",""id"":""25977""}]"	"[""25977""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080443""}]"
DOID:0080444	"[""developmental and epileptic encephalopathy 27"",""DEE27"",""early infantile epileptic encephalopathy 27""]"	"[{""label"":""GRIN2B"",""id"":""2904""}]"	"[""2904""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080444""}]"
DOID:0080445	"[""developmental and epileptic encephalopathy 13"",""DEE13"",""early infantile epileptic encephalopathy 13""]"	"[{""label"":""SCN8A"",""id"":""6334""}]"	"[""6334""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080445""}]"
DOID:0080446	"[""developmental and epileptic encephalopathy 66"",""DEE66"",""early infantile epileptic encephalopathy 66""]"	"[{""label"":""PACS2"",""id"":""23241""}]"	"[""23241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080446""}]"
DOID:0080447	"[""developmental and epileptic encephalopathy 43"",""DEE43"",""early infantile epileptic encephalopathy 43""]"	"[{""label"":""GABRB3"",""id"":""2562""}]"	"[""2562""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080447""}]"
DOID:0080448	"[""developmental and epileptic encephalopathy 48"",""DEE48"",""early infantile epileptic encephalopathy 48""]"	"[{""label"":""AP3B2"",""id"":""8120""}]"	"[""8120""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080448""}]"
DOID:0080450	"[""developmental and epileptic encephalopathy 17"",""DEE17"",""early infantile epileptic encephalopathy 17""]"	"[{""label"":""Gnao1"",""id"":""14681""}]"	"[""14681""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080450""}]"
DOID:0080451	"[""developmental and epileptic encephalopathy 29"",""DEE29"",""early infantile epileptic encephalopathy 29""]"	"[{""label"":""AARS1"",""id"":""16""}]"	"[""16""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080451""}]"
DOID:0080453	"[""developmental and epileptic encephalopathy 25"",""DEE25"",""developmental and epileptic encephalopathy 25, with amelogenesis imperfecta"",""early infantile epileptic encephalopathy 25""]"	"[{""label"":""SLC13A5"",""id"":""284111""}]"	"[""284111""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080453""}]"
DOID:0080454	"[""developmental and epileptic encephalopathy 42"",""DEE42"",""early infantile epileptic encephalopathy 42""]"	"[{""label"":""CACNA1A"",""id"":""773""}]"	"[""773""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080454""}]"
DOID:0080455	"[""developmental and epileptic encephalopathy 52"",""DEE52"",""early infantile epileptic encephalopathy 52""]"	"[{""label"":""SCN1B"",""id"":""6324""}]"	"[""6324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080455""}]"
DOID:0080456	"[""developmental and epileptic encephalopathy 46"",""DEE46"",""early infantile epileptic encephalopathy 46""]"	"[{""label"":""GRIN2D"",""id"":""2906""}]"	"[""2906""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080456""}]"
DOID:0080459	"[""developmental and epileptic encephalopathy 12"",""DEE12"",""early infantile epileptic encephalopathy 12""]"	"[{""label"":""PLCB1"",""id"":""23236""}]"	"[""23236""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080459""}]"
DOID:0080460	"[""developmental and epileptic encephalopathy 34"",""DEE34"",""early infantile epileptic encephalopathy 34""]"	"[{""label"":""SLC12A5"",""id"":""57468""}]"	"[""57468""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080460""}]"
DOID:0080462	"[""developmental and epileptic encephalopathy 7"",""KCNQ2-related epileptic encephalopathy"",""KCNQ2-related neonatal epileptic encephalopathy"",""early infantile epileptic encephalopathy 7""]"	"[{""label"":""KCNQ2"",""id"":""3785""}]"	"[""3785""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080462""}]"
DOID:0080462	"[""developmental and epileptic encephalopathy 7"",""KCNQ2-related epileptic encephalopathy"",""KCNQ2-related neonatal epileptic encephalopathy"",""early infantile epileptic encephalopathy 7""]"	"[{""label"":""Kcnq2"",""id"":""16536""}]"	"[""16536""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080462""}]"
DOID:0080463	"[""developmental and epileptic encephalopathy 33"",""DEE33"",""early infantile epileptic encephalopathy 33""]"	"[{""label"":""EEF1A2"",""id"":""1917""}]"	"[""1917""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080463""}]"
DOID:0080464	"[""developmental and epileptic encephalopathy 53"",""DEE53"",""early infantile epileptic encephalopathy 53""]"	"[{""label"":""SYNJ1"",""id"":""8867""}]"	"[""8867""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080464""}]"
DOID:0080465	"[""developmental and epileptic encephalopathy 30"",""DEE30"",""early infantile epileptic encephalopathy 30""]"	"[{""label"":""SIK1"",""id"":""150094""}]"	"[""150094""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080465""}]"
DOID:0080467	"[""developmental and epileptic encephalopathy 2"",""DEE2"",""EIEE2"",""X-linked infantile spasm syndrome 2"",""early infantile epileptic encephalopathy 2""]"	"[{""label"":""CDKL5"",""id"":""6792""}]"	"[""6792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080467""}]"
DOID:0080467	"[""developmental and epileptic encephalopathy 2"",""DEE2"",""EIEE2"",""X-linked infantile spasm syndrome 2"",""early infantile epileptic encephalopathy 2""]"	"[{""label"":""Cdkl5"",""id"":""382253""}]"	"[""382253""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080467""}]"
DOID:0080468	"[""developmental and epileptic encephalopathy 1"",""DEE1"",""X-linked infantile spasm syndrome 1"",""early infantile epileptic encephalopathy 1""]"	"[{""label"":""ARX"",""id"":""170302""}]"	"[""170302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080468""}]"
DOID:0080470	"[""developmental and epileptic encephalopathy 36"",""congenital disorder of glycosylation, type Is"",""early infantile epileptic encephalopathy 36""]"	"[{""label"":""ALG13"",""id"":""79868""}]"	"[""79868""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00624""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080470""}]"
DOID:0080471	"[""developmental and epileptic encephalopathy 92""]"	"[{""label"":""GABRB2"",""id"":""2561""}]"	"[""2561""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080471""}]"
DOID:0080472	"[""developmental and epileptic encephalopathy 91"",""infantile or early childhood epileptic encephalopathy 1""]"	"[{""label"":""PPP3CA"",""id"":""5530""}]"	"[""5530""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080472""}]"
DOID:0080473	"[""developmental delay and seizures with or without movement abnormalities""]"	"[{""label"":""DHDDS"",""id"":""79947""}]"	"[""79947""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080473""}]"
DOID:0080475	"[""psoriasis 2""]"	"[{""label"":""CARD14"",""id"":""79092""}]"	"[""79092""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080475""}]"
DOID:0080484	"[""peroxisome biogenesis disorder 10A"",""peroxisome biogenesis disorder 10A (Zellweger)""]"	"[{""label"":""PEX3"",""id"":""8504""}]"	"[""8504""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080484""}]"
DOID:0080486	"[""peroxisome biogenesis disorder 12A"",""peroxisome biogenesis disorder 12A (Zellweger)""]"	"[{""label"":""PEX19"",""id"":""5824""}]"	"[""5824""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080486""}]"
DOID:0080487	"[""peroxisome biogenesis disorder 13A"",""peroxisome biogenesis disorder 13A (Zellweger)""]"	"[{""label"":""PEX14"",""id"":""5195""}]"	"[""5195""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080487""}]"
DOID:0080488	"[""mucolipidosis""]"	"[{""label"":""gnptab"",""id"":""553365""}]"	"[""553365""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080488""}]"
DOID:0080488	"[""mucolipidosis""]"	"[{""label"":""NEU1"",""id"":""4758""}]"	"[""4758""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080488""}]"
DOID:0080489	"[""GM1 gangliosidosis type 3"",""adult-onset GM1 gangliosidosis""]"	"[{""label"":""GLB1"",""id"":""2720""}]"	"[""2720""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00053""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080489""}]"
DOID:0080490	"[""mucolipidosis type IV""]"	"[{""label"":""Mcoln1"",""id"":""94178""}]"	"[""94178""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080490""}]"
DOID:0080490	"[""mucolipidosis type IV""]"	"[{""label"":""MCOLN1"",""id"":""57192""}]"	"[""57192""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080490""}]"
DOID:0080490	"[""mucolipidosis type IV""]"	"[{""label"":""cup-5"",""id"":""176074""}]"	"[""176074""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080490""}]"
DOID:0080491	"[""cerebral cavernous malformation 1""]"	"[{""label"":""PTGIS"",""id"":""5740""}]"	"[""5740""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080491""}]"
DOID:0080493	"[""ovarian dysgenesis 1""]"	"[{""label"":""FSHR"",""id"":""2492""}]"	"[""2492""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080493""}]"
DOID:0080494	"[""ovarian dysgenesis 2""]"	"[{""label"":""BMP15"",""id"":""9210""}]"	"[""9210""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080494""}]"
DOID:0080498	"[""ovarian dysgenesis 6""]"	"[{""label"":""NUP107"",""id"":""57122""}]"	"[""57122""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080498""}]"
DOID:0080499	"[""ovarian dysgenesis 7""]"	"[{""label"":""MRPS22"",""id"":""56945""}]"	"[""56945""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080499""}]"
DOID:0080501	"[""GM1 gangliosidosis type 2"",""juvenile GM1 gangliosidosis""]"	"[{""label"":""GLB1"",""id"":""2720""}]"	"[""2720""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00052""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080501""}]"
DOID:0080502	"[""GM1 gangliosidosis type 1""]"	"[{""label"":""GLB1"",""id"":""2720""}]"	"[""2720""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00051""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080502""}]"
DOID:0080505	"[""Cornelia de Lange syndrome 1""]"	"[{""label"":""Nipbl"",""id"":""71175""}]"	"[""71175""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080505""}]"
DOID:0080505	"[""Cornelia de Lange syndrome 1""]"	"[{""label"":""NIPBL"",""id"":""25836""}]"	"[""25836""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080505""}]"
DOID:0080506	"[""Cornelia de Lange syndrome 2""]"	"[{""label"":""SMC1A"",""id"":""8243""}]"	"[""8243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080506""}]"
DOID:0080507	"[""Cornelia de Lange syndrome 3"",""CDLS3"",""Cornelia De Lange syndrome 3 with or without midline brain defects""]"	"[{""label"":""SMC3"",""id"":""9126""}]"	"[""9126""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080507""}]"
DOID:0080507	"[""Cornelia de Lange syndrome 3"",""CDLS3"",""Cornelia De Lange syndrome 3 with or without midline brain defects""]"	"[{""label"":""SMC3"",""id"":""32627""}]"	"[""32627""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080507""}]"
DOID:0080512	"[""Meier-Gorlin syndrome 1""]"	"[{""label"":""ORC1"",""id"":""4998""}]"	"[""4998""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080512""}]"
DOID:0080517	"[""Meier-Gorlin syndrome 6""]"	"[{""label"":""GMNN"",""id"":""51053""}]"	"[""51053""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080517""}]"
DOID:0080519	"[""PAPA syndrome"",""pyogenic arthritis, pyoderma gangrenosum and acne""]"	"[{""label"":""PSTPIP1"",""id"":""9051""}]"	"[""9051""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080519""}]"
DOID:0080520	"[""Tn polyagglutination syndrome"",""galactosyltransferase deficiency""]"	"[{""label"":""C1GALT1C1"",""id"":""29071""}]"	"[""29071""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00401""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080520""}]"
DOID:0080523	"[""adult-onset leukoencephalopathy with axonal spheroids and pigmented glia"",""hereditary diffuse leukoencephalopathy with spheroids""]"	"[{""label"":""CSF1R"",""id"":""1436""}]"	"[""1436""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080523""}]"
DOID:0080526	"[""bronchiectasis 1""]"	"[{""label"":""CFTR"",""id"":""1080""},{""label"":""SCNN1B"",""id"":""6338""}]"	"[""1080"",""6338""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080526""}]"
DOID:0080527	"[""bronchiectasis 2""]"	"[{""label"":""SCNN1A"",""id"":""6337""}]"	"[""6337""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080527""}]"
DOID:0080528	"[""bronchiectasis 3""]"	"[{""label"":""SCNN1G"",""id"":""6340""}]"	"[""6340""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080528""}]"
DOID:0080530	"[""granular corneal dystrophy 1"",""corneal dystrophy, Groenouw type I""]"	"[{""label"":""TGFBI"",""id"":""7045""}]"	"[""7045""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080530""}]"
DOID:0080533	"[""Carney-Stratakis syndrome""]"	"[{""label"":""SDHB"",""id"":""6390""},{""label"":""SDHC"",""id"":""6391""},{""label"":""SDHD"",""id"":""6392""}]"	"[""6390"",""6391"",""6392""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080533""}]"
DOID:0080537	"[""hypermanganesemia with dystonia 2""]"	"[{""label"":""SLC39A14"",""id"":""23516""}]"	"[""23516""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080537""}]"
DOID:0080538	"[""Sweeney-Cox syndrome""]"	"[{""label"":""TWIST1"",""id"":""7291""}]"	"[""7291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080538""}]"
DOID:0080540	"[""galactosialidosis""]"	"[{""label"":""CTSA"",""id"":""5476""}]"	"[""5476""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00023""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080540""}]"
DOID:0080545	"[""hyper IgE syndrome"",""hyper immunoglobulin E syndrome""]"	"[{""label"":""IL6R"",""id"":""3570""}]"	"[""3570""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080545""}]"
DOID:0080547	"[""metabolic dysfunction-associated steatohepatitis"",""MASH"",""NASH"",""non-alcoholic steatohepatitis"",""nonalcoholic steatohepatitis""]"	"[{""label"":""APOA1"",""id"":""335""},{""label"":""HTR2B"",""id"":""3357""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL6"",""id"":""3569""},{""label"":""LEPR"",""id"":""3953""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""SOD2"",""id"":""6648""}]"	"[""335"",""3357"",""3569"",""3586"",""3953"",""5176"",""6648""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080547""}]"
DOID:0080547	"[""metabolic dysfunction-associated steatohepatitis"",""MASH"",""NASH"",""non-alcoholic steatohepatitis"",""nonalcoholic steatohepatitis""]"	"[{""label"":""Krt18"",""id"":""16668""},{""label"":""Mc4r"",""id"":""17202""}]"	"[""16668"",""17202""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080547""}]"
DOID:0080548	"[""Noonan syndrome with multiple lentigines 1"",""LEOPARD syndrome 1""]"	"[{""label"":""PTPN11"",""id"":""5781""}]"	"[""5781""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080548""}]"
DOID:0080549	"[""Noonan syndrome with multiple lentigines 2"",""LEOPARD syndrome 2""]"	"[{""label"":""RAF1"",""id"":""5894""}]"	"[""5894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080549""}]"
DOID:0080551	"[""Naxos disease""]"	"[{""label"":""JUP"",""id"":""3728""}]"	"[""3728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080551""}]"
DOID:0080552	"[""congenital disorder of glycosylation Ia"",""PMM2-congenital disorder of glycosylation"",""congenital disorder of glycosylation 1a""]"	"[{""label"":""SEC53"",""id"":""850499""}]"	"[""850499""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080552""}]"
DOID:0080552	"[""congenital disorder of glycosylation Ia"",""PMM2-congenital disorder of glycosylation"",""congenital disorder of glycosylation 1a""]"	"[{""label"":""PMM2"",""id"":""5373""}]"	"[""5373""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00343""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00429""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00430""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00431""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080552""}]"
DOID:0080553	"[""congenital disorder of glycosylation Iaa"",""congenital disorder of glycosylation 1aa""]"	"[{""label"":""NUS1"",""id"":""116150""}]"	"[""116150""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080553""}]"
DOID:0080554	"[""congenital disorder of glycosylation Ib"",""congenital disorder of glycosylation 1b""]"	"[{""label"":""MPI"",""id"":""4351""}]"	"[""4351""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00344""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080554""}]"
DOID:0080555	"[""congenital disorder of glycosylation Ic"",""congenital disorder of glycosylation 1c""]"	"[{""label"":""ALG6"",""id"":""29929""}]"	"[""29929""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00345""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080555""}]"
DOID:0080556	"[""congenital disorder of glycosylation Id"",""congenital disorder of glycosylation 1d""]"	"[{""label"":""ALG3"",""id"":""852196""}]"	"[""852196""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080556""}]"
DOID:0080556	"[""congenital disorder of glycosylation Id"",""congenital disorder of glycosylation 1d""]"	"[{""label"":""ALG3"",""id"":""10195""}]"	"[""10195""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00346""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080556""}]"
DOID:0080557	"[""congenital disorder of glycosylation Ie"",""congenital disorder of glycosylation 1e""]"	"[{""label"":""DPM1"",""id"":""8813""}]"	"[""8813""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00347""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080557""}]"
DOID:0080558	"[""congenital disorder of glycosylation If"",""congenital disorder of glycosylation 1f""]"	"[{""label"":""MPDU1"",""id"":""9526""}]"	"[""9526""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00348""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080558""}]"
DOID:0080559	"[""congenital disorder of glycosylation Ig"",""ALG12-congenital disorder of glycosylation"",""congenital disorder of glycosylation 1g""]"	"[{""label"":""ALG12"",""id"":""79087""}]"	"[""79087""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00349""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080559""}]"
DOID:0080560	"[""congenital disorder of glycosylation Ih"",""congenital disorder of glycosylation 1h""]"	"[{""label"":""ALG8"",""id"":""79053""}]"	"[""79053""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00350""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080560""}]"
DOID:0080561	"[""congenital disorder of glycosylation Ii"",""congenital disorder of glycosylation 1i""]"	"[{""label"":""ALG2"",""id"":""85365""}]"	"[""85365""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00351""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080561""}]"
DOID:0080562	"[""congenital disorder of glycosylation Ij"",""Congenital disorder of glycosylation 1j""]"	"[{""label"":""Alg7"",""id"":""34711""}]"	"[""34711""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080562""}]"
DOID:0080562	"[""congenital disorder of glycosylation Ij"",""Congenital disorder of glycosylation 1j""]"	"[{""label"":""DPAGT1"",""id"":""1798""}]"	"[""1798""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00352""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080562""}]"
DOID:0080563	"[""congenital disorder of glycosylation Ik"",""congenital disorder of glycosylation 1k""]"	"[{""label"":""ALG1"",""id"":""852407""}]"	"[""852407""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080563""}]"
DOID:0080563	"[""congenital disorder of glycosylation Ik"",""congenital disorder of glycosylation 1k""]"	"[{""label"":""ALG1"",""id"":""56052""}]"	"[""56052""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00353""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080563""}]"
DOID:0080564	"[""congenital disorder of glycosylation Il"",""congenital disorder of glycosylation 1l""]"	"[{""label"":""ALG9"",""id"":""79796""}]"	"[""79796""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00354""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080564""}]"
DOID:0080565	"[""congenital disorder of glycosylation Im"",""DOLK-congenital disorder of glycosylation"",""congenital disorder of glycosylation 1m"",""dolichol kinase deficiency""]"	"[{""label"":""DOLK"",""id"":""22845""}]"	"[""22845""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00355""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080565""}]"
DOID:0080566	"[""congenital disorder of glycosylation In"",""congenital disorder of glycosylation 1n""]"	"[{""label"":""RFT1"",""id"":""91869""}]"	"[""91869""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00356""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080566""}]"
DOID:0080567	"[""congenital disorder of glycosylation Ip"",""congenital disorder of glycosylation 1p""]"	"[{""label"":""ALG11"",""id"":""440138""}]"	"[""440138""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00621""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080567""}]"
DOID:0080568	"[""congenital disorder of glycosylation Iq"",""congenital disorder of glycosylation 1q""]"	"[{""label"":""SRD5A3"",""id"":""79644""}]"	"[""79644""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00622""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080568""}]"
DOID:0080569	"[""congenital disorder of glycosylation Ir"",""congenital disorder of glycosylation 1r""]"	"[{""label"":""DDOST"",""id"":""1650""}]"	"[""1650""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00623""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080569""}]"
DOID:0080570	"[""congenital disorder of glycosylation It"",""congenital disorder of glycosylation 1t""]"	"[{""label"":""PGM1"",""id"":""853732""},{""label"":""PGM2"",""id"":""855131""}]"	"[""853732"",""855131""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080570""}]"
DOID:0080570	"[""congenital disorder of glycosylation It"",""congenital disorder of glycosylation 1t""]"	"[{""label"":""PGM1"",""id"":""5236""}]"	"[""5236""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00625""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080570""}]"
DOID:0080571	"[""congenital disorder of glycosylation Iu"",""congenital disorder of glycosylation 1u""]"	"[{""label"":""DPM2"",""id"":""8818""}]"	"[""8818""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080571""}]"
DOID:0080572	"[""congenital disorder of glycosylation Iw"",""congenital disorder of glycosylation 1w""]"	"[{""label"":""STT3A"",""id"":""3703""}]"	"[""3703""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080572""}]"
DOID:0080572	"[""congenital disorder of glycosylation Iw"",""congenital disorder of glycosylation 1w""]"	"[{""label"":""STT3"",""id"":""852862""}]"	"[""852862""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080572""}]"
DOID:0080573	"[""congenital disorder of glycosylation Ix"",""congenital disorder of glycosylation 1x""]"	"[{""label"":""STT3B"",""id"":""201595""}]"	"[""201595""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080573""}]"
DOID:0080575	"[""Larsen-like syndrome B3GAT3 type"",""Larsen-like syndrome, B3GAT3 type"",""multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome""]"	"[{""label"":""B3GAT3"",""id"":""26229""}]"	"[""26229""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00631""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080575""}]"
DOID:0080576	"[""spondyloepimetaphyseal dysplasia, Genevieve-type""]"	"[{""label"":""NANS"",""id"":""54187""}]"	"[""54187""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080576""}]"
DOID:0080579	"[""3-methylcrotonyl-CoA carboxylase 1 deficiency""]"	"[{""label"":""MCCC1"",""id"":""56922""}]"	"[""56922""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080579""}]"
DOID:0080581	"[""hyperekplexia 4""]"	"[{""label"":""ATAD1"",""id"":""84896""}]"	"[""84896""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080581""}]"
DOID:0080582	"[""hypotrichosis 14""]"	"[{""label"":""LSS"",""id"":""4047""}]"	"[""4047""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080582""}]"
DOID:0080584	"[""autosomal dominant Wolfram syndrome""]"	"[{""label"":""WFS1"",""id"":""7466""}]"	"[""7466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080584""}]"
DOID:0080585	"[""Van Maldergem syndrome 1""]"	"[{""label"":""DCHS1"",""id"":""8642""}]"	"[""8642""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080585""}]"
DOID:0080586	"[""Van Maldergem syndrome 2""]"	"[{""label"":""FAT4"",""id"":""79633""}]"	"[""79633""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080586""}]"
DOID:0080586	"[""Van Maldergem syndrome 2""]"	"[{""label"":""ft"",""id"":""33627""}]"	"[""33627""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080586""}]"
DOID:0080588	"[""agammaglobulinemia 5""]"	"[{""label"":""LRRC8A"",""id"":""56262""}]"	"[""56262""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080588""}]"
DOID:0080589	"[""Klippel-Feil syndrome 1""]"	"[{""label"":""GDF6"",""id"":""392255""}]"	"[""392255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080589""}]"
DOID:0080591	"[""Klippel-Feil syndrome 3""]"	"[{""label"":""GDF3"",""id"":""9573""}]"	"[""9573""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080591""}]"
DOID:0080592	"[""Klippel-Feil syndrome 4""]"	"[{""label"":""MYO18B"",""id"":""84700""}]"	"[""84700""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080592""}]"
DOID:0080594	"[""hyper IgE recurrent infection syndrome 2""]"	"[{""label"":""DOCK8"",""id"":""81704""}]"	"[""81704""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080594""}]"
DOID:0080596	"[""hyper IgE recurrent infection syndrome 4""]"	"[{""label"":""IL6ST"",""id"":""3572""}]"	"[""3572""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080596""}]"
DOID:0080597	"[""Kleefstra syndrome""]"	"[{""label"":""EHMT1"",""id"":""79813""}]"	"[""79813""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080597""}]"
DOID:0080598	"[""Kleefstra syndrome 2""]"	"[{""label"":""KMT2C"",""id"":""58508""}]"	"[""58508""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080598""}]"
DOID:0080599	"[""Coronavirus infectious disease""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""CD209"",""id"":""30835""},{""label"":""MBL2"",""id"":""4153""}]"	"[""1636"",""30835"",""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080599""}]"
DOID:0080599	"[""Coronavirus infectious disease""]"	"[{""label"":""Ccr5"",""id"":""12774""},{""label"":""Egfr"",""id"":""13649""},{""label"":""Muc4"",""id"":""140474""},{""label"":""Ppp1r14c"",""id"":""76142""}]"	"[""12774"",""13649"",""140474"",""76142""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080599""}]"
DOID:0080600	"[""COVID-19"",""2019 Novel Coronavirus (2019-nCoV)"",""2019-nCoV infection"",""COVID19"",""SARS-CoV-2 infection"",""Wuhan coronavirus infection"",""Wuhan seafood market pneumonia virus infection""]"	"[{""label"":""A2M"",""id"":""2""},{""label"":""ABO"",""id"":""28""},{""label"":""ACE2"",""id"":""59272""},{""label"":""ACE"",""id"":""1636""},{""label"":""AGTR1"",""id"":""185""},{""label"":""C3"",""id"":""718""},{""label"":""C4BPA"",""id"":""722""},{""label"":""C4BPB"",""id"":""725""},{""label"":""CFH"",""id"":""3075""},{""label"":""F3"",""id"":""2152""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-C"",""id"":""3107""},{""label"":""IFNB1"",""id"":""3456""},{""label"":""IFNL1"",""id"":""282618""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""PLG"",""id"":""5340""},{""label"":""SERPINF2"",""id"":""5345""},{""label"":""SERPING1"",""id"":""710""},{""label"":""TLR7"",""id"":""51284""}]"	"[""1636"",""185"",""2"",""2152"",""28"",""282618"",""3075"",""3106"",""3107"",""3456"",""3813"",""51284"",""5340"",""5345"",""59272"",""710"",""718"",""722"",""725""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080600""}]"
DOID:0080600	"[""COVID-19"",""2019 Novel Coronavirus (2019-nCoV)"",""2019-nCoV infection"",""COVID19"",""SARS-CoV-2 infection"",""Wuhan coronavirus infection"",""Wuhan seafood market pneumonia virus infection""]"	"[{""label"":""Ace2"",""id"":""70008""}]"	"[""70008""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080600""}]"
DOID:0080608	"[""anterior segment dysgenesis 3""]"	"[{""label"":""FOXC1"",""id"":""2296""}]"	"[""2296""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080608""}]"
DOID:0080609	"[""anterior segment dysgenesis 4""]"	"[{""label"":""PITX2"",""id"":""5308""}]"	"[""5308""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080609""}]"
DOID:0080611	"[""anterior segment dysgenesis 6""]"	"[{""label"":""CYP1B1"",""id"":""1545""}]"	"[""1545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080611""}]"
DOID:0080612	"[""anterior segment dysgenesis 7""]"	"[{""label"":""PXDN"",""id"":""7837""}]"	"[""7837""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080612""}]"
DOID:0080615	"[""nephroma"",""benign nephroma""]"	"[{""label"":""DICER1"",""id"":""23405""}]"	"[""23405""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080615""}]"
DOID:0080620	"[""familial glucocorticoid deficiency""]"	"[{""label"":""NNT"",""id"":""23530""}]"	"[""23530""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080620""}]"
DOID:0080621	"[""glucocorticoid deficiency 1""]"	"[{""label"":""MC2R"",""id"":""4158""}]"	"[""4158""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080621""}]"
DOID:0080625	"[""severe congenital neutropenia 1""]"	"[{""label"":""ELANE"",""id"":""1991""}]"	"[""1991""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080625""}]"
DOID:0080626	"[""corticosterone methyloxidase deficiency 1"",""aldosterone synthase deficiency""]"	"[{""label"":""CYP11B2"",""id"":""1585""}]"	"[""1585""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080626""}]"
DOID:0080628	"[""alopecia-mental retardation syndrome 1""]"	"[{""label"":""AHSG"",""id"":""197""}]"	"[""197""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080628""}]"
DOID:0080630	"[""B-lymphoblastic leukemia/lymphoma"",""B lymphoblastic leukemia/lymphoma"",""B-ALL"",""precursor B lymphoblastic lymphoma/leukemia""]"	"[{""label"":""ABL1"",""id"":""25""},{""label"":""AKR1C3"",""id"":""8644""},{""label"":""BRD2"",""id"":""6046""},{""label"":""CYP3A5"",""id"":""1577""},{""label"":""F3"",""id"":""2152""},{""label"":""IKZF1"",""id"":""10320""},{""label"":""TFPI"",""id"":""7035""},{""label"":""TNFSF13"",""id"":""8741""},{""label"":""TP53"",""id"":""7157""}]"	"[""10320"",""1577"",""2152"",""25"",""6046"",""7035"",""7157"",""8644"",""8741""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080630""}]"
DOID:0080631	"[""Elsahy-Waters syndrome"",""branchioskeletogenital syndrome""]"	"[{""label"":""CDH11"",""id"":""1009""}]"	"[""1009""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080631""}]"
DOID:0080632	"[""Fazio-Londe disease"",""riboflavin transporter deficiency neuronopathy""]"	"[{""label"":""SLC52A3"",""id"":""113278""}]"	"[""113278""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080632""}]"
DOID:0080633	"[""developmental cardiac valvular defect""]"	"[{""label"":""MTHFD1"",""id"":""4522""},{""label"":""PLD1"",""id"":""5337""}]"	"[""4522"",""5337""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080633""}]"
DOID:0080634	"[""nanophthalmos""]"	"[{""label"":""MFRP"",""id"":""83552""},{""label"":""MYRF"",""id"":""745""}]"	"[""745"",""83552""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080634""}]"
DOID:0080642	"[""Middle East respiratory syndrome""]"	"[{""label"":""DPP4"",""id"":""1803""}]"	"[""1803""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080642""}]"
DOID:0080642	"[""Middle East respiratory syndrome""]"	"[{""label"":""Dpp4"",""id"":""13482""}]"	"[""13482""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080642""}]"
DOID:0080652	"[""calcium oxalate nephrolithiasis""]"	"[{""label"":""CASR"",""id"":""846""},{""label"":""FN1"",""id"":""2335""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""OXGR1"",""id"":""27199""},{""label"":""SLC26A1"",""id"":""10861""}]"	"[""10861"",""2335"",""27199"",""3557"",""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080652""}]"
DOID:0080653	"[""urolithiasis""]"	"[{""label"":""PLAU"",""id"":""5328""}]"	"[""5328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080653""}]"
DOID:0080661	"[""nonsyndromic aplasia cutis congenita""]"	"[{""label"":""BMS1"",""id"":""9790""}]"	"[""9790""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080661""}]"
DOID:0080663	"[""atrial standstill 2""]"	"[{""label"":""NPPA"",""id"":""4878""}]"	"[""4878""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080663""}]"
DOID:0080664	"[""diaphyseal medullary stenosis with malignant fibrous histiocytoma"",""Hardcastle syndrome"",""bone dysplasia-medullary fibrosarcoma syndrome"",""diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome""]"	"[{""label"":""MTAP"",""id"":""4507""}]"	"[""4507""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080664""}]"
DOID:0080665	"[""warfarin resistance""]"	"[{""label"":""CYP2C9"",""id"":""1559""}]"	"[""1559""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080665""}]"
DOID:0080669	"[""posterior polymorphous corneal dystrophy 4""]"	"[{""label"":""GRHL2"",""id"":""79977""}]"	"[""79977""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080669""}]"
DOID:0080672	"[""fibrochondrogenesis 1""]"	"[{""label"":""COL11A1"",""id"":""1301""}]"	"[""1301""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080672""}]"
DOID:0080673	"[""fibrochondrogenesis 2""]"	"[{""label"":""COL11A2"",""id"":""1302""}]"	"[""1302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080673""}]"
DOID:0080675	"[""Stickler syndrome 2""]"	"[{""label"":""COL11A1"",""id"":""1301""}]"	"[""1301""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080675""}]"
DOID:0080676	"[""Stickler syndrome 1""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080676""}]"
DOID:0080677	"[""otospondylomegaepiphyseal dysplasia, autosomal dominant""]"	"[{""label"":""COL11A2"",""id"":""1302""}]"	"[""1302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080677""}]"
DOID:0080678	"[""mucolipidosis III gamma""]"	"[{""label"":""GNPTG"",""id"":""84572""}]"	"[""84572""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080678""}]"
DOID:0080679	"[""neuronal intestinal dysplasia type A""]"	"[{""label"":""ERBB3"",""id"":""2065""}]"	"[""2065""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080679""}]"
DOID:0080681	"[""X-linked chronic idiopathic intestinal pseudo-obstruction""]"	"[{""label"":""FLNA"",""id"":""2316""}]"	"[""2316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080681""}]"
DOID:0080686	"[""tubular aggregate myopathy 2""]"	"[{""label"":""ORAI1"",""id"":""84876""}]"	"[""84876""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080686""}]"
DOID:0080687	"[""reducing body myopathy 1B""]"	"[{""label"":""FHL1"",""id"":""2273""}]"	"[""2273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080687""}]"
DOID:0080688	"[""mosaic variegated aneuploidy syndrome""]"	"[{""label"":""SLF2"",""id"":""55719""},{""label"":""SMC5"",""id"":""23137""}]"	"[""23137"",""55719""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080688""}]"
DOID:0080689	"[""mosaic variegated aneuploidy syndrome 3""]"	"[{""label"":""TRIP13"",""id"":""9319""}]"	"[""9319""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080689""}]"
DOID:0080690	"[""RASopathy"",""RAS/mitogen-activated protein kinase syndrome""]"	"[{""label"":""Rreb1"",""id"":""68750""}]"	"[""68750""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080690""}]"
DOID:0080692	"[""Noonan syndrome-like disorder with loose anagen hair 1""]"	"[{""label"":""SHOC2"",""id"":""8036""}]"	"[""8036""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080692""}]"
DOID:0080693	"[""Noonan syndrome-like disorder with loose anagen hair 2""]"	"[{""label"":""PPP1CB"",""id"":""5500""}]"	"[""5500""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080693""}]"
DOID:0080694	"[""Galloway-Mowat syndrome""]"	"[{""label"":""NUP107"",""id"":""57122""},{""label"":""NUP133"",""id"":""55746""},{""label"":""YRDC"",""id"":""79693""}]"	"[""55746"",""57122"",""79693""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080694""}]"
DOID:0080695	"[""Burn-McKeown syndrome"",""Choanal atresia - deafness - cardiac defects - dysmorphism syndrome""]"	"[{""label"":""TXNL4A"",""id"":""10907""}]"	"[""10907""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080695""}]"
DOID:0080696	"[""Winchester syndrome""]"	"[{""label"":""MMP14"",""id"":""4323""}]"	"[""4323""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080696""}]"
DOID:0080697	"[""Opitz GBBB syndrome"",""Opitz G/BBB Syndrome"",""Opitz GBBB syndrome type I""]"	"[{""label"":""MID1"",""id"":""4281""}]"	"[""4281""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080697""}]"
DOID:0080698	"[""Teebi hypertelorism syndrome 1"",""Opitz GBBB syndrome type II"",""SPECC1L-related hypertelorism syndrome"",""Teebi hypertelorism syndrome-1""]"	"[{""label"":""Specc1l"",""id"":""74392""}]"	"[""74392""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080698""}]"
DOID:0080698	"[""Teebi hypertelorism syndrome 1"",""Opitz GBBB syndrome type II"",""SPECC1L-related hypertelorism syndrome"",""Teebi hypertelorism syndrome-1""]"	"[{""label"":""SPECC1L"",""id"":""23384""}]"	"[""23384""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080698""}]"
DOID:0080716	"[""infantile liver failure syndrome""]"	"[{""label"":""NBAS"",""id"":""51594""},{""label"":""RINT1"",""id"":""60561""}]"	"[""51594"",""60561""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080716""}]"
DOID:0080717	"[""infantile liver failure syndrome 1""]"	"[{""label"":""LARS1"",""id"":""51520""}]"	"[""51520""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080717""}]"
DOID:0080718	"[""GNE myopathy"",""Distal myopathy, Nonaka type"",""Hereditary Inclusion Body Myopathy"",""Nonaka myopathy"",""inclusion body myopathy 2""]"	"[{""label"":""GNE"",""id"":""10020""}]"	"[""10020""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00385""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00386""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080718""}]"
DOID:0080720	"[""autosomal dominant congenital deafness with onychodystrophy""]"	"[{""label"":""Atp6v1b2"",""id"":""11966""}]"	"[""11966""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080720""}]"
DOID:0080721	"[""calvarial doughnut lesions with bone fragility""]"	"[{""label"":""SGMS2"",""id"":""166929""}]"	"[""166929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080721""}]"
DOID:0080722	"[""Kenny-Caffey syndrome type 1""]"	"[{""label"":""TBCE"",""id"":""6905""}]"	"[""6905""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080722""}]"
DOID:0080726	"[""Ehlers-Danlos syndrome classic type 2""]"	"[{""label"":""COL5A2"",""id"":""1290""}]"	"[""1290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080726""}]"
DOID:0080727	"[""Ehlers-Danlos syndrome arthrochalasia type 1""]"	"[{""label"":""COL1A1"",""id"":""1277""}]"	"[""1277""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080727""}]"
DOID:0080728	"[""Ehlers-Danlos syndrome arthrochalasia type 2""]"	"[{""label"":""COL1A2"",""id"":""1278""}]"	"[""1278""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080728""}]"
DOID:0080730	"[""Ehlers-Danlos syndrome cardiac valvular type""]"	"[{""label"":""COL1A2"",""id"":""1278""}]"	"[""1278""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080730""}]"
DOID:0080732	"[""Ehlers-Danlos syndrome classic-like 2""]"	"[{""label"":""AEBP1"",""id"":""165""}]"	"[""165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080732""}]"
DOID:0080733	"[""Ehlers-Danlos syndrome dermatosparaxis type""]"	"[{""label"":""ADAMTS2"",""id"":""9509""}]"	"[""9509""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080733""}]"
DOID:0080734	"[""Ehlers-Danlos syndrome kyphoscoliotic type 1""]"	"[{""label"":""PLOD1"",""id"":""5351""}]"	"[""5351""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00407""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080734""}]"
DOID:0080735	"[""Ehlers-Danlos syndrome kyphoscoliotic type 2""]"	"[{""label"":""FKBP14"",""id"":""55033""}]"	"[""55033""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080735""}]"
DOID:0080736	"[""Ehlers-Danlos syndrome musculocontractural type 1""]"	"[{""label"":""CHST14"",""id"":""113189""}]"	"[""113189""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00634""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080736""}]"
DOID:0080737	"[""Ehlers-Danlos syndrome musculocontractural type 2""]"	"[{""label"":""DSE"",""id"":""29940""}]"	"[""29940""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080737""}]"
DOID:0080738	"[""Ehlers-Danlos syndrome spondylodysplastic type 1""]"	"[{""label"":""B4GALT7"",""id"":""11285""}]"	"[""11285""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00388""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080738""}]"
DOID:0080743	"[""transverse myelitis""]"	"[{""label"":""AQP4"",""id"":""361""}]"	"[""361""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080743""}]"
DOID:0080745	"[""polymyositis""]"	"[{""label"":""ELN"",""id"":""2006""},{""label"":""PMS1"",""id"":""5378""},{""label"":""STAT4"",""id"":""6775""}]"	"[""2006"",""5378"",""6775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080745""}]"
DOID:0080746	"[""Sweet syndrome"",""Acute Febrile Neutrophilic Dermatosis"",""Sweet's syndrome""]"	"[{""label"":""MEFV"",""id"":""4210""}]"	"[""4210""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080746""}]"
DOID:0080750	"[""erythema nodosum""]"	"[{""label"":""HLA-B"",""id"":""3106""},{""label"":""LTA"",""id"":""4049""},{""label"":""TNF"",""id"":""7124""}]"	"[""3106"",""4049"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080750""}]"
DOID:0080751	"[""keratosis pilaris atrophicans""]"	"[{""label"":""LRP1"",""id"":""4035""}]"	"[""4035""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080751""}]"
DOID:0080754	"[""X-linked keratosis follicularis spinulosa decalvans""]"	"[{""label"":""MBTPS2"",""id"":""51360""}]"	"[""51360""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080754""}]"
DOID:0080758	"[""Fanconi renotubular syndrome 2""]"	"[{""label"":""SLC34A1"",""id"":""6569""}]"	"[""6569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080758""}]"
DOID:0080759	"[""Fanconi renotubular syndrome 3""]"	"[{""label"":""EHHADH"",""id"":""1962""}]"	"[""1962""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080759""}]"
DOID:0080760	"[""Fanconi renotubular syndrome 4""]"	"[{""label"":""HNF4A"",""id"":""3172""}]"	"[""3172""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080760""}]"
DOID:0080762	"[""autosomal recessive limb-girdle muscular dystrophy type 2Z"",""limb-girdle muscular dystrophy 21""]"	"[{""label"":""POGLUT1"",""id"":""56983""}]"	"[""56983""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080762""}]"
DOID:0080763	"[""diffuse gastric cancer""]"	"[{""label"":""MAP3K1"",""id"":""4214""}]"	"[""4214""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080763""}]"
DOID:0080764	"[""hereditary diffuse gastric cancer""]"	"[{""label"":""CDH1"",""id"":""999""}]"	"[""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080764""}]"
DOID:0080766	"[""erythrokeratodermia variabilis et progressiva 6""]"	"[{""label"":""TRPM4"",""id"":""54795""}]"	"[""54795""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080766""}]"
DOID:0080768	"[""pyridoxine-dependent epilepsy""]"	"[{""label"":""Aldh7a1"",""id"":""110695""}]"	"[""110695""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080768""}]"
DOID:0080770	"[""autosomal dominant beta thalassemia"",""inclusion body beta-thalassemia""]"	"[{""label"":""HBB"",""id"":""3043""}]"	"[""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080770""}]"
DOID:0080773	"[""delta beta-thalassemia""]"	"[{""label"":""HBB"",""id"":""3043""}]"	"[""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080773""}]"
DOID:0080776	"[""partial androgen insensitivity syndrome"",""Reifenstein syndrome""]"	"[{""label"":""AR"",""id"":""367""}]"	"[""367""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080776""}]"
DOID:0080784	"[""urinary tract infection"",""UTI""]"	"[{""label"":""CXCR1"",""id"":""3577""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""LCN2"",""id"":""3934""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""}]"	"[""3304"",""3577"",""3934"",""7097"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080784""}]"
DOID:0080785	"[""Brown-Vialetto-Van Laere syndrome 1""]"	"[{""label"":""SLC52A3"",""id"":""113278""}]"	"[""113278""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080785""}]"
DOID:0080786	"[""Brown-Vialetto-Van Laere syndrome 2""]"	"[{""label"":""SLC52A2"",""id"":""79581""}]"	"[""79581""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080786""}]"
DOID:0080787	"[""proximal symphalangism 1""]"	"[{""label"":""NOG"",""id"":""9241""}]"	"[""9241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080787""}]"
DOID:0080788	"[""proximal symphalangism 2""]"	"[{""label"":""GDF5"",""id"":""8200""}]"	"[""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080788""}]"
DOID:0080789	"[""Treacher Collins syndrome 1""]"	"[{""label"":""TCOF1"",""id"":""6949""}]"	"[""6949""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080789""}]"
DOID:0080792	"[""Treacher Collins syndrome 4""]"	"[{""label"":""POLR1B"",""id"":""84172""}]"	"[""84172""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080792""}]"
DOID:0080797	"[""nasal type extranodal NK/T-cell lymphoma""]"	"[{""label"":""FAS"",""id"":""355""}]"	"[""355""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080797""}]"
DOID:0080804	"[""cranioectodermal dysplasia 2""]"	"[{""label"":""WDR35"",""id"":""57539""}]"	"[""57539""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080804""}]"
DOID:0080807	"[""autosomal dominant craniodiaphyseal dysplasia""]"	"[{""label"":""SOST"",""id"":""50964""}]"	"[""50964""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080807""}]"
DOID:0080809	"[""chronic asthma""]"	"[{""label"":""Ngf"",""id"":""310738""}]"	"[""310738""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080809""}]"
DOID:0080820	"[""occupational asthma""]"	"[{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DOA"",""id"":""3111""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-E"",""id"":""3133""}]"	"[""3106"",""3111"",""3115"",""3133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080820""}]"
DOID:0080821	"[""exercise-induced bronchoconstriction"",""exercise-induced asthma""]"	"[{""label"":""ALOX5"",""id"":""240""},{""label"":""TACR1"",""id"":""6869""}]"	"[""240"",""6869""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080821""}]"
DOID:0080822	"[""aspirin-induced respiratory disease"",""aspirin-sensitive asthma""]"	"[{""label"":""CYSLTR2"",""id"":""57105""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HLA-DRB3"",""id"":""3125""},{""label"":""HLA-DRB4"",""id"":""3126""},{""label"":""IL4"",""id"":""3565""},{""label"":""TBXA2R"",""id"":""6915""}]"	"[""3117"",""3119"",""3123"",""3125"",""3126"",""3565"",""57105"",""6915""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080822""}]"
DOID:0080827	"[""human cytomegalovirus infection""]"	"[{""label"":""KIR3DS1"",""id"":""3813""}]"	"[""3813""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080827""}]"
DOID:0080828	"[""VEXAS syndrome"",""vacuoles, E1 enzyme, X-linked, autoinflammatory and somatic syndrome""]"	"[{""label"":""UBA1"",""id"":""7317""}]"	"[""7317""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080828""}]"
DOID:0080832	"[""mild cognitive impairment""]"	"[{""label"":""AGER"",""id"":""177""},{""label"":""SLC6A3"",""id"":""6531""}]"	"[""177"",""6531""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080832""}]"
DOID:0080836	"[""growth hormone insensitivity syndrome with immune dysregulation 1""]"	"[{""label"":""STAT5B"",""id"":""6777""}]"	"[""6777""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080836""}]"
DOID:0080837	"[""growth hormone insensitivity syndrome with immune dysregulation 2""]"	"[{""label"":""STAT5B"",""id"":""6777""}]"	"[""6777""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080837""}]"
DOID:0080839	"[""X-linked warfarin sensitivity""]"	"[{""label"":""F9"",""id"":""2158""}]"	"[""2158""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080839""}]"
DOID:0080844	"[""omodysplasia 1""]"	"[{""label"":""GPC6"",""id"":""10082""}]"	"[""10082""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080844""}]"
DOID:0080845	"[""omodysplasia 2""]"	"[{""label"":""FZD2"",""id"":""2535""}]"	"[""2535""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080845""}]"
DOID:0080846	"[""latent autoimmune diabetes in adults"",""LADA"",""type 1.5 diabetes""]"	"[{""label"":""CTLA4"",""id"":""1493""}]"	"[""1493""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080846""}]"
DOID:0080855	"[""Parkinsonism""]"	"[{""label"":""Bad"",""id"":""64639""},{""label"":""Cnr1"",""id"":""25248""},{""label"":""Comt"",""id"":""24267""},{""label"":""Csf2"",""id"":""116630""},{""label"":""Drd2"",""id"":""24318""},{""label"":""Drd3"",""id"":""29238""},{""label"":""Esr1"",""id"":""24890""},{""label"":""Gdnf"",""id"":""25453""},{""label"":""Gfra1"",""id"":""25454""},{""label"":""Grm8"",""id"":""60590""},{""label"":""Ntrk1"",""id"":""59109""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Shh"",""id"":""29499""},{""label"":""Slc11a2"",""id"":""25715""},{""label"":""Vip"",""id"":""117064""}]"	"[""116630"",""117064"",""24267"",""24318"",""24890"",""25248"",""25453"",""25454"",""25715"",""29238"",""29499"",""29527"",""59109"",""60590"",""64639""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080855""}]"
DOID:0080855	"[""Parkinsonism""]"	"[{""label"":""BDNF"",""id"":""627""},{""label"":""GBA1"",""id"":""2629""},{""label"":""GDNF"",""id"":""2668""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""LRRK2"",""id"":""120892""},{""label"":""PARK7"",""id"":""11315""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""11315"",""120892"",""2629"",""2668"",""3303"",""627"",""7133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080855""}]"
DOID:0080857	"[""primary ovarian insufficiency 1"",""FMR1-related primary ovarian insufficiency"",""Fragile X-associated primary ovarian insufficiency"",""premature ovarian failure 1""]"	"[{""label"":""FMR1"",""id"":""2332""}]"	"[""2332""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080857""}]"
DOID:0080860	"[""primary ovarian insufficiency 3""]"	"[{""label"":""FOXL2"",""id"":""668""}]"	"[""668""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080860""}]"
DOID:0080862	"[""primary ovarian insufficiency 5""]"	"[{""label"":""NOBOX"",""id"":""135935""}]"	"[""135935""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080862""}]"
DOID:0080865	"[""primary ovarian insufficiency 8""]"	"[{""label"":""STAG3"",""id"":""10734""}]"	"[""10734""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080865""}]"
DOID:0080866	"[""primary ovarian insufficiency 9""]"	"[{""label"":""HFM1"",""id"":""164045""}]"	"[""164045""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080866""}]"
DOID:0080868	"[""primary ovarian insufficiency 11""]"	"[{""label"":""ERCC6"",""id"":""2074""}]"	"[""2074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080868""}]"
DOID:0080871	"[""primary ovarian insufficiency 14""]"	"[{""label"":""GDF9"",""id"":""2661""}]"	"[""2661""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080871""}]"
DOID:0080872	"[""primary ovarian insufficiency 15""]"	"[{""label"":""FANCM"",""id"":""57697""}]"	"[""57697""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080872""}]"
DOID:0080886	"[""vitamin D-dependent rickets type 1A""]"	"[{""label"":""CYP27B1"",""id"":""1594""}]"	"[""1594""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080886""}]"
DOID:0080887	"[""vitamin D-dependent rickets type 1B""]"	"[{""label"":""CYP2R1"",""id"":""120227""}]"	"[""120227""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080887""}]"
DOID:0080893	"[""Bainbridge-Ropers syndrome"",""ASXL3-related disorder""]"	"[{""label"":""ASXL3"",""id"":""80816""}]"	"[""80816""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080893""}]"
DOID:0080908	"[""Cockayne syndrome B"",""Cockayne syndrome 2"",""Cockayne syndrome type II""]"	"[{""label"":""ERCC6"",""id"":""2074""}]"	"[""2074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080908""}]"
DOID:0080909	"[""castration-resistant prostate carcinoma""]"	"[{""label"":""CCNE2"",""id"":""9134""},{""label"":""CHD1"",""id"":""1105""},{""label"":""NUF2"",""id"":""83540""}]"	"[""1105"",""83540"",""9134""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080909""}]"
DOID:0080911	"[""cerebrooculofacioskeletal syndrome 1""]"	"[{""label"":""ERCC6"",""id"":""2074""}]"	"[""2074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080911""}]"
DOID:0080913	"[""cerebrooculofacioskeletal syndrome 3""]"	"[{""label"":""ERCC5"",""id"":""2073""}]"	"[""2073""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080913""}]"
DOID:0080918	"[""polymicrogyria""]"	"[{""label"":""WDR62"",""id"":""284403""}]"	"[""284403""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080918""}]"
DOID:0080922	"[""bilateral frontoparietal polymicrogyria""]"	"[{""label"":""ADGRG1"",""id"":""9289""}]"	"[""9289""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080922""}]"
DOID:0080923	"[""bilateral parasagittal parieto-occipital polymicrogyria"",""bilateral temporooccipital polymicrogyria""]"	"[{""label"":""FIG4"",""id"":""9896""}]"	"[""9896""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080923""}]"
DOID:0080923	"[""bilateral parasagittal parieto-occipital polymicrogyria"",""bilateral temporooccipital polymicrogyria""]"	"[{""label"":""FIG4"",""id"":""855392""}]"	"[""855392""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080923""}]"
DOID:0080924	"[""bilateral perisylvian polymicrogyria""]"	"[{""label"":""ADGRG1"",""id"":""9289""}]"	"[""9289""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080924""}]"
DOID:0080925	"[""cytochrome P450 oxidoreductase deficiency""]"	"[{""label"":""POR"",""id"":""5447""}]"	"[""5447""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080925""}]"
DOID:0080930	"[""primary localized cutaneous amyloidosis 1"",""familial primary localized cutaneous amyloidosis-1""]"	"[{""label"":""OSMR"",""id"":""9180""}]"	"[""9180""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080930""}]"
DOID:0080931	"[""primary localized cutaneous amyloidosis 2""]"	"[{""label"":""IL31RA"",""id"":""133396""}]"	"[""133396""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080931""}]"
DOID:0080932	"[""primary localized cutaneous amyloidosis 3"",""Amyloidosis cutis dyschromica""]"	"[{""label"":""GPNMB"",""id"":""10457""}]"	"[""10457""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080932""}]"
DOID:0080939	"[""hereditary angioedema type I""]"	"[{""label"":""SERPING1"",""id"":""710""}]"	"[""710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080939""}]"
DOID:0080940	"[""hereditary angioedema type III""]"	"[{""label"":""F12"",""id"":""2161""}]"	"[""2161""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080940""}]"
DOID:0080941	"[""acquired angioedema""]"	"[{""label"":""XPNPEP2"",""id"":""7512""}]"	"[""7512""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080941""}]"
DOID:0080943	"[""46,XX sex reversal 5""]"	"[{""label"":""NR2F2"",""id"":""7026""}]"	"[""7026""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080943""}]"
DOID:0080944	"[""familial Behcet-like autoinflammatory syndrome"",""A20 haploinsufficiency""]"	"[{""label"":""TNFAIP3"",""id"":""7128""}]"	"[""7128""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080944""}]"
DOID:0080946	"[""retinal dystrophy with leukodystrophy"",""ACBD5 deficiency""]"	"[{""label"":""ACBD5"",""id"":""91452""}]"	"[""91452""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080946""}]"
DOID:0080948	"[""agenesis of corpus callosum, cardiac, ocular, and genital syndrome""]"	"[{""label"":""CDH2"",""id"":""1000""}]"	"[""1000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080948""}]"
DOID:0080950	"[""alopecia-mental retardation syndrome 4""]"	"[{""label"":""LSS"",""id"":""4047""}]"	"[""4047""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080950""}]"
DOID:0080952	"[""AMED syndrome"",""AMEDS""]"	"[{""label"":""ADH5"",""id"":""128""}]"	"[""128""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080952""}]"
DOID:0080953	"[""amelogenesis imperfecta type 1J"",""Amelogenesis imperfecta, type IJ""]"	"[{""label"":""ACP4"",""id"":""93650""}]"	"[""93650""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080953""}]"
DOID:0080954	"[""arthrogryposis multiplex congenita""]"	"[{""label"":""SYNE1"",""id"":""23345""},{""label"":""VPS33B"",""id"":""26276""}]"	"[""23345"",""26276""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080954""}]"
DOID:0080957	"[""primary hypoalphalipoproteinemia 1"",""familial HDL deficiency"",""familial hypoalphalipoproteinemia""]"	"[{""label"":""ABCA1"",""id"":""19""}]"	"[""19""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080957""}]"
DOID:0080958	"[""primary hypoalphalipoproteinemia 2"",""Apolipoprotein A-I deficiency""]"	"[{""label"":""APOA1"",""id"":""335""}]"	"[""335""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080958""}]"
DOID:0080959	"[""arrhythmogenic right ventricular dysplasia 14""]"	"[{""label"":""CDH2"",""id"":""1000""}]"	"[""1000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080959""}]"
DOID:0080960	"[""amelogenesis imperfecta type 2A6"",""Amelogenesis imperfecta, hypomaturation type, IIA6""]"	"[{""label"":""GPR68"",""id"":""8111""}]"	"[""8111""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080960""}]"
DOID:0080962	"[""anauxetic dysplasia 2""]"	"[{""label"":""POP1"",""id"":""10940""}]"	"[""10940""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080962""}]"
DOID:0080975	"[""intracranial berry aneurysm 12""]"	"[{""label"":""THSD1"",""id"":""55901""}]"	"[""55901""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080975""}]"
DOID:0080977	"[""aortic valve disease 3""]"	"[{""label"":""ROBO4"",""id"":""54538""}]"	"[""54538""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080977""}]"
DOID:0080978	"[""arthrogryposis multiplex congenita-1""]"	"[{""label"":""LGI4"",""id"":""163175""}]"	"[""163175""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080978""}]"
DOID:0080979	"[""arthrogryposis multiplex congenita-3""]"	"[{""label"":""SYNE1"",""id"":""23345""}]"	"[""23345""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080979""}]"
DOID:0080980	"[""arthrogryposis multiplex congenita-4"",""Zain syndrome""]"	"[{""label"":""SCYL2"",""id"":""55681""}]"	"[""55681""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080980""}]"
DOID:0080981	"[""arthrogryposis multiplex congenita-5""]"	"[{""label"":""TOR1A"",""id"":""1861""}]"	"[""1861""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080981""}]"
DOID:0080982	"[""X-linked mental retardation-hypotonic facies syndrome-1""]"	"[{""label"":""ATRX"",""id"":""546""}]"	"[""546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080982""}]"
DOID:0080984	"[""X-linked intellectual developmental disorder 109"",""Fragile XE syndrome"",""fragile site on chromosome Xq28""]"	"[{""label"":""AFF2"",""id"":""2334""}]"	"[""2334""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080984""}]"
DOID:0080985	"[""syndromic X-linked intellectual disorder Lujan-Fryns-type""]"	"[{""label"":""MED12"",""id"":""9968""}]"	"[""9968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080985""}]"
DOID:0080986	"[""Ehlers-Danlos syndrome periodontal type 1""]"	"[{""label"":""C1R"",""id"":""715""}]"	"[""715""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080986""}]"
DOID:0080987	"[""Ehlers-Danlos syndrome periodontal type 2""]"	"[{""label"":""C1S"",""id"":""716""}]"	"[""716""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080987""}]"
DOID:0080988	"[""pretibial dystrophic epidermolysis bullosa""]"	"[{""label"":""COL7A1"",""id"":""1294""}]"	"[""1294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080988""}]"
DOID:0080990	"[""King Denborough syndrome""]"	"[{""label"":""RYR1"",""id"":""6261""}]"	"[""6261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080990""}]"
DOID:0080991	"[""congenital myopathy 1B"",""multiminicore disease""]"	"[{""label"":""RYR1"",""id"":""6261""}]"	"[""6261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080991""}]"
DOID:0080991	"[""congenital myopathy 1B"",""multiminicore disease""]"	"[{""label"":""Ryr1"",""id"":""20190""}]"	"[""20190""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080991""}]"
DOID:0080998	"[""acute necrotizing pancreatitis""]"	"[{""label"":""Calca"",""id"":""24241""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Nos1"",""id"":""24598""},{""label"":""Selp"",""id"":""25651""}]"	"[""24241"",""24598"",""24770"",""25651""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080998""}]"
DOID:0080998	"[""acute necrotizing pancreatitis""]"	"[{""label"":""IL1RN"",""id"":""3557""}]"	"[""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0080998""}]"
DOID:0081001	"[""Cowden syndrome 5""]"	"[{""label"":""PIK3CA"",""id"":""5290""}]"	"[""5290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081001""}]"
DOID:0081002	"[""Cowden syndrome 6"",""CWS6""]"	"[{""label"":""AKT1"",""id"":""207""}]"	"[""207""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081002""}]"
DOID:0081003	"[""Cowden syndrome 7""]"	"[{""label"":""SEC23B"",""id"":""10483""}]"	"[""10483""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081003""}]"
DOID:0081007	"[""RNASET2-deficient cystic leukoencephalopathy"",""cystic leukoencephalopathy without megalencephaly"",""infantile-onset RNASET2 deficient cystic leukoencephalopathy""]"	"[{""label"":""rnaset2"",""id"":""791890""}]"	"[""791890""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081007""}]"
DOID:0081007	"[""RNASET2-deficient cystic leukoencephalopathy"",""cystic leukoencephalopathy without megalencephaly"",""infantile-onset RNASET2 deficient cystic leukoencephalopathy""]"	"[{""label"":""RNASET2"",""id"":""8635""}]"	"[""8635""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081007""}]"
DOID:0081011	"[""Bardet-Biedl syndrome 22""]"	"[{""label"":""IFT74"",""id"":""80173""}]"	"[""80173""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081011""}]"
DOID:0081015	"[""congenital fibrosis of the extraocular muscles 1""]"	"[{""label"":""KIF21A"",""id"":""55605""}]"	"[""55605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081015""}]"
DOID:0081017	"[""congenital fibrosis of the extraocular muscles 3A""]"	"[{""label"":""TUBB3"",""id"":""10381""}]"	"[""10381""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081017""}]"
DOID:0081020	"[""congenital fibrosis of the extraocular muscles 5""]"	"[{""label"":""COL25A1"",""id"":""84570""}]"	"[""84570""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081020""}]"
DOID:0081022	"[""retinal cone dystrophy 3B"",""cone dystrophy with supernormal rod responses""]"	"[{""label"":""KCNV2"",""id"":""169522""}]"	"[""169522""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081022""}]"
DOID:0081023	"[""retinal cone dystrophy 4""]"	"[{""label"":""CACNA2D4"",""id"":""93589""}]"	"[""93589""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081023""}]"
DOID:0081030	"[""central conducting lymphatic anomaly"",""lymphatic malformation-7""]"	"[{""label"":""EPHB4"",""id"":""2050""}]"	"[""2050""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081030""}]"
DOID:0081042	"[""T-cell prolymphocytic leukemia"",""Prolymphocytic leukemia, T-cell type"",""T Cell Prolymphocytic Leukemia""]"	"[{""label"":""JAK3"",""id"":""3718""}]"	"[""3718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081042""}]"
DOID:0081046	"[""frontonasal dysplasia 2""]"	"[{""label"":""ALX4"",""id"":""60529""}]"	"[""60529""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081046""}]"
DOID:0081048	"[""congenital limbs-face contractures-hypotonia-developmental delay syndrome"",""CLIFAHDD syndrome"",""congenital contractures of the limbs and face, hypotonia, and developmental delay""]"	"[{""label"":""NALCN"",""id"":""259232""}]"	"[""259232""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081048""}]"
DOID:0081060	"[""X-linked nephrogenic diabetes insipidus"",""nephrogenic diabetes insipidus type 1""]"	"[{""label"":""Avpr2"",""id"":""12000""}]"	"[""12000""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081060""}]"
DOID:0081060	"[""X-linked nephrogenic diabetes insipidus"",""nephrogenic diabetes insipidus type 1""]"	"[{""label"":""AVPR2"",""id"":""554""}]"	"[""554""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081060""}]"
DOID:0081061	"[""nephrogenic diabetes insipidus type 2"",""autosomal nephrogenic diabetes insipidus-2""]"	"[{""label"":""AQP2"",""id"":""359""}]"	"[""359""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081061""}]"
DOID:0081063	"[""DICER1 syndrome"",""PPB familial tumor susceptibility syndrome"",""Pleuro-pulmonary blastoma familial tumor susceptibility"",""Pleuro-pulmonary blastoma familial tumor susceptibility syndrome"",""Pleuropulmonary blastoma familial tumor susceptibility syndrome""]"	"[{""label"":""DICER1"",""id"":""23405""}]"	"[""23405""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081063""}]"
DOID:0081074	"[""Teebi hypertelorism syndrome 2""]"	"[{""label"":""CDH11"",""id"":""1009""}]"	"[""1009""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081074""}]"
DOID:0081075	"[""Marsili syndrome"",""congenital analgesia"",""congenital insensitivity to pain""]"	"[{""label"":""ZFHX2"",""id"":""85446""}]"	"[""85446""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081075""}]"
DOID:0081075	"[""Marsili syndrome"",""congenital analgesia"",""congenital insensitivity to pain""]"	"[{""label"":""Zfhx2"",""id"":""239102""}]"	"[""239102""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081075""}]"
DOID:0081082	"[""acute myelomonocytic leukemia""]"	"[{""label"":""ARHGAP26"",""id"":""23092""},{""label"":""CBFB"",""id"":""865""},{""label"":""FLT3"",""id"":""2322""},{""label"":""GMPS"",""id"":""8833""}]"	"[""23092"",""2322"",""865"",""8833""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081082""}]"
DOID:0081097	"[""Rafiq syndrome"",""MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15""]"	"[{""label"":""MAN1B1"",""id"":""11253""}]"	"[""11253""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00629""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081097""}]"
DOID:0081101	"[""nonautoimmune hyperthyroidism"",""Congenital nonautoimmune hyperthyroidism""]"	"[{""label"":""TSHR"",""id"":""7253""}]"	"[""7253""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081101""}]"
DOID:0081102	"[""familial gestational hyperthyroidism""]"	"[{""label"":""TSHR"",""id"":""7253""}]"	"[""7253""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081102""}]"
DOID:0081108	"[""keratosis palmoplantaris striata 1""]"	"[{""label"":""DSG1"",""id"":""1828""}]"	"[""1828""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081108""}]"
DOID:0081109	"[""keratosis palmoplantaris striata 2""]"	"[{""label"":""DSP"",""id"":""1832""}]"	"[""1832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081109""}]"
DOID:0081110	"[""keratosis palmoplantaris striata 3""]"	"[{""label"":""KRT1"",""id"":""3848""}]"	"[""3848""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081110""}]"
DOID:0081111	"[""osteosclerotic metaphyseal dysplasia""]"	"[{""label"":""LRRK1"",""id"":""79705""}]"	"[""79705""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081111""}]"
DOID:0081112	"[""Baraitser-Winter syndrome 1""]"	"[{""label"":""ACTB"",""id"":""60""}]"	"[""60""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081112""}]"
DOID:0081113	"[""Baraitser-Winter syndrome 2""]"	"[{""label"":""ACTG1"",""id"":""71""}]"	"[""71""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081113""}]"
DOID:0081116	"[""benign familial infantile seizures 3"",""Benign Familial Infantile Seizures, 3"",""benign familial neonatal-infantile seizures""]"	"[{""label"":""SCN2A"",""id"":""6326""}]"	"[""6326""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081116""}]"
DOID:0081118	"[""benign familial infantile seizures 5"",""Benign Familial Infantile Seizures, 5""]"	"[{""label"":""SCN8A"",""id"":""6334""}]"	"[""6334""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081118""}]"
DOID:0081119	"[""benign familial infantile seizures 6"",""Autosomal dominant nocturnal frontal lobe epilepsy"",""Benign Familial Infantile Seizures, 6"",""nocturnal frontal lobe epilepsy-4""]"	"[{""label"":""CHRNA2"",""id"":""1135""}]"	"[""1135""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081119""}]"
DOID:0081120	"[""Graves ophthalmopathy"",""Graves orbitopathy"",""Thyroid associated ophthalmopathy"",""thyroid eye disease""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL3"",""id"":""3562""},{""label"":""TNF"",""id"":""7124""},{""label"":""TSHR"",""id"":""7253""}]"	"[""149233"",""1493"",""3383"",""3557"",""3558"",""3562"",""3586"",""7124"",""7253""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081120""}]"
DOID:0081122	"[""Catel Manzke syndrome"",""Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome"",""Micrognathia digital syndrome""]"	"[{""label"":""TGDS"",""id"":""23483""}]"	"[""23483""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081122""}]"
DOID:0081123	"[""X-linked mental retardation Gustavson type"",""mental retardation with optic atrophy, deafness and seizures""]"	"[{""label"":""RBMX"",""id"":""27316""}]"	"[""27316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081123""}]"
DOID:0081124	"[""craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1""]"	"[{""label"":""TMCO1"",""id"":""54499""}]"	"[""54499""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081124""}]"
DOID:0081125	"[""craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2""]"	"[{""label"":""RAB5IF"",""id"":""55969""}]"	"[""55969""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081125""}]"
DOID:0081126	"[""DeSanto-Shinawi syndrome"",""Chromosome 10p12-p11 deletion syndrome"",""Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion"",""Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation"",""WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome""]"	"[{""label"":""WAC"",""id"":""51322""}]"	"[""51322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081126""}]"
DOID:0081128	"[""mandibuloacral dysplasia type A lipodystrophy""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081128""}]"
DOID:0081135	"[""agammaglobulinemia 2""]"	"[{""label"":""IGLL1"",""id"":""3543""}]"	"[""3543""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081135""}]"
DOID:0081137	"[""agammaglobulinemia 3""]"	"[{""label"":""CD79A"",""id"":""973""}]"	"[""973""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081137""}]"
DOID:0081138	"[""agammaglobulinemia 6""]"	"[{""label"":""CD79B"",""id"":""974""}]"	"[""974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081138""}]"
DOID:0081140	"[""agammaglobulinemia 8A""]"	"[{""label"":""TCF3"",""id"":""6929""}]"	"[""6929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081140""}]"
DOID:0081141	"[""agammaglobulinemia 9""]"	"[{""label"":""SLC39A7"",""id"":""7922""}]"	"[""7922""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081141""}]"
DOID:0081143	"[""agammaglobulinemia 8B""]"	"[{""label"":""TCF3"",""id"":""6929""}]"	"[""6929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081143""}]"
DOID:0081144	"[""common variable immunodeficiency 1""]"	"[{""label"":""ICOS"",""id"":""29851""}]"	"[""29851""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081144""}]"
DOID:0081145	"[""common variable immunodeficiency 2""]"	"[{""label"":""TNFRSF13B"",""id"":""23495""}]"	"[""23495""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081145""}]"
DOID:0081146	"[""common variable immunodeficiency 3""]"	"[{""label"":""CD19"",""id"":""930""}]"	"[""930""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081146""}]"
DOID:0081147	"[""common variable immunodeficiency 4""]"	"[{""label"":""TNFRSF13C"",""id"":""115650""}]"	"[""115650""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081147""}]"
DOID:0081148	"[""common variable immunodeficiency 5""]"	"[{""label"":""MS4A1"",""id"":""931""}]"	"[""931""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081148""}]"
DOID:0081150	"[""common variable immunodeficiency 7""]"	"[{""label"":""CR2"",""id"":""1380""}]"	"[""1380""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081150""}]"
DOID:0081151	"[""common variable immunodeficiency 8"",""common variable immunodeficiency-8 (CVID8) with autoimmunity""]"	"[{""label"":""LRBA"",""id"":""987""}]"	"[""987""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081151""}]"
DOID:0081152	"[""common variable immunodeficiency 10""]"	"[{""label"":""NFKB2"",""id"":""4791""}]"	"[""4791""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081152""}]"
DOID:0081153	"[""common variable immunodeficiency 11""]"	"[{""label"":""IL21"",""id"":""59067""}]"	"[""59067""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081153""}]"
DOID:0081154	"[""common variable immunodeficiency 12""]"	"[{""label"":""NFKB1"",""id"":""4790""}]"	"[""4790""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081154""}]"
DOID:0081155	"[""common variable immunodeficiency 13""]"	"[{""label"":""IKZF1"",""id"":""10320""}]"	"[""10320""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081155""}]"
DOID:0081156	"[""common variable immunodeficiency 14""]"	"[{""label"":""IRF2BP2"",""id"":""359948""}]"	"[""359948""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081156""}]"
DOID:0081157	"[""dilated cardiomyopathy 1LL""]"	"[{""label"":""PRDM16"",""id"":""63976""}]"	"[""63976""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081157""}]"
DOID:0081158	"[""dilated cardiomyopathy 1MM""]"	"[{""label"":""MYBPC3"",""id"":""4607""}]"	"[""4607""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081158""}]"
DOID:0081163	"[""dilated cardiomyopathy 2G""]"	"[{""label"":""LMOD2"",""id"":""442721""}]"	"[""442721""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081163""}]"
DOID:0081168	"[""HMG-CoA synthase 2 deficiency"",""3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency""]"	"[{""label"":""HMGCS2"",""id"":""3158""}]"	"[""3158""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081168""}]"
DOID:0081168	"[""HMG-CoA synthase 2 deficiency"",""3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency""]"	"[{""label"":""Hmgcs2"",""id"":""15360""}]"	"[""15360""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081168""}]"
DOID:0081169	"[""Leber congenital amaurosis 19""]"	"[{""label"":""Usp45"",""id"":""77593""}]"	"[""77593""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081169""}]"
DOID:0081175	"[""short stature, hearing loss, retinitis pigmentosa, and distinctive facies""]"	"[{""label"":""EXOSC2"",""id"":""23404""}]"	"[""23404""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081175""}]"
DOID:0081177	"[""autosomal recessive intellectual developmental disorder 1""]"	"[{""label"":""PRSS12"",""id"":""8492""}]"	"[""8492""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081177""}]"
DOID:0081179	"[""autosomal recessive intellectual developmental disorder 3""]"	"[{""label"":""CC2D1A"",""id"":""54862""}]"	"[""54862""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081179""}]"
DOID:0081180	"[""autosomal recessive intellectual developmental disorder 12""]"	"[{""label"":""ST3GAL3"",""id"":""6487""}]"	"[""6487""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00630""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081180""}]"
DOID:0081181	"[""autosomal recessive intellectual developmental disorder 5""]"	"[{""label"":""NSUN2"",""id"":""54888""}]"	"[""54888""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081181""}]"
DOID:0081182	"[""autosomal recessive intellectual developmental disorder 6""]"	"[{""label"":""GRIK2"",""id"":""2898""}]"	"[""2898""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081182""}]"
DOID:0081183	"[""autosomal recessive intellectual developmental disorder 7""]"	"[{""label"":""TUSC3"",""id"":""7991""}]"	"[""7991""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00369""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081183""}]"
DOID:0081188	"[""autosomal recessive intellectual developmental disorder 14""]"	"[{""label"":""TECR"",""id"":""9524""}]"	"[""9524""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081188""}]"
DOID:0081190	"[""autosomal recessive intellectual developmental disorder 18""]"	"[{""label"":""MED23"",""id"":""9439""}]"	"[""9439""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081190""}]"
DOID:0081202	"[""autosomal recessive intellectual developmental disorder 37""]"	"[{""label"":""ANK3"",""id"":""288""}]"	"[""288""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081202""}]"
DOID:0081203	"[""autosomal recessive intellectual developmental disorder 38""]"	"[{""label"":""HERC2"",""id"":""8924""}]"	"[""8924""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081203""}]"
DOID:0081205	"[""autosomal recessive intellectual developmental disorder 40""]"	"[{""label"":""TAF2"",""id"":""6873""}]"	"[""6873""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081205""}]"
DOID:0081209	"[""autosomal recessive intellectual developmental disorder 45""]"	"[{""label"":""FBXO31"",""id"":""79791""}]"	"[""79791""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081209""}]"
DOID:0081210	"[""autosomal recessive intellectual developmental disorder 46""]"	"[{""label"":""NDST1"",""id"":""3340""}]"	"[""3340""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081210""}]"
DOID:0081212	"[""autosomal recessive intellectual developmental disorder 48""]"	"[{""label"":""SLC6A17"",""id"":""388662""}]"	"[""388662""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081212""}]"
DOID:0081213	"[""autosomal recessive intellectual developmental disorder 50""]"	"[{""label"":""EDC3"",""id"":""80153""}]"	"[""80153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081213""}]"
DOID:0081215	"[""autosomal recessive intellectual developmental disorder 52""]"	"[{""label"":""LMAN2L"",""id"":""81562""}]"	"[""81562""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081215""}]"
DOID:0081216	"[""autosomal recessive intellectual developmental disorder 54""]"	"[{""label"":""TNIK"",""id"":""23043""}]"	"[""23043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081216""}]"
DOID:0081217	"[""autosomal recessive intellectual developmental disorder 56""]"	"[{""label"":""ZC3H14"",""id"":""79882""}]"	"[""79882""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081217""}]"
DOID:0081218	"[""autosomal recessive intellectual developmental disorder 74""]"	"[{""label"":""APC2"",""id"":""10297""}]"	"[""10297""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081218""}]"
DOID:0081219	"[""autosomal recessive intellectual developmental disorder 57""]"	"[{""label"":""MBOAT7"",""id"":""79143""}]"	"[""79143""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081219""}]"
DOID:0081220	"[""autosomal recessive intellectual developmental disorder 58""]"	"[{""label"":""ELP2"",""id"":""55250""}]"	"[""55250""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081220""}]"
DOID:0081221	"[""autosomal recessive intellectual developmental disorder 59""]"	"[{""label"":""IMPA1"",""id"":""3612""}]"	"[""3612""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081221""}]"
DOID:0081223	"[""glycosylphosphatidylinositol biosynthesis defect 16"",""Intellectual developmental disorder, autosomal recessive 62""]"	"[{""label"":""PIGC"",""id"":""5279""}]"	"[""5279""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081223""}]"
DOID:0081224	"[""autosomal recessive intellectual developmental disorder 63""]"	"[{""label"":""CAMK2A"",""id"":""815""}]"	"[""815""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081224""}]"
DOID:0081225	"[""autosomal recessive intellectual developmental disorder 64""]"	"[{""label"":""LINGO1"",""id"":""84894""}]"	"[""84894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081225""}]"
DOID:0081226	"[""autosomal recessive intellectual developmental disorder 65""]"	"[{""label"":""KDM5B"",""id"":""10765""}]"	"[""10765""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081226""}]"
DOID:0081228	"[""autosomal recessive intellectual developmental disorder 67""]"	"[{""label"":""EIF3F"",""id"":""8665""}]"	"[""8665""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081228""}]"
DOID:0081230	"[""autosomal recessive intellectual developmental disorder 69""]"	"[{""label"":""ZBTB11"",""id"":""27107""}]"	"[""27107""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081230""}]"
DOID:0081231	"[""autosomal recessive intellectual developmental disorder 70""]"	"[{""label"":""RSRC1"",""id"":""51319""}]"	"[""51319""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081231""}]"
DOID:0081234	"[""autosomal recessive intellectual developmental disorder 75""]"	"[{""label"":""PIDD1"",""id"":""55367""}]"	"[""55367""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081234""}]"
DOID:0081235	"[""autosomal recessive intellectual developmental disorder 76""]"	"[{""label"":""GRIA1"",""id"":""2890""}]"	"[""2890""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081235""}]"
DOID:0081236	"[""autosomal recessive intellectual developmental disorder 77""]"	"[{""label"":""CEP104"",""id"":""9731""}]"	"[""9731""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081236""}]"
DOID:0081237	"[""acromesomelic dysplasia 3"",""Demirhan-type acromesomelic dysplasia""]"	"[{""label"":""BMPR1B"",""id"":""658""}]"	"[""658""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081237""}]"
DOID:0081242	"[""autoimmune interstitial lung, joint, and kidney disease"",""Autoimmune interstitial lung disease-arthritis syndrome"",""COPA syndrome""]"	"[{""label"":""Copa"",""id"":""12847""}]"	"[""12847""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081242""}]"
DOID:0081242	"[""autoimmune interstitial lung, joint, and kidney disease"",""Autoimmune interstitial lung disease-arthritis syndrome"",""COPA syndrome""]"	"[{""label"":""COPA"",""id"":""1314""}]"	"[""1314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081242""}]"
DOID:0081243	"[""rhizomelic chondrodysplasia punctate type 4""]"	"[{""label"":""FAR1"",""id"":""84188""}]"	"[""84188""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081243""}]"
DOID:0081263	"[""neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities"",""NEDMCR syndrome""]"	"[{""label"":""GEMIN4"",""id"":""50628""}]"	"[""50628""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081263""}]"
DOID:0081265	"[""intellectual developmental disorder with abnormal behavior, microcephaly, and short stature"",""IDDBAS""]"	"[{""label"":""PUS7"",""id"":""54517""}]"	"[""54517""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081265""}]"
DOID:0081266	"[""pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures"",""PAMDDFS""]"	"[{""label"":""TUBGCP2"",""id"":""10844""}]"	"[""10844""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081266""}]"
DOID:0081267	"[""graft-versus-host disease"",""GvHD"",""graft versus host disease""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HGF"",""id"":""3082""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL10RB"",""id"":""3588""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL2"",""id"":""3558""},{""label"":""MKI67"",""id"":""4288""},{""label"":""NOD2"",""id"":""64127""}]"	"[""1493"",""2214"",""28"",""3082"",""3115"",""3458"",""3552"",""3557"",""3558"",""3586"",""3588"",""4288"",""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081267""}]"
DOID:0081268	"[""pulmonary venoocclusive disease 1""]"	"[{""label"":""BMPR2"",""id"":""659""}]"	"[""659""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081268""}]"
DOID:0081270	"[""Smith-McCort dysplasia 1""]"	"[{""label"":""DYM"",""id"":""54808""}]"	"[""54808""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081270""}]"
DOID:0081271	"[""Smith-McCort dysplasia 2""]"	"[{""label"":""RAB33B"",""id"":""83452""}]"	"[""83452""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081271""}]"
DOID:0081272	"[""Sandestig-Stefanova syndrome""]"	"[{""label"":""NUP188"",""id"":""23511""}]"	"[""23511""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081272""}]"
DOID:0081274	"[""peroxisome biogenesis disorder 14B""]"	"[{""label"":""PEX11B"",""id"":""8799""}]"	"[""8799""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081274""}]"
DOID:0081276	"[""cerebellar atrophy, visual impairment, and psychomotor retardation"",""CAVIPMR""]"	"[{""label"":""EMC1"",""id"":""23065""}]"	"[""23065""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081276""}]"
DOID:0081288	"[""white sponge nevus 2""]"	"[{""label"":""KRT13"",""id"":""3860""}]"	"[""3860""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081288""}]"
DOID:0081289	"[""Antley-Bixler syndrome"",""Antley Bixler syndrome"",""Antley and Bixler's syndrome""]"	"[{""label"":""FGFR2"",""id"":""2263""}]"	"[""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081289""}]"
DOID:0081290	"[""Antley-Bixler syndrome without disordered steroidogenesis""]"	"[{""label"":""FGFR2"",""id"":""2263""}]"	"[""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081290""}]"
DOID:0081292	"[""traumatic brain injury""]"	"[{""label"":""APP"",""id"":""351""}]"	"[""351""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081292""}]"
DOID:0081292	"[""traumatic brain injury""]"	"[{""label"":""Ngf"",""id"":""310738""},{""label"":""Tp53"",""id"":""24842""}]"	"[""24842"",""310738""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081292""}]"
DOID:0081297	"[""oculopharyngodistal myopathy 1""]"	"[{""label"":""LRP12"",""id"":""29967""}]"	"[""29967""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081297""}]"
DOID:0081301	"[""intellectual developmental disorder with ocular anomalies and distinctive facial features"",""IDDOF"",""MTSS2-related neurodevelopmental disorder""]"	"[{""label"":""MTSS2"",""id"":""92154""}]"	"[""92154""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081301""}]"
DOID:0081312	"[""T-cell non-Hodgkin lymphoma""]"	"[{""label"":""FGFR1"",""id"":""2260""},{""label"":""IER3"",""id"":""8870""},{""label"":""JAK3"",""id"":""3718""},{""label"":""TMEM260"",""id"":""54916""}]"	"[""2260"",""3718"",""54916"",""8870""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081312""}]"
DOID:0081317	"[""multiple synostoses syndrome 1""]"	"[{""label"":""GDF5"",""id"":""8200""},{""label"":""NOG"",""id"":""9241""}]"	"[""8200"",""9241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081317""}]"
DOID:0081318	"[""multiple synostoses syndrome 2""]"	"[{""label"":""GDF5"",""id"":""8200""}]"	"[""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081318""}]"
DOID:0081319	"[""multiple synostoses syndrome 3""]"	"[{""label"":""FGF9"",""id"":""2254""}]"	"[""2254""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081319""}]"
DOID:0081320	"[""multiple synostoses syndrome 4""]"	"[{""label"":""GDF6"",""id"":""392255""}]"	"[""392255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081320""}]"
DOID:0081325	"[""developmental and epileptic encephalopathy 94""]"	"[{""label"":""CHD2"",""id"":""1106""}]"	"[""1106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081325""}]"
DOID:0081326	"[""oxoglutarate dehydrogenase deficiency"",""Oxoglutaric aciduria"",""alpha-ketoglutarate dehydrogenase deficiency""]"	"[{""label"":""OGDH"",""id"":""4967""}]"	"[""4967""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081326""}]"
DOID:0081327	"[""neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures"",""NEDAMSS""]"	"[{""label"":""IRF2BPL"",""id"":""64207""}]"	"[""64207""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081327""}]"
DOID:0081330	"[""glycogen storage disease Ib""]"	"[{""label"":""SLC37A4"",""id"":""2542""}]"	"[""2542""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081330""}]"
DOID:0081331	"[""glycogen storage disease Ic""]"	"[{""label"":""SLC37A4"",""id"":""2542""}]"	"[""2542""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081331""}]"
DOID:0081333	"[""Wiedemann-Rautenstrauch syndrome"",""Neonatal progeroid syndrome"",""PROGEROID SYNDROME, NEONATAL""]"	"[{""label"":""POLR3A"",""id"":""11128""}]"	"[""11128""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081333""}]"
DOID:0081337	"[""congenital myopathy""]"	"[{""label"":""Ldb3"",""id"":""24131""}]"	"[""24131""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081337""}]"
DOID:0081337	"[""congenital myopathy""]"	"[{""label"":""HACD1"",""id"":""9200""}]"	"[""9200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081337""}]"
DOID:0081339	"[""congenital myopathy 2B""]"	"[{""label"":""ACTA1"",""id"":""58""}]"	"[""58""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081339""}]"
DOID:0081340	"[""congenital myopathy 2C""]"	"[{""label"":""ACTA1"",""id"":""58""}]"	"[""58""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081340""}]"
DOID:0081341	"[""congenital myopathy 5"",""Salih myopathy"",""congenital myopathy-5 with cardiomyopathy""]"	"[{""label"":""TTN"",""id"":""7273""}]"	"[""7273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081341""}]"
DOID:0081342	"[""congenital myopathy 8""]"	"[{""label"":""ACTN2"",""id"":""88""}]"	"[""88""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081342""}]"
DOID:0081343	"[""congenital myopathy 9A""]"	"[{""label"":""FXR1"",""id"":""8087""}]"	"[""8087""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081343""}]"
DOID:0081344	"[""congenital myopathy 9B""]"	"[{""label"":""FXR1"",""id"":""8087""}]"	"[""8087""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081344""}]"
DOID:0081345	"[""congenital myopathy 10B""]"	"[{""label"":""MEGF10"",""id"":""84466""}]"	"[""84466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081345""}]"
DOID:0081348	"[""congenital myopathy 16""]"	"[{""label"":""MYBPC1"",""id"":""4604""}]"	"[""4604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081348""}]"
DOID:0081350	"[""congenital myopathy 18""]"	"[{""label"":""CACNA1S"",""id"":""779""}]"	"[""779""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081350""}]"
DOID:0081352	"[""congenital myopathy 20""]"	"[{""label"":""RYR3"",""id"":""6263""}]"	"[""6263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081352""}]"
DOID:0081354	"[""congenital myopathy 22A""]"	"[{""label"":""SCN4A"",""id"":""6329""}]"	"[""6329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081354""}]"
DOID:0081355	"[""congenital myopathy 22B""]"	"[{""label"":""SCN4A"",""id"":""6329""}]"	"[""6329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081355""}]"
DOID:0081358	"[""epidermolytic hyperkeratosis 1""]"	"[{""label"":""KRT1"",""id"":""3848""}]"	"[""3848""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081358""}]"
DOID:0081359	"[""epidermolytic hyperkeratosis 2""]"	"[{""label"":""KRT10"",""id"":""3858""}]"	"[""3858""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081359""}]"
DOID:0081360	"[""spastic quadriplegic cerebral palsy 2""]"	"[{""label"":""KANK1"",""id"":""23189""}]"	"[""23189""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081360""}]"
DOID:0081361	"[""spastic quadriplegic cerebral palsy 3"",""CPSQ3""]"	"[{""label"":""ADD3"",""id"":""120""}]"	"[""120""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081361""}]"
DOID:0081363	"[""distal myopathy with rimmed vacuoles""]"	"[{""label"":""SQSTM1"",""id"":""8878""}]"	"[""8878""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081363""}]"
DOID:0081364	"[""neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset""]"	"[{""label"":""SQSTM1"",""id"":""8878""}]"	"[""8878""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081364""}]"
DOID:0081365	"[""Paget's disease of bone 2"",""Paget disease of bone-2""]"	"[{""label"":""TNFRSF11A"",""id"":""8792""}]"	"[""8792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081365""}]"
DOID:0081366	"[""Paget's disease of bone 3"",""Paget disease of bone-3""]"	"[{""label"":""SQSTM1"",""id"":""8878""}]"	"[""8878""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081366""}]"
DOID:0081368	"[""Paget's disease of bone 5"",""Familial osteoectasia"",""Hereditary hyperphosphatasia"",""Hyperostosis corticalis deformans juvenilis"",""Juvenile Paget disease"",""Paget disease of bone-5""]"	"[{""label"":""TNFRSF11B"",""id"":""4982""}]"	"[""4982""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081368""}]"
DOID:0081369	"[""Paget's disease of bone 6"",""Paget disease of bone-6""]"	"[{""label"":""ZNF687"",""id"":""57592""}]"	"[""57592""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081369""}]"
DOID:0081371	"[""lacrimoauriculodentodigital syndrome 2"",""Lacrimo-auriculo-dento-digital syndrome 2""]"	"[{""label"":""FGFR3"",""id"":""2261""}]"	"[""2261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081371""}]"
DOID:0081372	"[""lacrimoauriculodentodigital syndrome 3"",""Lacrimo-auriculo-dento-digital syndrome 3""]"	"[{""label"":""FGF10"",""id"":""2255""}]"	"[""2255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081372""}]"
DOID:0081373	"[""disabling pansclerotic morphea"",""disabling pansclerotic morphea of childhood""]"	"[{""label"":""STAT4"",""id"":""6775""}]"	"[""6775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081373""}]"
DOID:0081378	"[""amyotrophic lateral sclerosis type 24""]"	"[{""label"":""NEK1"",""id"":""4750""}]"	"[""4750""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081378""}]"
DOID:0081381	"[""juvenile amyotrophic lateral sclerosis type 27""]"	"[{""label"":""SPTLC1"",""id"":""10558""}]"	"[""10558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081381""}]"
DOID:0081382	"[""amyotrophic lateral sclerosis type 28""]"	"[{""label"":""LRP12"",""id"":""29967""}]"	"[""29967""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081382""}]"
DOID:0081384	"[""ataxia-telangiectasia-like disorder-1""]"	"[{""label"":""MRE11"",""id"":""4361""}]"	"[""4361""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081384""}]"
DOID:0081385	"[""ataxia-telangiectasia-like disorder-2"",""PCNA-related progressive neurodegenerative photosensitivity syndrome""]"	"[{""label"":""PCNA"",""id"":""5111""}]"	"[""5111""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081385""}]"
DOID:0081386	"[""TANGO2-related metabolic encephalopathy and arrythmias"",""TANGO2 deficiency"",""metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration""]"	"[{""label"":""TANGO2"",""id"":""128989""}]"	"[""128989""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081386""}]"
DOID:0081394	"[""Caroli syndrome""]"	"[{""label"":""Pkhd1"",""id"":""241035""}]"	"[""241035""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081394""}]"
DOID:0081395	"[""Harel-Yoon syndrome"",""Ocular anomalies-axonal neuropathy-developmental delay syndrome""]"	"[{""label"":""ATAD3A"",""id"":""55210""}]"	"[""55210""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081395""}]"
DOID:0081396	"[""neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome"",""PHRINL syndrome""]"	"[{""label"":""ATAD3A"",""id"":""55210""}]"	"[""55210""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081396""}]"
DOID:0081397	"[""Vissers-Bodmer syndrome""]"	"[{""label"":""CNOT1"",""id"":""23019""}]"	"[""23019""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081397""}]"
DOID:0081398	"[""holoprosencephaly 12"",""holoprosencephaly-12 with or without pancreatic agenesis""]"	"[{""label"":""CNOT1"",""id"":""23019""}]"	"[""23019""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081398""}]"
DOID:0081399	"[""autosomal dominant distal hereditary motor neuronopathy 10""]"	"[{""label"":""EMILIN1"",""id"":""11117""}]"	"[""11117""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081399""}]"
DOID:0081400	"[""autosomal dominant distal hereditary motor neuronopathy 11""]"	"[{""label"":""SPTAN1"",""id"":""6709""}]"	"[""6709""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081400""}]"
DOID:0081401	"[""autosomal dominant distal hereditary motor neuronopathy 13""]"	"[{""label"":""BSCL2"",""id"":""26580""}]"	"[""26580""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081401""}]"
DOID:0081419	"[""childhood-onset dystonia with optic atrophy and basal ganglia abnormalities"",""DYSTONIA 29, CHILDHOOD-ONSET"",""DYTOABG"",""MECR-related neurologic disorder"",""MEPAN syndrome"",""Mitochondrial Enoyl CoA Reductase Protein-Associated Neurodegeneration""]"	"[{""label"":""MECR"",""id"":""51102""}]"	"[""51102""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081419""}]"
DOID:0081421	"[""familial focal epilepsy with variable foci 1""]"	"[{""label"":""DEPDC5"",""id"":""9681""}]"	"[""9681""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081421""}]"
DOID:0081423	"[""familial focal epilepsy with variable foci 3""]"	"[{""label"":""NPRL3"",""id"":""8131""}]"	"[""8131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081423""}]"
DOID:0081424	"[""familial focal epilepsy with variable foci 4""]"	"[{""label"":""SCN3A"",""id"":""6328""}]"	"[""6328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081424""}]"
DOID:0081426	"[""autosomal recessive distal hereditary motor neuronopathy 7""]"	"[{""label"":""VWA1"",""id"":""64856""}]"	"[""64856""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081426""}]"
DOID:0081427	"[""autosomal recessive distal hereditary motor neuronopathy 8"",""SORDD"",""sorbitol dehydrogenase deficiency with peripheral neuropathy""]"	"[{""label"":""SORD"",""id"":""6652""}]"	"[""6652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081427""}]"
DOID:0081430	"[""intellectual developmental disorder with autistic features and language delay, with or without seizures"",""IDDALDS""]"	"[{""label"":""TANC2"",""id"":""26115""}]"	"[""26115""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081430""}]"
DOID:0081440	"[""Peroxisome biogenesis disorder 10B""]"	"[{""label"":""PEX3"",""id"":""8504""}]"	"[""8504""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081440""}]"
DOID:0081441	"[""Nicolaides-Baraitser syndrome"",""Intellectual disability-sparse hair-brachydactyly syndrome"",""SPARSE HAIR-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME""]"	"[{""label"":""SMARCA2"",""id"":""6595""}]"	"[""6595""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081441""}]"
DOID:0081442	"[""blepharophimosis-impaired intellectual development syndrome"",""SMARCA2-related blepharophimosis-intellectual disability syndrome""]"	"[{""label"":""SMARCA2"",""id"":""6595""}]"	"[""6595""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081442""}]"
DOID:0081443	"[""Stolerman neurodevelopmental syndrome""]"	"[{""label"":""KDM6B"",""id"":""23135""}]"	"[""23135""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081443""}]"
DOID:0081445	"[""sickle cell disease""]"	"[{""label"":""HBB"",""id"":""3043""}]"	"[""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081445""}]"
DOID:0081450	"[""hyperimmunoglobulinemia D periodic fever syndrome"",""HYPER-IgD SYNDROME""]"	"[{""label"":""MVK"",""id"":""4598""}]"	"[""4598""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081450""}]"
DOID:0081451	"[""PFAPA syndrome"",""Marshall syndrome with periodic fever"",""Periodic fever-aphtous stomatitis-pharyngitis-adenopathy syndrome""]"	"[{""label"":""NOD2"",""id"":""64127""}]"	"[""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081451""}]"
DOID:0081453	"[""Dent disease 1""]"	"[{""label"":""CLCN5"",""id"":""1184""}]"	"[""1184""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081453""}]"
DOID:0081454	"[""Dent disease 2""]"	"[{""label"":""OCRL"",""id"":""4952""}]"	"[""4952""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0081454""}]"
DOID:0090001	"[""Fraser syndrome"",""cryptophthalmos with other malformations""]"	"[{""label"":""Fras1"",""id"":""231470""},{""label"":""Frem1"",""id"":""329872""},{""label"":""Frem2"",""id"":""242022""},{""label"":""Grip1"",""id"":""74053""}]"	"[""231470"",""242022"",""329872"",""74053""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090001""}]"
DOID:0090002	"[""Tietz syndrome"",""Tietz albinism-deafness syndrome"",""albinism-deafness of Tietz"",""hypopigmentation/deafness of Tietz""]"	"[{""label"":""Mitf"",""id"":""17342""}]"	"[""17342""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090002""}]"
DOID:0090002	"[""Tietz syndrome"",""Tietz albinism-deafness syndrome"",""albinism-deafness of Tietz"",""hypopigmentation/deafness of Tietz""]"	"[{""label"":""MITF"",""id"":""4286""}]"	"[""4286""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090002""}]"
DOID:0090003	"[""agenesis of the corpus callosum with peripheral neuropathy"",""Andermann syndrome"",""Charlevoix disease"",""corpus callosum agenesis-neuronopathy syndrome""]"	"[{""label"":""Slc12a6"",""id"":""107723""}]"	"[""107723""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090003""}]"
DOID:0090003	"[""agenesis of the corpus callosum with peripheral neuropathy"",""Andermann syndrome"",""Charlevoix disease"",""corpus callosum agenesis-neuronopathy syndrome""]"	"[{""label"":""SLC12A6"",""id"":""9990""}]"	"[""9990""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090003""}]"
DOID:0090004	"[""progressive pseudorheumatoid arthropathy of childhood"",""spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome""]"	"[{""label"":""CCN6"",""id"":""8838""}]"	"[""8838""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090004""}]"
DOID:0090004	"[""progressive pseudorheumatoid arthropathy of childhood"",""spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome""]"	"[{""label"":""Ccn6"",""id"":""327743""}]"	"[""327743""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090004""}]"
DOID:0090005	"[""Schwartz-Jampel syndrome 1"",""Aberfeld syndrome"",""Burton skeletal dysplasia"",""Burton syndrome"",""Catel-Hempel syndrome"",""Catel-Hempel type dysostosis enchondralis metaepiphysaria"",""Schwartz-Jampel syndrome type 1"",""Schwartz-Jampel-Aberfeld syndrome"",""myotonic chondrodystrophy"",""myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies"",""osteochondromuscular dystrophy""]"	"[{""label"":""Hspg2"",""id"":""15530""}]"	"[""15530""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090005""}]"
DOID:0090005	"[""Schwartz-Jampel syndrome 1"",""Aberfeld syndrome"",""Burton skeletal dysplasia"",""Burton syndrome"",""Catel-Hempel syndrome"",""Catel-Hempel type dysostosis enchondralis metaepiphysaria"",""Schwartz-Jampel syndrome type 1"",""Schwartz-Jampel-Aberfeld syndrome"",""myotonic chondrodystrophy"",""myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies"",""osteochondromuscular dystrophy""]"	"[{""label"":""HSPG2"",""id"":""3339""}]"	"[""3339""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090005""}]"
DOID:0090006	"[""renal coloboma syndrome"",""CAKUT with or without ocular abnormalities"",""coloboma of optic nerve with renal disease"",""congenital anomalies of the kidney and urinary tract with or without ocular abnormalities"",""optic coloboma, vesicoureteral reflux and renal anomalies"",""papillo-renal syndrome, optic nerve coloboma with renal disease"",""papillorenal syndrome"",""renal-coloboma syndrome with macular abnormalities""]"	"[{""label"":""PAX2"",""id"":""5076""}]"	"[""5076""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090006""}]"
DOID:0090011	"[""immunodeficiency-centromeric instability-facial anomalies syndrome 4"",""ICF syndrome 4""]"	"[{""label"":""HELLS"",""id"":""3070""}]"	"[""3070""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090011""}]"
DOID:0090012	"[""severe combined immunodeficiency with sensitivity to ionizing radiation"",""SCID due to DCLRE1C deficiency"",""SCID due to artemis deficiency"",""SCID, Athabascan type"",""SCID, Athabaskan type"",""Severe combined immunodeficiency due to DCLRE1C deficiency"",""Severe combined immunodeficiency due to artemis deficiency"",""Severe combined immunodeficiency, Athabascan type"",""Severe combined immunodeficiency, Athabaskan type"",""artemis deficiency""]"	"[{""label"":""DCLRE1C"",""id"":""64421""}]"	"[""64421""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090012""}]"
DOID:0090014	"[""severe combined immunodeficiency 104"",""autosomal recessive T cell-negative, B-cell positive, NK cell-positive SCID"",""interleukin-7 receptor alpha deficiency"",""severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive""]"	"[{""label"":""Coro1a"",""id"":""12721""}]"	"[""12721""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090014""}]"
DOID:0090015	"[""Cenani-Lenz syndactyly syndrome"",""syndactyly type 7""]"	"[{""label"":""LRP4"",""id"":""4038""}]"	"[""4038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090015""}]"
DOID:0090016	"[""chromosome 5q deletion syndrome"",""5q- syndrome, refractory macrocytic anemia due to 5q deletion"",""myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality""]"	"[{""label"":""RPS14"",""id"":""6208""}]"	"[""6208""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090016""}]"
DOID:0090017	"[""epidermolysis bullosa simplex with muscular dystrophy"",""epidermolysis bullosa simplex and limb-girdle muscular dystrophy"",""limb-girdle muscular dystrophy with epidermolysis bullosa simplex""]"	"[{""label"":""PLEC"",""id"":""5339""}]"	"[""5339""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090017""}]"
DOID:0090017	"[""epidermolysis bullosa simplex with muscular dystrophy"",""epidermolysis bullosa simplex and limb-girdle muscular dystrophy"",""limb-girdle muscular dystrophy with epidermolysis bullosa simplex""]"	"[{""label"":""Plec"",""id"":""18810""}]"	"[""18810""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090017""}]"
DOID:0090018	"[""TNF receptor–associated periodic syndrome"",""FHF"",""FPF"",""TRAPS"",""autosomal dominant familial periodic fever"",""familial Hibernian fever"",""hibernian fever"",""tumor necrosis factor receptor associated periodic syndrome""]"	"[{""label"":""TNFRSF1A"",""id"":""7132""}]"	"[""7132""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090018""}]"
DOID:0090018	"[""TNF receptor–associated periodic syndrome"",""FHF"",""FPF"",""TRAPS"",""autosomal dominant familial periodic fever"",""familial Hibernian fever"",""hibernian fever"",""tumor necrosis factor receptor associated periodic syndrome""]"	"[{""label"":""Tnfrsf1a"",""id"":""21937""}]"	"[""21937""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090018""}]"
DOID:0090019	"[""sitosterolemia 1"",""phytosterolemia""]"	"[{""label"":""ABCG5"",""id"":""64240""},{""label"":""ABCG8"",""id"":""64241""}]"	"[""64240"",""64241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090019""}]"
DOID:0090019	"[""sitosterolemia 1"",""phytosterolemia""]"	"[{""label"":""Abcg8"",""id"":""67470""}]"	"[""67470""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090019""}]"
DOID:0090019	"[""sitosterolemia 1"",""phytosterolemia""]"	"[{""label"":""Abcg5"",""id"":""114628""}]"	"[""114628""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090019""}]"
DOID:0090026	"[""split hand-foot malformation 6"",""SHFM6""]"	"[{""label"":""WNT10B"",""id"":""7480""}]"	"[""7480""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090026""}]"
DOID:0090030	"[""corticosteroid-binding globulin deficiency"",""CBG deficiency"",""transcortin deficiency""]"	"[{""label"":""SERPINA6"",""id"":""866""}]"	"[""866""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090030""}]"
DOID:0090030	"[""corticosteroid-binding globulin deficiency"",""CBG deficiency"",""transcortin deficiency""]"	"[{""label"":""Serpina6"",""id"":""12401""}]"	"[""12401""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090030""}]"
DOID:0090031	"[""D-bifunctional protein deficiency""]"	"[{""label"":""Hsd17b4"",""id"":""15488""}]"	"[""15488""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090031""}]"
DOID:0090031	"[""D-bifunctional protein deficiency""]"	"[{""label"":""HSD17B4"",""id"":""3295""}]"	"[""3295""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090031""}]"
DOID:0090032	"[""Silverman-Handmaker type dyssegmental dysplasia""]"	"[{""label"":""HSPG2"",""id"":""3339""}]"	"[""3339""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090032""}]"
DOID:0090032	"[""Silverman-Handmaker type dyssegmental dysplasia""]"	"[{""label"":""Hspg2"",""id"":""15530""}]"	"[""15530""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090032""}]"
DOID:0090034	"[""myoclonic dystonia 11""]"	"[{""label"":""Sgce"",""id"":""20392""}]"	"[""20392""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090034""}]"
DOID:0090034	"[""myoclonic dystonia 11""]"	"[{""label"":""SGCE"",""id"":""8910""}]"	"[""8910""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090034""}]"
DOID:0090041	"[""torsion dystonia 4""]"	"[{""label"":""TUBB4A"",""id"":""10382""}]"	"[""10382""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090041""}]"
DOID:0090044	"[""dystonia 9"",""paroxysmal choreoathetosis with spasticity""]"	"[{""label"":""SLC2A1"",""id"":""6513""}]"	"[""6513""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090044""}]"
DOID:0090045	"[""glucose transporter type 1 deficiency syndrome 2"",""DYT18"",""GLUT1 deficiency syndrome 2"",""GLUT1DS2"",""childhood-onset GLUT1 deficiency syndrome 2"",""dystonia 18""]"	"[{""label"":""SLC2A1"",""id"":""6513""}]"	"[""6513""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090045""}]"
DOID:0090048	"[""dystonia 16""]"	"[{""label"":""PRKRA"",""id"":""8575""}]"	"[""8575""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090048""}]"
DOID:0090050	"[""dystonia 27""]"	"[{""label"":""COL6A3"",""id"":""1293""}]"	"[""1293""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090050""}]"
DOID:0090052	"[""dystonia 24""]"	"[{""label"":""ANO3"",""id"":""63982""}]"	"[""63982""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090052""}]"
DOID:0090053	"[""episodic kinesigenic dyskinesia 1"",""Paroxysmal kinesigenic choreoathetosis""]"	"[{""label"":""Prrt2"",""id"":""69017""}]"	"[""69017""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090053""}]"
DOID:0090056	"[""dystonia 12""]"	"[{""label"":""PLA2G6"",""id"":""8398""}]"	"[""8398""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090056""}]"
DOID:0090059	"[""enhanced S-cone syndrome""]"	"[{""label"":""NR2E3"",""id"":""10002""}]"	"[""10002""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090059""}]"
DOID:0090060	"[""Wolcott-Rallison syndrome""]"	"[{""label"":""EIF2AK3"",""id"":""9451""}]"	"[""9451""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090060""}]"
DOID:0090060	"[""Wolcott-Rallison syndrome""]"	"[{""label"":""Eif2ak3"",""id"":""13666""}]"	"[""13666""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090060""}]"
DOID:0090064	"[""familial cold autoinflammatory syndrome 3"",""FACU"",""FCAS3"",""PLAID"",""PLCG2-associated antibody deficiency and immune dysregulation"",""familial atypical cold urticaria"",""phospholipase C gamma 2-associated antibody deficiency and immune dysregulation""]"	"[{""label"":""PLCG2"",""id"":""5336""}]"	"[""5336""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090064""}]"
DOID:0090067	"[""Fuhrmann syndrome""]"	"[{""label"":""Wnt7a"",""id"":""22421""}]"	"[""22421""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090067""}]"
DOID:0090067	"[""Fuhrmann syndrome""]"	"[{""label"":""WNT7A"",""id"":""7476""}]"	"[""7476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090067""}]"
DOID:0090068	"[""giant axonal neuropathy 1""]"	"[{""label"":""GAN"",""id"":""8139""}]"	"[""8139""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090068""}]"
DOID:0090070	"[""hypogonadotropic hypogonadism"",""congenital idiopathic hypogonadotropic hypogonadism"",""hypogonadotropism"",""isolated congenital gonadotropin deficiency""]"	"[{""label"":""NDNF"",""id"":""79625""},{""label"":""TCF12"",""id"":""6938""}]"	"[""6938"",""79625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090070""}]"
DOID:0090071	"[""hypogonadotropic hypogonadism 11 with or without anosmia""]"	"[{""label"":""TACR3"",""id"":""6870""}]"	"[""6870""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090071""}]"
DOID:0090071	"[""hypogonadotropic hypogonadism 11 with or without anosmia""]"	"[{""label"":""Tacr3"",""id"":""21338""}]"	"[""21338""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090071""}]"
DOID:0090074	"[""hypogonadotropic hypogonadism 8 with or without anosmia""]"	"[{""label"":""Kiss1r"",""id"":""114229""}]"	"[""114229""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090074""}]"
DOID:0090074	"[""hypogonadotropic hypogonadism 8 with or without anosmia""]"	"[{""label"":""KISS1R"",""id"":""84634""}]"	"[""84634""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090074""}]"
DOID:0090075	"[""hypogonadotropic hypogonadism 15 with or without anosmia""]"	"[{""label"":""HS6ST1"",""id"":""9394""}]"	"[""9394""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090075""}]"
DOID:0090076	"[""hypogonadotropic hypogonadism 18 with or without anosmia""]"	"[{""label"":""IL17RD"",""id"":""54756""}]"	"[""54756""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090076""}]"
DOID:0090078	"[""hypogonadotropic hypogonadism 7 with or without anosmia""]"	"[{""label"":""FGFR1"",""id"":""2260""},{""label"":""GNRHR"",""id"":""2798""},{""label"":""NSMF"",""id"":""26012""}]"	"[""2260"",""26012"",""2798""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090078""}]"
DOID:0090078	"[""hypogonadotropic hypogonadism 7 with or without anosmia""]"	"[{""label"":""Gnrhr"",""id"":""14715""}]"	"[""14715""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090078""}]"
DOID:0090080	"[""hypogonadotropic hypogonadism 16 with or without anosmia""]"	"[{""label"":""SEMA3A"",""id"":""10371""}]"	"[""10371""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090080""}]"
DOID:0090081	"[""hypogonadotropic hypogonadism 22 with or without anosmia""]"	"[{""label"":""FEZF1"",""id"":""389549""}]"	"[""389549""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090081""}]"
DOID:0090082	"[""hypogonadotropic hypogonadism 20 with or without anosmia""]"	"[{""label"":""FGF17"",""id"":""8822""}]"	"[""8822""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090082""}]"
DOID:0090083	"[""hypogonadotropic hypogonadism 2 with or without anosmia""]"	"[{""label"":""FGFR1"",""id"":""2260""}]"	"[""2260""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090083""}]"
DOID:0090084	"[""hypogonadotropic hypogonadism 5 with or without anosmia""]"	"[{""label"":""CHD7"",""id"":""55636""}]"	"[""55636""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090084""}]"
DOID:0090085	"[""hypogonadotropic hypogonadism 9 with or without anosmia""]"	"[{""label"":""NSMF"",""id"":""26012""}]"	"[""26012""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090085""}]"
DOID:0090086	"[""hypogonadotropic hypogonadism 6 with or without anosmia""]"	"[{""label"":""FGF8"",""id"":""2253""}]"	"[""2253""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090086""}]"
DOID:0090088	"[""hypogonadotropic hypogonadism 24 without anosmia"",""isolated follicle-stimulating hormone deficiency""]"	"[{""label"":""FSHB"",""id"":""2488""}]"	"[""2488""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090088""}]"
DOID:0090091	"[""hypogonadotropic hypogonadism 23 with or without anosmia"",""46,XY DSD due to LHB deficiency"",""46,XY DSD due to luteinizing hormone subunit beta deficiency"",""46,XY disorder of sex development due to LHB deficiency"",""46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency"",""Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency"",""Pasqualini syndrome"",""fertile eunuch syndrome"",""leydig cell hypoplasia due to LHB deficiency""]"	"[{""label"":""LHB"",""id"":""3972""}]"	"[""3972""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090091""}]"
DOID:0090092	"[""hypogonadotropic hypogonadism 3 with or without anosmia""]"	"[{""label"":""PROKR2"",""id"":""128674""}]"	"[""128674""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090092""}]"
DOID:0090093	"[""hypogonadotropic hypogonadism 21 with or without anosmia""]"	"[{""label"":""FLRT3"",""id"":""23767""}]"	"[""23767""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090093""}]"
DOID:0090094	"[""hypogonadotropic hypogonadism 1 with or without anosmia"",""dysplasia olfactogenitalis of de morsier""]"	"[{""label"":""ANOS1"",""id"":""3730""}]"	"[""3730""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090094""}]"
DOID:0090100	"[""ocular albinism with sensorineural deafness"",""WS2-OA"",""autosomal recessive Waardenburg syndrome type 2 with ocular albinism"",""digenic Waardenburg syndrome/albinism"",""digenic Waardenburg syndrome/ocular albinism""]"	"[{""label"":""Mitf"",""id"":""17342""}]"	"[""17342""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090100""}]"
DOID:0090101	"[""lethal congenital glycogen storage disease of heart"",""fatal congenital hypertrophic cardiomyopathy due to GSD"",""fatal congenital hypertrophic cardiomyopathy due to glycogenosis"",""fatal congenital nonlysosomal cardiac glycogenosis"",""phosphorylase kinase deficiency of heart""]"	"[{""label"":""PRKAG2"",""id"":""51422""}]"	"[""51422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090101""}]"
DOID:0090102	"[""autosomal dominant isolated macrothrombocytopenia 1"",""MACTHC1""]"	"[{""label"":""TUBB1"",""id"":""81027""}]"	"[""81027""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090102""}]"
DOID:0090103	"[""Huntington's disease-like 1"",""HDL1"",""HLN1"",""Huntington disease-like 1"",""Huntington-like neurodegenerative disorder 1"",""autosomal dominant Huntington-like neurodegenerative disorder"",""early-onset prion disease with prominent psychiatric features""]"	"[{""label"":""PRNP"",""id"":""5621""}]"	"[""5621""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090103""}]"
DOID:0090107	"[""autosomal dominant hypocalcemia 1"",""HYPOC1""]"	"[{""label"":""Casr"",""id"":""12374""}]"	"[""12374""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090107""}]"
DOID:0090107	"[""autosomal dominant hypocalcemia 1"",""HYPOC1""]"	"[{""label"":""CASR"",""id"":""846""}]"	"[""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090107""}]"
DOID:0090109	"[""autosomal dominant hypocalcemia"",""HYPOC""]"	"[{""label"":""CASR"",""id"":""846""}]"	"[""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090109""}]"
DOID:0090110	"[""immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome"",""Autoimmune enteropathy type 1"",""DMSD"",""IDDM-secretory diarrhea syndrome"",""IPEX"",""X-linked autoimmunity-allergic dysregulation syndrome"",""XLAAD"",""XPID"",""autoimmunity-immunodeficiency syndrome, X-linked"",""diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea"",""diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked"",""immunodeficiency, polyendocrinopathy, and enteropathy, X-linked"",""immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked""]"	"[{""label"":""Foxp3"",""id"":""20371""}]"	"[""20371""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090110""}]"
DOID:0090110	"[""immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome"",""Autoimmune enteropathy type 1"",""DMSD"",""IDDM-secretory diarrhea syndrome"",""IPEX"",""X-linked autoimmunity-allergic dysregulation syndrome"",""XLAAD"",""XPID"",""autoimmunity-immunodeficiency syndrome, X-linked"",""diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea"",""diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked"",""immunodeficiency, polyendocrinopathy, and enteropathy, X-linked"",""immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked""]"	"[{""label"":""DOCK8"",""id"":""81704""}]"	"[""81704""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090110""}]"
DOID:0090111	"[""PCWH syndrome"",""Neurologic Waardenburg-Shah syndrome"",""PCWH"",""Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease"",""Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Hirschsprung disease-Waardenburg syndrome""]"	"[{""label"":""Mpz"",""id"":""17528""}]"	"[""17528""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090111""}]"
DOID:0090113	"[""RIDDLE syndrome"",""RNF168 deficiency"",""Radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome""]"	"[{""label"":""RNF168"",""id"":""165918""}]"	"[""165918""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090113""}]"
DOID:0090114	"[""Sorsby's fundus dystrophy"",""SFD"",""hemorrhagic macular dystrophy"",""pseudoinflammatory fundus dystrophy of Sorsby""]"	"[{""label"":""TIMP3"",""id"":""7078""}]"	"[""7078""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090114""}]"
DOID:0090114	"[""Sorsby's fundus dystrophy"",""SFD"",""hemorrhagic macular dystrophy"",""pseudoinflammatory fundus dystrophy of Sorsby""]"	"[{""label"":""Timp3"",""id"":""21859""}]"	"[""21859""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090114""}]"
DOID:0090115	"[""spinocerebellar ataxia with axonal neuropathy 1"",""SCAN1"",""autosomal recessive spinocerebellar ataxia with axonal neuropathy 1"",""spinocerebellar ataxia with axonal neuropathy type 1""]"	"[{""label"":""TDP1"",""id"":""55775""}]"	"[""55775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090115""}]"
DOID:0090116	"[""spondylocarpotarsal synostosis syndrome"",""SCT"",""congenital scoliosis with unilateral unsegmented bar"",""congenital synspondylism"",""spondylocarpotarsal syndrome"",""spondylocarpotarsal synostosis"",""vertebral fusion with carpal coalition""]"	"[{""label"":""Flnb"",""id"":""286940""}]"	"[""286940""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090116""}]"
DOID:0090116	"[""spondylocarpotarsal synostosis syndrome"",""SCT"",""congenital scoliosis with unilateral unsegmented bar"",""congenital synspondylism"",""spondylocarpotarsal syndrome"",""spondylocarpotarsal synostosis"",""vertebral fusion with carpal coalition""]"	"[{""label"":""FLNB"",""id"":""2317""}]"	"[""2317""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090116""}]"
DOID:0090117	"[""thiamine-responsive megaloblastic anemia syndrome"",""Rogers syndrome"",""THMD1"",""TRMA"",""thiamine metabolism dysfunction syndrome 1"",""thiamine-responsive anaemia syndrome"",""thiamine-responsive anemia syndrome"",""thiamine-responsive megaloblastic anaemia syndrome"",""thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness"",""thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness"",""thiamine-responsive myelodysplasia""]"	"[{""label"":""folt-2"",""id"":""178745""}]"	"[""178745""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090117""}]"
DOID:0090117	"[""thiamine-responsive megaloblastic anemia syndrome"",""Rogers syndrome"",""THMD1"",""TRMA"",""thiamine metabolism dysfunction syndrome 1"",""thiamine-responsive anaemia syndrome"",""thiamine-responsive anemia syndrome"",""thiamine-responsive megaloblastic anaemia syndrome"",""thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness"",""thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness"",""thiamine-responsive myelodysplasia""]"	"[{""label"":""Slc19a2"",""id"":""116914""}]"	"[""116914""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090117""}]"
DOID:0090117	"[""thiamine-responsive megaloblastic anemia syndrome"",""Rogers syndrome"",""THMD1"",""TRMA"",""thiamine metabolism dysfunction syndrome 1"",""thiamine-responsive anaemia syndrome"",""thiamine-responsive anemia syndrome"",""thiamine-responsive megaloblastic anaemia syndrome"",""thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness"",""thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness"",""thiamine-responsive myelodysplasia""]"	"[{""label"":""SLC19A2"",""id"":""10560""}]"	"[""10560""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090117""}]"
DOID:0090118	"[""congenital amegakaryocytic thrombocytopenia"",""CAMT"",""congenital amegakaryocytic thrombocytopenic purpura""]"	"[{""label"":""Mpl"",""id"":""17480""}]"	"[""17480""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090118""}]"
DOID:0090120	"[""hereditary neutrophilia""]"	"[{""label"":""Csf3r"",""id"":""12986""}]"	"[""12986""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090120""}]"
DOID:0090120	"[""hereditary neutrophilia""]"	"[{""label"":""CSF3R"",""id"":""1441""}]"	"[""1441""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090120""}]"
DOID:0090122	"[""aromatase excess syndrome"",""AEXS"",""familial hyperestrogenism"",""hereditary prepubertal gynecomastia"",""increased aromatase activity""]"	"[{""label"":""CYP19A1"",""id"":""1588""}]"	"[""1588""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090122""}]"
DOID:0090124	"[""neurogenic-type arthrogryposis multiplex congenita-2"",""AMC neurogenic type"",""AMC2"",""AMCN"",""arthrogryposis multiplex congenita 2, neurogenic type"",""arthrogryposis multiplex congenita neurogenic type""]"	"[{""label"":""ERGIC1"",""id"":""57222""}]"	"[""57222""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090124""}]"
DOID:0090125	"[""brain small vessel disease 1"",""BSVD1"",""COL4A1-related brain small vessel disease with hemorrhage"",""COL4A1-related familial vascular leukoencephalopathy"",""COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome"",""autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy"",""brain small vessel disease with Axenfeld-Riegar anomaly"",""brain small vessel disease with hemorrhage"",""brain small vessel disease with or without ocular anomalies"",""infantile hemiparesis"",""leukoencephalopathy with Axenfeld-Riegar anomaly""]"	"[{""label"":""Col4a1"",""id"":""12826""}]"	"[""12826""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090125""}]"
DOID:0090125	"[""brain small vessel disease 1"",""BSVD1"",""COL4A1-related brain small vessel disease with hemorrhage"",""COL4A1-related familial vascular leukoencephalopathy"",""COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome"",""autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy"",""brain small vessel disease with Axenfeld-Riegar anomaly"",""brain small vessel disease with hemorrhage"",""brain small vessel disease with or without ocular anomalies"",""infantile hemiparesis"",""leukoencephalopathy with Axenfeld-Riegar anomaly""]"	"[{""label"":""COL4A1"",""id"":""1282""}]"	"[""1282""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090125""}]"
DOID:0090126	"[""branched-chain keto acid dehydrogenase kinase deficiency"",""BCKDK deficiency"",""BCKDKD"",""autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency""]"	"[{""label"":""Bckdk"",""id"":""12041""}]"	"[""12041""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090126""}]"
DOID:0090127	"[""camptodactyly-arthropathy-coxa vara-pericarditis syndrome"",""CACP"",""CACP syndrome"",""CAP syndrome"",""Jacobs syndrome"",""PAC syndrome"",""arthropathy-camptodactyly syndrome"",""camptodactyly-arthropathy-pericarditis syndrome"",""congenital familial hypertrophic synovitis"",""familial fibrosing serositis"",""pericarditis-arthropathy-camptodactyly syndrome""]"	"[{""label"":""PRG4"",""id"":""10216""}]"	"[""10216""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090127""}]"
DOID:0090128	"[""Carvajal syndrome"",""DCWHK"",""dilated cardiomyopathy with woolly hair and keratoderma"",""palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair""]"	"[{""label"":""DSP"",""id"":""1832""}]"	"[""1832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090128""}]"
DOID:0090129	"[""carnitine palmitoyltransferase I deficiency"",""CPT I deficiency"",""CPT1A deficiency"",""L-CPT1 deficiency"",""carnitine palmitoyl transferase 1A deficiency"",""carnitine palmitoyl transferase IA deficiency"",""hepatic CPT deficiency type I"",""hepatic carnitine palmitoyl transferase 1 deficiency"",""hepatic carnitine palmitoyl transferase I deficiency""]"	"[{""label"":""Cpt1a"",""id"":""12894""}]"	"[""12894""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090129""}]"
DOID:0090129	"[""carnitine palmitoyltransferase I deficiency"",""CPT I deficiency"",""CPT1A deficiency"",""L-CPT1 deficiency"",""carnitine palmitoyl transferase 1A deficiency"",""carnitine palmitoyl transferase IA deficiency"",""hepatic CPT deficiency type I"",""hepatic carnitine palmitoyl transferase 1 deficiency"",""hepatic carnitine palmitoyl transferase I deficiency""]"	"[{""label"":""CPT1A"",""id"":""1374""}]"	"[""1374""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090129""}]"
DOID:0090130	"[""cortical dysplasia-focal epilepsy syndrome"",""CDFE syndrome"",""CDFES"",""PTHSL1"",""Pitt-Hopkins-like syndrome-1""]"	"[{""label"":""CNTNAP2"",""id"":""26047""}]"	"[""26047""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090130""}]"
DOID:0090130	"[""cortical dysplasia-focal epilepsy syndrome"",""CDFE syndrome"",""CDFES"",""PTHSL1"",""Pitt-Hopkins-like syndrome-1""]"	"[{""label"":""Cntnap2"",""id"":""66797""}]"	"[""66797""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090130""}]"
DOID:0090131	"[""complex cortical dysplasia with other brain malformations"",""CDCBM""]"	"[{""label"":""APC2"",""id"":""10297""},{""label"":""CAMSAP1"",""id"":""157922""}]"	"[""10297"",""157922""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090131""}]"
DOID:0090132	"[""complex cortical dysplasia with other brain malformations 7"",""CDCBM7"",""polymicrogyria due to TUBB2B mutation""]"	"[{""label"":""Tubb2b"",""id"":""73710""}]"	"[""73710""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090132""}]"
DOID:0090132	"[""complex cortical dysplasia with other brain malformations 7"",""CDCBM7"",""polymicrogyria due to TUBB2B mutation""]"	"[{""label"":""TUBB2B"",""id"":""347733""}]"	"[""347733""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090132""}]"
DOID:0090134	"[""complex cortical dysplasia with other brain malformations 3"",""CDCBM3""]"	"[{""label"":""KIF2A"",""id"":""3796""}]"	"[""3796""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090134""}]"
DOID:0090135	"[""complex cortical dysplasia with other brain malformations 5"",""CDCBM5""]"	"[{""label"":""TUBB2A"",""id"":""7280""}]"	"[""7280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090135""}]"
DOID:0090136	"[""complex cortical dysplasia with other brain malformations 6"",""CDCBM56""]"	"[{""label"":""TUBB"",""id"":""203068""}]"	"[""203068""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090136""}]"
DOID:0090137	"[""complex cortical dysplasia with other brain malformations 1"",""CDCBM1"",""cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation""]"	"[{""label"":""TUBB3"",""id"":""10381""}]"	"[""10381""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090137""}]"
DOID:0090139	"[""cortisone reductase deficiency"",""CORTRD""]"	"[{""label"":""H6PD"",""id"":""9563""},{""label"":""HSD11B1"",""id"":""3290""}]"	"[""3290"",""9563""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090139""}]"
DOID:0090140	"[""cortisone reductase deficiency 2"",""CORTRD2""]"	"[{""label"":""HSD11B1"",""id"":""3290""}]"	"[""3290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090140""}]"
DOID:0090140	"[""cortisone reductase deficiency 2"",""CORTRD2""]"	"[{""label"":""Hsd11b1"",""id"":""15483""}]"	"[""15483""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090140""}]"
DOID:0090141	"[""cortisone reductase deficiency 1"",""CORTRD1""]"	"[{""label"":""H6PD"",""id"":""9563""}]"	"[""9563""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090141""}]"
DOID:0090142	"[""cystathioninuria"",""cystathionase deficiency"",""cystathione gamma-lyase deficiency syndrome"",""gamma-cystathionase deficiency""]"	"[{""label"":""CTH"",""id"":""1491""}]"	"[""1491""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090142""}]"
DOID:0090142	"[""cystathioninuria"",""cystathionase deficiency"",""cystathione gamma-lyase deficiency syndrome"",""gamma-cystathionase deficiency""]"	"[{""label"":""Cth"",""id"":""107869""}]"	"[""107869""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090142""}]"
DOID:0090143	"[""brachyolmia-amelogenesis imperfecta syndrome"",""DASS"",""STHAG6"",""dental anomalies and short stature"",""platyspondyly with amelogenesis imperfecta"",""selective tooth agenesis 5""]"	"[{""label"":""LTBP3"",""id"":""4054""}]"	"[""4054""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090143""}]"
DOID:0090143	"[""brachyolmia-amelogenesis imperfecta syndrome"",""DASS"",""STHAG6"",""dental anomalies and short stature"",""platyspondyly with amelogenesis imperfecta"",""selective tooth agenesis 5""]"	"[{""label"":""Ltbp3"",""id"":""16998""}]"	"[""16998""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090143""}]"
DOID:0090144	"[""Donnai-Barrow syndrome"",""DBS/FOAR syndrome"",""FOAR syndrome"",""Holmes-Schepens syndrome"",""diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and proteinuria"",""diaphragmatic hernia-exomphalos-hypertelorism syndrome"",""diaphragmatic hernia-hypertelorism-myopia-deafness syndrome"",""facio-oculo-acoustico-renal syndrome"",""faciooculoacousticorenal syndrome"",""syndrome of ocular and facial anomalies, telecanthus and deafness""]"	"[{""label"":""LRP2"",""id"":""4036""}]"	"[""4036""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090144""}]"
DOID:0090144	"[""Donnai-Barrow syndrome"",""DBS/FOAR syndrome"",""FOAR syndrome"",""Holmes-Schepens syndrome"",""diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and proteinuria"",""diaphragmatic hernia-exomphalos-hypertelorism syndrome"",""diaphragmatic hernia-hypertelorism-myopia-deafness syndrome"",""facio-oculo-acoustico-renal syndrome"",""faciooculoacousticorenal syndrome"",""syndrome of ocular and facial anomalies, telecanthus and deafness""]"	"[{""label"":""Lrp2"",""id"":""14725""}]"	"[""14725""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090144""}]"
DOID:0090145	"[""dopamine beta-hydroxylase deficiency"",""congenital dopamine beta-hydroxylase deficiency"",""noradrenaline deficiency"",""norepinephrine deficiency""]"	"[{""label"":""dat-1"",""id"":""176304""}]"	"[""176304""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090145""}]"
DOID:0090145	"[""dopamine beta-hydroxylase deficiency"",""congenital dopamine beta-hydroxylase deficiency"",""noradrenaline deficiency"",""norepinephrine deficiency""]"	"[{""label"":""DBH"",""id"":""1621""},{""label"":""HSPA5"",""id"":""3309""}]"	"[""1621"",""3309""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090145""}]"
DOID:0090145	"[""dopamine beta-hydroxylase deficiency"",""congenital dopamine beta-hydroxylase deficiency"",""noradrenaline deficiency"",""norepinephrine deficiency""]"	"[{""label"":""Dbh"",""id"":""13166""}]"	"[""13166""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0090145""}]"
DOID:0110004	"[""3-methylglutaconic aciduria type 3"",""3-methylglutaconic aciduria type III"",""Costeff optic atrophy syndrome"",""Costeff syndrome"",""Iraqi-Jewish optic atrophy plus"",""MGA3"",""autosomal recessive optic atrophy plus syndrome"",""autosomal recessive optic atrophy type 3"",""infantile optic atrophy with chorea and spastic paraplegia""]"	"[{""label"":""OPA3"",""id"":""80207""}]"	"[""80207""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110004""}]"
DOID:0110007	"[""achromatopsia 2"",""ACHM2"",""RMCH2"",""rod monochromacy 2"",""rod monochromatism 2""]"	"[{""label"":""CNGA3"",""id"":""1261""}]"	"[""1261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110007""}]"
DOID:0110007	"[""achromatopsia 2"",""ACHM2"",""RMCH2"",""rod monochromacy 2"",""rod monochromatism 2""]"	"[{""label"":""Cnga3"",""id"":""12790""}]"	"[""12790""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110007""}]"
DOID:0110009	"[""achromatopsia 7"",""ACHM7""]"	"[{""label"":""ATF6"",""id"":""22926""}]"	"[""22926""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110009""}]"
DOID:0110009	"[""achromatopsia 7"",""ACHM7""]"	"[{""label"":""Atf6"",""id"":""226641""}]"	"[""226641""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110009""}]"
DOID:0110011	"[""advanced sleep phase syndrome 1"",""FASPS1"",""familial advanced sleep phase syndrome 1""]"	"[{""label"":""Per2"",""id"":""18627""}]"	"[""18627""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110011""}]"
DOID:0110011	"[""advanced sleep phase syndrome 1"",""FASPS1"",""familial advanced sleep phase syndrome 1""]"	"[{""label"":""PER2"",""id"":""8864""}]"	"[""8864""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110011""}]"
DOID:0110013	"[""advanced sleep phase syndrome 3"",""FASPS3"",""familial advanced sleep phase syndrome 3""]"	"[{""label"":""PER3"",""id"":""8863""}]"	"[""8863""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110013""}]"
DOID:0110014	"[""age related macular degeneration 1"",""ARMD1"",""age related maculopathy 1""]"	"[{""label"":""Vldlr"",""id"":""22359""}]"	"[""22359""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110014""}]"
DOID:0110014	"[""age related macular degeneration 1"",""ARMD1"",""age related maculopathy 1""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""CFHR1"",""id"":""3078""},{""label"":""CFHR3"",""id"":""10878""},{""label"":""HMCN1"",""id"":""83872""}]"	"[""10878"",""3078"",""348"",""83872""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110014""}]"
DOID:0110015	"[""age related macular degeneration 2"",""ARMD2""]"	"[{""label"":""ABCA4"",""id"":""24""}]"	"[""24""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110015""}]"
DOID:0110017	"[""age related macular degeneration 4"",""ARMD4""]"	"[{""label"":""CFH"",""id"":""3075""}]"	"[""3075""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110017""}]"
DOID:0110017	"[""age related macular degeneration 4"",""ARMD4""]"	"[{""label"":""Cfh"",""id"":""12628""}]"	"[""12628""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110017""}]"
DOID:0110019	"[""age related macular degeneration 7"",""ARMD7""]"	"[{""label"":""C3"",""id"":""718""}]"	"[""718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110019""}]"
DOID:0110021	"[""age related macular degeneration 9"",""ARMD9""]"	"[{""label"":""C3"",""id"":""718""}]"	"[""718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110021""}]"
DOID:0110025	"[""age related macular degeneration 13"",""ARMD13""]"	"[{""label"":""CFI"",""id"":""3426""}]"	"[""3426""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110025""}]"
DOID:0110026	"[""age related macular degeneration 14"",""ARMD14""]"	"[{""label"":""C2"",""id"":""717""},{""label"":""CFB"",""id"":""629""}]"	"[""629"",""717""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110026""}]"
DOID:0110027	"[""age related macular degeneration 15"",""ARMD15""]"	"[{""label"":""C9"",""id"":""735""}]"	"[""735""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110027""}]"
DOID:0110028	"[""age related macular degeneration 5"",""ARMD5""]"	"[{""label"":""ERCC6"",""id"":""2074""}]"	"[""2074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110028""}]"
DOID:0110030	"[""alpha thalassemia-X-linked intellectual disability syndrome"",""ATR, nondeletion type"",""ATR-X syndrome"",""alpha-thalassemia/mental retardation syndrome nondeletion type""]"	"[{""label"":""Atrx"",""id"":""22589""}]"	"[""22589""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110030""}]"
DOID:0110030	"[""alpha thalassemia-X-linked intellectual disability syndrome"",""ATR, nondeletion type"",""ATR-X syndrome"",""alpha-thalassemia/mental retardation syndrome nondeletion type""]"	"[{""label"":""ATRX"",""id"":""546""}]"	"[""546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110030""}]"
DOID:0110031	"[""hemoglobin H disease"",""HBH"",""alpha thalassemia, haemoglobin H type"",""alpha thalassemia, hemoglobin H type"",""alpha-thalassemia intermedia"",""haemoglobin H disease"",""haemoglobin H disease, deletional"",""hemoglobin H disease, deletional""]"	"[{""label"":""HBA1"",""id"":""3039""},{""label"":""HBA2"",""id"":""3040""}]"	"[""3039"",""3040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110031""}]"
DOID:0110032	"[""autosomal dominant Alport syndrome""]"	"[{""label"":""COL4A3"",""id"":""1285""},{""label"":""MYH9"",""id"":""4627""}]"	"[""1285"",""4627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110032""}]"
DOID:0110033	"[""autosomal recessive Alport syndrome""]"	"[{""label"":""COL4A3"",""id"":""1285""},{""label"":""COL4A4"",""id"":""1286""}]"	"[""1285"",""1286""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110033""}]"
DOID:0110033	"[""autosomal recessive Alport syndrome""]"	"[{""label"":""Col4a3"",""id"":""12828""},{""label"":""Col4a4"",""id"":""12829""}]"	"[""12828"",""12829""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110033""}]"
DOID:0110034	"[""X-linked Alport syndrome"",""nephropathy and deafness, X-linked""]"	"[{""label"":""COL4A5"",""id"":""1287""}]"	"[""1287""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110034""}]"
DOID:0110035	"[""Alzheimer's disease 2"",""AD2"",""Alzheimer disease 2, late onset"",""Alzheimer disease associated with APOE4"",""Alzheimer disease-2""]"	"[{""label"":""APOE"",""id"":""348""}]"	"[""348""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110035""}]"
DOID:0110042	"[""Alzheimer's disease 3"",""AD3"",""Alzheimer disease 3"",""Alzheimer disease 3, early onset"",""Alzheimer disease familial 3""]"	"[{""label"":""Psn"",""id"":""40260""}]"	"[""40260""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110042""}]"
DOID:0110042	"[""Alzheimer's disease 3"",""AD3"",""Alzheimer disease 3"",""Alzheimer disease 3, early onset"",""Alzheimer disease familial 3""]"	"[{""label"":""APOE"",""id"":""348""}]"	"[""348""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110042""}]"
DOID:0110049	"[""Alzheimer's disease 17"",""AD17"",""Alzheimer disease 17"",""Alzheimer disease 17, late onset""]"	"[{""label"":""TREM2"",""id"":""54209""}]"	"[""54209""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110049""}]"
DOID:0110050	"[""Alzheimer's disease 18"",""AD18"",""Alzheimer disease 18"",""Alzheimer's disease 18, late onset""]"	"[{""label"":""ADAM10"",""id"":""102""}]"	"[""102""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110050""}]"
DOID:0110052	"[""amelogenesis imperfecta type 1B"",""AI1B"",""AIH2"",""amelogenesis imperfecta type IB"",""autosomal dominant hypoplastic local amelogenesis imperfecta"",""hereditary localized enamel hypoplasia""]"	"[{""label"":""Enam"",""id"":""13801""}]"	"[""13801""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110052""}]"
DOID:0110052	"[""amelogenesis imperfecta type 1B"",""AI1B"",""AIH2"",""amelogenesis imperfecta type IB"",""autosomal dominant hypoplastic local amelogenesis imperfecta"",""hereditary localized enamel hypoplasia""]"	"[{""label"":""ENAM"",""id"":""10117""}]"	"[""10117""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110052""}]"
DOID:0110054	"[""amelogenesis imperfecta type 1A"",""AI1A"",""amelogenesis imperfecta hypoplastic type IA"",""amelogenesis imperfecta type IA""]"	"[{""label"":""LAMB3"",""id"":""3914""}]"	"[""3914""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110054""}]"
DOID:0110056	"[""amelogenesis imperfecta type 1C"",""AI1C"",""amelogenesis imperfecta type IC"",""autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion"",""autosomal recessive amelogenesis imperfecta local hypoplastic type""]"	"[{""label"":""ENAM"",""id"":""10117""}]"	"[""10117""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110056""}]"
DOID:0110057	"[""amelogenesis imperfecta type 2A1"",""AI2A1"",""amelogenesis imperfecta pigmented hypomaturation type 1"",""amelogenesis imperfecta type IIA1""]"	"[{""label"":""KLK4"",""id"":""9622""}]"	"[""9622""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110057""}]"
DOID:0110060	"[""amelogenesis imperfecta hypomaturation type 2A2"",""AI2A2"",""amelogenesis imperfecta hypomaturation type IIA2"",""amelogenesis imperfecta pigmented hypomaturation type 2"",""amelogenesis imperfecta type IIA2""]"	"[{""label"":""MMP20"",""id"":""9313""}]"	"[""9313""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110060""}]"
DOID:0110061	"[""amelogenesis imperfecta hypomaturation type 2A3"",""AI2A3"",""amelogenesis imperfecta hypomaturation type IIA3"",""amelogenesis imperfecta type IIA3""]"	"[{""label"":""WDR72"",""id"":""256764""}]"	"[""256764""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110061""}]"
DOID:0110063	"[""amelogenesis imperfecta hypomaturation type 2A5"",""AI2A5"",""amelogenesis imperfecta hypomaturation type IIA5"",""amelogenesis imperfecta type IIA5""]"	"[{""label"":""SLC24A4"",""id"":""123041""}]"	"[""123041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110063""}]"
DOID:0110064	"[""amelogenesis imperfecta type 1H"",""AI1H"",""amelogenesis imperfecta type IH""]"	"[{""label"":""ITGB6"",""id"":""3694""}]"	"[""3694""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110064""}]"
DOID:0110065	"[""amelogenesis imperfecta type 1F"",""AI1F"",""amelogenesis imperfecta hypoplastic type IF"",""amelogenesis imperfecta type IF""]"	"[{""label"":""AMBN"",""id"":""258""}]"	"[""258""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110065""}]"
DOID:0110066	"[""amelogenesis imperfecta type 1G"",""AI1G"",""AIGFS"",""ERS"",""amelogenesis imperfecta and gingival fibromatosis syndrome"",""amelogenesis imperfecta hypoplastic with nephrocalcinosis"",""amelogenesis imperfecta type IG"",""enamel-renal syndrome"",""enamel-renal-gingival syndrome""]"	"[{""label"":""FAM20A"",""id"":""54757""}]"	"[""54757""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110066""}]"
DOID:0110068	"[""frontotemporal dementia and/or amyotrophic lateral sclerosis 3"",""FTDALS3""]"	"[{""label"":""SQSTM1"",""id"":""8878""}]"	"[""8878""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110068""}]"
DOID:0110070	"[""arrhythmogenic right ventricular dysplasia 1"",""ARVC1"",""Uhl anomaly"",""arrhythmogenic right ventricular cardiomyopathy 1""]"	"[{""label"":""TGFB3"",""id"":""7043""}]"	"[""7043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110070""}]"
DOID:0110074	"[""arrhythmogenic right ventricular dysplasia 5"",""ARVC5"",""ARVD5"",""arrhythmogenic right ventricular cardiomyopathy 5"",""familial arrhythmogenic right ventricular dysplasia 5""]"	"[{""label"":""TMEM43"",""id"":""79188""}]"	"[""79188""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110074""}]"
DOID:0110076	"[""arrhythmogenic right ventricular dysplasia 8"",""ARVC8"",""ARVD8"",""arrhythmogenic right ventricular cardiomyopathy 8"",""familial arrhythmogenic right ventricular dysplasia 8""]"	"[{""label"":""DSP"",""id"":""1832""}]"	"[""1832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110076""}]"
DOID:0110077	"[""arrhythmogenic right ventricular dysplasia 9"",""ARVC9"",""ARVD9"",""arrhythmogenic right ventricular cardiomyopathy 9"",""familial arrhythmogenic right ventricular dysplasia 9""]"	"[{""label"":""PKP2"",""id"":""5318""}]"	"[""5318""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110077""}]"
DOID:0110078	"[""Leber congenital amaurosis 1"",""LCA1"",""amaurosis congenita of Leber I""]"	"[{""label"":""GUCY2D"",""id"":""3000""}]"	"[""3000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110078""}]"
DOID:0110078	"[""Leber congenital amaurosis 1"",""LCA1"",""amaurosis congenita of Leber I""]"	"[{""label"":""Gucy2e"",""id"":""14919""}]"	"[""14919""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110078""}]"
DOID:0110079	"[""Leber congenital amaurosis 8"",""LCA8""]"	"[{""label"":""CRB1"",""id"":""23418""}]"	"[""23418""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110079""}]"
DOID:0110079	"[""Leber congenital amaurosis 8"",""LCA8""]"	"[{""label"":""Crb1"",""id"":""170788""}]"	"[""170788""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110079""}]"
DOID:0110081	"[""arrhythmogenic right ventricular dysplasia 10"",""ARVC10"",""ARVD10"",""arrhythmogenic right ventricular cardiomyopathy 10"",""familial arrhythmogenic right ventricular dysplasia 10""]"	"[{""label"":""Dsg2"",""id"":""13511""}]"	"[""13511""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110081""}]"
DOID:0110081	"[""arrhythmogenic right ventricular dysplasia 10"",""ARVC10"",""ARVD10"",""arrhythmogenic right ventricular cardiomyopathy 10"",""familial arrhythmogenic right ventricular dysplasia 10""]"	"[{""label"":""DSG2"",""id"":""1829""}]"	"[""1829""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110081""}]"
DOID:0110082	"[""arrhythmogenic right ventricular dysplasia 11"",""ARVC11"",""ARVD11"",""arrhythmogenic right ventricular cardiomyopathy 11"",""familial arrhythmogenic right ventricular dysplasia 11""]"	"[{""label"":""DSC2"",""id"":""1824""}]"	"[""1824""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110082""}]"
DOID:0110083	"[""arrhythmogenic right ventricular dysplasia 12"",""ARVC12"",""ARVD12"",""arrhythmogenic right ventricular cardiomyopathy 12"",""familial arrhythmogenic right ventricular dysplasia 12""]"	"[{""label"":""Jup"",""id"":""16480""}]"	"[""16480""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110083""}]"
DOID:0110083	"[""arrhythmogenic right ventricular dysplasia 12"",""ARVC12"",""ARVD12"",""arrhythmogenic right ventricular cardiomyopathy 12"",""familial arrhythmogenic right ventricular dysplasia 12""]"	"[{""label"":""JUP"",""id"":""3728""}]"	"[""3728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110083""}]"
DOID:0110084	"[""arrhythmogenic right ventricular dysplasia 13"",""ARVC13"",""ARVD13"",""arrhythmogenic right ventricular cardiomyopathy 13"",""familial arrhythmogenic right ventricular dysplasia 13""]"	"[{""label"":""CTNNA3"",""id"":""29119""}]"	"[""29119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110084""}]"
DOID:0110087	"[""asphyxiating thoracic dystrophy 3"",""ATD3"",""SRPS1"",""SRPS2B"",""SRPS3"",""SRTD3"",""Saldino-Noonan syndrome"",""Verma-Naumoff syndrome"",""polydactyly with neonatal chondrodystrophy, type I"",""polydactyly with neonatal chondrodystrophy, type III"",""short rib-polydactyly syndrome, type I"",""short rib-polydactyly syndrome, type IIB"",""short-rib thoracic dysplasia 3 with or without polydactyly""]"	"[{""label"":""Dync2h1"",""id"":""110350""}]"	"[""110350""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110087""}]"
DOID:0110087	"[""asphyxiating thoracic dystrophy 3"",""ATD3"",""SRPS1"",""SRPS2B"",""SRPS3"",""SRTD3"",""Saldino-Noonan syndrome"",""Verma-Naumoff syndrome"",""polydactyly with neonatal chondrodystrophy, type I"",""polydactyly with neonatal chondrodystrophy, type III"",""short rib-polydactyly syndrome, type I"",""short rib-polydactyly syndrome, type IIB"",""short-rib thoracic dysplasia 3 with or without polydactyly""]"	"[{""label"":""DYNC2H1"",""id"":""79659""}]"	"[""79659""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110087""}]"
DOID:0110090	"[""short-rib thoracic dysplasia 7 with or without polydactyly"",""SRPS5"",""SRTD7"",""short rib-polydactyly syndrome type V""]"	"[{""label"":""WDR35"",""id"":""57539""}]"	"[""57539""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110090""}]"
DOID:0110092	"[""short-rib thoracic dysplasia 6 with or without polydactyly"",""Majewski syndrome"",""SRPS2A"",""SRTD6"",""polydactyly with neonatal chondrodystrophy, type II"",""short rib-polydactyly syndrome type IIA""]"	"[{""label"":""NEK1"",""id"":""4750""}]"	"[""4750""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110092""}]"
DOID:0110098	"[""atopic dermatitis 2"",""ATOD2""]"	"[{""label"":""FLG"",""id"":""2312""}]"	"[""2312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110098""}]"
DOID:0110106	"[""atrial heart septal defect 1"",""ASD1"",""atrial septal defect 1""]"	"[{""label"":""Ntf3"",""id"":""18205""}]"	"[""18205""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110106""}]"
DOID:0110107	"[""atrial heart septal defect 2"",""ASD2"",""atrial septal defect 2""]"	"[{""label"":""Gata4"",""id"":""14463""}]"	"[""14463""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110107""}]"
DOID:0110107	"[""atrial heart septal defect 2"",""ASD2"",""atrial septal defect 2""]"	"[{""label"":""GATA4"",""id"":""2626""}]"	"[""2626""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110107""}]"
DOID:0110110	"[""atrial heart septal defect 5"",""ASD5"",""atrial septal defect 5""]"	"[{""label"":""ACTC1"",""id"":""70""}]"	"[""70""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110110""}]"
DOID:0110111	"[""atrial heart septal defect 6"",""ASD6"",""atrial septal defect 6""]"	"[{""label"":""TLL1"",""id"":""7092""}]"	"[""7092""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110111""}]"
DOID:0110117	"[""autoimmune lymphoproliferative syndrome type 4"",""ALPS type 4"",""ALPS type IV"",""ALPS4"",""RALD"",""RAS-associated autoimmune leukoproliferative disease"",""RAS-associated autoimmune leukoproliferative disorder"",""autoimmune lymphoproliferative syndrome type IV""]"	"[{""label"":""KRAS"",""id"":""3845""},{""label"":""NRAS"",""id"":""4893""}]"	"[""3845"",""4893""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110117""}]"
DOID:0110120	"[""Axenfeld-Rieger syndrome type 1"",""RIEG1"",""Rieger syndrome type 1""]"	"[{""label"":""PITX2"",""id"":""5308""}]"	"[""5308""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110120""}]"
DOID:0110122	"[""Axenfeld-Rieger syndrome type 3"",""Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss"",""RIEG3"",""Rieger syndrome type 3"",""anterior chamber cleavage syndrome"",""anterior segment mesenchymal dysgenesis""]"	"[{""label"":""FOXC1"",""id"":""2296""}]"	"[""2296""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110122""}]"
DOID:0110122	"[""Axenfeld-Rieger syndrome type 3"",""Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss"",""RIEG3"",""Rieger syndrome type 3"",""anterior chamber cleavage syndrome"",""anterior segment mesenchymal dysgenesis""]"	"[{""label"":""Bmp4"",""id"":""12159""}]"	"[""12159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110122""}]"
DOID:0110124	"[""Bardet-Biedl syndrome 2"",""BBS2""]"	"[{""label"":""BBS2"",""id"":""583""}]"	"[""583""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110124""}]"
DOID:0110125	"[""Bardet-Biedl syndrome 3"",""BBS3""]"	"[{""label"":""Arl6"",""id"":""56297""}]"	"[""56297""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110125""}]"
DOID:0110130	"[""Bardet-Biedl syndrome 8"",""BBS8""]"	"[{""label"":""TTC8"",""id"":""123016""}]"	"[""123016""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110130""}]"
DOID:0110131	"[""Bardet-Biedl syndrome 9"",""BBS9""]"	"[{""label"":""BBS9"",""id"":""27241""}]"	"[""27241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110131""}]"
DOID:0110136	"[""Bardet-Biedl syndrome 14"",""BBS14""]"	"[{""label"":""TMEM67"",""id"":""91147""}]"	"[""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110136""}]"
DOID:0110142	"[""Bartter disease type 1"",""BARTS1"",""Bartter syndrome type 1"",""Bartter syndrome type 1 antenatal"",""hyperprostaglandin E syndrome 1"",""hypokalemic alkalosis with hypercalciuria 1 antenatal""]"	"[{""label"":""SLC12A1"",""id"":""6557""}]"	"[""6557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110142""}]"
DOID:0110142	"[""Bartter disease type 1"",""BARTS1"",""Bartter syndrome type 1"",""Bartter syndrome type 1 antenatal"",""hyperprostaglandin E syndrome 1"",""hypokalemic alkalosis with hypercalciuria 1 antenatal""]"	"[{""label"":""Slc12a1"",""id"":""20495""}]"	"[""20495""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110142""}]"
DOID:0110143	"[""Bartter disease type 2"",""BARTS2"",""Bartter syndrome type 2"",""Bartter syndrome type 2 antenatal"",""hyperprostaglandin E syndrome 2"",""hypokalemic alkalosis with hypercalciuria 2 antenatal""]"	"[{""label"":""KCNJ1"",""id"":""3758""}]"	"[""3758""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110143""}]"
DOID:0110143	"[""Bartter disease type 2"",""BARTS2"",""Bartter syndrome type 2"",""Bartter syndrome type 2 antenatal"",""hyperprostaglandin E syndrome 2"",""hypokalemic alkalosis with hypercalciuria 2 antenatal""]"	"[{""label"":""Kcnj1"",""id"":""56379""}]"	"[""56379""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110143""}]"
DOID:0110144	"[""Bartter disease type 3"",""BARTS3"",""Bartter syndrome type 3"",""classic Bartter syndrome""]"	"[{""label"":""CLCNKB"",""id"":""1188""}]"	"[""1188""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110144""}]"
DOID:0110144	"[""Bartter disease type 3"",""BARTS3"",""Bartter syndrome type 3"",""classic Bartter syndrome""]"	"[{""label"":""Clcnkb"",""id"":""56365""}]"	"[""56365""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110144""}]"
DOID:0110146	"[""Bartter disease type 4b"",""BARTS4B"",""Bartter syndrome, type 4b, digenic"",""neonatal Bartter syndrome type 4B with sensorineural deafness""]"	"[{""label"":""CLCNKB"",""id"":""1188""}]"	"[""1188""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110146""}]"
DOID:0110147	"[""Bartter disease type 5"",""BARTS5"",""Bartter syndrome, type 5, antenatal, transient""]"	"[{""label"":""MAGED2"",""id"":""10916""}]"	"[""10916""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110147""}]"
DOID:0110148	"[""Charcot-Marie-Tooth disease type 1A"",""CMT1A"",""Charcot-Marie-Tooth neuropathy type 1A"",""HMSN1A"",""autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A"",""hereditary motor and sensory neuropathy 1A"",""microduplication 17p12""]"	"[{""label"":""Pmp22"",""id"":""18858""}]"	"[""18858""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110148""}]"
DOID:0110148	"[""Charcot-Marie-Tooth disease type 1A"",""CMT1A"",""Charcot-Marie-Tooth neuropathy type 1A"",""HMSN1A"",""autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A"",""hereditary motor and sensory neuropathy 1A"",""microduplication 17p12""]"	"[{""label"":""PMP22"",""id"":""5376""}]"	"[""5376""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110148""}]"
DOID:0110149	"[""Charcot-Marie-Tooth disease type 1F"",""CMT1F"",""Charcot-Marie-Tooth neuropathy type 1F""]"	"[{""label"":""NEFL"",""id"":""4747""}]"	"[""4747""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110149""}]"
DOID:0110150	"[""Charcot-Marie-Tooth disease type 1D"",""CMT1D"",""Charcot-Marie-Tooth neuropathy type 1D"",""HMSN ID"",""HMSN1D"",""hereditary motor and sensory neuropathy 1D""]"	"[{""label"":""EGR2"",""id"":""1959""}]"	"[""1959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110150""}]"
DOID:0110151	"[""Charcot-Marie-Tooth disease type 1C"",""CMT slow nerve conduction type C"",""CMT1C"",""Charcot-Marie-Tooth neuropathy type 1C"",""HMSN IC"",""HMSN1C"",""neuropathy hereditary motor and sensory type 1C""]"	"[{""label"":""LITAF"",""id"":""9516""}]"	"[""9516""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110151""}]"
DOID:0110152	"[""Charcot-Marie-Tooth disease type 1B"",""CMT1B"",""Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy"",""Charcot-Marie-Tooth neuropathy type 1B"",""HMSN IB"",""HMSN1B"",""autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B"",""hereditary motor and sensory neuropathy IB"",""peroneal muscular atrophy""]"	"[{""label"":""MPZ"",""id"":""4359""}]"	"[""4359""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110152""}]"
DOID:0110152	"[""Charcot-Marie-Tooth disease type 1B"",""CMT1B"",""Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy"",""Charcot-Marie-Tooth neuropathy type 1B"",""HMSN IB"",""HMSN1B"",""autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B"",""hereditary motor and sensory neuropathy IB"",""peroneal muscular atrophy""]"	"[{""label"":""Mpz"",""id"":""17528""}]"	"[""17528""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110152""}]"
DOID:0110153	"[""Charcot-Marie-Tooth disease type 1E"",""CMT1E"",""Charcot-Marie-Tooth disease and deafness"",""Charcot-Marie-Tooth disease demyelinating type 1E"",""Charcot-Marie-Tooth disease-deafness"",""autosomal dominant Charcot-Marie-Tooth neuropathy and deafness""]"	"[{""label"":""Pmp22"",""id"":""18858""}]"	"[""18858""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110153""}]"
DOID:0110153	"[""Charcot-Marie-Tooth disease type 1E"",""CMT1E"",""Charcot-Marie-Tooth disease and deafness"",""Charcot-Marie-Tooth disease demyelinating type 1E"",""Charcot-Marie-Tooth disease-deafness"",""autosomal dominant Charcot-Marie-Tooth neuropathy and deafness""]"	"[{""label"":""PMP22"",""id"":""5376""}]"	"[""5376""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110153""}]"
DOID:0110154	"[""Charcot-Marie-Tooth disease type 2A1"",""CMT2A1"",""Charcot-Marie-Tooth disease neuronal type 2A1"",""Charcot-Marie-Tooth neuropathy type 2A1"",""HMSN IIA1"",""HMSN2A1"",""autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1"",""hereditary motor and sensory neuropathy IIA1""]"	"[{""label"":""KIF1B"",""id"":""23095""}]"	"[""23095""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110154""}]"
DOID:0110156	"[""Charcot-Marie-Tooth disease type 2B1"",""CMT2B1"",""Charcot-Marie-Tooth disease neuronal type 2B1"",""Charcot-Marie-Tooth neuropathy type 2B1"",""autosomal recessive Charcot-Marie-Tooth disease type 2B1"",""autosomal recessive axonal CMT4C1"",""autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110156""}]"
DOID:0110156	"[""Charcot-Marie-Tooth disease type 2B1"",""CMT2B1"",""Charcot-Marie-Tooth disease neuronal type 2B1"",""Charcot-Marie-Tooth neuropathy type 2B1"",""autosomal recessive Charcot-Marie-Tooth disease type 2B1"",""autosomal recessive axonal CMT4C1"",""autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1""]"	"[{""label"":""Lmna"",""id"":""16905""}]"	"[""16905""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110156""}]"
DOID:0110157	"[""Charcot-Marie-Tooth disease type 2J"",""CMT2J"",""Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities"",""Charcot-Marie-Tooth neuropathy type 2J""]"	"[{""label"":""MPZ"",""id"":""4359""}]"	"[""4359""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110157""}]"
DOID:0110158	"[""Charcot-Marie-Tooth disease type 2I"",""CMT2I"",""Charcot-Marie-Tooth neuropathy type 2I""]"	"[{""label"":""MPZ"",""id"":""4359""}]"	"[""4359""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110158""}]"
DOID:0110159	"[""Charcot-Marie-Tooth disease type 2B"",""CMT2B"",""Charcot-Marie-Tooth neuropathy type 2B"",""HMSN IIB"",""HMSN2B"",""autosomal dominant Charcot-Marie-Tooth disease type 2B"",""hereditary motor and sensory nueropathy IIB""]"	"[{""label"":""RAB7A"",""id"":""7879""}]"	"[""7879""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110159""}]"
DOID:0110160	"[""Charcot-Marie-Tooth disease axonal type 2T"",""AR-CMT2T"",""CMT2T"",""Charcot-Marie-Tooth neuropathy type 2T"",""autosomal recessive axonal Charcot-Marie-Tooth disease type 2T""]"	"[{""label"":""MME"",""id"":""4311""}]"	"[""4311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110160""}]"
DOID:0110163	"[""Charcot-Marie-Tooth disease axonal type 2F"",""CMT2F"",""Charcot-Marie-Tooth neuronal type 2F"",""Charcot-Marie-Tooth neuropathy type 2F"",""autosomal dominant Charcot-Marie-Tooth disease type 2F""]"	"[{""label"":""HSPB1"",""id"":""3315""}]"	"[""3315""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110163""}]"
DOID:0110165	"[""Charcot-Marie-Tooth disease type 2E"",""CMT2E"",""Charcot-Marie-Tooth neuropathy type 2E"",""autosomal dominant Charcot-Marie-Tooth disease type 2E""]"	"[{""label"":""Nefl"",""id"":""18039""}]"	"[""18039""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110165""}]"
DOID:0110165	"[""Charcot-Marie-Tooth disease type 2E"",""CMT2E"",""Charcot-Marie-Tooth neuropathy type 2E"",""autosomal dominant Charcot-Marie-Tooth disease type 2E""]"	"[{""label"":""NEFL"",""id"":""4747""}]"	"[""4747""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110165""}]"
DOID:0110167	"[""Charcot-Marie-Tooth disease axonal type 2K"",""ARCMT2K"",""Charcot-Marie-Tooth neuropathy axonal type 2K"",""autosomal recessive Charcot-Marie-Tooth disease with hoarseness"",""autosomal recessive axonal CMT4C4"",""autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K"",""autosomal recessive axonal Charcot-Marie-Tooth disease type 2K""]"	"[{""label"":""JPH1"",""id"":""56704""}]"	"[""56704""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110167""}]"
DOID:0110168	"[""Charcot-Marie-Tooth disease type 2Y"",""CMT2 due to VCP mutation"",""CMT2Y"",""Charcot-Marie-Tooth neuropathy type 2Y"",""autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation"",""autosomal dominant axonal Charcot-Marie-Tooth type 2Y""]"	"[{""label"":""VCP"",""id"":""7415""}]"	"[""7415""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110168""}]"
DOID:0110169	"[""Charcot-Marie-Tooth disease axonal type 2P"",""CMT2P"",""Charcot-Marie-Tooth disease type 2P"",""Charcot-Marie-Tooth neuropathy type 2P""]"	"[{""label"":""LRSAM1"",""id"":""90678""}]"	"[""90678""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110169""}]"
DOID:0110170	"[""Charcot-Marie-Tooth disease axonal type 2Q"",""CMT2Q"",""Charcot-Marie-Tooth neuropathy type 2Q"",""autosomal dominant Charcot-Marie-Tooth disease type 2Q"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q""]"	"[{""label"":""Dhtkd1"",""id"":""209692""}]"	"[""209692""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110170""}]"
DOID:0110170	"[""Charcot-Marie-Tooth disease axonal type 2Q"",""CMT2Q"",""Charcot-Marie-Tooth neuropathy type 2Q"",""autosomal dominant Charcot-Marie-Tooth disease type 2Q"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q""]"	"[{""label"":""DHTKD1"",""id"":""55526""}]"	"[""55526""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110170""}]"
DOID:0110170	"[""Charcot-Marie-Tooth disease axonal type 2Q"",""CMT2Q"",""Charcot-Marie-Tooth neuropathy type 2Q"",""autosomal dominant Charcot-Marie-Tooth disease type 2Q"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q""]"	"[{""label"":""CG1544"",""id"":""43689""}]"	"[""43689""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110170""}]"
DOID:0110171	"[""Charcot-Marie-Tooth disease axonal type 2S"",""CMT2S"",""Charcot-Marie-Tooth disease type 2S"",""Charcot-Marie-Tooth neuropathy type 2S"",""autosomal recessive axonal Charcot-Marie-Tooth type 2S""]"	"[{""label"":""IGHMBP2"",""id"":""3508""}]"	"[""3508""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110171""}]"
DOID:0110173	"[""Charcot-Marie-Tooth disease axonal type 2U"",""CMT2U"",""Charcot-Marie-Tooth neuropathy type 2U"",""autosomal dominant Charcot-Marie-Tooth disease type 2U"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2U""]"	"[{""label"":""MARS1"",""id"":""4141""}]"	"[""4141""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110173""}]"
DOID:0110174	"[""Charcot-Marie-Tooth disease axonal type 2L"",""CMT2L"",""Charcot-Marie-Tooth neuropathy axonal type 2L"",""autosomal dominant Charcot-Marie-Tooth disease type 2L"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2L""]"	"[{""label"":""HSPB8"",""id"":""26353""}]"	"[""26353""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110174""}]"
DOID:0110175	"[""Charcot-Marie-Tooth disease axonal type 2O"",""Charcot-Marie-Tooth neuropathy axonal type 2O"",""autosomal dominant Charcot-Marie-Tooth disease type 2O"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2O""]"	"[{""label"":""Dync1h1"",""id"":""13424""}]"	"[""13424""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110175""}]"
DOID:0110175	"[""Charcot-Marie-Tooth disease axonal type 2O"",""Charcot-Marie-Tooth neuropathy axonal type 2O"",""autosomal dominant Charcot-Marie-Tooth disease type 2O"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2O""]"	"[{""label"":""DYNC1H1"",""id"":""1778""}]"	"[""1778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110175""}]"
DOID:0110176	"[""Charcot-Marie-Tooth disease axonal type 2X"",""Charcot-Marie-Tooth neuropathy type 2X"",""autosomal recessive axonal Charcot-Marie-Tooth disease type 2X""]"	"[{""label"":""SPG11"",""id"":""80208""}]"	"[""80208""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110176""}]"
DOID:0110177	"[""Charcot-Marie-Tooth disease axonal type 2N"",""CMT2N"",""Charcot-Marie-Tooth neuropathy axonal type 2N"",""autosomal dominant Charcot-Marie-Tooth disease type 2N"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2N""]"	"[{""label"":""AARS1"",""id"":""16""}]"	"[""16""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110177""}]"
DOID:0110178	"[""Charcot-Marie-Tooth disease axonal type 2V"",""CMT2V"",""Charcot-Marie-Tooth neuropathy type 2V"",""autosomal dominant Charcot-Marie-Tooth disease type 2V"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2V""]"	"[{""label"":""NAGLU"",""id"":""4669""}]"	"[""4669""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110178""}]"
DOID:0110180	"[""Charcot-Marie-Tooth disease axonal type 2CC"",""CMT2CC"",""Charcot-Marie-Tooth neuropathy type 2CC""]"	"[{""label"":""NEFH"",""id"":""4744""}]"	"[""4744""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110180""}]"
DOID:0110181	"[""Charcot-Marie-Tooth disease axonal type 2Z"",""CMT2Z"",""Charcot-Marie-Tooth neuropathy type 2Z"",""autosomal dominant axonal Charcot-Marie-Tooth disease type 2Z""]"	"[{""label"":""MORC2"",""id"":""22880""}]"	"[""22880""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110181""}]"
DOID:0110184	"[""Charcot-Marie-Tooth disease type 4J"",""CMT4J"",""autosomal recessive Charcot-Marie-Tooth disease type 4J""]"	"[{""label"":""FIG4"",""id"":""33658""}]"	"[""33658""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110184""}]"
DOID:0110184	"[""Charcot-Marie-Tooth disease type 4J"",""CMT4J"",""autosomal recessive Charcot-Marie-Tooth disease type 4J""]"	"[{""label"":""FIG4"",""id"":""855392""}]"	"[""855392""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110184""}]"
DOID:0110184	"[""Charcot-Marie-Tooth disease type 4J"",""CMT4J"",""autosomal recessive Charcot-Marie-Tooth disease type 4J""]"	"[{""label"":""FIG4"",""id"":""9896""}]"	"[""9896""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110184""}]"
DOID:0110186	"[""Charcot-Marie-Tooth disease type 4D"",""CMT4D"",""Charcot-Marie-Tooth neuropathy type 4D"",""HMSN Lom type"",""HMSN-Lom"",""HMSN4D"",""HMSNL"",""autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D"",""hereditary motor and sensory neuropathy LOM type""]"	"[{""label"":""NDRG1"",""id"":""10397""}]"	"[""10397""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110186""}]"
DOID:0110187	"[""Charcot-Marie-Tooth disease type 4K"",""CMT4K"",""SURF1-related CMT4"",""SURF1-related Charcot-Marie-Tooth disease type 4"",""SURF1-related severe demyelinating Charcot-Marie-Tooth disease"",""autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K"",""autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K""]"	"[{""label"":""SURF1"",""id"":""6834""}]"	"[""6834""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110187""}]"
DOID:0110191	"[""Charcot-Marie-Tooth disease type 4B1"",""CMT4B1"",""Charcot-Marie-Tooth neuropathy type 4B1"",""autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1""]"	"[{""label"":""MTMR2"",""id"":""8898""}]"	"[""8898""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110191""}]"
DOID:0110194	"[""Charcot-Marie-Tooth disease type 4B3"",""CMT4B3""]"	"[{""label"":""Sbf1"",""id"":""77980""}]"	"[""77980""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110194""}]"
DOID:0110195	"[""Charcot-Marie-Tooth disease type 4E"",""CMT4E"",""Charcot-Marie-Tooth neuropathy type 4E"",""Neuropathy, congenital hypomyelinating, 1"",""autosomal recessive congenital hypomyelinating or amyelinating neuropathy""]"	"[{""label"":""EGR2"",""id"":""1959""}]"	"[""1959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110195""}]"
DOID:0110196	"[""Charcot-Marie-Tooth disease type 4G"",""CMT4G"",""Charcot-Marie-Tooth neuropathy type 4G"",""HMSNR"",""autosomal recessive Charcot-Marie-Tooth disease type 4G"",""hereditary motor and sensory neuropathy Russe type""]"	"[{""label"":""HK1"",""id"":""3098""}]"	"[""3098""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110196""}]"
DOID:0110197	"[""Charcot-Marie-Tooth disease dominant intermediate B"",""CMTDI1"",""CMTDIB"",""Charcot-Marie-Tooth neuropathy dominant intermediate B"",""DI-CMTB""]"	"[{""label"":""DNM2"",""id"":""1785""}]"	"[""1785""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110197""}]"
DOID:0110197	"[""Charcot-Marie-Tooth disease dominant intermediate B"",""CMTDI1"",""CMTDIB"",""Charcot-Marie-Tooth neuropathy dominant intermediate B"",""DI-CMTB""]"	"[{""label"":""VPS1"",""id"":""853870""}]"	"[""853870""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110197""}]"
DOID:0110199	"[""Charcot-Marie-Tooth disease dominant intermediate C"",""CMTDIC"",""Charcot-Marie-Tooth neuropathy dominant intermediate C"",""DI-CMTC"",""autosomal dominant intermediate Charcot-Marie-Tooth disease type C""]"	"[{""label"":""YARS1"",""id"":""8565""}]"	"[""8565""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110199""}]"
DOID:0110199	"[""Charcot-Marie-Tooth disease dominant intermediate C"",""CMTDIC"",""Charcot-Marie-Tooth neuropathy dominant intermediate C"",""DI-CMTC"",""autosomal dominant intermediate Charcot-Marie-Tooth disease type C""]"	"[{""label"":""Yars1"",""id"":""107271""}]"	"[""107271""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110199""}]"
DOID:0110200	"[""Charcot-Marie-Tooth disease dominant intermediate D"",""CMTDID"",""Charcot-Marie-Tooth neuropathy dominant intermediate D"",""DI-CMTD"",""autosomal dominant intermediate Charcot-Marie-Tooth disease type D""]"	"[{""label"":""MPZ"",""id"":""4359""}]"	"[""4359""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110200""}]"
DOID:0110202	"[""Charcot-Marie-Tooth disease dominant intermediate A"",""CMTDIA"",""Charcot-Marie-Tooth neuropathy dominant intermediate A"",""DI-CMTA"",""autosomal dominant intermediate Charcot-Marie-Tooth disease type A""]"	"[{""label"":""GBF1"",""id"":""8729""}]"	"[""8729""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110202""}]"
DOID:0110204	"[""Charcot-Marie-Tooth disease recessive intermediate B"",""CMTRIB"",""Charcot-Marie-Tooth neuropathy recessive intermediate B"",""RI-CMTB"",""autosomal recessive intermediate Charcot-Marie-Tooth disease type B""]"	"[{""label"":""KARS1"",""id"":""3735""}]"	"[""3735""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110204""}]"
DOID:0110205	"[""Charcot-Marie-Tooth disease dominant intermediate E"",""CMTDIE"",""Charcot-Marie-Tooth disease-nephropathy syndrome"",""Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis"",""autosomal dominant intermediate Charcot-Marie-Tooth disease type E""]"	"[{""label"":""INF2"",""id"":""64423""}]"	"[""64423""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110205""}]"
DOID:0110206	"[""Charcot-Marie-Tooth disease dominant intermediate F"",""CMTDIF"",""autosomal dominant intermediate Charcot-Marie-Tooth disease type F""]"	"[{""label"":""GNB4"",""id"":""59345""}]"	"[""59345""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110206""}]"
DOID:0110207	"[""Charcot-Marie-Tooth disease X-linked dominant 6"",""CMT6X"",""CMTX6"",""Charcot-Marie-Tooth neuropathy X-linked dominant 6"",""X-linked Charcot-Marie-Tooth disease type 6""]"	"[{""label"":""PDK3"",""id"":""5165""}]"	"[""5165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110207""}]"
DOID:0110210	"[""Charcot-Marie-Tooth disease X-linked recessive 5"",""CMT5X"",""CMTX5"",""Charcot-Marie-Tooth neuropathy X-linked recessive 5"",""Rosenberg-Chutorian syndrome"",""X-linked Charcot-Marie-Tooth disease type 5"",""optic atrophy, polyneuropathy, and deafness""]"	"[{""label"":""PRPS1"",""id"":""5631""}]"	"[""5631""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110210""}]"
DOID:0110212	"[""Charcot-Marie-Tooth disease X-linked recessive 4"",""CMT4X"",""CMTX4"",""Charcot-Marie-Tooth disease with deafness and mental retardation"",""Cowchock syndrome"",""NADMR"",""NAMSD"",""X-linked Charcot-Marie-Tooth disease type 4"",""axonal motor sensory neuropathy with deafness and mental retardation""]"	"[{""label"":""AIFM1"",""id"":""9131""}]"	"[""9131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110212""}]"
DOID:0110214	"[""cleft soft palate"",""cleft velum"",""cleft velum palatinum"",""soft cleft palate""]"	"[{""label"":""Tgfbr2"",""id"":""21813""}]"	"[""21813""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110214""}]"
DOID:0110217	"[""Leber congenital amaurosis 17"",""LCA17""]"	"[{""label"":""GDF6"",""id"":""392255""}]"	"[""392255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110217""}]"
DOID:0110218	"[""Brugada syndrome 1"",""BRGDA1""]"	"[{""label"":""Scn5a"",""id"":""20271""}]"	"[""20271""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110218""}]"
DOID:0110218	"[""Brugada syndrome 1"",""BRGDA1""]"	"[{""label"":""SCN5A"",""id"":""6331""}]"	"[""6331""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110218""}]"
DOID:0110219	"[""Brugada syndrome 2"",""BRGDA2""]"	"[{""label"":""GPD1L"",""id"":""23171""}]"	"[""23171""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110219""}]"
DOID:0110220	"[""Brugada syndrome 3"",""BRGDA3""]"	"[{""label"":""CACNA1C"",""id"":""775""}]"	"[""775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110220""}]"
DOID:0110221	"[""Brugada syndrome 4"",""BRGDA4""]"	"[{""label"":""CACNB2"",""id"":""783""}]"	"[""783""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110221""}]"
DOID:0110222	"[""Brugada syndrome 5"",""BRGDA5""]"	"[{""label"":""SCN1B"",""id"":""6324""}]"	"[""6324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110222""}]"
DOID:0110223	"[""Brugada syndrome 6"",""BRGDA6""]"	"[{""label"":""KCNE3"",""id"":""10008""}]"	"[""10008""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110223""}]"
DOID:0110224	"[""Brugada syndrome 7"",""BRGDA7""]"	"[{""label"":""SCN3B"",""id"":""55800""}]"	"[""55800""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110224""}]"
DOID:0110224	"[""Brugada syndrome 7"",""BRGDA7""]"	"[{""label"":""Scn3b"",""id"":""235281""}]"	"[""235281""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110224""}]"
DOID:0110225	"[""Brugada syndrome 8"",""BRGDA8""]"	"[{""label"":""HCN4"",""id"":""10021""}]"	"[""10021""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110225""}]"
DOID:0110229	"[""cataract 6 multiple types"",""CTRCT6""]"	"[{""label"":""Epha2"",""id"":""13836""}]"	"[""13836""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110229""}]"
DOID:0110229	"[""cataract 6 multiple types"",""CTRCT6""]"	"[{""label"":""EPHA2"",""id"":""1969""}]"	"[""1969""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110229""}]"
DOID:0110241	"[""cataract 41"",""CTRCT41"",""congenital nuclear type cataract 41""]"	"[{""label"":""WFS1"",""id"":""7466""}]"	"[""7466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110241""}]"
DOID:0110242	"[""cataract 13 with adult i phenotype"",""CTRCT13""]"	"[{""label"":""GCNT2"",""id"":""2651""}]"	"[""2651""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110242""}]"
DOID:0110243	"[""cataract 46 juvenile-onset"",""CTRCT46"",""juvenilae cataract Hutterite type""]"	"[{""label"":""LEMD2"",""id"":""221496""}]"	"[""221496""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110243""}]"
DOID:0110245	"[""cataract 38"",""CATC5"",""CTRCT38"",""autosomal recessive congenital cataract 5""]"	"[{""label"":""AGK"",""id"":""55750""}]"	"[""55750""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110245""}]"
DOID:0110247	"[""cataract 36"",""CATC4"",""CTRCT36"",""autosomal recessive congenital cataract 4""]"	"[{""label"":""TDRD7"",""id"":""23424""}]"	"[""23424""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110247""}]"
DOID:0110248	"[""cataract 30"",""CTRCT30"",""Dusty cataract"",""cataract 30 pulverulent"",""cataract Coppock-like""]"	"[{""label"":""VIM"",""id"":""7431""}]"	"[""7431""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110248""}]"
DOID:0110248	"[""cataract 30"",""CTRCT30"",""Dusty cataract"",""cataract 30 pulverulent"",""cataract Coppock-like""]"	"[{""label"":""Vim"",""id"":""22352""}]"	"[""22352""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110248""}]"
DOID:0110250	"[""cataract 16 multiple types"",""CTRCT16""]"	"[{""label"":""Cryab"",""id"":""12955""}]"	"[""12955""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110250""}]"
DOID:0110250	"[""cataract 16 multiple types"",""CTRCT16""]"	"[{""label"":""CRYAB"",""id"":""1410""}]"	"[""1410""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110250""}]"
DOID:0110255	"[""cataract 5 multiple types"",""CTRCT5""]"	"[{""label"":""HSF4"",""id"":""3299""}]"	"[""3299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110255""}]"
DOID:0110262	"[""cataract 45"",""CTRCT45""]"	"[{""label"":""SIPA1L3"",""id"":""23094""}]"	"[""23094""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110262""}]"
DOID:0110263	"[""cataract 19 multiple types"",""CTRCT19""]"	"[{""label"":""Lim2"",""id"":""233187""}]"	"[""233187""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110263""}]"
DOID:0110263	"[""cataract 19 multiple types"",""CTRCT19""]"	"[{""label"":""LIM2"",""id"":""3982""}]"	"[""3982""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110263""}]"
DOID:0110264	"[""cataract 33"",""CTRCT33""]"	"[{""label"":""BFSP1"",""id"":""631""}]"	"[""631""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110264""}]"
DOID:0110265	"[""cataract 31 multiple types"",""CTRCT31""]"	"[{""label"":""CHMP4B"",""id"":""128866""}]"	"[""128866""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110265""}]"
DOID:0110266	"[""cataract 9 multiple types"",""CTRCT9"",""cataract 9 multiple types with or without microcornea""]"	"[{""label"":""Cryaa"",""id"":""12954""}]"	"[""12954""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110266""}]"
DOID:0110266	"[""cataract 9 multiple types"",""CTRCT9"",""cataract 9 multiple types with or without microcornea""]"	"[{""label"":""CRYAA"",""id"":""1409""}]"	"[""1409""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110266""}]"
DOID:0110267	"[""cataract 44"",""CTRCT44"",""total early-onset cataract""]"	"[{""label"":""LSS"",""id"":""4047""}]"	"[""4047""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110267""}]"
DOID:0110272	"[""cataract 40"",""CTRCT40"",""cataract 40 X-linked"",""cataract 40 with or without microcornea""]"	"[{""label"":""NHS"",""id"":""4810""}]"	"[""4810""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110272""}]"
DOID:0110273	"[""autosomal dominant limb-girdle muscular dystrophy""]"	"[{""label"":""CAPN3"",""id"":""825""}]"	"[""825""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110273""}]"
DOID:0110274	"[""autosomal recessive limb-girdle muscular dystrophy""]"	"[{""label"":""HMGCR"",""id"":""3156""},{""label"":""JAG2"",""id"":""3714""},{""label"":""LAMA2"",""id"":""3908""},{""label"":""POMT2"",""id"":""29954""},{""label"":""POPDC3"",""id"":""64208""}]"	"[""29954"",""3156"",""3714"",""3908"",""64208""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110274""}]"
DOID:0110274	"[""autosomal recessive limb-girdle muscular dystrophy""]"	"[{""label"":""rumi"",""id"":""326122""},{""label"":""tn"",""id"":""37190""}]"	"[""326122"",""37190""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110274""}]"
DOID:0110275	"[""autosomal recessive limb-girdle muscular dystrophy type 2A"",""LGMD2A"",""Leyden-Moebius muscular dystrophy"",""limb-girdle muscular dystrophy due to calpain deficiency"",""muscular dystrophy, limb-girdle, type 2A"",""pelvofemoral muscular dystrophy"",""primary calpainopathy""]"	"[{""label"":""CAPN3"",""id"":""825""}]"	"[""825""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110275""}]"
DOID:0110276	"[""autosomal recessive limb-girdle muscular dystrophy type 2B"",""LGMD2B"",""LGMD3"",""limb-girdle muscular dystrophy due to dysferlin deficiency"",""limb-girdle muscular dystrophy type 3""]"	"[{""label"":""Dysf"",""id"":""26903""}]"	"[""26903""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110276""}]"
DOID:0110276	"[""autosomal recessive limb-girdle muscular dystrophy type 2B"",""LGMD2B"",""LGMD3"",""limb-girdle muscular dystrophy due to dysferlin deficiency"",""limb-girdle muscular dystrophy type 3""]"	"[{""label"":""DYSF"",""id"":""8291""}]"	"[""8291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110276""}]"
DOID:0110277	"[""autosomal recessive limb-girdle muscular dystrophy type 2C"",""DMDA1"",""LGMD2C"",""Maghrebian myopathy"",""SCARMD"",""autosomal recessive Duchenne-like muscular dystrophy type 1"",""deficiency of sarcoglycan gamma"",""gamma-sarcoglycanopathy"",""limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency"",""muscular dystrophy, limb-girdle, type 2C"",""severe childhood autosomal recessive muscular dystrophy North African type""]"	"[{""label"":""Sgcg"",""id"":""24053""}]"	"[""24053""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110277""}]"
DOID:0110277	"[""autosomal recessive limb-girdle muscular dystrophy type 2C"",""DMDA1"",""LGMD2C"",""Maghrebian myopathy"",""SCARMD"",""autosomal recessive Duchenne-like muscular dystrophy type 1"",""deficiency of sarcoglycan gamma"",""gamma-sarcoglycanopathy"",""limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency"",""muscular dystrophy, limb-girdle, type 2C"",""severe childhood autosomal recessive muscular dystrophy North African type""]"	"[{""label"":""SGCG"",""id"":""6445""}]"	"[""6445""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110277""}]"
DOID:0110278	"[""autosomal recessive limb-girdle muscular dystrophy type 2D"",""Alpha-sarcoglycanopathy"",""DMDA2"",""Duchenne-like autosomal recessive muscular dystrophy type 2"",""LGMD2D"",""muscular dystrophy, limb-girdle, type 2D"",""primary adhalinopathy""]"	"[{""label"":""Sgca"",""id"":""20391""}]"	"[""20391""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110278""}]"
DOID:0110278	"[""autosomal recessive limb-girdle muscular dystrophy type 2D"",""Alpha-sarcoglycanopathy"",""DMDA2"",""Duchenne-like autosomal recessive muscular dystrophy type 2"",""LGMD2D"",""muscular dystrophy, limb-girdle, type 2D"",""primary adhalinopathy""]"	"[{""label"":""DAG1"",""id"":""1605""},{""label"":""SGCA"",""id"":""6442""}]"	"[""1605"",""6442""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110278""}]"
DOID:0110279	"[""autosomal recessive limb-girdle muscular dystrophy type 2E"",""Beta-sarcoglycanopathy"",""LGMD2E"",""Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency"",""muscular dystrophy, limb-girdle, type 2E""]"	"[{""label"":""SGCB"",""id"":""6443""}]"	"[""6443""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110279""}]"
DOID:0110279	"[""autosomal recessive limb-girdle muscular dystrophy type 2E"",""Beta-sarcoglycanopathy"",""LGMD2E"",""Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency"",""muscular dystrophy, limb-girdle, type 2E""]"	"[{""label"":""Sgcb"",""id"":""24051""}]"	"[""24051""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110279""}]"
DOID:0110280	"[""autosomal recessive limb-girdle muscular dystrophy type 2F"",""LGMD2F"",""delta-sarcoglycanopathy"",""limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency""]"	"[{""label"":""Sgcd"",""id"":""24052""}]"	"[""24052""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110280""}]"
DOID:0110280	"[""autosomal recessive limb-girdle muscular dystrophy type 2F"",""LGMD2F"",""delta-sarcoglycanopathy"",""limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency""]"	"[{""label"":""SGCD"",""id"":""6444""}]"	"[""6444""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110280""}]"
DOID:0110282	"[""autosomal recessive limb-girdle muscular dystrophy type 2H"",""LGMD2H"",""limb-girdle muscular dystrophy due to TRIM32 deficiency"",""muscular dystrophy Hutterite type"",""sarcotubular myopathy""]"	"[{""label"":""tn"",""id"":""37190""}]"	"[""37190""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110282""}]"
DOID:0110283	"[""autosomal recessive limb-girdle muscular dystrophy type 2J"",""LGMD2J"",""muscular dystrophy, limb-girdle, type 2J""]"	"[{""label"":""Ttn"",""id"":""22138""}]"	"[""22138""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110283""}]"
DOID:0110283	"[""autosomal recessive limb-girdle muscular dystrophy type 2J"",""LGMD2J"",""muscular dystrophy, limb-girdle, type 2J""]"	"[{""label"":""TTN"",""id"":""7273""}]"	"[""7273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110283""}]"
DOID:0110284	"[""autosomal recessive limb-girdle muscular dystrophy type 2L"",""LGMD2L"",""muscular dystrophy, limb-girdle, type 2L""]"	"[{""label"":""ANO5"",""id"":""203859""},{""label"":""FKTN"",""id"":""2218""}]"	"[""203859"",""2218""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110284""}]"
DOID:0110284	"[""autosomal recessive limb-girdle muscular dystrophy type 2L"",""LGMD2L"",""muscular dystrophy, limb-girdle, type 2L""]"	"[{""label"":""Ano5"",""id"":""233246""}]"	"[""233246""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110284""}]"
DOID:0110285	"[""autosomal recessive limb-girdle muscular dystrophy type 2Q"",""LGMD2Q"",""autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency"",""muscular dystrophy, limb-girdle, type 2Q""]"	"[{""label"":""PLEC"",""id"":""5339""}]"	"[""5339""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110285""}]"
DOID:0110288	"[""autosomal recessive limb-girdle muscular dystrophy type 2W"",""LGMD2W"",""muscular dystrophy, limb-girdle, type 2W""]"	"[{""label"":""LIMS2"",""id"":""55679""}]"	"[""55679""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110288""}]"
DOID:0110289	"[""autosomal recessive limb-girdle muscular dystrophy type 2Y"",""LGMD2Y"",""autosomal recessive muscular dystrophy due to LAP1B deficiency"",""autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency"",""muscular dystrophy with progressive weakness, distal contractures and rigid spine"",""muscular dystrophy, limb-girdle, type 2Y""]"	"[{""label"":""TOR1AIP1"",""id"":""26092""}]"	"[""26092""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110289""}]"
DOID:0110290	"[""autosomal recessive limb-girdle muscular dystrophy type 2X"",""LGMD2X"",""muscular dystrophy, limb-girdle, type 2X""]"	"[{""label"":""POPDC1"",""id"":""11149""}]"	"[""11149""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110290""}]"
DOID:0110291	"[""Leber congenital amaurosis 10"",""LCA10""]"	"[{""label"":""Cep290"",""id"":""216274""}]"	"[""216274""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110291""}]"
DOID:0110292	"[""autosomal recessive limb-girdle muscular dystrophy type 2O"",""LGMD2O"",""MDDGC3"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C3"",""muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related""]"	"[{""label"":""POMGNT1"",""id"":""55624""}]"	"[""55624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110292""}]"
DOID:0110293	"[""autosomal recessive limb-girdle muscular dystrophy type 2P"",""LGMD2P"",""MDDGC9"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C9"",""muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related""]"	"[{""label"":""Dag1"",""id"":""13138""}]"	"[""13138""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110293""}]"
DOID:0110293	"[""autosomal recessive limb-girdle muscular dystrophy type 2P"",""LGMD2P"",""MDDGC9"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C9"",""muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related""]"	"[{""label"":""DAG1"",""id"":""1605""}]"	"[""1605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110293""}]"
DOID:0110294	"[""autosomal recessive limb-girdle muscular dystrophy type 2T"",""LGMD2T"",""MDDGC14"",""muscular dystrophy limb-girdle type 2T"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C14"",""muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related""]"	"[{""label"":""GMPPB"",""id"":""29925""}]"	"[""29925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110294""}]"
DOID:0110295	"[""autosomal recessive limb-girdle muscular dystrophy type 2U"",""LGMD2U"",""MDDGC7"",""autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency"",""muscular dystrophy limb-girdle type 2U"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C7""]"	"[{""label"":""Crppa"",""id"":""75847""}]"	"[""75847""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110295""}]"
DOID:0110295	"[""autosomal recessive limb-girdle muscular dystrophy type 2U"",""LGMD2U"",""MDDGC7"",""autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency"",""muscular dystrophy limb-girdle type 2U"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C7""]"	"[{""label"":""CRPPA"",""id"":""729920""}]"	"[""729920""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110295""}]"
DOID:0110296	"[""autosomal recessive limb-girdle muscular dystrophy type 2M"",""LGMD2M"",""MDDGC4"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4""]"	"[{""label"":""FKTN"",""id"":""2218""}]"	"[""2218""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00379""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110296""}]"
DOID:0110297	"[""autosomal recessive limb-girdle muscular dystrophy type 2K"",""LGMD2K"",""MDDGC1"",""limb-girdle muscular dystrophy-intellectual disability syndrome"",""muscular dystrophy limb-girdle type 2K"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1""]"	"[{""label"":""POMT1"",""id"":""10585""}]"	"[""10585""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110297""}]"
DOID:0110298	"[""autosomal recessive limb-girdle muscular dystrophy type 2N"",""LGMD2N"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2"",""muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related""]"	"[{""label"":""POMT2"",""id"":""29954""}]"	"[""29954""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110298""}]"
DOID:0110299	"[""autosomal recessive limb-girdle muscular dystrophy type 2I"",""LGMD2I"",""Limb-girdle muscular dystrophy due to FKRP deficiency"",""MDDGC5"",""muscular dystrophy limb-girdle type 2I"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5"",""muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related""]"	"[{""label"":""Fkrp"",""id"":""243853""}]"	"[""243853""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110299""}]"
DOID:0110299	"[""autosomal recessive limb-girdle muscular dystrophy type 2I"",""LGMD2I"",""Limb-girdle muscular dystrophy due to FKRP deficiency"",""MDDGC5"",""muscular dystrophy limb-girdle type 2I"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5"",""muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related""]"	"[{""label"":""FKRP"",""id"":""79147""}]"	"[""79147""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00382""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110299""}]"
DOID:0110307	"[""hypertrophic cardiomyopathy 1"",""CMH1"",""cardiomyopathy, familial hypertrophic 1"",""hypertrophic cardiomyopathy 19""]"	"[{""label"":""MYH7"",""id"":""4625""}]"	"[""4625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110307""}]"
DOID:0110310	"[""hypertrophic cardiomyopathy 4"",""CMH4"",""cardiomyopathy, familial hypertrophic, 4""]"	"[{""label"":""MYBPC3"",""id"":""4607""}]"	"[""4607""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110310""}]"
DOID:0110312	"[""hypertrophic cardiomyopathy 6"",""CMH6"",""cardiomyopathy, familial hypertrophic 6""]"	"[{""label"":""PRKAG2"",""id"":""51422""}]"	"[""51422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110312""}]"
DOID:0110313	"[""hypertrophic cardiomyopathy 7"",""CMH7"",""cardiomyopathy, familial hypertrophic 7""]"	"[{""label"":""TNNI3"",""id"":""7137""}]"	"[""7137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110313""}]"
DOID:0110313	"[""hypertrophic cardiomyopathy 7"",""CMH7"",""cardiomyopathy, familial hypertrophic 7""]"	"[{""label"":""Tnni3"",""id"":""21954""}]"	"[""21954""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110313""}]"
DOID:0110315	"[""hypertrophic cardiomyopathy 9"",""CMH9"",""cardiomyopathy, familial hypertrophic, 9""]"	"[{""label"":""TTN"",""id"":""7273""}]"	"[""7273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110315""}]"
DOID:0110317	"[""hypertrophic cardiomyopathy 11"",""CMH11"",""cardiomyopathy familial hypertrophic 11""]"	"[{""label"":""ACTC1"",""id"":""70""}]"	"[""70""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110317""}]"
DOID:0110320	"[""hypertrophic cardiomyopathy 14"",""CMH14"",""cardiomyopathy familial hypertrophic 14""]"	"[{""label"":""Myh6"",""id"":""17888""}]"	"[""17888""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110320""}]"
DOID:0110321	"[""hypertrophic cardiomyopathy 15"",""CMH15"",""cardiomyopathy familial hypertrophic 15""]"	"[{""label"":""VCL"",""id"":""7414""}]"	"[""7414""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110321""}]"
DOID:0110326	"[""hypertrophic cardiomyopathy 20"",""CMH20"",""cardiomyopathy familial hypertrophic 20""]"	"[{""label"":""NEXN"",""id"":""91624""}]"	"[""91624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110326""}]"
DOID:0110327	"[""hypertrophic cardiomyopathy 26"",""CMH26"",""cardiomyopathy familial hypertrophic 26""]"	"[{""label"":""FLNC"",""id"":""2318""}]"	"[""2318""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110327""}]"
DOID:0110334	"[""osteogenesis imperfecta type 1"",""OI1"",""osteogenesis imperfecta type I""]"	"[{""label"":""Col1a1"",""id"":""12842""}]"	"[""12842""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110334""}]"
DOID:0110334	"[""osteogenesis imperfecta type 1"",""OI1"",""osteogenesis imperfecta type I""]"	"[{""label"":""COL1A1"",""id"":""1277""}]"	"[""1277""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110334""}]"
DOID:0110336	"[""osteogenesis imperfecta type 8"",""OI8"",""osteogenesis imperfecta type VIII""]"	"[{""label"":""P3h1"",""id"":""56401""}]"	"[""56401""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110336""}]"
DOID:0110336	"[""osteogenesis imperfecta type 8"",""OI8"",""osteogenesis imperfecta type VIII""]"	"[{""label"":""P3H1"",""id"":""64175""}]"	"[""64175""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110336""}]"
DOID:0110337	"[""osteogenesis imperfecta type 7"",""OI7"",""osteogenesis imperfecta type VII""]"	"[{""label"":""Crtap"",""id"":""56693""}]"	"[""56693""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110337""}]"
DOID:0110337	"[""osteogenesis imperfecta type 7"",""OI7"",""osteogenesis imperfecta type VII""]"	"[{""label"":""CRTAP"",""id"":""10491""}]"	"[""10491""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110337""}]"
DOID:0110338	"[""osteogenesis imperfecta type 17"",""OI17"",""osteogenesis imperfecta type XVII""]"	"[{""label"":""SPARC"",""id"":""6678""}]"	"[""6678""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110338""}]"
DOID:0110339	"[""osteogenesis imperfecta type 3"",""OI3"",""osteogenesis imperfecta type III"",""progressively deforming osteogenesis imperfecta with normal sclera""]"	"[{""label"":""Col1a1"",""id"":""12842""},{""label"":""Col1a2"",""id"":""12843""}]"	"[""12842"",""12843""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110339""}]"
DOID:0110339	"[""osteogenesis imperfecta type 3"",""OI3"",""osteogenesis imperfecta type III"",""progressively deforming osteogenesis imperfecta with normal sclera""]"	"[{""label"":""COL1A1"",""id"":""1277""},{""label"":""COL1A2"",""id"":""1278""}]"	"[""1277"",""1278""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110339""}]"
DOID:0110340	"[""osteogenesis imperfecta type 4"",""OI4"",""osteogenesis imperfecta type IV"",""osteogenesis imperfecta with normal sclera""]"	"[{""label"":""COL1A1"",""id"":""1277""},{""label"":""COL1A2"",""id"":""1278""}]"	"[""1277"",""1278""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110340""}]"
DOID:0110340	"[""osteogenesis imperfecta type 4"",""OI4"",""osteogenesis imperfecta type IV"",""osteogenesis imperfecta with normal sclera""]"	"[{""label"":""Col1a1"",""id"":""12842""}]"	"[""12842""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110340""}]"
DOID:0110341	"[""osteogenesis imperfecta type 2"",""OI2"",""Vrolik type of osteogenesis imperfecta"",""osteogenesis imperfecta type II"",""perinatal lethal osteogenesis imperfecta congenita""]"	"[{""label"":""Col1a1"",""id"":""12842""}]"	"[""12842""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110341""}]"
DOID:0110341	"[""osteogenesis imperfecta type 2"",""OI2"",""Vrolik type of osteogenesis imperfecta"",""osteogenesis imperfecta type II"",""perinatal lethal osteogenesis imperfecta congenita""]"	"[{""label"":""COL1A1"",""id"":""1277""},{""label"":""COL1A2"",""id"":""1278""}]"	"[""1277"",""1278""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110341""}]"
DOID:0110342	"[""osteogenesis imperfecta type 13"",""OI13"",""osteogenesis imperfecta type XIII""]"	"[{""label"":""BMP1"",""id"":""649""}]"	"[""649""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110342""}]"
DOID:0110344	"[""osteogenesis imperfecta type 5"",""OI5"",""osteogenesis imperfecta type V""]"	"[{""label"":""Suco"",""id"":""226551""}]"	"[""226551""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110344""}]"
DOID:0110345	"[""osteogenesis imperfecta type 16"",""OI16"",""chromosome 11p11.2 deletion syndrome 91.3-KB"",""osteogenesis imperfecta type XVI""]"	"[{""label"":""CREB3L1"",""id"":""90993""}]"	"[""90993""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110345""}]"
DOID:0110346	"[""osteogenesis imperfecta type 10"",""OI10"",""osteogenesis imperfecta type X""]"	"[{""label"":""SERPINH1"",""id"":""871""}]"	"[""871""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110346""}]"
DOID:0110346	"[""osteogenesis imperfecta type 10"",""OI10"",""osteogenesis imperfecta type X""]"	"[{""label"":""Serpinh1"",""id"":""12406""}]"	"[""12406""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110346""}]"
DOID:0110347	"[""osteogenesis imperfecta type 15"",""OI15"",""osteogenesis imperfecta type XV""]"	"[{""label"":""WNT1"",""id"":""7471""}]"	"[""7471""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110347""}]"
DOID:0110348	"[""osteogenesis imperfecta type 12"",""OI12"",""osteogenesis imperfecta type XII""]"	"[{""label"":""SP7"",""id"":""121340""}]"	"[""121340""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110348""}]"
DOID:0110349	"[""osteogenesis imperfecta type 9"",""OI9"",""osteogenesis imperfecta type IX""]"	"[{""label"":""Ppib"",""id"":""19035""}]"	"[""19035""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110349""}]"
DOID:0110349	"[""osteogenesis imperfecta type 9"",""OI9"",""osteogenesis imperfecta type IX""]"	"[{""label"":""PPIB"",""id"":""5479""}]"	"[""5479""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110349""}]"
DOID:0110350	"[""osteogenesis imperfecta type 6"",""OI6"",""osteogenesis imperfecta type VI""]"	"[{""label"":""Serpinf1"",""id"":""20317""}]"	"[""20317""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110350""}]"
DOID:0110350	"[""osteogenesis imperfecta type 6"",""OI6"",""osteogenesis imperfecta type VI""]"	"[{""label"":""SERPINF1"",""id"":""5176""}]"	"[""5176""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110350""}]"
DOID:0110351	"[""osteogenesis imperfecta type 11"",""OI11"",""osteogenesis imperfecta type XI""]"	"[{""label"":""FKBP10"",""id"":""60681""}]"	"[""60681""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110351""}]"
DOID:0110352	"[""retinitis pigmentosa 59"",""RP59""]"	"[{""label"":""DHDDS"",""id"":""79947""}]"	"[""79947""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110352""}]"
DOID:0110354	"[""retinitis pigmentosa 19"",""RP19""]"	"[{""label"":""Abca4"",""id"":""11304""}]"	"[""11304""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110354""}]"
DOID:0110354	"[""retinitis pigmentosa 19"",""RP19""]"	"[{""label"":""ABCA4"",""id"":""24""}]"	"[""24""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110354""}]"
DOID:0110355	"[""retinitis pigmentosa 32"",""RP32""]"	"[{""label"":""CLCC1"",""id"":""23155""}]"	"[""23155""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110355""}]"
DOID:0110356	"[""retinitis pigmentosa 18"",""RP18""]"	"[{""label"":""PRPF3"",""id"":""9129""}]"	"[""9129""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110356""}]"
DOID:0110357	"[""retinitis pigmentosa 35"",""RP35""]"	"[{""label"":""SEMA4A"",""id"":""64218""}]"	"[""64218""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110357""}]"
DOID:0110358	"[""retinitis pigmentosa 12"",""RP12""]"	"[{""label"":""CRB1"",""id"":""23418""}]"	"[""23418""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110358""}]"
DOID:0110358	"[""retinitis pigmentosa 12"",""RP12""]"	"[{""label"":""Crb1"",""id"":""170788""}]"	"[""170788""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110358""}]"
DOID:0110360	"[""retinitis pigmentosa 39"",""RP39""]"	"[{""label"":""USH2A"",""id"":""7399""}]"	"[""7399""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110360""}]"
DOID:0110361	"[""retinitis pigmentosa 75"",""RP75""]"	"[{""label"":""AGBL5"",""id"":""60509""}]"	"[""60509""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110361""}]"
DOID:0110365	"[""retinitis pigmentosa 28"",""RP28""]"	"[{""label"":""FAM161A"",""id"":""84140""}]"	"[""84140""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110365""}]"
DOID:0110366	"[""retinitis pigmentosa 33"",""RP33""]"	"[{""label"":""SNRNP200"",""id"":""23020""}]"	"[""23020""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110366""}]"
DOID:0110367	"[""retinitis pigmentosa 38"",""RP38""]"	"[{""label"":""MERTK"",""id"":""10461""}]"	"[""10461""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110367""}]"
DOID:0110371	"[""retinitis pigmentosa 56"",""RP56""]"	"[{""label"":""IMPG2"",""id"":""50939""}]"	"[""50939""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110371""}]"
DOID:0110371	"[""retinitis pigmentosa 56"",""RP56""]"	"[{""label"":""Impg2"",""id"":""224224""}]"	"[""224224""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110371""}]"
DOID:0110372	"[""retinitis pigmentosa 4"",""RP4""]"	"[{""label"":""Rho"",""id"":""212541""}]"	"[""212541""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110372""}]"
DOID:0110372	"[""retinitis pigmentosa 4"",""RP4""]"	"[{""label"":""ninaE"",""id"":""42367""}]"	"[""42367""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110372""}]"
DOID:0110372	"[""retinitis pigmentosa 4"",""RP4""]"	"[{""label"":""RHO"",""id"":""6010""}]"	"[""6010""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110372""}]"
DOID:0110373	"[""retinitis pigmentosa 61"",""RP61""]"	"[{""label"":""CLRN1"",""id"":""7401""}]"	"[""7401""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110373""}]"
DOID:0110374	"[""retinitis pigmentosa 68"",""RP68""]"	"[{""label"":""SLC7A14"",""id"":""57709""}]"	"[""57709""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110374""}]"
DOID:0110375	"[""retinitis pigmentosa 40"",""RP40""]"	"[{""label"":""PDE6B"",""id"":""5158""}]"	"[""5158""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110375""}]"
DOID:0110376	"[""retinitis pigmentosa 41"",""RP41""]"	"[{""label"":""Prom1"",""id"":""19126""}]"	"[""19126""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110376""}]"
DOID:0110376	"[""retinitis pigmentosa 41"",""RP41""]"	"[{""label"":""PROM1"",""id"":""8842""}]"	"[""8842""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110376""}]"
DOID:0110377	"[""retinitis pigmentosa 49"",""RP49""]"	"[{""label"":""Cnga1"",""id"":""12788""}]"	"[""12788""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110377""}]"
DOID:0110377	"[""retinitis pigmentosa 49"",""RP49""]"	"[{""label"":""CNGA1"",""id"":""1259""}]"	"[""1259""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110377""}]"
DOID:0110381	"[""retinitis pigmentosa 14"",""RP14""]"	"[{""label"":""Tulp1"",""id"":""22157""}]"	"[""22157""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110381""}]"
DOID:0110383	"[""retinitis pigmentosa 7"",""RP7""]"	"[{""label"":""Prph2"",""id"":""19133""}]"	"[""19133""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110383""}]"
DOID:0110383	"[""retinitis pigmentosa 7"",""RP7""]"	"[{""label"":""PRPH2"",""id"":""5961""},{""label"":""ROM1"",""id"":""6094""}]"	"[""5961"",""6094""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110383""}]"
DOID:0110384	"[""retinitis pigmentosa 25"",""RP25""]"	"[{""label"":""EYS"",""id"":""346007""}]"	"[""346007""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110384""}]"
DOID:0110386	"[""retinitis pigmentosa 42"",""RP42""]"	"[{""label"":""KLHL7"",""id"":""55975""}]"	"[""55975""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110386""}]"
DOID:0110389	"[""retinitis pigmentosa 73"",""RP73""]"	"[{""label"":""HGSNAT"",""id"":""138050""}]"	"[""138050""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110389""}]"
DOID:0110390	"[""retinitis pigmentosa 1"",""RP1""]"	"[{""label"":""RP1"",""id"":""6101""}]"	"[""6101""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110390""}]"
DOID:0110392	"[""retinitis pigmentosa 70"",""RP70""]"	"[{""label"":""PRPF4"",""id"":""9128""}]"	"[""9128""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110392""}]"
DOID:0110393	"[""retinitis pigmentosa 66"",""RP66""]"	"[{""label"":""RBP3"",""id"":""5949""}]"	"[""5949""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110393""}]"
DOID:0110394	"[""retinitis pigmentosa 44"",""RP44""]"	"[{""label"":""RGR"",""id"":""5995""}]"	"[""5995""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110394""}]"
DOID:0110395	"[""retinitis pigmentosa 72"",""RP72""]"	"[{""label"":""ZNF408"",""id"":""79797""}]"	"[""79797""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110395""}]"
DOID:0110398	"[""retinitis pigmentosa 51"",""RP51""]"	"[{""label"":""TTC8"",""id"":""123016""}]"	"[""123016""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110398""}]"
DOID:0110399	"[""retinitis pigmentosa 37"",""RP37""]"	"[{""label"":""NR2E3"",""id"":""10002""}]"	"[""10002""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110399""}]"
DOID:0110401	"[""retinitis pigmentosa 74"",""RP74""]"	"[{""label"":""BBS2"",""id"":""583""}]"	"[""583""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110401""}]"
DOID:0110402	"[""retinitis pigmentosa 45"",""RP45""]"	"[{""label"":""CNGB1"",""id"":""1258""}]"	"[""1258""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110402""}]"
DOID:0110403	"[""retinitis pigmentosa 13"",""RP13""]"	"[{""label"":""Prpf8"",""id"":""192159""}]"	"[""192159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110403""}]"
DOID:0110403	"[""retinitis pigmentosa 13"",""RP13""]"	"[{""label"":""PRPF8"",""id"":""10594""}]"	"[""10594""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110403""}]"
DOID:0110409	"[""retinitis pigmentosa 46"",""RP46""]"	"[{""label"":""IDH3B"",""id"":""3420""}]"	"[""3420""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110409""}]"
DOID:0110411	"[""retinitis pigmentosa 60"",""RP60""]"	"[{""label"":""PRPF6"",""id"":""24148""}]"	"[""24148""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110411""}]"
DOID:0110414	"[""retinitis pigmentosa 3"",""RP3""]"	"[{""label"":""Rpgr"",""id"":""19893""}]"	"[""19893""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110414""}]"
DOID:0110414	"[""retinitis pigmentosa 3"",""RP3""]"	"[{""label"":""RPGRIP1L"",""id"":""23322""}]"	"[""23322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110414""}]"
DOID:0110415	"[""retinitis pigmentosa 2"",""RP2""]"	"[{""label"":""Arl3"",""id"":""56350""}]"	"[""56350""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110415""}]"
DOID:0110423	"[""dilated cardiomyopathy 1C"",""CMDC1"",""dilated cardiomyopathy 1C with or without left ventricular noncompaction""]"	"[{""label"":""Ldb3"",""id"":""24131""}]"	"[""24131""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110423""}]"
DOID:0110423	"[""dilated cardiomyopathy 1C"",""CMDC1"",""dilated cardiomyopathy 1C with or without left ventricular noncompaction""]"	"[{""label"":""LDB3"",""id"":""11155""}]"	"[""11155""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110423""}]"
DOID:0110424	"[""dilated cardiomyopathy 1CC"",""CMD1CC""]"	"[{""label"":""NEXN"",""id"":""91624""}]"	"[""91624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110424""}]"
DOID:0110425	"[""dilated cardiomyopathy 1A"",""CDCD1"",""dilated cardiomyopathy with conduction defect 1"",""familial dilated cardiomyopathy with conduction defect due to LMNA mutation""]"	"[{""label"":""Dot1l"",""id"":""208266""},{""label"":""Lmna"",""id"":""16905""}]"	"[""16905"",""208266""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110425""}]"
DOID:0110425	"[""dilated cardiomyopathy 1A"",""CDCD1"",""dilated cardiomyopathy with conduction defect 1"",""familial dilated cardiomyopathy with conduction defect due to LMNA mutation""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110425""}]"
DOID:0110428	"[""dilated cardiomyopathy 1AA"",""CMD1AA"",""dilated cardiomyopathy 1AA with or without left ventricular noncompaction""]"	"[{""label"":""ACTN2"",""id"":""88""}]"	"[""88""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110428""}]"
DOID:0110429	"[""dilated cardiomyopathy 1H"",""dilated cardiomyopathy with conduction defect""]"	"[{""label"":""ADRB3"",""id"":""155""},{""label"":""CYP11B2"",""id"":""1585""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""155"",""1585"",""3117"",""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110429""}]"
DOID:0110430	"[""dilated cardiomyopathy 1G"",""CMD1G""]"	"[{""label"":""TTN"",""id"":""7273""}]"	"[""7273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110430""}]"
DOID:0110430	"[""dilated cardiomyopathy 1G"",""CMD1G""]"	"[{""label"":""Ttn"",""id"":""22138""}]"	"[""22138""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110430""}]"
DOID:0110431	"[""dilated cardiomyopathy 1I"",""CMD1I""]"	"[{""label"":""DES"",""id"":""1674""}]"	"[""1674""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110431""}]"
DOID:0110431	"[""dilated cardiomyopathy 1I"",""CMD1I""]"	"[{""label"":""Des"",""id"":""13346""}]"	"[""13346""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110431""}]"
DOID:0110432	"[""dilated cardiomyopathy 1NN"",""CMD1NN""]"	"[{""label"":""RAF1"",""id"":""5894""}]"	"[""5894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110432""}]"
DOID:0110433	"[""dilated cardiomyopathy 1E"",""CDCD2"",""CMD1E"",""dilated cardiomyopathy with conduction defect 2"",""dilated cardiomyopathy with conduction disorder and arrhythmia""]"	"[{""label"":""SCN5A"",""id"":""6331""}]"	"[""6331""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110433""}]"
DOID:0110435	"[""dilated cardiomyopathy 1GG"",""CMD1GG""]"	"[{""label"":""SDHA"",""id"":""6389""}]"	"[""6389""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110435""}]"
DOID:0110436	"[""dilated cardiomyopathy 1L"",""CMD1L""]"	"[{""label"":""Sgcd"",""id"":""24052""}]"	"[""24052""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110436""}]"
DOID:0110436	"[""dilated cardiomyopathy 1L"",""CMD1L""]"	"[{""label"":""SGCD"",""id"":""6444""}]"	"[""6444""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110436""}]"
DOID:0110438	"[""dilated cardiomyopathy 1JJ"",""CMD1JJ""]"	"[{""label"":""LAMA4"",""id"":""3910""}]"	"[""3910""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110438""}]"
DOID:0110440	"[""dilated cardiomyopathy 1J"",""CMD1J"",""autosomal dominant dilated cardiomyopathy with sensorineural hearing loss"",""neurosensory deafness with dilated cardiomyopathy"",""neurosensory hearing loss with dilated cardiomyopathy"",""sensorineural deafness with dilated cardiomyopathy"",""sensorineural hearing loss with dilated cardiomyopathy""]"	"[{""label"":""EYA4"",""id"":""2070""}]"	"[""2070""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110440""}]"
DOID:0110441	"[""dilated cardiomyopathy 2B"",""CMD2B""]"	"[{""label"":""GATAD1"",""id"":""57798""}]"	"[""57798""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110441""}]"
DOID:0110443	"[""dilated cardiomyopathy 1B""]"	"[{""label"":""FKTN"",""id"":""2218""}]"	"[""2218""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110443""}]"
DOID:0110444	"[""dilated cardiomyopathy 1X"",""CMD1X"",""dilated cardiomyopathy with mild or no proximal muscle weakness""]"	"[{""label"":""FKTN"",""id"":""2218""}]"	"[""2218""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00380""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110444""}]"
DOID:0110445	"[""dilated cardiomyopathy 1KK"",""CMD1KK""]"	"[{""label"":""MYPN"",""id"":""84665""}]"	"[""84665""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110445""}]"
DOID:0110446	"[""dilated cardiomyopathy 1W"",""CMD1W""]"	"[{""label"":""VCL"",""id"":""7414""}]"	"[""7414""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110446""}]"
DOID:0110447	"[""dilated cardiomyopathy 1DD"",""CMD1DD""]"	"[{""label"":""RBM20"",""id"":""282996""}]"	"[""282996""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110447""}]"
DOID:0110448	"[""dilated cardiomyopathy 1HH"",""CMD1HH""]"	"[{""label"":""Bag3"",""id"":""29810""}]"	"[""29810""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110448""}]"
DOID:0110448	"[""dilated cardiomyopathy 1HH"",""CMD1HH""]"	"[{""label"":""BAG3"",""id"":""9531""}]"	"[""9531""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110448""}]"
DOID:0110450	"[""dilated cardiomyopathy 1II"",""CMD1II""]"	"[{""label"":""CRYAB"",""id"":""1410""}]"	"[""1410""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110450""}]"
DOID:0110451	"[""dilated cardiomyopathy 1O"",""CMD1O"",""dilated cardiomyopathy with ventricular tachycardia""]"	"[{""label"":""ABCC9"",""id"":""10060""}]"	"[""10060""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110451""}]"
DOID:0110453	"[""dilated cardiomyopathy 1EE"",""CMD1EE""]"	"[{""label"":""Myh6"",""id"":""17888""}]"	"[""17888""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110453""}]"
DOID:0110454	"[""dilated cardiomyopathy 1S"",""CMD1S""]"	"[{""label"":""MYH7"",""id"":""4625""}]"	"[""4625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110454""}]"
DOID:0110456	"[""dilated cardiomyopathy 1R"",""CMD1R""]"	"[{""label"":""Actc1"",""id"":""11464""}]"	"[""11464""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110456""}]"
DOID:0110456	"[""dilated cardiomyopathy 1R"",""CMD1R""]"	"[{""label"":""ACTC1"",""id"":""70""}]"	"[""70""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110456""}]"
DOID:0110458	"[""dilated cardiomyopathy 1BB"",""CMD1BB""]"	"[{""label"":""DSG2"",""id"":""1829""}]"	"[""1829""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110458""}]"
DOID:0110459	"[""dilated cardiomyopathy 1FF"",""CMD1FF""]"	"[{""label"":""TNNI3"",""id"":""7137""}]"	"[""7137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110459""}]"
DOID:0110460	"[""dilated cardiomyopathy 2A"",""CMD2A""]"	"[{""label"":""TNNI3"",""id"":""7137""}]"	"[""7137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110460""}]"
DOID:0110461	"[""X-linked dilated cardiomyopathy"",""CMD3B"",""DMD-related dilated cardiomyopathy"",""XLCM"",""dilated cardiomyopathy 3B""]"	"[{""label"":""DMD"",""id"":""1756""}]"	"[""1756""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110461""}]"
DOID:0110463	"[""autosomal recessive nonsyndromic deafness 102"",""DFNB102"",""autosomal recessive deafness 102""]"	"[{""label"":""EPS8"",""id"":""2059""}]"	"[""2059""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110463""}]"
DOID:0110465	"[""autosomal recessive nonsyndromic deafness 104"",""DFNB104"",""autosomal recessive deafness 104""]"	"[{""label"":""RIPOR2"",""id"":""9750""}]"	"[""9750""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110465""}]"
DOID:0110467	"[""autosomal recessive nonsyndromic deafness 12"",""DFNB12"",""autosomal recessive deafness 12""]"	"[{""label"":""Cdh23"",""id"":""22295""}]"	"[""22295""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110467""}]"
DOID:0110467	"[""autosomal recessive nonsyndromic deafness 12"",""DFNB12"",""autosomal recessive deafness 12""]"	"[{""label"":""CDH23"",""id"":""64072""}]"	"[""64072""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110467""}]"
DOID:0110471	"[""autosomal recessive nonsyndromic deafness 16"",""DFNB16"",""autosomal recessive deafness 16""]"	"[{""label"":""STRC"",""id"":""161497""}]"	"[""161497""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110471""}]"
DOID:0110471	"[""autosomal recessive nonsyndromic deafness 16"",""DFNB16"",""autosomal recessive deafness 16""]"	"[{""label"":""Strc"",""id"":""140476""}]"	"[""140476""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110471""}]"
DOID:0110474	"[""autosomal recessive nonsyndromic deafness 18B"",""DFNB18B"",""autosomal recessive deafness 18B""]"	"[{""label"":""OTOG"",""id"":""340990""}]"	"[""340990""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110474""}]"
DOID:0110474	"[""autosomal recessive nonsyndromic deafness 18B"",""DFNB18B"",""autosomal recessive deafness 18B""]"	"[{""label"":""Otog"",""id"":""18419""}]"	"[""18419""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110474""}]"
DOID:0110475	"[""autosomal recessive nonsyndromic deafness 1A"",""DFNB1A"",""autosomal recessive deafness 1A""]"	"[{""label"":""Gjb6"",""id"":""14623""}]"	"[""14623""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110475""}]"
DOID:0110477	"[""autosomal recessive nonsyndromic deafness 2"",""DFNB2"",""autosomal recessive deafness 2""]"	"[{""label"":""MYO7A"",""id"":""4647""}]"	"[""4647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110477""}]"
DOID:0110479	"[""autosomal recessive nonsyndromic deafness 21"",""DFNB21"",""autosomal recessive deafness 21""]"	"[{""label"":""TECTA"",""id"":""7007""}]"	"[""7007""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110479""}]"
DOID:0110480	"[""autosomal recessive nonsyndromic deafness 22"",""DFNB22"",""autosomal recessive deafness 22""]"	"[{""label"":""Otoa"",""id"":""246190""}]"	"[""246190""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110480""}]"
DOID:0110480	"[""autosomal recessive nonsyndromic deafness 22"",""DFNB22"",""autosomal recessive deafness 22""]"	"[{""label"":""OTOA"",""id"":""146183""}]"	"[""146183""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110480""}]"
DOID:0110481	"[""autosomal recessive nonsyndromic deafness 23"",""DFNB23"",""autosomal recessive deafness 23""]"	"[{""label"":""PCDH15"",""id"":""65217""}]"	"[""65217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110481""}]"
DOID:0110481	"[""autosomal recessive nonsyndromic deafness 23"",""DFNB23"",""autosomal recessive deafness 23""]"	"[{""label"":""Pcdh15"",""id"":""11994""}]"	"[""11994""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110481""}]"
DOID:0110482	"[""autosomal recessive nonsyndromic deafness 24"",""DFNB24"",""autosomal recessive deafness 24""]"	"[{""label"":""RDX"",""id"":""5962""}]"	"[""5962""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110482""}]"
DOID:0110484	"[""autosomal recessive nonsyndromic deafness 26"",""DFNB26"",""autosomal recessive deafness 26""]"	"[{""label"":""GAB1"",""id"":""2549""}]"	"[""2549""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110484""}]"
DOID:0110486	"[""autosomal recessive nonsyndromic deafness 28"",""DFNB28"",""autosomal recessive deafness 28""]"	"[{""label"":""Triobp"",""id"":""110253""}]"	"[""110253""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110486""}]"
DOID:0110486	"[""autosomal recessive nonsyndromic deafness 28"",""DFNB28"",""autosomal recessive deafness 28""]"	"[{""label"":""TRIOBP"",""id"":""11078""}]"	"[""11078""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110486""}]"
DOID:0110488	"[""autosomal recessive nonsyndromic deafness 3"",""DFNB3"",""NRSD3"",""autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3""]"	"[{""label"":""MYO15A"",""id"":""51168""}]"	"[""51168""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110488""}]"
DOID:0110490	"[""autosomal recessive nonsyndromic deafness 31"",""DFNB31"",""autosomal recessive deafness 31""]"	"[{""label"":""WHRN"",""id"":""25861""}]"	"[""25861""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110490""}]"
DOID:0110495	"[""autosomal recessive nonsyndromic deafness 37"",""DFNB37"",""autosomal recessive deafness 37""]"	"[{""label"":""Myo6"",""id"":""17920""}]"	"[""17920""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110495""}]"
DOID:0110495	"[""autosomal recessive nonsyndromic deafness 37"",""DFNB37"",""autosomal recessive deafness 37""]"	"[{""label"":""MYO6"",""id"":""4646""}]"	"[""4646""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110495""}]"
DOID:0110497	"[""autosomal recessive nonsyndromic deafness 39"",""DFNB39"",""autosomal recessive deafness 39""]"	"[{""label"":""HGF"",""id"":""3082""}]"	"[""3082""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110497""}]"
DOID:0110497	"[""autosomal recessive nonsyndromic deafness 39"",""DFNB39"",""autosomal recessive deafness 39""]"	"[{""label"":""Hgf"",""id"":""15234""}]"	"[""15234""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110497""}]"
DOID:0110500	"[""autosomal recessive nonsyndromic deafness 42"",""DFNB42"",""autosomal recessive deafness 42""]"	"[{""label"":""ILDR1"",""id"":""286676""}]"	"[""286676""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110500""}]"
DOID:0110500	"[""autosomal recessive nonsyndromic deafness 42"",""DFNB42"",""autosomal recessive deafness 42""]"	"[{""label"":""Ildr1"",""id"":""106347""}]"	"[""106347""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110500""}]"
DOID:0110501	"[""autosomal recessive nonsyndromic deafness 44"",""DFNB44"",""autosomal recessive deafness 44""]"	"[{""label"":""ADCY1"",""id"":""107""}]"	"[""107""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110501""}]"
DOID:0110509	"[""autosomal recessive nonsyndromic deafness 53"",""DFNB53"",""autosomal recessive deafness 53""]"	"[{""label"":""COL11A2"",""id"":""1302""}]"	"[""1302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110509""}]"
DOID:0110513	"[""autosomal recessive nonsyndromic deafness 61"",""DFNB61"",""autosomal recessive deafness 61""]"	"[{""label"":""SLC26A5"",""id"":""375611""}]"	"[""375611""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110513""}]"
DOID:0110515	"[""autosomal recessive nonsyndromic deafness 63"",""DFNB63"",""autosomal recessive deafness 63""]"	"[{""label"":""LRTOMT"",""id"":""220074""}]"	"[""220074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110515""}]"
DOID:0110519	"[""autosomal recessive nonsyndromic deafness 68"",""DFNB68"",""autosomal recessive deafness 68""]"	"[{""label"":""S1PR2"",""id"":""9294""}]"	"[""9294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110519""}]"
DOID:0110519	"[""autosomal recessive nonsyndromic deafness 68"",""DFNB68"",""autosomal recessive deafness 68""]"	"[{""label"":""S1pr2"",""id"":""14739""}]"	"[""14739""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110519""}]"
DOID:0110521	"[""autosomal recessive nonsyndromic deafness 70"",""DFNB70"",""autosomal recessive deafness 70""]"	"[{""label"":""PNPT1"",""id"":""87178""}]"	"[""87178""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110521""}]"
DOID:0110525	"[""autosomal recessive nonsyndromic deafness 77"",""DFNB77"",""autosomal recessive deafness 77""]"	"[{""label"":""LOXHD1"",""id"":""125336""}]"	"[""125336""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110525""}]"
DOID:0110526	"[""autosomal recessive nonsyndromic deafness 79"",""DFNB79"",""autosomal recessive deafness 79""]"	"[{""label"":""TPRN"",""id"":""286262""}]"	"[""286262""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110526""}]"
DOID:0110527	"[""autosomal recessive nonsyndromic deafness 8"",""DFNB10"",""DFNB8"",""NRSD8"",""autosomal recessive deafness 10"",""autosomal recessive deafness 8"",""childhood-onset neurosensory autosomal recessive deafness 8"",""neurosensory nonsyndromic recessive deafness 8""]"	"[{""label"":""TMPRSS3"",""id"":""64699""}]"	"[""64699""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110527""}]"
DOID:0110534	"[""autosomal recessive nonsyndromic deafness 89"",""DFNB89"",""autosomal recessive deafness 89""]"	"[{""label"":""KARS1"",""id"":""3735""}]"	"[""3735""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110534""}]"
DOID:0110536	"[""autosomal recessive nonsyndromic deafness 91"",""DFNB91"",""autosomal recessive deafness 91""]"	"[{""label"":""SERPINB6"",""id"":""5269""}]"	"[""5269""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110536""}]"
DOID:0110539	"[""autosomal recessive nonsyndromic deafness 97"",""DFNB97"",""autosomal recessive deafness 97""]"	"[{""label"":""MET"",""id"":""4233""}]"	"[""4233""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110539""}]"
DOID:0110540	"[""autosomal recessive nonsyndromic deafness 98"",""DFNB98"",""autosomal recessive deafness 98""]"	"[{""label"":""TSPEAR"",""id"":""54084""}]"	"[""54084""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110540""}]"
DOID:0110541	"[""autosomal dominant nonsyndromic deafness 1"",""DFNA1"",""Konigsmark syndrome"",""LFHL1"",""autosomal dominant deafness 1"",""autosomal dominant deafness 1, with or without thrombocytopenia"",""hereditary low frequency hearing loss 1""]"	"[{""label"":""DIAPH1"",""id"":""1729""}]"	"[""1729""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110541""}]"
DOID:0110542	"[""autosomal dominant nonsyndromic deafness 10"",""DFNA10"",""autosomal dominant deafness 10""]"	"[{""label"":""EYA4"",""id"":""2070""}]"	"[""2070""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110542""}]"
DOID:0110543	"[""autosomal dominant nonsyndromic deafness 11"",""DFNA11"",""autosomal dominant deafness 11""]"	"[{""label"":""MYO7A"",""id"":""4647""}]"	"[""4647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110543""}]"
DOID:0110544	"[""autosomal dominant nonsyndromic deafness 12"",""DFNA12"",""DFNA8"",""autosomal dominant deafness 12"",""autosomal dominant deafness 8""]"	"[{""label"":""TECTA"",""id"":""7007""}]"	"[""7007""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110544""}]"
DOID:0110544	"[""autosomal dominant nonsyndromic deafness 12"",""DFNA12"",""DFNA8"",""autosomal dominant deafness 12"",""autosomal dominant deafness 8""]"	"[{""label"":""Tecta"",""id"":""21683""}]"	"[""21683""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110544""}]"
DOID:0110545	"[""autosomal dominant nonsyndromic deafness 13"",""DFNA13"",""autosomal dominant deafness 13""]"	"[{""label"":""COL11A2"",""id"":""1302""}]"	"[""1302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110545""}]"
DOID:0110545	"[""autosomal dominant nonsyndromic deafness 13"",""DFNA13"",""autosomal dominant deafness 13""]"	"[{""label"":""Col11a2"",""id"":""12815""}]"	"[""12815""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110545""}]"
DOID:0110548	"[""autosomal dominant nonsyndromic deafness 17"",""DFNA17"",""autosomal dominant deafness 17""]"	"[{""label"":""MYH9"",""id"":""4627""}]"	"[""4627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110548""}]"
DOID:0110550	"[""autosomal dominant nonsyndromic deafness 20"",""DFNA20"",""DFNA26"",""autosomal dominant deafness 20""]"	"[{""label"":""ACTG1"",""id"":""71""}]"	"[""71""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110550""}]"
DOID:0110551	"[""autosomal dominant nonsyndromic deafness 21"",""DFNA21"",""autosomal dominant deafness 21""]"	"[{""label"":""RIPOR2"",""id"":""9750""}]"	"[""9750""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110551""}]"
DOID:0110552	"[""autosomal dominant nonsyndromic deafness 22"",""DFNA22"",""autosomal dominant deafness 22""]"	"[{""label"":""Myo6"",""id"":""17920""}]"	"[""17920""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110552""}]"
DOID:0110552	"[""autosomal dominant nonsyndromic deafness 22"",""DFNA22"",""autosomal dominant deafness 22""]"	"[{""label"":""MYO6"",""id"":""4646""}]"	"[""4646""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110552""}]"
DOID:0110553	"[""autosomal dominant nonsyndromic deafness 23"",""DFNA23"",""autosomal dominant deafness 23""]"	"[{""label"":""SIX1"",""id"":""6495""}]"	"[""6495""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110553""}]"
DOID:0110555	"[""autosomal dominant nonsyndromic deafness 25"",""DFNA25"",""autosomal dominant deafness 25""]"	"[{""label"":""Slc17a8"",""id"":""216227""},{""label"":""Trpv4"",""id"":""63873""}]"	"[""216227"",""63873""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110555""}]"
DOID:0110555	"[""autosomal dominant nonsyndromic deafness 25"",""DFNA25"",""autosomal dominant deafness 25""]"	"[{""label"":""SLC17A8"",""id"":""246213""}]"	"[""246213""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110555""}]"
DOID:0110556	"[""autosomal dominant nonsyndromic deafness 27"",""DFNA27"",""autosomal dominant deafness 27""]"	"[{""label"":""REST"",""id"":""5978""}]"	"[""5978""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110556""}]"
DOID:0110557	"[""autosomal dominant nonsyndromic deafness 28"",""DFNA28"",""autosomal dominant deafness 28""]"	"[{""label"":""GRHL2"",""id"":""79977""}]"	"[""79977""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110557""}]"
DOID:0110566	"[""autosomal dominant nonsyndromic deafness 40"",""DFNA40"",""autosomal dominant deafness 40""]"	"[{""label"":""CRYM"",""id"":""1428""}]"	"[""1428""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110566""}]"
DOID:0110567	"[""autosomal dominant nonsyndromic deafness 41"",""DFNA41"",""autosomal dominant deafness 41""]"	"[{""label"":""P2RX2"",""id"":""22953""}]"	"[""22953""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110567""}]"
DOID:0110567	"[""autosomal dominant nonsyndromic deafness 41"",""DFNA41"",""autosomal dominant deafness 41""]"	"[{""label"":""P2rx2"",""id"":""231602""}]"	"[""231602""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110567""}]"
DOID:0110569	"[""autosomal dominant nonsyndromic deafness 44"",""DFNA44"",""autosomal dominant deafness 44""]"	"[{""label"":""CCDC50"",""id"":""152137""}]"	"[""152137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110569""}]"
DOID:0110573	"[""autosomal dominant nonsyndromic deafness 4A"",""DFNA4A"",""autosomal dominant deafness 4A""]"	"[{""label"":""Ceacam16"",""id"":""330483""}]"	"[""330483""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110573""}]"
DOID:0110573	"[""autosomal dominant nonsyndromic deafness 4A"",""DFNA4A"",""autosomal dominant deafness 4A""]"	"[{""label"":""MYH14"",""id"":""79784""}]"	"[""79784""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110573""}]"
DOID:0110574	"[""autosomal dominant nonsyndromic deafness 4B"",""DFNA4B"",""autosomal dominant deafness 4B""]"	"[{""label"":""CEACAM16"",""id"":""388551""}]"	"[""388551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110574""}]"
DOID:0110581	"[""autosomal dominant nonsyndromic deafness 56"",""DFNA56"",""autosomal dominant deafness 56""]"	"[{""label"":""TNC"",""id"":""3371""}]"	"[""3371""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110581""}]"
DOID:0110584	"[""autosomal dominant nonsyndromic deafness 6"",""DFNA14"",""DFNA38"",""DFNA6"",""DFNA6/14/38"",""autosomal dominant deafness 14"",""autosomal dominant deafness 38"",""autosomal dominant deafness 6""]"	"[{""label"":""WFS1"",""id"":""7466""}]"	"[""7466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110584""}]"
DOID:0110587	"[""autosomal dominant nonsyndromic deafness 66"",""DFNA66"",""autosomal dominant deafness 66""]"	"[{""label"":""CD164"",""id"":""8763""}]"	"[""8763""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110587""}]"
DOID:0110589	"[""autosomal dominant nonsyndromic deafness 68"",""DFNA68"",""autosomal dominant deafness 68""]"	"[{""label"":""HOMER2"",""id"":""9455""}]"	"[""9455""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110589""}]"
DOID:0110590	"[""autosomal dominant nonsyndromic deafness 69"",""DCUA"",""DFNA69"",""autosomal dominant deafness 69"",""unilateral or asymmetric congenital deafness""]"	"[{""label"":""KITLG"",""id"":""4254""}]"	"[""4254""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110590""}]"
DOID:0110591	"[""autosomal dominant nonsyndromic deafness 7"",""DFNA7"",""autosomal dominant deafness 7""]"	"[{""label"":""LMX1A"",""id"":""4009""}]"	"[""4009""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110591""}]"
DOID:0110592	"[""autosomal dominant nonsyndromic deafness 70"",""DFNA70"",""autosomal dominant deafness 70""]"	"[{""label"":""MCM2"",""id"":""4171""}]"	"[""4171""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110592""}]"
DOID:0110593	"[""autosomal dominant nonsyndromic deafness 9"",""DFNA9"",""autosomal dominant deafness 9""]"	"[{""label"":""COCH"",""id"":""1690""}]"	"[""1690""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110593""}]"
DOID:0110593	"[""autosomal dominant nonsyndromic deafness 9"",""DFNA9"",""autosomal dominant deafness 9""]"	"[{""label"":""Coch"",""id"":""12810""}]"	"[""12810""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110593""}]"
DOID:0110594	"[""primary ciliary dyskinesia 1"",""CILD1"",""primary ciliary dyskinesia 1 with or without situs inversus""]"	"[{""label"":""Dnai1"",""id"":""68922""}]"	"[""68922""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110594""}]"
DOID:0110595	"[""Stromme syndrome"",""CILD31"",""apple peel syndrome with microcephaly and ocular anomalies"",""jejunal atresia with microcephaly and ocular anomalies"",""lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome"",""primary ciliary dyskinesia 31""]"	"[{""label"":""CENPF"",""id"":""1063""}]"	"[""1063""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110595""}]"
DOID:0110596	"[""primary ciliary dyskinesia 21"",""CILD21"",""primary ciliary dyskinesia 21 without situs inversus""]"	"[{""label"":""Drc1"",""id"":""381738""}]"	"[""381738""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110596""}]"
DOID:0110596	"[""primary ciliary dyskinesia 21"",""CILD21"",""primary ciliary dyskinesia 21 without situs inversus""]"	"[{""label"":""DRC1"",""id"":""92749""}]"	"[""92749""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110596""}]"
DOID:0110598	"[""primary ciliary dyskinesia 14"",""CILD14"",""primary ciliary dyskinesia 14 with or without situs inversus""]"	"[{""label"":""CCDC39"",""id"":""339829""}]"	"[""339829""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110598""}]"
DOID:0110599	"[""primary ciliary dyskinesia 3"",""CILD3"",""primary ciliary dyskinesia 3 with or without situs inversus""]"	"[{""label"":""Dnah5"",""id"":""110082""}]"	"[""110082""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110599""}]"
DOID:0110599	"[""primary ciliary dyskinesia 3"",""CILD3"",""primary ciliary dyskinesia 3 with or without situs inversus""]"	"[{""label"":""DNAH5"",""id"":""1767""}]"	"[""1767""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110599""}]"
DOID:0110605	"[""primary ciliary dyskinesia 7"",""CILD7"",""primary ciliary dyskinesia 7 with or without situs inversus""]"	"[{""label"":""Dnah11"",""id"":""13411""}]"	"[""13411""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110605""}]"
DOID:0110605	"[""primary ciliary dyskinesia 7"",""CILD7"",""primary ciliary dyskinesia 7 with or without situs inversus""]"	"[{""label"":""DNAH11"",""id"":""8701""}]"	"[""8701""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110605""}]"
DOID:0110607	"[""primary ciliary dyskinesia 28"",""CILD28"",""primary ciliary dyskinesia 28 with or without situs inversus""]"	"[{""label"":""SPAG1"",""id"":""6674""}]"	"[""6674""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110607""}]"
DOID:0110609	"[""primary ciliary dyskinesia 23"",""CILD23"",""primary ciliary dyskinesia 23 with or without situs inversus""]"	"[{""label"":""ODAD2"",""id"":""55130""}]"	"[""55130""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110609""}]"
DOID:0110612	"[""primary ciliary dyskinesia 10"",""CILD10"",""primary ciliary dyskinesia 10 with or without situs inversus""]"	"[{""label"":""DNAAF2"",""id"":""55172""}]"	"[""55172""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110612""}]"
DOID:0110612	"[""primary ciliary dyskinesia 10"",""CILD10"",""primary ciliary dyskinesia 10 with or without situs inversus""]"	"[{""label"":""Dnaaf2"",""id"":""109065""}]"	"[""109065""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110612""}]"
DOID:0110615	"[""primary ciliary dyskinesia 25"",""CILD25"",""primary ciliary dyskinesia 25 with or without situs inversus""]"	"[{""label"":""DNAAF4"",""id"":""161582""}]"	"[""161582""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110615""}]"
DOID:0110617	"[""primary ciliary dyskinesia 5"",""CILD5"",""primary ciliary dyskinesia 5 without situs inversus""]"	"[{""label"":""HYDIN"",""id"":""54768""}]"	"[""54768""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110617""}]"
DOID:0110624	"[""primary ciliary dyskinesia 30"",""CILD30"",""primary ciliary dyskinesia 30 without situs inversus""]"	"[{""label"":""ODAD3"",""id"":""115948""}]"	"[""115948""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110624""}]"
DOID:0110626	"[""primary ciliary dyskinesia 2"",""CILD2"",""primary ciliary dyskinesia 2 with or without situs inversus""]"	"[{""label"":""DNAAF3"",""id"":""352909""}]"	"[""352909""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110626""}]"
DOID:0110629	"[""Wolfram syndrome 1"",""DIDMOAD"",""WFS1"",""diabetes mellitus AND insipidus with optic atrophy AND deafness""]"	"[{""label"":""wfs1"",""id"":""42679""}]"	"[""42679""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110629""}]"
DOID:0110629	"[""Wolfram syndrome 1"",""DIDMOAD"",""WFS1"",""diabetes mellitus AND insipidus with optic atrophy AND deafness""]"	"[{""label"":""Wfs1"",""id"":""22393""}]"	"[""22393""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110629""}]"
DOID:0110629	"[""Wolfram syndrome 1"",""DIDMOAD"",""WFS1"",""diabetes mellitus AND insipidus with optic atrophy AND deafness""]"	"[{""label"":""WFS1"",""id"":""7466""}]"	"[""7466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110629""}]"
DOID:0110632	"[""megaconial type congenital muscular dystrophy"",""congenital megaconial myopathy"",""congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect"",""congenital muscular dystrophy with mitochondrial structural abnormalities"",""megaconial congenital muscular dystrophy""]"	"[{""label"":""CHKB"",""id"":""1120""}]"	"[""1120""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110632""}]"
DOID:0110633	"[""rigid spine muscular dystrophy 1"",""Eichsfeld type congenital muscular dystrophy"",""MDRS1"",""RSMD1"",""RSS"",""SEPN1-related myopathy"",""classic MmD"",""classic multiminicore disease"",""classic multiminicore myopathy"",""congenital merosin-positive muscular dystrophy with early spine rigidity"",""desmin-related myopathy with Mallory bodies"",""desmin-related myopathy with Mallory body-like inclusions"",""early-onset desmin-related myopathy"",""rigid spine syndrome"",""severe classic form minicore myopathy"",""severe classic form multicore myopathy"",""severe classic form multiminicore disease""]"	"[{""label"":""SELENON"",""id"":""57190""}]"	"[""57190""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110633""}]"
DOID:0110633	"[""rigid spine muscular dystrophy 1"",""Eichsfeld type congenital muscular dystrophy"",""MDRS1"",""RSMD1"",""RSS"",""SEPN1-related myopathy"",""classic MmD"",""classic multiminicore disease"",""classic multiminicore myopathy"",""congenital merosin-positive muscular dystrophy with early spine rigidity"",""desmin-related myopathy with Mallory bodies"",""desmin-related myopathy with Mallory body-like inclusions"",""early-onset desmin-related myopathy"",""rigid spine syndrome"",""severe classic form minicore myopathy"",""severe classic form multicore myopathy"",""severe classic form multiminicore disease""]"	"[{""label"":""Selenon"",""id"":""74777""}]"	"[""74777""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110633""}]"
DOID:0110635	"[""muscular dystrophy-dystroglycanopathy type B5"",""FKRP-related congenital muscular dystrophy"",""MDC1C"",""MDDGB5"",""congenital muscular dystrophy 1C"",""muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5"",""muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5""]"	"[{""label"":""Fkrp"",""id"":""243853""}]"	"[""243853""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110635""}]"
DOID:0110635	"[""muscular dystrophy-dystroglycanopathy type B5"",""FKRP-related congenital muscular dystrophy"",""MDC1C"",""MDDGB5"",""congenital muscular dystrophy 1C"",""muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5"",""muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5""]"	"[{""label"":""FKRP"",""id"":""79147""}]"	"[""79147""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00381""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110635""}]"
DOID:0110636	"[""congenital merosin-deficient muscular dystrophy 1A"",""CMD1A"",""MDC1A"",""Merosin-negative congenital muscular dystrophy"",""congenital muscular dystrophy due to laminin alpha2 deficiency""]"	"[{""label"":""Lama2"",""id"":""16773""}]"	"[""16773""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110636""}]"
DOID:0110636	"[""congenital merosin-deficient muscular dystrophy 1A"",""CMD1A"",""MDC1A"",""Merosin-negative congenital muscular dystrophy"",""congenital muscular dystrophy due to laminin alpha2 deficiency""]"	"[{""label"":""LAMA2"",""id"":""3908""}]"	"[""3908""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110636""}]"
DOID:0110637	"[""muscular dystrophy-dystroglycanopathy type B6"",""MDC1D"",""MDDGB6"",""congenital muscular dystrophy LARGE-related"",""congenital muscular dystrophy type 1D"",""muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6"",""muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6""]"	"[{""label"":""LARGE1"",""id"":""9215""}]"	"[""9215""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00383""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110637""}]"
DOID:0110637	"[""muscular dystrophy-dystroglycanopathy type B6"",""MDC1D"",""MDDGB6"",""congenital muscular dystrophy LARGE-related"",""congenital muscular dystrophy type 1D"",""muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6"",""muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6""]"	"[{""label"":""Large1"",""id"":""16795""}]"	"[""16795""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110637""}]"
DOID:0110639	"[""congenital muscular dystrophy due to integrin alpha-7 deficiency"",""congenital muscular dystrophy with ITGA7 deficiency"",""congenital muscular dystrophy with integrin alpha-7 deficiency"",""congenital myopathy due to integrin alpha-7 deficiency""]"	"[{""label"":""ITGA7"",""id"":""3679""}]"	"[""3679""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110639""}]"
DOID:0110639	"[""congenital muscular dystrophy due to integrin alpha-7 deficiency"",""congenital muscular dystrophy with ITGA7 deficiency"",""congenital muscular dystrophy with integrin alpha-7 deficiency"",""congenital myopathy due to integrin alpha-7 deficiency""]"	"[{""label"":""Itga7"",""id"":""16404""}]"	"[""16404""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110639""}]"
DOID:0110640	"[""congenital muscular dystrophy due to LMNA mutation"",""L-CMD"",""LMNA-related congenital muscular dystrophy"",""congenital muscular dystrophy LMNA-related""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110640""}]"
DOID:0110640	"[""congenital muscular dystrophy due to LMNA mutation"",""L-CMD"",""LMNA-related congenital muscular dystrophy"",""congenital muscular dystrophy LMNA-related""]"	"[{""label"":""Lmna"",""id"":""16905""}]"	"[""16905""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110640""}]"
DOID:0110644	"[""long QT syndrome 1"",""LQT1"",""ventricular fibrillation with prolonged QT interval""]"	"[{""label"":""Kcnq1"",""id"":""16535""}]"	"[""16535""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110644""}]"
DOID:0110644	"[""long QT syndrome 1"",""LQT1"",""ventricular fibrillation with prolonged QT interval""]"	"[{""label"":""KCNQ1"",""id"":""3784""}]"	"[""3784""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110644""}]"
DOID:0110645	"[""long QT syndrome 2"",""LQT2""]"	"[{""label"":""ALG10B"",""id"":""144245""},{""label"":""KCNH2"",""id"":""3757""}]"	"[""144245"",""3757""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110645""}]"
DOID:0110646	"[""long QT syndrome 3"",""LQT3""]"	"[{""label"":""Scn5a"",""id"":""20271""}]"	"[""20271""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110646""}]"
DOID:0110646	"[""long QT syndrome 3"",""LQT3""]"	"[{""label"":""SCN5A"",""id"":""6331""}]"	"[""6331""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110646""}]"
DOID:0110647	"[""long QT syndrome 5"",""LQT5""]"	"[{""label"":""KCNE1"",""id"":""3753""}]"	"[""3753""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110647""}]"
DOID:0110648	"[""long QT syndrome 6"",""LQT6""]"	"[{""label"":""KCNE2"",""id"":""9992""}]"	"[""9992""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110648""}]"
DOID:0110649	"[""long QT syndrome 8"",""LQT8""]"	"[{""label"":""CACNA1C"",""id"":""775""}]"	"[""775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110649""}]"
DOID:0110651	"[""long QT syndrome 10"",""LQT10""]"	"[{""label"":""SCN4B"",""id"":""6330""}]"	"[""6330""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110651""}]"
DOID:0110652	"[""long QT syndrome 11"",""LQT11""]"	"[{""label"":""AKAP9"",""id"":""10142""}]"	"[""10142""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110652""}]"
DOID:0110654	"[""long QT syndrome 13"",""LQT13""]"	"[{""label"":""KCNJ5"",""id"":""3762""}]"	"[""3762""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110654""}]"
DOID:0110657	"[""congenital myasthenic syndrome 8"",""CMS8"",""congenital myasthenic syndrome 8 with pre- and postsynaptic defects"",""congenital myasthenic syndrome due to agrin deficiency""]"	"[{""label"":""Agrn"",""id"":""11603""}]"	"[""11603""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110657""}]"
DOID:0110657	"[""congenital myasthenic syndrome 8"",""CMS8"",""congenital myasthenic syndrome 8 with pre- and postsynaptic defects"",""congenital myasthenic syndrome due to agrin deficiency""]"	"[{""label"":""AGRN"",""id"":""375790""}]"	"[""375790""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110657""}]"
DOID:0110658	"[""congenital myasthenic syndrome 15"",""CMS15"",""congenital myasthenic syndrome 15 without tubular aggregates""]"	"[{""label"":""ALG14"",""id"":""199857""}]"	"[""199857""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110658""}]"
DOID:0110659	"[""congenital myasthenic syndrome 7"",""CMS7"",""congenital myasthenic syndrome 7 presynaptic""]"	"[{""label"":""SYT2"",""id"":""127833""}]"	"[""127833""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110659""}]"
DOID:0110660	"[""congenital myasthenic syndrome 12"",""CMS12"",""congenital myasthenia 12 with tubular aggregates""]"	"[{""label"":""GFPT1"",""id"":""2673""}]"	"[""2673""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00628""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110660""}]"
DOID:0110660	"[""congenital myasthenic syndrome 12"",""CMS12"",""congenital myasthenia 12 with tubular aggregates""]"	"[{""label"":""Gfpt1"",""id"":""14583""}]"	"[""14583""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110660""}]"
DOID:0110661	"[""congenital myasthenic syndrome 20"",""CMS20"",""congenital myasthenic syndrome 20 presynaptic""]"	"[{""label"":""SLC5A7"",""id"":""60482""}]"	"[""60482""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110661""}]"
DOID:0110662	"[""congenital myasthenic syndrome 1B"",""CMS1B"",""congenital myasthenic syndrome 1B, fast-channel""]"	"[{""label"":""CHRNA1"",""id"":""1134""}]"	"[""1134""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110662""}]"
DOID:0110663	"[""congenital myasthenic syndrome 1A"",""CMS IIa"",""CMS1A"",""congenital myasthenic syndrome 1A, slow-channel"",""congenital myasthenic syndrome type IIa""]"	"[{""label"":""CAST"",""id"":""831""},{""label"":""CHRNA1"",""id"":""1134""}]"	"[""1134"",""831""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110663""}]"
DOID:0110664	"[""congenital myasthenic syndrome 3C"",""congenital myasthenic syndrome 3C associated with acetylcholine receptor deficiency""]"	"[{""label"":""CHRND"",""id"":""1144""}]"	"[""1144""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110664""}]"
DOID:0110665	"[""congenital myasthenic syndrome 3B"",""CMS3B"",""congenital myasthenic syndrome 3B, fast-channel""]"	"[{""label"":""CHRND"",""id"":""1144""}]"	"[""1144""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110665""}]"
DOID:0110666	"[""congenital myasthenic syndrome 3A"",""CMS3A"",""congenital myasthenic syndrome 3A, slow-channel""]"	"[{""label"":""CHRND"",""id"":""1144""}]"	"[""1144""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110666""}]"
DOID:0110666	"[""congenital myasthenic syndrome 3A"",""CMS3A"",""congenital myasthenic syndrome 3A, slow-channel""]"	"[{""label"":""Chrnd"",""id"":""11447""}]"	"[""11447""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110666""}]"
DOID:0110668	"[""congenital myasthenic syndrome 10"",""CMS10"",""LGM"",""congenital muscular dystrophy merosin-positive"",""familial limb-girdle myasthenia""]"	"[{""label"":""DOK7"",""id"":""285489""}]"	"[""285489""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110668""}]"
DOID:0110669	"[""congenital myasthenic syndrome 14"",""CMS14"",""CMSTA3"",""congenital myasthenic syndrome 14, with tubular aggregates"",""congenital myasthenic syndrome with tubular aggregates 3""]"	"[{""label"":""ALG2"",""id"":""85365""}]"	"[""85365""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110669""}]"
DOID:0110670	"[""congenital myasthenic syndrome 9"",""CMS9"",""congenital myasthenic syndrome 9, associated with acetylcholine receptor deficiency""]"	"[{""label"":""Musk"",""id"":""18198""}]"	"[""18198""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110670""}]"
DOID:0110670	"[""congenital myasthenic syndrome 9"",""CMS9"",""congenital myasthenic syndrome 9, associated with acetylcholine receptor deficiency""]"	"[{""label"":""MUSK"",""id"":""4593""}]"	"[""4593""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110670""}]"
DOID:0110671	"[""congenital myasthenic syndrome 6"",""CMS Ia2"",""CMS1A2"",""CMS6"",""CMSEA"",""FIM"",""FIMG2"",""congenital myasthenic syndrome 6, presynaptic"",""congenital myasthenic syndrome type Ia2"",""congenital presynaptic myasthenic syndrome associated with episodic apnea"",""familial infantile myasthenia"",""familial infantile myasthenia gravis 2""]"	"[{""label"":""CHAT"",""id"":""1103""}]"	"[""1103""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110671""}]"
DOID:0110672	"[""congenital myasthenic syndrome 21"",""CMS21"",""congenital myasthenic syndrome 21, presynaptic""]"	"[{""label"":""SLC18A3"",""id"":""6572""}]"	"[""6572""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110672""}]"
DOID:0110673	"[""congenital myasthenic syndrome 19"",""CMS19""]"	"[{""label"":""Col13a1"",""id"":""12817""}]"	"[""12817""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110673""}]"
DOID:0110674	"[""congenital myasthenic syndrome 17"",""CMS17""]"	"[{""label"":""LRP4"",""id"":""4038""}]"	"[""4038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110674""}]"
DOID:0110676	"[""congenital myasthenic syndrome 13"",""CMS13"",""CMSTA2"",""congenital myasthenic syndrome 13 with tubular aggregates"",""congenital myasthenic syndrome with tubular aggregates 2""]"	"[{""label"":""DPAGT1"",""id"":""1798""}]"	"[""1798""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110676""}]"
DOID:0110677	"[""congenital myasthenic syndrome 4B"",""CMS4B"",""congenital myasthenic syndrome 4B fast-channel""]"	"[{""label"":""CHRNE"",""id"":""1145""}]"	"[""1145""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110677""}]"
DOID:0110678	"[""congenital myasthenic syndrome 4A"",""CMS Ia1"",""CMS1A1"",""CMS4A"",""congenital myasthenic syndrome 4A slow-channel"",""congenital myasthenic syndrometype Ia1""]"	"[{""label"":""Chrne"",""id"":""11448""}]"	"[""11448""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110678""}]"
DOID:0110678	"[""congenital myasthenic syndrome 4A"",""CMS Ia1"",""CMS1A1"",""CMS4A"",""congenital myasthenic syndrome 4A slow-channel"",""congenital myasthenic syndrometype Ia1""]"	"[{""label"":""CHRNE"",""id"":""1145""}]"	"[""1145""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110678""}]"
DOID:0110679	"[""congenital myasthenic syndrome 4C"",""CMS Id"",""CMS1D"",""CMS4C"",""FIM1"",""congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency"",""congenital myasthenic syndrome type Id"",""familial infantile myasthenia 1""]"	"[{""label"":""CHRNE"",""id"":""1145""}]"	"[""1145""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110679""}]"
DOID:0110679	"[""congenital myasthenic syndrome 4C"",""CMS Id"",""CMS1D"",""CMS4C"",""FIM1"",""congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency"",""congenital myasthenic syndrome type Id"",""familial infantile myasthenia 1""]"	"[{""label"":""Chrne"",""id"":""11448""}]"	"[""11448""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110679""}]"
DOID:0110680	"[""congenital myasthenic syndrome 2C"",""CMS2C"",""congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency""]"	"[{""label"":""CHRNB1"",""id"":""1140""}]"	"[""1140""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110680""}]"
DOID:0110681	"[""congenital myasthenic syndrome 2A"",""CMS2A"",""congenital myasthenic syndrome 2A slow-channel""]"	"[{""label"":""CHRNB1"",""id"":""1140""}]"	"[""1140""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110681""}]"
DOID:0110682	"[""congenital myasthenic syndrome 16"",""CMS16"",""congenital myasthenic syndrome acetazolamide-responsive""]"	"[{""label"":""SCN4A"",""id"":""6329""}]"	"[""6329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110682""}]"
DOID:0110683	"[""congenital myasthenic syndrome 18"",""CMS18""]"	"[{""label"":""SNAP25"",""id"":""6616""}]"	"[""6616""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110683""}]"
DOID:0110698	"[""hypotrichosis 1"",""HHS"",""HTS"",""HYPT1"",""hereditary generalized hypotrichosis simplex""]"	"[{""label"":""APCDD1"",""id"":""147495""},{""label"":""SNRPE"",""id"":""6635""}]"	"[""147495"",""6635""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110698""}]"
DOID:0110699	"[""hypotrichosis 2"",""HTSS1"",""HYPT2"",""Spanish type hypotrichosis"",""hypotrichosis simplex of the scalp 1""]"	"[{""label"":""CDSN"",""id"":""1041""}]"	"[""1041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110699""}]"
DOID:0110703	"[""hypotrichosis 6"",""HYPT6"",""Hypotrichosis, Localized, Autosomal Recessive 1"",""LAH1"",""Monilethrix-like hypotrichosis"",""autosomal recessive localized hypotrichosis""]"	"[{""label"":""Dsg4"",""id"":""16769""}]"	"[""16769""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110703""}]"
DOID:0110703	"[""hypotrichosis 6"",""HYPT6"",""Hypotrichosis, Localized, Autosomal Recessive 1"",""LAH1"",""Monilethrix-like hypotrichosis"",""autosomal recessive localized hypotrichosis""]"	"[{""label"":""DSG4"",""id"":""147409""}]"	"[""147409""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110703""}]"
DOID:0110704	"[""hypotrichosis 7"",""HYPT7"",""LAH2"",""hypotrichosis, localized, autosomal recessive 2"",""total hyptrichosis, Mari type""]"	"[{""label"":""LIPH"",""id"":""200879""}]"	"[""200879""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110704""}]"
DOID:0110705	"[""hypotrichosis 8"",""HYPT8"",""LAH3"",""hypotrichosis, localized, autosomal recessive 3""]"	"[{""label"":""LPAR6"",""id"":""10161""}]"	"[""10161""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110705""}]"
DOID:0110708	"[""hypotrichosis 11"",""HYPT11""]"	"[{""label"":""SNRPE"",""id"":""6635""}]"	"[""6635""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110708""}]"
DOID:0110709	"[""hypotrichosis 12"",""HYPT12""]"	"[{""label"":""RPL21"",""id"":""6144""}]"	"[""6144""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110709""}]"
DOID:0110710	"[""hypotrichosis 13"",""HYPT13"",""hypotrichosis with woolly hair""]"	"[{""label"":""KRT71"",""id"":""112802""}]"	"[""112802""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110710""}]"
DOID:0110711	"[""congenital hypotrichosis with juvenile macular dystrophy"",""HJMD"",""hypotrichosis with cone-rod dystrophy""]"	"[{""label"":""CDH3"",""id"":""1001""}]"	"[""1001""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110711""}]"
DOID:0110713	"[""Oguchi disease-2"",""CSNBO2"",""congenital stationary night blindness Oguchi type 2""]"	"[{""label"":""GRK1"",""id"":""6011""}]"	"[""6011""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110713""}]"
DOID:0110721	"[""neuronal ceroid lipofuscinosis 1"",""CLN1"",""neuronal ceroid lipofuscinosis 1 variable age of onset""]"	"[{""label"":""PPT1"",""id"":""5538""}]"	"[""5538""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110721""}]"
DOID:0110721	"[""neuronal ceroid lipofuscinosis 1"",""CLN1"",""neuronal ceroid lipofuscinosis 1 variable age of onset""]"	"[{""label"":""Ppt1"",""id"":""31805""}]"	"[""31805""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110721""}]"
DOID:0110721	"[""neuronal ceroid lipofuscinosis 1"",""CLN1"",""neuronal ceroid lipofuscinosis 1 variable age of onset""]"	"[{""label"":""Ppt1"",""id"":""19063""}]"	"[""19063""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110721""}]"
DOID:0110722	"[""neuronal ceroid lipofuscinosis 7"",""CLN7""]"	"[{""label"":""MFSD8"",""id"":""256471""}]"	"[""256471""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110722""}]"
DOID:0110722	"[""neuronal ceroid lipofuscinosis 7"",""CLN7""]"	"[{""label"":""Mfsd8"",""id"":""72175""}]"	"[""72175""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110722""}]"
DOID:0110725	"[""neuronal ceroid lipofuscinosis 10"",""CLN10"",""Cathepsin D deficiency"",""neuronal ceroid lipofuscinosis cathepsin D-deficient"",""neuronal ceroid lipofuscinosis due to cathepsin D deficiency""]"	"[{""label"":""Ctsd"",""id"":""13033""}]"	"[""13033""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110725""}]"
DOID:0110725	"[""neuronal ceroid lipofuscinosis 10"",""CLN10"",""Cathepsin D deficiency"",""neuronal ceroid lipofuscinosis cathepsin D-deficient"",""neuronal ceroid lipofuscinosis due to cathepsin D deficiency""]"	"[{""label"":""CTSD"",""id"":""1509""}]"	"[""1509""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110725""}]"
DOID:0110726	"[""neuronal ceroid lipofuscinosis 2"",""CLN2"",""neuronal ceroid lipofuscinosis 2 variable age at onset""]"	"[{""label"":""Tpp1"",""id"":""12751""}]"	"[""12751""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110726""}]"
DOID:0110726	"[""neuronal ceroid lipofuscinosis 2"",""CLN2"",""neuronal ceroid lipofuscinosis 2 variable age at onset""]"	"[{""label"":""TPP1"",""id"":""1200""}]"	"[""1200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110726""}]"
DOID:0110726	"[""neuronal ceroid lipofuscinosis 2"",""CLN2"",""neuronal ceroid lipofuscinosis 2 variable age at onset""]"	"[{""label"":""tpp1"",""id"":""798347""}]"	"[""798347""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110726""}]"
DOID:0110727	"[""neuronal ceroid lipofuscinosis 13"",""CLN13"",""neuronal ceroid lipofuscinosis 13 Kufs type""]"	"[{""label"":""CTSF"",""id"":""8722""}]"	"[""8722""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110727""}]"
DOID:0110728	"[""neuronal ceroid lipofuscinosis 5"",""CLN5"",""neuronal ceroid lipofuscinosis 5 variable age of onset""]"	"[{""label"":""Cln5"",""id"":""211286""}]"	"[""211286""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110728""}]"
DOID:0110728	"[""neuronal ceroid lipofuscinosis 5"",""CLN5"",""neuronal ceroid lipofuscinosis 5 variable age of onset""]"	"[{""label"":""CLN5"",""id"":""1203""}]"	"[""1203""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110728""}]"
DOID:0110731	"[""neuronal ceroid lipofuscinosis 3"",""Batten disease"",""CLN3"",""juvenile neuronal ceroid lipofuscinosis""]"	"[{""label"":""CLN3"",""id"":""1201""}]"	"[""1201""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110731""}]"
DOID:0110731	"[""neuronal ceroid lipofuscinosis 3"",""Batten disease"",""CLN3"",""juvenile neuronal ceroid lipofuscinosis""]"	"[{""label"":""Clcn3"",""id"":""12725""},{""label"":""Clcn6"",""id"":""26372""},{""label"":""Cln3"",""id"":""12752""},{""label"":""Ppt1"",""id"":""19063""}]"	"[""12725"",""12752"",""19063"",""26372""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110731""}]"
DOID:0110732	"[""neuronal ceroid lipofuscinosis 11"",""CLN11""]"	"[{""label"":""GRN"",""id"":""2896""}]"	"[""2896""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110732""}]"
DOID:0110734	"[""neurodegeneration with brain iron accumulation"",""NBIA""]"	"[{""label"":""CRAT"",""id"":""1384""},{""label"":""FTH1"",""id"":""2495""},{""label"":""REPS1"",""id"":""85021""}]"	"[""1384"",""2495"",""85021""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110734""}]"
DOID:0110735	"[""neurodegeneration with brain iron accumulation 2a"",""INAD1"",""Infantile Neuroaxonal Dystrophy 1"",""NBIA2a"",""Neurodegeneration, Pla2g6-Associated"",""Seitelberger Disease""]"	"[{""label"":""Pla2g6"",""id"":""53357""}]"	"[""53357""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110735""}]"
DOID:0110735	"[""neurodegeneration with brain iron accumulation 2a"",""INAD1"",""Infantile Neuroaxonal Dystrophy 1"",""NBIA2a"",""Neurodegeneration, Pla2g6-Associated"",""Seitelberger Disease""]"	"[{""label"":""PLA2G6"",""id"":""8398""}]"	"[""8398""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110735""}]"
DOID:0110736	"[""neurodegeneration with brain iron accumulation 2b"",""NBIA2b"",""Neuroaxonal Dystrophy, Atypical"",""Neurodegeneration With Brain Iron Accumulation, Pla2g6-Related""]"	"[{""label"":""PLA2G6"",""id"":""8398""}]"	"[""8398""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110736""}]"
DOID:0110739	"[""neurodegeneration with brain iron accumulation 5"",""BPAN"",""Beta-Propeller Protein-Associated Neurodegeneration"",""NBIA5"",""SENDA"",""Static Encephalopathy Of Childhood With Neurodegeneration In Adulthood""]"	"[{""label"":""WDR45"",""id"":""11152""}]"	"[""11152""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110739""}]"
DOID:0110741	"[""type 1 diabetes mellitus 2"",""IDDM2"",""Insulin-Dependent Diabetes Mellitus 2""]"	"[{""label"":""INS"",""id"":""3630""}]"	"[""3630""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110741""}]"
DOID:0110741	"[""type 1 diabetes mellitus 2"",""IDDM2"",""Insulin-Dependent Diabetes Mellitus 2""]"	"[{""label"":""Igf2"",""id"":""16002""}]"	"[""16002""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110741""}]"
DOID:0110749	"[""type 1 diabetes mellitus 10"",""IDDM10"",""Insulin-Dependent Diabetes Mellitus 10""]"	"[{""label"":""IL2RA"",""id"":""3559""}]"	"[""3559""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110749""}]"
DOID:0110751	"[""type 1 diabetes mellitus 12"",""IDDM12"",""Insulin-Dependent Diabetes Mellitus 12""]"	"[{""label"":""CTLA4"",""id"":""1493""}]"	"[""1493""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110751""}]"
DOID:0110757	"[""type 1 diabetes mellitus 20"",""IDDM20"",""Insulin-Dependent Diabetes Mellitus 20""]"	"[{""label"":""HNF1A"",""id"":""6927""}]"	"[""6927""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110757""}]"
DOID:0110759	"[""type 1 diabetes mellitus 22"",""IDDM22"",""Insulin-Dependent Diabetes Mellitus 22""]"	"[{""label"":""CCR5"",""id"":""1234""}]"	"[""1234""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110759""}]"
DOID:0110764	"[""hereditary spastic paraplegia 11"",""HSP-TCC"",""Nakamura-Osame syndrome"",""SPG11"",""autosomal recessive spastic paraplegia 11"",""autosomal recessive spastic paraplegia complicated with thin corpus callosum"",""autosomal recessive spastic paraplegia type 11"",""autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum"",""spastic paraplegia-intellectual disability-thin corpus callosum syndrome""]"	"[{""label"":""SPG11"",""id"":""80208""}]"	"[""80208""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110764""}]"
DOID:0110765	"[""hereditary spastic paraplegia 12"",""SPG12"",""autosomal dominant spastic paraplegia 12"",""autosomal dominant spastic paraplegia type 12""]"	"[{""label"":""RTN2"",""id"":""6253""}]"	"[""6253""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110765""}]"
DOID:0110766	"[""hereditary spastic paraplegia 13"",""SPG13"",""autosomal dominant spastic paraplegia 13""]"	"[{""label"":""Hspd1"",""id"":""15510""}]"	"[""15510""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110766""}]"
DOID:0110766	"[""hereditary spastic paraplegia 13"",""SPG13"",""autosomal dominant spastic paraplegia 13""]"	"[{""label"":""HSPD1"",""id"":""3329""}]"	"[""3329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110766""}]"
DOID:0110768	"[""hereditary spastic paraplegia 15"",""Kjellin syndrome"",""SPG15"",""autosomal recessive spastic paraplegia 15"",""autosomal recessive spastic paraplegia type 15"",""hereditary spastic paraparesis type 15"",""spastic paraplegia and retinal degeneration"",""spastic paraplegia-retinal degeneration syndrome""]"	"[{""label"":""ZFYVE26"",""id"":""23503""}]"	"[""23503""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110768""}]"
DOID:0110770	"[""hereditary spastic paraplegia 17"",""SPG17"",""Silver spastic paraplegia syndrome"",""Silver syndrome"",""autosomal dominant spastic paraplegia 17"",""autosomal dominant spastic paraplegia type 17"",""dHMN5B"",""distal hereditary motor neuropathy type 5B"",""spastic paraplegia with amyotrophy of hands and feet"",""spastic paraplegia-amyotrophy of hands and feet""]"	"[{""label"":""BSCL2"",""id"":""26580""}]"	"[""26580""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110770""}]"
DOID:0110771	"[""hereditary spastic paraplegia 18"",""IDMDC"",""SPG18"",""autosomal recessive spastic paraplegia 18"",""autosomal recessive spastic paraplegia type 18"",""intellectual disability, motor dysfunction and joint contractures""]"	"[{""label"":""ERLIN2"",""id"":""11160""}]"	"[""11160""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110771""}]"
DOID:0110773	"[""hereditary spastic paraplegia 2"",""SPG2"",""X-linked spastic paraplegia 2"",""spastic paraplegia type 2""]"	"[{""label"":""PLP1"",""id"":""5354""}]"	"[""5354""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110773""}]"
DOID:0110773	"[""hereditary spastic paraplegia 2"",""SPG2"",""X-linked spastic paraplegia 2"",""spastic paraplegia type 2""]"	"[{""label"":""Plp1"",""id"":""18823""}]"	"[""18823""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110773""}]"
DOID:0110774	"[""hereditary spastic paraplegia 23"",""Lison syndrome"",""SPG23"",""Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome"",""spastic paraplegia 23"",""spastic paraplegia with pigmentary abnormalities""]"	"[{""label"":""DSTYK"",""id"":""25778""}]"	"[""25778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110774""}]"
DOID:0110777	"[""hereditary spastic paraplegia 26"",""GM2 synthase deficiency"",""SPG26"",""autosomal recessive spastic paraplegia 26"",""autosomal recessive spastic paraplegia type 26""]"	"[{""label"":""B4GALNT1"",""id"":""2583""}]"	"[""2583""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110777""}]"
DOID:0110779	"[""hereditary spastic paraplegia 28"",""SPG28"",""autosomal recessive spastic paraplegia 28"",""autosomal recessive spastic paraplegia type 28""]"	"[{""label"":""DDHD1"",""id"":""80821""}]"	"[""80821""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110779""}]"
DOID:0110786	"[""hereditary spastic paraplegia 35"",""FAHN"",""SPG35"",""autosomal recessive spastic paraplegia 35"",""autosomal recessive spastic paraplegia type 35"",""fatty acid hydroxylase-associated neurodegeneration"",""leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia""]"	"[{""label"":""FA2H"",""id"":""79152""}]"	"[""79152""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110786""}]"
DOID:0110790	"[""hereditary spastic paraplegia 39"",""NTE-related motor neuron disorder"",""NTEMND"",""SPG39"",""autosomal recessive spastic paraplegia 39"",""autosomal recessive spastic paraplegia type 39"",""spastic paraplegia due to NTE mutation"",""spastic paraplegia due to neuropathy target esterase mutation""]"	"[{""label"":""PNPLA6"",""id"":""10908""}]"	"[""10908""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110790""}]"
DOID:0110792	"[""hereditary spastic paraplegia 4"",""SPG4"",""autosomal dominant spastic paraplegia 4"",""autosomal dominant spastic paraplegia type 4""]"	"[{""label"":""SPAST"",""id"":""6683""}]"	"[""6683""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110792""}]"
DOID:0110794	"[""hereditary spastic paraplegia 42"",""SPG42"",""autosomal dominant spastic paraplegia 42"",""autosomal dominant spastic paraplegia type 42""]"	"[{""label"":""SLC33A1"",""id"":""9197""}]"	"[""9197""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110794""}]"
DOID:0110796	"[""hereditary spastic paraplegia 44"",""SPG44"",""autosomal recessive spastic paraplegia 44""]"	"[{""label"":""GJC2"",""id"":""57165""}]"	"[""57165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110796""}]"
DOID:0110798	"[""hereditary spastic paraplegia 46"",""SPG46"",""autosomal recessive spastic paraplegia 46"",""autosomal recessive spastic paraplegia type 46""]"	"[{""label"":""GBA2"",""id"":""57704""}]"	"[""57704""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110798""}]"
DOID:0110800	"[""hereditary spastic paraplegia 48"",""SPG48"",""autosomal recessive spastic paraplegia 48"",""autosomal recessive spastic paraplegia type 48""]"	"[{""label"":""AP5Z1"",""id"":""9907""}]"	"[""9907""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110800""}]"
DOID:0110801	"[""hereditary spastic paraplegia 49"",""SPG49"",""autosomal recessive spastic paraplegia 49"",""autosomal recessive spastic paraplegia type 49""]"	"[{""label"":""TECPR2"",""id"":""9895""}]"	"[""9895""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110801""}]"
DOID:0110805	"[""hereditary spastic paraplegia 53"",""SPG53"",""autosomal recessive spastic paraplegia 53"",""autosomal recessive spastic paraplegia type 53""]"	"[{""label"":""VPS37A"",""id"":""137492""}]"	"[""137492""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110805""}]"
DOID:0110807	"[""hereditary spastic paraplegia 55"",""SPG55"",""autosomal recessive spastic paraplegia 55"",""autosomal recessive spastic paraplegia type 55""]"	"[{""label"":""MTRFR"",""id"":""91574""}]"	"[""91574""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110807""}]"
DOID:0110808	"[""hereditary spastic paraplegia 56"",""SPG56"",""autosomal recessive spastic paraplegia 56"",""autosomal recessive spastic paraplegia type 56""]"	"[{""label"":""CYP2U1"",""id"":""113612""}]"	"[""113612""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110808""}]"
DOID:0110809	"[""hereditary spastic paraplegia 57"",""SPG57"",""autosomal recessive spastic paraplegia 57"",""autosomal recessive spastic paraplegia type 57""]"	"[{""label"":""TFG"",""id"":""10342""}]"	"[""10342""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110809""}]"
DOID:0110810	"[""hereditary spastic paraplegia 5A"",""SPG5A"",""autosomal recessive spastic paraplegia 5A"",""autosomal recessive spastic paraplegia type 5A""]"	"[{""label"":""CYP7B1"",""id"":""9420""}]"	"[""9420""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110810""}]"
DOID:0110813	"[""hereditary spastic paraplegia 62"",""SPG62"",""autosomal recessive spastic paraplegia 62"",""autosomal recessive spastic paraplegia type 62""]"	"[{""label"":""ERLIN1"",""id"":""10613""}]"	"[""10613""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110813""}]"
DOID:0110814	"[""hereditary spastic paraplegia 63"",""SPG63"",""autosomal recessive spastic paraplegia 63"",""spastic paraplegia 63""]"	"[{""label"":""AMPD2"",""id"":""271""}]"	"[""271""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110814""}]"
DOID:0110815	"[""hereditary spastic paraplegia 64"",""SPG64"",""autosomal recessive spastic paraplegia 64"",""autosomal recessive spastic paraplegia type 64""]"	"[{""label"":""ENTPD1"",""id"":""953""}]"	"[""953""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110815""}]"
DOID:0110816	"[""hereditary spastic paraplegia 7"",""SPG7"",""autosomal recessive spastic paraplegia 7"",""spastic paraplegia type 7""]"	"[{""label"":""SPG7"",""id"":""6687""}]"	"[""6687""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110816""}]"
DOID:0110818	"[""hereditary spastic paraplegia 73"",""SPG73"",""autosomal dominant spastic paraplegia 73"",""autosomal dominant spastic paraplegia type 73""]"	"[{""label"":""CPT1C"",""id"":""126129""}]"	"[""126129""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110818""}]"
DOID:0110819	"[""hereditary spastic paraplegia 74"",""SPG74"",""autosomal recessive spastic paraplegia 74""]"	"[{""label"":""IBA57"",""id"":""200205""}]"	"[""200205""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110819""}]"
DOID:0110820	"[""hereditary spastic paraplegia 75"",""SPG75"",""autosomal recessive spastic paraplegia 75"",""autosomal recessive spastic paraplegia type 75""]"	"[{""label"":""MAG"",""id"":""4099""}]"	"[""4099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110820""}]"
DOID:0110821	"[""hereditary spastic paraplegia 76"",""SPG76"",""autosomal recessive spastic paraplegia 76""]"	"[{""label"":""CAPN1"",""id"":""823""}]"	"[""823""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110821""}]"
DOID:0110823	"[""hereditary spastic paraplegia 8"",""SPG8"",""autosomal dominant spastic paraplegia 8"",""autosomal dominant spastic paraplegia type 8""]"	"[{""label"":""WASHC5"",""id"":""9897""}]"	"[""9897""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110823""}]"
DOID:0110824	"[""hereditary spastic paraplegia 9A"",""AD-SPG9A"",""Cataracts motor neuropathy-short stature-skeletal anomalies syndrome"",""SPG9A"",""autosomal dominant complex spastic paraplegia type 9A"",""autosomal dominant spastic paraplegia 9A"",""cataracts with motor neuronopathy, short stature and skeletal abnormalities"",""spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux"",""spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome""]"	"[{""label"":""ALDH18A1"",""id"":""5832""}]"	"[""5832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110824""}]"
DOID:0110825	"[""hereditary spastic paraplegia 9B"",""SPG9B"",""autosomal recessive complex spastic paraplegia type 9B"",""autosomal recessive spastic paraplegia 9B""]"	"[{""label"":""ALDH18A1"",""id"":""5832""}]"	"[""5832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110825""}]"
DOID:0110826	"[""Usher syndrome type 1"",""US1"",""USH1""]"	"[{""label"":""MYO7A"",""id"":""4647""}]"	"[""4647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110826""}]"
DOID:0110827	"[""Usher syndrome type 2"",""USH2""]"	"[{""label"":""USH2A"",""id"":""7399""}]"	"[""7399""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110827""}]"
DOID:0110828	"[""Usher syndrome type 3"",""USH3""]"	"[{""label"":""Clrn1"",""id"":""229320""}]"	"[""229320""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110828""}]"
DOID:0110831	"[""Usher syndrome type 1D"",""USH1D"",""Usher syndrome type ID""]"	"[{""label"":""Cdh23"",""id"":""22295""}]"	"[""22295""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110831""}]"
DOID:0110831	"[""Usher syndrome type 1D"",""USH1D"",""Usher syndrome type ID""]"	"[{""label"":""CDH23"",""id"":""64072""},{""label"":""PCDH15"",""id"":""65217""}]"	"[""64072"",""65217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110831""}]"
DOID:0110832	"[""Usher syndrome type 1F"",""USH1F"",""Usher syndrome type IF""]"	"[{""label"":""PCDH15"",""id"":""65217""}]"	"[""65217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110832""}]"
DOID:0110832	"[""Usher syndrome type 1F"",""USH1F"",""Usher syndrome type IF""]"	"[{""label"":""Pcdh15"",""id"":""11994""}]"	"[""11994""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110832""}]"
DOID:0110838	"[""Usher syndrome type 2A"",""USH2A"",""Usher syndrome type IIA""]"	"[{""label"":""PDZD7"",""id"":""79955""},{""label"":""USH2A"",""id"":""7399""}]"	"[""7399"",""79955""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110838""}]"
DOID:0110838	"[""Usher syndrome type 2A"",""USH2A"",""Usher syndrome type IIA""]"	"[{""label"":""Ush2a"",""id"":""22283""}]"	"[""22283""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110838""}]"
DOID:0110839	"[""Usher syndrome type 2C"",""USH2C"",""Usher syndrome IIC"",""Usher syndrome type IIC""]"	"[{""label"":""ADGRV1"",""id"":""84059""},{""label"":""PDZD7"",""id"":""79955""}]"	"[""79955"",""84059""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110839""}]"
DOID:0110840	"[""Usher syndrome type 2D"",""USH2D"",""Usher syndrome type IID""]"	"[{""label"":""WHRN"",""id"":""25861""}]"	"[""25861""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110840""}]"
DOID:0110841	"[""Usher syndrome type 3A"",""USH3A"",""Usher syndrome type IIIA""]"	"[{""label"":""CLRN1"",""id"":""7401""}]"	"[""7401""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110841""}]"
DOID:0110841	"[""Usher syndrome type 3A"",""USH3A"",""Usher syndrome type IIIA""]"	"[{""label"":""Clrn1"",""id"":""229320""}]"	"[""229320""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110841""}]"
DOID:0110844	"[""xeroderma pigmentosum group C"",""XP group C"",""XP3"",""XPC"",""XPCC"",""xeroderma pigmentosum III""]"	"[{""label"":""XPC"",""id"":""7508""}]"	"[""7508""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110844""}]"
DOID:0110847	"[""xeroderma pigmentosum variant type"",""XPV"",""photosensitivity with defective DNA synthesis"",""xeroderma pigmentosum with normal DNA repair rates""]"	"[{""label"":""POLH"",""id"":""5429""}]"	"[""5429""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110847""}]"
DOID:0110849	"[""xeroderma pigmentosum group G"",""XP group G"",""XP7"",""XPG"",""xeroderma pigmentosum VII""]"	"[{""label"":""ERCC5"",""id"":""2073""}]"	"[""2073""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110849""}]"
DOID:0110852	"[""rhizomelic chondrodysplasia punctata type 2"",""Chondrodysplasia Punctata, Rhizomelic, Due To Dihydroxyacetonephosphate Acyltransferase Deficiency"",""DHAPAT deficiency"",""Dihydroxyacetonephosphate Acyltransferase Deficiency"",""GNPAT deficiency"",""Glyceronephosphate O-Acyltransferase Deficiency"",""Peroxisomal Dihydroxyacetonephosphate Acyltransferase Deficiency"",""RCDP2""]"	"[{""label"":""GNPAT"",""id"":""8443""}]"	"[""8443""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110852""}]"
DOID:0110853	"[""rhizomelic chondrodysplasia punctata type 3"",""AGPS deficiency"",""Alkyldihydroxyacetonephosphate Synthase Deficiency"",""Alkylglycerone-Phosphate Synthase Deficiency"",""RCDP3""]"	"[{""label"":""AGPS"",""id"":""8540""}]"	"[""8540""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110853""}]"
DOID:0110856	"[""posterior polymorphous corneal dystrophy 2"",""PPCD2""]"	"[{""label"":""COL8A2"",""id"":""1296""}]"	"[""1296""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110856""}]"
DOID:0110857	"[""posterior polymorphous corneal dystrophy 3"",""PPCD3""]"	"[{""label"":""ZEB1"",""id"":""6935""}]"	"[""6935""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110857""}]"
DOID:0110858	"[""polycystic kidney disease 1"",""APKD1"",""PKD1"",""Polycystic Kidney Disease, Adult, Type I""]"	"[{""label"":""PKD1"",""id"":""5310""}]"	"[""5310""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110858""}]"
DOID:0110858	"[""polycystic kidney disease 1"",""APKD1"",""PKD1"",""Polycystic Kidney Disease, Adult, Type I""]"	"[{""label"":""Pkd1"",""id"":""18763""}]"	"[""18763""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110858""}]"
DOID:0110859	"[""polycystic kidney disease 2"",""APKD2"",""PKD2"",""Polycystic Kidney Disease, Adult, Type II""]"	"[{""label"":""PKD2"",""id"":""5311""}]"	"[""5311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110859""}]"
DOID:0110859	"[""polycystic kidney disease 2"",""APKD2"",""PKD2"",""Polycystic Kidney Disease, Adult, Type II""]"	"[{""label"":""Pkd2"",""id"":""18764""}]"	"[""18764""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110859""}]"
DOID:0110860	"[""polycystic kidney disease 3"",""APKD3"",""PKD3"",""Polycystic Kidney Disease, Adult, Type III""]"	"[{""label"":""GANAB"",""id"":""23193""}]"	"[""23193""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110860""}]"
DOID:0110861	"[""autosomal recessive polycystic kidney disease"",""AR-PKD""]"	"[{""label"":""Arl3"",""id"":""56350""},{""label"":""Pkd1"",""id"":""18763""},{""label"":""Pkhd1"",""id"":""241035""},{""label"":""Tsc1"",""id"":""64930""}]"	"[""18763"",""241035"",""56350"",""64930""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110861""}]"
DOID:0110861	"[""autosomal recessive polycystic kidney disease"",""AR-PKD""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Akt1"",""id"":""24185""}]"	"[""24185"",""24310""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110861""}]"
DOID:0110861	"[""autosomal recessive polycystic kidney disease"",""AR-PKD""]"	"[{""label"":""PKHD1"",""id"":""5314""}]"	"[""5314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110861""}]"
DOID:0110862	"[""congenital stationary night blindness autosomal dominant 1"",""CSNBAD1"",""rhodopsin-related congenital stationary night blindness""]"	"[{""label"":""RHO"",""id"":""6010""}]"	"[""6010""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110862""}]"
DOID:0110862	"[""congenital stationary night blindness autosomal dominant 1"",""CSNBAD1"",""rhodopsin-related congenital stationary night blindness""]"	"[{""label"":""Rho"",""id"":""212541""}]"	"[""212541""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110862""}]"
DOID:0110863	"[""congenital stationary night blindness autosomal dominant 2"",""CSNBAD2"",""Rambusch type congenital stationary night blindness""]"	"[{""label"":""PDE6B"",""id"":""5158""}]"	"[""5158""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110863""}]"
DOID:0110864	"[""congenital stationary night blindness 1F"",""CSNB1F"",""congenital stationary night blindness 1F autosomal recessive""]"	"[{""label"":""Lrit3"",""id"":""242235""}]"	"[""242235""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110864""}]"
DOID:0110864	"[""congenital stationary night blindness 1F"",""CSNB1F"",""congenital stationary night blindness 1F autosomal recessive""]"	"[{""label"":""LRIT3"",""id"":""345193""}]"	"[""345193""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110864""}]"
DOID:0110865	"[""congenital stationary night blindness 1B"",""CSNB1B"",""autosomal recessive complete congenital stationary night blindness"",""congenital stationary night blindness 1B autosomal recessive""]"	"[{""label"":""Grm6"",""id"":""108072""}]"	"[""108072""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110865""}]"
DOID:0110865	"[""congenital stationary night blindness 1B"",""CSNB1B"",""autosomal recessive complete congenital stationary night blindness"",""congenital stationary night blindness 1B autosomal recessive""]"	"[{""label"":""GRM6"",""id"":""2916""}]"	"[""2916""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110865""}]"
DOID:0110867	"[""congenital stationary night blindness 1C"",""CSNB1C"",""congenital stationary night blindness 1C autosomal recessive""]"	"[{""label"":""Trpm1"",""id"":""17364""}]"	"[""17364""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110867""}]"
DOID:0110867	"[""congenital stationary night blindness 1C"",""CSNB1C"",""congenital stationary night blindness 1C autosomal recessive""]"	"[{""label"":""TRPM1"",""id"":""4308""}]"	"[""4308""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110867""}]"
DOID:0110868	"[""congenital stationary night blindness 1D"",""CSNB1D"",""congenital stationary night blindness 1D autosomal recessive""]"	"[{""label"":""Slc24a1"",""id"":""214111""}]"	"[""214111""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110868""}]"
DOID:0110868	"[""congenital stationary night blindness 1D"",""CSNB1D"",""congenital stationary night blindness 1D autosomal recessive""]"	"[{""label"":""SLC24A1"",""id"":""9187""}]"	"[""9187""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110868""}]"
DOID:0110869	"[""congenital stationary night blindness 1E"",""CSNB1E"",""congenital stationary night blindness 1E autosomal recessive""]"	"[{""label"":""GPR179"",""id"":""440435""}]"	"[""440435""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110869""}]"
DOID:0110869	"[""congenital stationary night blindness 1E"",""CSNB1E"",""congenital stationary night blindness 1E autosomal recessive""]"	"[{""label"":""Gpr179"",""id"":""217143""}]"	"[""217143""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110869""}]"
DOID:0110870	"[""congenital stationary night blindness 1A"",""CSNB1A"",""NBMI"",""complete CSNB X-linked"",""congenital stationary night blindness 1A X-linked"",""congenital stationary night blindness with myopia"",""hemeralopia-myopia"",""myopia-night blindness""]"	"[{""label"":""NYX"",""id"":""60506""}]"	"[""60506""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110870""}]"
DOID:0110870	"[""congenital stationary night blindness 1A"",""CSNB1A"",""NBMI"",""complete CSNB X-linked"",""congenital stationary night blindness 1A X-linked"",""congenital stationary night blindness with myopia"",""hemeralopia-myopia"",""myopia-night blindness""]"	"[{""label"":""Nyx"",""id"":""236690""}]"	"[""236690""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110870""}]"
DOID:0110871	"[""congenital stationary night blindness 2A"",""congenital stationary night blindness 2A X-linked""]"	"[{""label"":""Cacna1f"",""id"":""54652""}]"	"[""54652""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110871""}]"
DOID:0110871	"[""congenital stationary night blindness 2A"",""congenital stationary night blindness 2A X-linked""]"	"[{""label"":""CACNA1F"",""id"":""778""}]"	"[""778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110871""}]"
DOID:0110873	"[""holoprosencephaly 9"",""HPE9"",""holoprosencephaly with microphthalmia and first branchial arch anomalies"",""pituitary anomalies with holoprosencephaly-like features""]"	"[{""label"":""GLI2"",""id"":""2736""}]"	"[""2736""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110873""}]"
DOID:0110875	"[""holoprosencephaly 3"",""HLP3"",""HPE3""]"	"[{""label"":""SHH"",""id"":""6469""}]"	"[""6469""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110875""}]"
DOID:0110875	"[""holoprosencephaly 3"",""HLP3"",""HPE3""]"	"[{""label"":""Shh"",""id"":""20423""}]"	"[""20423""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110875""}]"
DOID:0110876	"[""holoprosencephaly 7"",""HPE7""]"	"[{""label"":""PTCH1"",""id"":""5727""}]"	"[""5727""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110876""}]"
DOID:0110877	"[""holoprosencephaly 11"",""HPE11""]"	"[{""label"":""CDON"",""id"":""50937""}]"	"[""50937""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110877""}]"
DOID:0110877	"[""holoprosencephaly 11"",""HPE11""]"	"[{""label"":""Cdon"",""id"":""57810""}]"	"[""57810""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110877""}]"
DOID:0110880	"[""holoprosencephaly 4"",""HPE4""]"	"[{""label"":""TGIF1"",""id"":""7050""}]"	"[""7050""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110880""}]"
DOID:0110883	"[""inflammatory bowel disease 17"",""IBD17""]"	"[{""label"":""IL23R"",""id"":""149233""}]"	"[""149233""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110883""}]"
DOID:0110887	"[""inflammatory bowel disease 12"",""IBD12""]"	"[{""label"":""Gnai2"",""id"":""14678""}]"	"[""14678""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110887""}]"
DOID:0110893	"[""inflammatory bowel disease 13"",""IBD13""]"	"[{""label"":""ABCB1"",""id"":""5243""}]"	"[""5243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110893""}]"
DOID:0110893	"[""inflammatory bowel disease 13"",""IBD13""]"	"[{""label"":""Abcb1a"",""id"":""18671""}]"	"[""18671""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110893""}]"
DOID:0110895	"[""inflammatory bowel disease 14"",""IBD14""]"	"[{""label"":""IRF5"",""id"":""3663""}]"	"[""3663""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110895""}]"
DOID:0110896	"[""inflammatory bowel disease 16"",""IBD16""]"	"[{""label"":""Tnfsf15"",""id"":""326623""}]"	"[""326623""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110896""}]"
DOID:0110899	"[""inflammatory bowel disease 28"",""IBD28"",""early onset autosomal recessive inflammatory bowel disease 28""]"	"[{""label"":""IL10RA"",""id"":""3587""}]"	"[""3587""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110899""}]"
DOID:0110909	"[""inflammatory bowel disease 25"",""IBD25"",""early onset autosomal recessive inflammatory bowel disease 25""]"	"[{""label"":""IL10RB"",""id"":""3588""}]"	"[""3588""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110909""}]"
DOID:0110910	"[""leukocyte adhesion deficiency 1"",""LAD1"",""LFA1 immunodeficiency"",""leukocyte adhesion deficiency type I"",""lymphocyte function-associated antigen 1 immunodeficiency""]"	"[{""label"":""Itgb2"",""id"":""16414""}]"	"[""16414""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110910""}]"
DOID:0110910	"[""leukocyte adhesion deficiency 1"",""LAD1"",""LFA1 immunodeficiency"",""leukocyte adhesion deficiency type I"",""lymphocyte function-associated antigen 1 immunodeficiency""]"	"[{""label"":""ITGB2"",""id"":""3689""}]"	"[""3689""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110910""}]"
DOID:0110913	"[""adult hypophosphatasia"",""mild hypophosphatasia""]"	"[{""label"":""ALPL"",""id"":""249""}]"	"[""249""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110913""}]"
DOID:0110913	"[""adult hypophosphatasia"",""mild hypophosphatasia""]"	"[{""label"":""Alpl"",""id"":""11647""}]"	"[""11647""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110913""}]"
DOID:0110914	"[""infantile hypophosphatasia"",""HOPS"",""HPPI"",""phosphoethanolaminuria""]"	"[{""label"":""Alpl"",""id"":""11647""}]"	"[""11647""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110914""}]"
DOID:0110914	"[""infantile hypophosphatasia"",""HOPS"",""HPPI"",""phosphoethanolaminuria""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110914""}]"
DOID:0110914	"[""infantile hypophosphatasia"",""HOPS"",""HPPI"",""phosphoethanolaminuria""]"	"[{""label"":""ALPL"",""id"":""249""}]"	"[""249""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110914""}]"
DOID:0110915	"[""childhood hypophosphatasia""]"	"[{""label"":""Alpl"",""id"":""11647""}]"	"[""11647""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110915""}]"
DOID:0110915	"[""childhood hypophosphatasia""]"	"[{""label"":""ALPL"",""id"":""249""}]"	"[""249""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110915""}]"
DOID:0110916	"[""hereditary spherocytosis type 1"",""HS1"",""SPH1"",""hereditary spherocytosis 1""]"	"[{""label"":""ANK1"",""id"":""286""}]"	"[""286""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110916""}]"
DOID:0110916	"[""hereditary spherocytosis type 1"",""HS1"",""SPH1"",""hereditary spherocytosis 1""]"	"[{""label"":""Spta1"",""id"":""20739""}]"	"[""20739""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110916""}]"
DOID:0110917	"[""hereditary spherocytosis type 2"",""HS2"",""SPH2"",""hereditary spherocytosis 2""]"	"[{""label"":""SPTB"",""id"":""6710""}]"	"[""6710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110917""}]"
DOID:0110918	"[""hereditary spherocytosis type 3"",""HS3"",""SPH3"",""hereditary spherocytosis 3""]"	"[{""label"":""Spta1"",""id"":""20739""}]"	"[""20739""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110918""}]"
DOID:0110918	"[""hereditary spherocytosis type 3"",""HS3"",""SPH3"",""hereditary spherocytosis 3""]"	"[{""label"":""SPTA1"",""id"":""6708""}]"	"[""6708""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110918""}]"
DOID:0110919	"[""hereditary spherocytosis type 4"",""HS4"",""SPH4"",""hereditary spherocytosis 4""]"	"[{""label"":""Slc4a1"",""id"":""20533""}]"	"[""20533""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110919""}]"
DOID:0110920	"[""hereditary spherocytosis type 5"",""HS5"",""SPH5"",""hereditary spherocytosis 5""]"	"[{""label"":""EPB42"",""id"":""2038""}]"	"[""2038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110920""}]"
DOID:0110922	"[""familial hemophagocytic lymphohistiocytosis 2"",""FHL2"",""HLH2"",""HPLH2""]"	"[{""label"":""PRF1"",""id"":""5551""}]"	"[""5551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110922""}]"
DOID:0110922	"[""familial hemophagocytic lymphohistiocytosis 2"",""FHL2"",""HLH2"",""HPLH2""]"	"[{""label"":""Prf1"",""id"":""18646""}]"	"[""18646""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110922""}]"
DOID:0110923	"[""familial hemophagocytic lymphohistiocytosis 3"",""FHL3"",""HLH3"",""HPLH3""]"	"[{""label"":""UNC13D"",""id"":""201294""}]"	"[""201294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110923""}]"
DOID:0110925	"[""familial hemophagocytic lymphohistiocytosis 5"",""FHL5"",""HLH5"",""HPLH5""]"	"[{""label"":""STXBP2"",""id"":""6813""}]"	"[""6813""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110925""}]"
DOID:0110927	"[""nemaline myopathy 3"",""NEM3"",""congenital myopathy 2A"",""nemaline myopathy 3, autosomal dominant or recessive""]"	"[{""label"":""ACTA1"",""id"":""58""}]"	"[""58""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110927""}]"
DOID:0110927	"[""nemaline myopathy 3"",""NEM3"",""congenital myopathy 2A"",""nemaline myopathy 3, autosomal dominant or recessive""]"	"[{""label"":""Acta1"",""id"":""11459""}]"	"[""11459""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110927""}]"
DOID:0110928	"[""nemaline myopathy 2"",""NEM2"",""congenital myopathy 2"",""nemaline myopathy 2, autosomal recessive""]"	"[{""label"":""NEB"",""id"":""4703""}]"	"[""4703""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110928""}]"
DOID:0110928	"[""nemaline myopathy 2"",""NEM2"",""congenital myopathy 2"",""nemaline myopathy 2, autosomal recessive""]"	"[{""label"":""Neb"",""id"":""17996""}]"	"[""17996""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110928""}]"
DOID:0110929	"[""nemaline myopathy 9"",""NEM9""]"	"[{""label"":""KLHL41"",""id"":""10324""}]"	"[""10324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110929""}]"
DOID:0110933	"[""nemaline myopathy 11"",""NEM11"",""nemaline myopathy 11, autosomal recessive""]"	"[{""label"":""Mypn"",""id"":""68802""}]"	"[""68802""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110933""}]"
DOID:0110933	"[""nemaline myopathy 11"",""NEM11"",""nemaline myopathy 11, autosomal recessive""]"	"[{""label"":""MYPN"",""id"":""84665""}]"	"[""84665""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110933""}]"
DOID:0110934	"[""nemaline myopathy 7"",""NEM7"",""nemaline myopathy 7, autosomal recessive""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110934""}]"
DOID:0110937	"[""autosomal dominant osteopetrosis 1"",""OPTA1"",""autosomal dominant osteopetrosis type 1""]"	"[{""label"":""LRP5"",""id"":""4041""}]"	"[""4041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110937""}]"
DOID:0110939	"[""autosomal recessive osteopetrosis 5"",""OPTB5"",""infantile malignant osteopetrosis 3""]"	"[{""label"":""OSTM1"",""id"":""28962""}]"	"[""28962""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110939""}]"
DOID:0110939	"[""autosomal recessive osteopetrosis 5"",""OPTB5"",""infantile malignant osteopetrosis 3""]"	"[{""label"":""Ostm1"",""id"":""14628""}]"	"[""14628""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110939""}]"
DOID:0110943	"[""autosomal recessive osteopetrosis 2"",""OPTB2"",""mild autosomal recessive form osteopetrosis"",""osteoclast-poor osteopetrosis""]"	"[{""label"":""TNFSF11"",""id"":""8600""}]"	"[""8600""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110943""}]"
DOID:0110943	"[""autosomal recessive osteopetrosis 2"",""OPTB2"",""mild autosomal recessive form osteopetrosis"",""osteoclast-poor osteopetrosis""]"	"[{""label"":""Tnfsf11"",""id"":""21943""}]"	"[""21943""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110943""}]"
DOID:0110945	"[""autosomal recessive osteopetrosis 6"",""OPTB6"",""autosomal recessive osteopetrosis intermediate form""]"	"[{""label"":""PLEKHM1"",""id"":""9842""}]"	"[""9842""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110945""}]"
DOID:0110946	"[""autosomal recessive osteopetrosis 7"",""OPTB7"",""autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia"",""autosomal recessive osteopetrosis type 7"",""osteoclast-poor osteopetrosis with hypogammaglobulinemia"",""osteopetrosis-hypogammaglobulinemia syndrome""]"	"[{""label"":""TNFRSF11A"",""id"":""8792""}]"	"[""8792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110946""}]"
DOID:0110948	"[""Waardenburg syndrome type 1"",""WS1"",""Waardenburg syndrome type I""]"	"[{""label"":""Mitf"",""id"":""17342""}]"	"[""17342""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110948""}]"
DOID:0110950	"[""Waardenburg syndrome type 2A"",""WS2A"",""Waardenburg syndrome type IIA""]"	"[{""label"":""MITF"",""id"":""4286""}]"	"[""4286""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110950""}]"
DOID:0110950	"[""Waardenburg syndrome type 2A"",""WS2A"",""Waardenburg syndrome type IIA""]"	"[{""label"":""Mitf"",""id"":""17342""}]"	"[""17342""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110950""}]"
DOID:0110953	"[""Waardenburg syndrome type 4A"",""WS4A"",""Waardenburg syndrome type IVA"",""Waardenburg syndrome with Hirschsprung disease type 4A""]"	"[{""label"":""EDNRB"",""id"":""1910""}]"	"[""1910""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110953""}]"
DOID:0110953	"[""Waardenburg syndrome type 4A"",""WS4A"",""Waardenburg syndrome type IVA"",""Waardenburg syndrome with Hirschsprung disease type 4A""]"	"[{""label"":""Ednrb"",""id"":""13618""}]"	"[""13618""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110953""}]"
DOID:0110957	"[""Gaucher's disease type I"",""Acid Beta-Glucosidase Deficiency"",""GD I"",""GD1"",""Gaucher Disease, Noncerebral Juvenile"",""Gba Deficiency"",""Glucocerebrosidase Deficiency""]"	"[{""label"":""Gba1"",""id"":""14466""}]"	"[""14466""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110957""}]"
DOID:0110957	"[""Gaucher's disease type I"",""Acid Beta-Glucosidase Deficiency"",""GD I"",""GD1"",""Gaucher Disease, Noncerebral Juvenile"",""Gba Deficiency"",""Glucocerebrosidase Deficiency""]"	"[{""label"":""GBA1"",""id"":""2629""}]"	"[""2629""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00066""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110957""}]"
DOID:0110958	"[""Gaucher's disease type II"",""GD II"",""GD2"",""Gaucher Disease, Acute Neuronopathic Type"",""Infantile Cerebral Gaucher Disease""]"	"[{""label"":""GBA1"",""id"":""2629""}]"	"[""2629""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00068""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110958""}]"
DOID:0110958	"[""Gaucher's disease type II"",""GD II"",""GD2"",""Gaucher Disease, Acute Neuronopathic Type"",""Infantile Cerebral Gaucher Disease""]"	"[{""label"":""Gba1"",""id"":""14466""}]"	"[""14466""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110958""}]"
DOID:0110959	"[""Gaucher's disease type III"",""GD III"",""Gaucher Disease, Chronic Neuronopathic Type"",""Gaucher Disease, Juvenile And Adult, Cerebral"",""Gaucher Disease, Subacute Neuronopathic Type""]"	"[{""label"":""GBA1"",""id"":""2629""}]"	"[""2629""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00070""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110959""}]"
DOID:0110960	"[""Gaucher's disease perinatal lethal"",""Fetal Gaucher Disease"",""Gaucher Disease, Collodion Type""]"	"[{""label"":""GBA1"",""id"":""2629""}]"	"[""2629""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00069""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110960""}]"
DOID:0110961	"[""atypical Gaucher's disease due to saposin c deficiency""]"	"[{""label"":""PSAP"",""id"":""5660""}]"	"[""5660""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00072""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110961""}]"
DOID:0110964	"[""brachydactyly type A1"",""BDA1"",""Farabee type brachydactyly""]"	"[{""label"":""GDF5"",""id"":""8200""},{""label"":""IHH"",""id"":""3549""}]"	"[""3549"",""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110964""}]"
DOID:0110964	"[""brachydactyly type A1"",""BDA1"",""Farabee type brachydactyly""]"	"[{""label"":""Ihh"",""id"":""16147""}]"	"[""16147""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110964""}]"
DOID:0110965	"[""brachydactyly type A2"",""BDA2"",""Mohr-Wriedt type brachydactyly"",""brachymesophalangy II""]"	"[{""label"":""BMP2"",""id"":""650""},{""label"":""BMPR1B"",""id"":""658""},{""label"":""GDF5"",""id"":""8200""}]"	"[""650"",""658"",""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110965""}]"
DOID:0110965	"[""brachydactyly type A2"",""BDA2"",""Mohr-Wriedt type brachydactyly"",""brachymesophalangy II""]"	"[{""label"":""Gdf5"",""id"":""14563""}]"	"[""14563""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110965""}]"
DOID:0110967	"[""brachydactyly type A4"",""BDA4"",""Temtamy type brachydactyly"",""brachymesophalangy II and V""]"	"[{""label"":""HOXD13"",""id"":""3239""}]"	"[""3239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110967""}]"
DOID:0110969	"[""brachydactyly type B1"",""BDB1""]"	"[{""label"":""ROR2"",""id"":""4920""}]"	"[""4920""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110969""}]"
DOID:0110970	"[""brachydactyly type C"",""BDC""]"	"[{""label"":""Gdf5"",""id"":""14563""}]"	"[""14563""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110970""}]"
DOID:0110970	"[""brachydactyly type C"",""BDC""]"	"[{""label"":""GDF5"",""id"":""8200""}]"	"[""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110970""}]"
DOID:0110971	"[""brachydactyly type D"",""BDD""]"	"[{""label"":""HOXD13"",""id"":""3239""}]"	"[""3239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110971""}]"
DOID:0110972	"[""brachydactyly type E1"",""BDE1""]"	"[{""label"":""HOXD13"",""id"":""3239""}]"	"[""3239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110972""}]"
DOID:0110975	"[""brachydactyly type B2"",""BDB2""]"	"[{""label"":""NOG"",""id"":""9241""}]"	"[""9241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110975""}]"
DOID:0110976	"[""brachydactyly type E2"",""BDE2""]"	"[{""label"":""PTHLH"",""id"":""5744""}]"	"[""5744""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110976""}]"
DOID:0110977	"[""brachydactyly type A1C"",""BDA1C""]"	"[{""label"":""Gdf5"",""id"":""14563""}]"	"[""14563""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110977""}]"
DOID:0110977	"[""brachydactyly type A1C"",""BDA1C""]"	"[{""label"":""GDF5"",""id"":""8200""}]"	"[""8200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110977""}]"
DOID:0110978	"[""brachydactyly type A1D"",""BDA1D""]"	"[{""label"":""BMPR1B"",""id"":""658""}]"	"[""658""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110978""}]"
DOID:0110980	"[""Joubert syndrome 1"",""CORS1"",""CPD4"",""JBTS1"",""cerebellooculorenal syndrome 1"",""cerebelloparenchymal disorder IV""]"	"[{""label"":""INPP5E"",""id"":""56623""}]"	"[""56623""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110980""}]"
DOID:0110982	"[""Joubert syndrome 13"",""JBTS13""]"	"[{""label"":""TCTN1"",""id"":""79600""}]"	"[""79600""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110982""}]"
DOID:0110984	"[""Joubert syndrome 15"",""JBTS15""]"	"[{""label"":""CEP41"",""id"":""95681""}]"	"[""95681""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110984""}]"
DOID:0110985	"[""Joubert syndrome 16"",""JBTS16""]"	"[{""label"":""TMEM138"",""id"":""51524""}]"	"[""51524""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110985""}]"
DOID:0110987	"[""Joubert syndrome 18"",""JBTS18""]"	"[{""label"":""TCTN3"",""id"":""26123""}]"	"[""26123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110987""}]"
DOID:0110989	"[""Joubert syndrome 20"",""JBTS20""]"	"[{""label"":""TMEM231"",""id"":""79583""}]"	"[""79583""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110989""}]"
DOID:0110993	"[""Joubert syndrome 24"",""JBTS24""]"	"[{""label"":""TCTN2"",""id"":""79867""}]"	"[""79867""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110993""}]"
DOID:0110994	"[""Joubert syndrome 25"",""JBTS25""]"	"[{""label"":""CEP104"",""id"":""9731""}]"	"[""9731""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110994""}]"
DOID:0110995	"[""Joubert syndrome 26"",""JBTS26""]"	"[{""label"":""KATNIP"",""id"":""23247""}]"	"[""23247""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0110995""}]"
DOID:0111000	"[""Joubert syndrome 5"",""JBTS5""]"	"[{""label"":""Cep290"",""id"":""216274""}]"	"[""216274""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111000""}]"
DOID:0111001	"[""Joubert syndrome 6"",""JBTS6""]"	"[{""label"":""TMEM67"",""id"":""91147""}]"	"[""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111001""}]"
DOID:0111001	"[""Joubert syndrome 6"",""JBTS6""]"	"[{""label"":""Tmem67"",""id"":""329795""}]"	"[""329795""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111001""}]"
DOID:0111002	"[""Joubert syndrome 7"",""JBTS7""]"	"[{""label"":""RPGRIP1L"",""id"":""23322""}]"	"[""23322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111002""}]"
DOID:0111004	"[""Joubert syndrome 9"",""JBTS9""]"	"[{""label"":""CC2D2A"",""id"":""57545""}]"	"[""57545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111004""}]"
DOID:0111007	"[""X-linked cone-rod dystrophy 3"",""CORDX3""]"	"[{""label"":""CACNA1F"",""id"":""778""}]"	"[""778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111007""}]"
DOID:0111008	"[""X-linked cone-rod dystrophy 1"",""COD1"",""CORDX1"",""X-linked cone dystrophy 1""]"	"[{""label"":""Rpgr"",""id"":""19893""}]"	"[""19893""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111008""}]"
DOID:0111010	"[""cone-rod dystrophy 5"",""CORD5""]"	"[{""label"":""PITPNM3"",""id"":""83394""}]"	"[""83394""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111010""}]"
DOID:0111011	"[""cone-rod dystrophy 6"",""CORD6"",""RCD2"",""retinal cone dystrophy 2""]"	"[{""label"":""GUCY2D"",""id"":""3000""}]"	"[""3000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111011""}]"
DOID:0111011	"[""cone-rod dystrophy 6"",""CORD6"",""RCD2"",""retinal cone dystrophy 2""]"	"[{""label"":""Gucy2e"",""id"":""14919""}]"	"[""14919""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111011""}]"
DOID:0111013	"[""cone-rod dystrophy 3"",""CORD3""]"	"[{""label"":""ABCA4"",""id"":""24""}]"	"[""24""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111013""}]"
DOID:0111013	"[""cone-rod dystrophy 3"",""CORD3""]"	"[{""label"":""Abca4"",""id"":""11304""}]"	"[""11304""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111013""}]"
DOID:0111015	"[""Newfoundland cone-rod dystrophy"",""NFRCD""]"	"[{""label"":""RLBP1"",""id"":""6017""}]"	"[""6017""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111015""}]"
DOID:0111017	"[""cone-rod dystrophy 10"",""CORD10""]"	"[{""label"":""SEMA4A"",""id"":""64218""}]"	"[""64218""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111017""}]"
DOID:0111019	"[""cone-rod dystrophy 12"",""CORD12""]"	"[{""label"":""PROM1"",""id"":""8842""}]"	"[""8842""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111019""}]"
DOID:0111020	"[""cone-rod dystrophy 9"",""CORD9""]"	"[{""label"":""ADAM9"",""id"":""8754""}]"	"[""8754""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111020""}]"
DOID:0111020	"[""cone-rod dystrophy 9"",""CORD9""]"	"[{""label"":""Adam9"",""id"":""11502""}]"	"[""11502""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111020""}]"
DOID:0111021	"[""cone-rod dystrophy 15"",""CORD15""]"	"[{""label"":""CDHR1"",""id"":""92211""}]"	"[""92211""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111021""}]"
DOID:0111025	"[""cone-rod dystrophy 19"",""CORD19""]"	"[{""label"":""TTLL5"",""id"":""23093""}]"	"[""23093""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111025""}]"
DOID:0111027	"[""hemochromatosis type 2A"",""HFE2A""]"	"[{""label"":""HJV"",""id"":""148738""}]"	"[""148738""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111027""}]"
DOID:0111027	"[""hemochromatosis type 2A"",""HFE2A""]"	"[{""label"":""Hjv"",""id"":""69585""}]"	"[""69585""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111027""}]"
DOID:0111028	"[""hemochromatosis type 4"",""HFE4"",""autosomal dominant hereditary hemochromatosis"",""ferroportin disease"",""hemochromatosis due to defect in ferroportin""]"	"[{""label"":""SLC40A1"",""id"":""30061""}]"	"[""30061""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111028""}]"
DOID:0111028	"[""hemochromatosis type 4"",""HFE4"",""autosomal dominant hereditary hemochromatosis"",""ferroportin disease"",""hemochromatosis due to defect in ferroportin""]"	"[{""label"":""Slc40a1"",""id"":""53945""}]"	"[""53945""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111028""}]"
DOID:0111029	"[""hemochromatosis type 1"",""HFE1"",""symptomatic form of HFE-related hereditary hemochromatosis"",""symptomatic form of classic hemochromatosis"",""symptomatic form of hemochromatosis type 1""]"	"[{""label"":""Hfe"",""id"":""15216""}]"	"[""15216""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111029""}]"
DOID:0111029	"[""hemochromatosis type 1"",""HFE1"",""symptomatic form of HFE-related hereditary hemochromatosis"",""symptomatic form of classic hemochromatosis"",""symptomatic form of hemochromatosis type 1""]"	"[{""label"":""BMP2"",""id"":""650""},{""label"":""HFE"",""id"":""3077""}]"	"[""3077"",""650""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111029""}]"
DOID:0111030	"[""hemochromatosis type 3"",""HFE3"",""TFR2-related hemochromatosis"",""hemochromatosis due to defect in transferrin receptor 2""]"	"[{""label"":""Tfr2"",""id"":""288562""}]"	"[""288562""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111030""}]"
DOID:0111030	"[""hemochromatosis type 3"",""HFE3"",""TFR2-related hemochromatosis"",""hemochromatosis due to defect in transferrin receptor 2""]"	"[{""label"":""Tfr2"",""id"":""50765""}]"	"[""50765""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111030""}]"
DOID:0111030	"[""hemochromatosis type 3"",""HFE3"",""TFR2-related hemochromatosis"",""hemochromatosis due to defect in transferrin receptor 2""]"	"[{""label"":""TFR2"",""id"":""7036""}]"	"[""7036""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111030""}]"
DOID:0111031	"[""hemochromatosis type 5"",""FTH1-associated iron overload"",""FTH1-related iron overload"",""HFE5""]"	"[{""label"":""FTH1"",""id"":""2495""}]"	"[""2495""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111031""}]"
DOID:0111035	"[""CADASIL 1"",""autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1""]"	"[{""label"":""NOTCH3"",""id"":""4854""}]"	"[""4854""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111035""}]"
DOID:0111035	"[""CADASIL 1"",""autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1""]"	"[{""label"":""Notch3"",""id"":""18131""}]"	"[""18131""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111035""}]"
DOID:0111037	"[""glycine N-methyltransferase deficiency"",""GNMT deficiency"",""hypermethioninemia due to GNMT deficiency"",""hypermethioninemia due to glycine N-methyltransferase deficiency""]"	"[{""label"":""Gnmt"",""id"":""14711""}]"	"[""14711""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111037""}]"
DOID:0111037	"[""glycine N-methyltransferase deficiency"",""GNMT deficiency"",""hypermethioninemia due to GNMT deficiency"",""hypermethioninemia due to glycine N-methyltransferase deficiency""]"	"[{""label"":""GNMT"",""id"":""27232""}]"	"[""27232""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111037""}]"
DOID:0111039	"[""hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase"",""hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency"",""psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency""]"	"[{""label"":""AHCY"",""id"":""191""}]"	"[""191""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111039""}]"
DOID:0111040	"[""glycogen storage disease IXd"",""GSD IXd"",""GSD due to muscle phosphorylase kinase deficiency"",""GSD type 9D"",""GSD type 9E"",""GSD type IXd"",""GSD type IXe"",""GSD9D"",""X-linked muscke glycogenosis"",""glycogen storage disease due to muscle phosphorylase kinase deficiency"",""glycogen storage disease type 9D"",""glycogen storage disease type 9E"",""glycogen storage disease type IXd"",""glycogen storage disease type IXe"",""glycogenosis due to muscle phosphorylase kinase deficiency"",""glycogenosis type 9D"",""glycogenosis type 9E"",""glycogenosis type IXd"",""glycogenosis type IXe"",""muscle phosphorylase kinase deficiency""]"	"[{""label"":""PHKA1"",""id"":""5255""}]"	"[""5255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111040""}]"
DOID:0111040	"[""glycogen storage disease IXd"",""GSD IXd"",""GSD due to muscle phosphorylase kinase deficiency"",""GSD type 9D"",""GSD type 9E"",""GSD type IXd"",""GSD type IXe"",""GSD9D"",""X-linked muscke glycogenosis"",""glycogen storage disease due to muscle phosphorylase kinase deficiency"",""glycogen storage disease type 9D"",""glycogen storage disease type 9E"",""glycogen storage disease type IXd"",""glycogen storage disease type IXe"",""glycogenosis due to muscle phosphorylase kinase deficiency"",""glycogenosis type 9D"",""glycogenosis type 9E"",""glycogenosis type IXd"",""glycogenosis type IXe"",""muscle phosphorylase kinase deficiency""]"	"[{""label"":""Phka1"",""id"":""18679""}]"	"[""18679""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111040""}]"
DOID:0111041	"[""glycogen storage disease IXb"",""GSD IXb"",""GSD due to liver and muscle phosphorylase kinase deficiency"",""GSD type 9B"",""GSD type IXb"",""GSD9B"",""glycogen storage disease type 9B"",""glycogen storage disease type IXb"",""glycogenosis due to liver and muscle phosphorylase kinase deficiency"",""glycogenosis type 9B"",""glycogenosis type IXb""]"	"[{""label"":""Phkb"",""id"":""102093""}]"	"[""102093""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111041""}]"
DOID:0111041	"[""glycogen storage disease IXb"",""GSD IXb"",""GSD due to liver and muscle phosphorylase kinase deficiency"",""GSD type 9B"",""GSD type IXb"",""GSD9B"",""glycogen storage disease type 9B"",""glycogen storage disease type IXb"",""glycogenosis due to liver and muscle phosphorylase kinase deficiency"",""glycogenosis type 9B"",""glycogenosis type IXb""]"	"[{""label"":""PHKB"",""id"":""5257""}]"	"[""5257""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111041""}]"
DOID:0111042	"[""glycogen storage disease IXa"",""GSD type 9A"",""GSD type IXa"",""GSD9A"",""glycogen storage disease type 9A"",""glycogen storage disease type IXa"",""glycogenosis type 9A"",""glycogenosis type IXa""]"	"[{""label"":""PHKA2"",""id"":""5256""}]"	"[""5256""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111042""}]"
DOID:0111043	"[""glycogen storage disease IXc"",""GSD type 9C"",""GSD type IXc"",""GSD9C"",""glycogen storage disease type 9C"",""glycogen storage disease type IXc"",""glycogenosis type 9C"",""glycogenosis type IXc""]"	"[{""label"":""PHKG2"",""id"":""5261""}]"	"[""5261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111043""}]"
DOID:0111044	"[""gray platelet syndrome"",""BDPLT4"",""GPS"",""platelet alpha-granule deficiency"",""platelet-type bleeding disorder 4""]"	"[{""label"":""NBEAL2"",""id"":""23218""}]"	"[""23218""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111044""}]"
DOID:0111046	"[""platelet-type bleeding disorder 10"",""BDPLT10"",""CD36 deficiency"",""platelet glycoprotein IV deficiency""]"	"[{""label"":""Cd36"",""id"":""12491""}]"	"[""12491""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111046""}]"
DOID:0111046	"[""platelet-type bleeding disorder 10"",""BDPLT10"",""CD36 deficiency"",""platelet glycoprotein IV deficiency""]"	"[{""label"":""CD36"",""id"":""948""}]"	"[""948""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111046""}]"
DOID:0111050	"[""Quebec platelet disorder"",""BDPLT5"",""factor V Quebec"",""platelet-type bleeding disorder 5""]"	"[{""label"":""PLAU"",""id"":""5328""}]"	"[""5328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111050""}]"
DOID:0111051	"[""platelet-type bleeding disorder 18"",""BDPLT18"",""bleeding disorder due to CalDAG-GEFI deficiency"",""bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency""]"	"[{""label"":""RASGRP2"",""id"":""10235""}]"	"[""10235""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111051""}]"
DOID:0111052	"[""Scott syndrome"",""BDPLT7"",""SCTS"",""bleeding abnormality due to deficiency of platelet biding of factor X"",""familial prothrombin consumption inhibitor"",""familial prothrombin conversion defect"",""platelet-type bleeding disorder 7"",""prothrombin consumption deficiency""]"	"[{""label"":""ANO6"",""id"":""196527""}]"	"[""196527""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111052""}]"
DOID:0111053	"[""platelet-type bleeding disorder 15"",""BDPLT15"",""autosomal dominant macrothrombocytopenia ACTN1-related""]"	"[{""label"":""ACTN1"",""id"":""87""}]"	"[""87""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111053""}]"
DOID:0111054	"[""von Willebrand's disease 3"",""VWD type 3"",""VWD3"",""von Willebrand disease type 3"",""von Willebrand disease type III""]"	"[{""label"":""VWF"",""id"":""7450""}]"	"[""7450""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111054""}]"
DOID:0111056	"[""platelet-type bleeding disorder 3"",""BDPLT3"",""PT-VWD"",""platelet type-von Willebrand disease"",""pseudo-von Willebrand disease"",""von Willebrand disease platelet-type""]"	"[{""label"":""GP1BA"",""id"":""2811""}]"	"[""2811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111056""}]"
DOID:0111057	"[""platelet-type bleeding disorder 11"",""BDPLT11"",""GP VI deficiency"",""glycoprotein VI deficiency""]"	"[{""label"":""GP6"",""id"":""51206""}]"	"[""51206""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111057""}]"
DOID:0111059	"[""Bernard-Soulier syndrome type A2"",""BSSA2""]"	"[{""label"":""GP1BA"",""id"":""2811""}]"	"[""2811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111059""}]"
DOID:0111061	"[""familial hypobetalipoproteinemia 2"",""FHBL2"",""combined familial hypolipidemia""]"	"[{""label"":""ANGPTL3"",""id"":""27329""}]"	"[""27329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111061""}]"
DOID:0111061	"[""familial hypobetalipoproteinemia 2"",""FHBL2"",""combined familial hypolipidemia""]"	"[{""label"":""Apob"",""id"":""238055""}]"	"[""238055""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111061""}]"
DOID:0111062	"[""familial hypobetalipoproteinemia 1"",""FHBL1""]"	"[{""label"":""APOB"",""id"":""338""}]"	"[""338""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111062""}]"
DOID:0111063	"[""hyperphosphatemic familial tumoral calcinosis"",""HFTC"",""PHPTC"",""cortical hyperostosis with hyperphosphatemia"",""familial Teutschlaender disease"",""familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome"",""hypercalcemic tumoral calcinosis"",""hyperostosis with hyperphosphatemia"",""hyperphosphatemia hyperostosis"",""hyperphosphatemia hyperostosis syndrome"",""hyperphosphatemia tumoral calcinosis"",""lipocalcinogranulomatosis"",""morbus Teutschlaender"",""primary hyperphosphatemic tumoral calcinosis"",""tumoral calcinosis with hyperphosphatemia""]"	"[{""label"":""Galnt3"",""id"":""14425""},{""label"":""Kl"",""id"":""16591""}]"	"[""14425"",""16591""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111063""}]"
DOID:0111063	"[""hyperphosphatemic familial tumoral calcinosis"",""HFTC"",""PHPTC"",""cortical hyperostosis with hyperphosphatemia"",""familial Teutschlaender disease"",""familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome"",""hypercalcemic tumoral calcinosis"",""hyperostosis with hyperphosphatemia"",""hyperphosphatemia hyperostosis"",""hyperphosphatemia hyperostosis syndrome"",""hyperphosphatemia tumoral calcinosis"",""lipocalcinogranulomatosis"",""morbus Teutschlaender"",""primary hyperphosphatemic tumoral calcinosis"",""tumoral calcinosis with hyperphosphatemia""]"	"[{""label"":""GALNT3"",""id"":""2591""}]"	"[""2591""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00402""}]"
DOID:0111064	"[""autosomal recessive distal hereditary motor neuronopathy 1"",""DSMA1"",""SIANRF"",""SMARD1"",""autosomal recessive distal spinal muscular atrophy 1"",""autosomal recessive spinal muscular atrophy with respiratory distress"",""dHMN6"",""diaphragmatic spinal muscular atrophy"",""distal hereditary motor neuropathy type 6"",""distal spinal muscular atrophy 1"",""distal-HMN type 6"",""severe infantile axonal neuropathy with respiratory failure type 1"",""spinal muscular atrophy with respiratory distress type 1""]"	"[{""label"":""IGHMBP2"",""id"":""3508""}]"	"[""3508""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111064""}]"
DOID:0111066	"[""congenital bile acid synthesis defect 5"",""CBAS5""]"	"[{""label"":""Abcd3"",""id"":""19299""}]"	"[""19299""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111066""}]"
DOID:0111066	"[""congenital bile acid synthesis defect 5"",""CBAS5""]"	"[{""label"":""ABCD3"",""id"":""5825""}]"	"[""5825""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111066""}]"
DOID:0111067	"[""congenital bile acid synthesis defect 6"",""CBAS6""]"	"[{""label"":""ACOX2"",""id"":""8309""}]"	"[""8309""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111067""}]"
DOID:0111068	"[""congenital bile acid synthesis defect 4"",""CBAS4"",""intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid"",""trihydroxycoprostanic acid in bile""]"	"[{""label"":""AMACR"",""id"":""23600""}]"	"[""23600""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111068""}]"
DOID:0111069	"[""congenital bile acid synthesis defect 2"",""CBAS2"",""cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency""]"	"[{""label"":""AKR1D1"",""id"":""6718""}]"	"[""6718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111069""}]"
DOID:0111070	"[""congenital bile acid synthesis defect 3"",""CBAS3"",""oxysterol 7-alpha-hydroxylase deficiency""]"	"[{""label"":""CYP7B1"",""id"":""9420""}]"	"[""9420""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111070""}]"
DOID:0111071	"[""congenital bile acid synthesis defect 1"",""CBAS1""]"	"[{""label"":""HSD3B7"",""id"":""80270""}]"	"[""80270""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111071""}]"
DOID:0111072	"[""myostatin-related muscle hypertrophy"",""MSLHP""]"	"[{""label"":""Mstn"",""id"":""17700""}]"	"[""17700""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111072""}]"
DOID:0111072	"[""myostatin-related muscle hypertrophy"",""MSLHP""]"	"[{""label"":""MSTN"",""id"":""2660""}]"	"[""2660""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111072""}]"
DOID:0111074	"[""progressive familial heart block type IA"",""PFHB1A""]"	"[{""label"":""SCN5A"",""id"":""6331""}]"	"[""6331""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111074""}]"
DOID:0111074	"[""progressive familial heart block type IA"",""PFHB1A""]"	"[{""label"":""Scn5a"",""id"":""20271""}]"	"[""20271""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111074""}]"
DOID:0111076	"[""progressive familial heart block type IB"",""PFHB1B""]"	"[{""label"":""TRPM4"",""id"":""54795""}]"	"[""54795""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111076""}]"
DOID:0111077	"[""congenital nonspherocytic hemolytic anemia 2"",""PK deficiency"",""Red cell pyruvate kinase deficiency"",""hemolytic anemia due to red cell pyruvate kinase deficiency"",""pyruvate kinase deficiency of erythrocyte"",""pyruvate kinase deficiency of red cells""]"	"[{""label"":""PKLR"",""id"":""5313""}]"	"[""5313""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111077""}]"
DOID:0111078	"[""tibial muscular dystrophy"",""Finnish tibial muscular dystrophy"",""TMD"",""Tardive tibial muscular dystrophy"",""Udd myopathy"",""Udd type distal myopathy"",""distal titinopathy""]"	"[{""label"":""Ttn"",""id"":""22138""}]"	"[""22138""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111078""}]"
DOID:0111078	"[""tibial muscular dystrophy"",""Finnish tibial muscular dystrophy"",""TMD"",""Tardive tibial muscular dystrophy"",""Udd myopathy"",""Udd type distal myopathy"",""distal titinopathy""]"	"[{""label"":""TTN"",""id"":""7273""}]"	"[""7273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111078""}]"
DOID:0111079	"[""birdshot chorioretinopathy"",""BSCR"",""birdshot chorioretinitis"",""birdshot retinochoroiditis"",""birdshot retinochoroidopathy"",""vitiliginous choroiditis""]"	"[{""label"":""HLA-B"",""id"":""3106""}]"	"[""3106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111079""}]"
DOID:0111081	"[""Fanconi anemia complementation group T"",""FANCT""]"	"[{""label"":""UBE2T"",""id"":""29089""}]"	"[""29089""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111081""}]"
DOID:0111083	"[""Fanconi anemia complementation group D2"",""FA4"",""FAD2"",""FANCD2"",""Fanconi pancytopenia type 4""]"	"[{""label"":""FANCD2"",""id"":""2177""}]"	"[""2177""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111083""}]"
DOID:0111086	"[""Fanconi anemia complementation group G"",""FANCG""]"	"[{""label"":""FANCG"",""id"":""2189""}]"	"[""2189""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111086""}]"
DOID:0111089	"[""Fanconi anemia complementation group D1"",""FAD1"",""FANCD1""]"	"[{""label"":""BRCA2"",""id"":""675""}]"	"[""675""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111089""}]"
DOID:0111091	"[""Fanconi anemia complementation group I"",""FANCI""]"	"[{""label"":""FANCI"",""id"":""55215""}]"	"[""55215""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111091""}]"
DOID:0111094	"[""Fanconi anemia complementation group N"",""FANCN""]"	"[{""label"":""PALB2"",""id"":""79728""}]"	"[""79728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111094""}]"
DOID:0111095	"[""Fanconi anemia complementation group A"",""FANCA""]"	"[{""label"":""Fanca"",""id"":""14087""}]"	"[""14087""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111095""}]"
DOID:0111096	"[""Fanconi anemia complementation group O"",""FANCO""]"	"[{""label"":""RAD51C"",""id"":""5889""}]"	"[""5889""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111096""}]"
DOID:0111098	"[""Fanconi anemia complementation group B"",""FACB"",""FANCB"",""Fanconi pancytopenia type 2""]"	"[{""label"":""FANCB"",""id"":""2187""}]"	"[""2187""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111098""}]"
DOID:0111099	"[""maturity-onset diabetes of the young type 1"",""Diabetes Mellitus Type 2"",""MODY type 1"",""MODY1"",""mild juvenile diabetes mellitus""]"	"[{""label"":""HNF4A"",""id"":""3172""}]"	"[""3172""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111099""}]"
DOID:0111100	"[""maturity-onset diabetes of the young type 2"",""MODY glucokinase-related"",""MODY type 2"",""MODY2""]"	"[{""label"":""Gck"",""id"":""103988""}]"	"[""103988""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111100""}]"
DOID:0111100	"[""maturity-onset diabetes of the young type 2"",""MODY glucokinase-related"",""MODY type 2"",""MODY2""]"	"[{""label"":""GCK"",""id"":""2645""}]"	"[""2645""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111100""}]"
DOID:0111102	"[""maturity-onset diabetes of the young type 3"",""MODY type 3"",""MODY3""]"	"[{""label"":""HNF1A"",""id"":""6927""}]"	"[""6927""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111102""}]"
DOID:0111103	"[""maturity-onset diabetes of the young type 4"",""MODY type 4"",""MODY4""]"	"[{""label"":""PDX1"",""id"":""3651""}]"	"[""3651""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111103""}]"
DOID:0111103	"[""maturity-onset diabetes of the young type 4"",""MODY type 4"",""MODY4""]"	"[{""label"":""Pdx1"",""id"":""18609""}]"	"[""18609""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111103""}]"
DOID:0111105	"[""maturity-onset diabetes of the young type 8"",""MODY type 8"",""MODY8"",""diabetes and pancreatic exocrine"",""maturity-onset diabetes of the young type 8 with exocrine dysfunction""]"	"[{""label"":""CEL"",""id"":""1056""}]"	"[""1056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111105""}]"
DOID:0111108	"[""maturity-onset diabetes of the young type 10"",""MODY10""]"	"[{""label"":""INS"",""id"":""3630""}]"	"[""3630""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111108""}]"
DOID:0111110	"[""maturity-onset diabetes of the young type 13"",""MODY type 13"",""MODY13""]"	"[{""label"":""KCNJ11"",""id"":""3767""}]"	"[""3767""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111110""}]"
DOID:0111111	"[""maturity-onset diabetes of the young type 14"",""MODY14""]"	"[{""label"":""APPL1"",""id"":""26060""}]"	"[""26060""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111111""}]"
DOID:0111113	"[""nephronophthisis 2"",""NPH2"",""NPHP2"",""infantile nephronophthisis 2""]"	"[{""label"":""INVS"",""id"":""27130""}]"	"[""27130""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111113""}]"
DOID:0111114	"[""nephronophthisis 3"",""NPH3"",""NPHP3""]"	"[{""label"":""NPHP3"",""id"":""27031""}]"	"[""27031""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111114""}]"
DOID:0111118	"[""nephronophthisis 11"",""NPHP11""]"	"[{""label"":""TMEM67"",""id"":""91147""}]"	"[""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111118""}]"
DOID:0111122	"[""nephronophthisis 14"",""NPHP14""]"	"[{""label"":""ZNF423"",""id"":""23090""}]"	"[""23090""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111122""}]"
DOID:0111123	"[""nephronophthisis 15"",""NPHP15""]"	"[{""label"":""CEP164"",""id"":""22897""}]"	"[""22897""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111123""}]"
DOID:0111127	"[""nephronophthisis 20"",""NPHP20""]"	"[{""label"":""MAPKBP1"",""id"":""23005""}]"	"[""23005""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111127""}]"
DOID:0111128	"[""focal segmental glomerulosclerosis 1"",""FSGS1""]"	"[{""label"":""Ace"",""id"":""24310""}]"	"[""24310""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111128""}]"
DOID:0111128	"[""focal segmental glomerulosclerosis 1"",""FSGS1""]"	"[{""label"":""Actn4"",""id"":""60595""}]"	"[""60595""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111128""}]"
DOID:0111128	"[""focal segmental glomerulosclerosis 1"",""FSGS1""]"	"[{""label"":""ACTN4"",""id"":""81""}]"	"[""81""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111128""}]"
DOID:0111129	"[""focal segmental glomerulosclerosis 2"",""FSGS2""]"	"[{""label"":""TRPC6"",""id"":""7225""}]"	"[""7225""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111129""}]"
DOID:0111129	"[""focal segmental glomerulosclerosis 2"",""FSGS2""]"	"[{""label"":""Trpc6"",""id"":""22068""}]"	"[""22068""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111129""}]"
DOID:0111130	"[""focal segmental glomerulosclerosis 5"",""FSGS5""]"	"[{""label"":""INF2"",""id"":""64423""}]"	"[""64423""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111130""}]"
DOID:0111131	"[""focal segmental glomerulosclerosis 6"",""FSGS6""]"	"[{""label"":""MYO1E"",""id"":""4643""}]"	"[""4643""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111131""}]"
DOID:0111132	"[""focal segmental glomerulosclerosis 7"",""FSGS7""]"	"[{""label"":""PAX2"",""id"":""5076""}]"	"[""5076""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111132""}]"
DOID:0111133	"[""focal segmental glomerulosclerosis 8"",""FSGS8""]"	"[{""label"":""ANLN"",""id"":""54443""}]"	"[""54443""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111133""}]"
DOID:0111134	"[""focal segmental glomerulosclerosis 9"",""FSGS9""]"	"[{""label"":""CRB2"",""id"":""286204""}]"	"[""286204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111134""}]"
DOID:0111135	"[""congenital generalized lipodystrophy type 1"",""Berardinelli-Seip Congenital Lipodystrophy, Type 1"",""Brunzell syndrome AGPAT2-related""]"	"[{""label"":""AGPAT2"",""id"":""10555""}]"	"[""10555""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111135""}]"
DOID:0111136	"[""congenital generalized lipodystrophy type 2"",""Berardinelli-Seip congenital lipodystrophy type 2"",""Berardinelli-Seip syndrome"",""Brunzell syndrome BSCL2-related"",""CGL2"",""congenital lipoatrophic diabetes"",""total lipodystrophy and acromegaloid gigantism""]"	"[{""label"":""Bscl2"",""id"":""14705""},{""label"":""Pparg"",""id"":""19016""}]"	"[""14705"",""19016""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111136""}]"
DOID:0111136	"[""congenital generalized lipodystrophy type 2"",""Berardinelli-Seip congenital lipodystrophy type 2"",""Berardinelli-Seip syndrome"",""Brunzell syndrome BSCL2-related"",""CGL2"",""congenital lipoatrophic diabetes"",""total lipodystrophy and acromegaloid gigantism""]"	"[{""label"":""BSCL2"",""id"":""26580""}]"	"[""26580""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111136""}]"
DOID:0111138	"[""congenital generalized lipodystrophy type 4"",""Berardinelli-Seip congenital lipodystrophy type 4 with muscular dystrophy"",""congenital generalised lipodystrophy type 4"",""generalised congenital lipodystrophy type 4"",""generalised congenital lipodystrophy with myopathy"",""generalized congenital lipodystrophy type 4"",""generalized congenital lipodystrophy with myopathy""]"	"[{""label"":""Cavin1"",""id"":""19285""}]"	"[""19285""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111138""}]"
DOID:0111138	"[""congenital generalized lipodystrophy type 4"",""Berardinelli-Seip congenital lipodystrophy type 4 with muscular dystrophy"",""congenital generalised lipodystrophy type 4"",""generalised congenital lipodystrophy type 4"",""generalised congenital lipodystrophy with myopathy"",""generalized congenital lipodystrophy type 4"",""generalized congenital lipodystrophy with myopathy""]"	"[{""label"":""CAVIN1"",""id"":""284119""}]"	"[""284119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111138""}]"
DOID:0111139	"[""mitochondrial complex III deficiency""]"	"[{""label"":""UQCRFS1"",""id"":""7386""}]"	"[""7386""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111139""}]"
DOID:0111140	"[""IGSF1 deficiency syndrome"",""CHTE"",""X-linked central congenital hypothyroidism with late-onset macroorchidism"",""X-linked central congenital hypothyroidism with late-onset testicular enlargement"",""central hypothyroidism and testicular enlargement""]"	"[{""label"":""IGSF1"",""id"":""3547""}]"	"[""3547""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111140""}]"
DOID:0111140	"[""IGSF1 deficiency syndrome"",""CHTE"",""X-linked central congenital hypothyroidism with late-onset macroorchidism"",""X-linked central congenital hypothyroidism with late-onset testicular enlargement"",""central hypothyroidism and testicular enlargement""]"	"[{""label"":""Igsf1"",""id"":""209268""}]"	"[""209268""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111140""}]"
DOID:0111141	"[""delayed sleep phase syndrome"",""DSPD""]"	"[{""label"":""CRY1"",""id"":""1407""}]"	"[""1407""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111141""}]"
DOID:0111144	"[""preterm premature rupture of the membranes"",""PPROM""]"	"[{""label"":""SERPINH1"",""id"":""871""}]"	"[""871""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111144""}]"
DOID:0111149	"[""autosomal recessive isolated ectopia lentis 2"",""ECTOL2""]"	"[{""label"":""Adamtsl4"",""id"":""229595""}]"	"[""229595""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111149""}]"
DOID:0111149	"[""autosomal recessive isolated ectopia lentis 2"",""ECTOL2""]"	"[{""label"":""ADAMTSL4"",""id"":""54507""}]"	"[""54507""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111149""}]"
DOID:0111150	"[""autosomal dominant isolated ectopia lentis 1"",""ECTOL1""]"	"[{""label"":""FBN1"",""id"":""2200""}]"	"[""2200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111150""}]"
DOID:0111153	"[""congenital mirror movement disorder"",""familial congenital controlateral synkinesia"",""familial congenital mirror movements"",""hereditary congenital controlateral synkinesia"",""hereditary congenital mirror movements"",""isolated congenital controlateral synkinesia"",""isolated congenital mirror movements""]"	"[{""label"":""DCC"",""id"":""1630""},{""label"":""NTN1"",""id"":""9423""}]"	"[""1630"",""9423""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111153""}]"
DOID:0111155	"[""autosomal recessive spinocerebellar ataxia 21"",""SCAR21"",""acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome"",""autosomal recessive spinocerebellar ataxia 21 with hepatopathy""]"	"[{""label"":""SCYL1"",""id"":""57410""}]"	"[""57410""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111155""}]"
DOID:0111156	"[""spermatogenic failure 9"",""globozoospermia"",""male infertility due to round-headed spermatozoa""]"	"[{""label"":""DPY19L2"",""id"":""283417""}]"	"[""283417""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111156""}]"
DOID:0111158	"[""SADDAN"",""SADDAN dysplasia"",""severe achondroplasia with developmental delay and acanthosis nigricans""]"	"[{""label"":""FGFR3"",""id"":""2261""}]"	"[""2261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111158""}]"
DOID:0111160	"[""camptodactyly-tall stature-scoliosis-hearing loss syndrome"",""CATSHL syndrome""]"	"[{""label"":""FGFR3"",""id"":""2261""}]"	"[""2261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111160""}]"
DOID:0111161	"[""Crouzon syndrome-acanthosis nigricans syndrome"",""CAN"",""Crouzon-dermoskeletal syndrome"",""Crouzonodermoskeletal syndrome""]"	"[{""label"":""FGFR3"",""id"":""2261""}]"	"[""2261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111161""}]"
DOID:0111162	"[""epidermal nevus"",""nonepidermolytic keratinocytic nevus""]"	"[{""label"":""FGFR3"",""id"":""2261""},{""label"":""HRAS"",""id"":""3265""},{""label"":""NRAS"",""id"":""4893""},{""label"":""PIK3CA"",""id"":""5290""}]"	"[""2261"",""3265"",""4893"",""5290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111162""}]"
DOID:0111166	"[""molybdenum cofactor deficiency type C"",""MOCOD type C"",""MOCODC"",""combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C"",""molybdenum cofactor deficiency complementation group C""]"	"[{""label"":""GPHN"",""id"":""10243""}]"	"[""10243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111166""}]"
DOID:0111167	"[""Dyggve-Melchior-Clausen disease"",""DMC disease"",""pseudo-Morquio disease type I""]"	"[{""label"":""DYM"",""id"":""54808""}]"	"[""54808""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111167""}]"
DOID:0111169	"[""subcortical band heterotopia"",""HeCo"",""band heterotopia"",""double cortex syndrome"",""heterotopic cortex"",""subcortical laminar heterotopia""]"	"[{""label"":""Eml1"",""id"":""68519""}]"	"[""68519""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111169""}]"
DOID:0111180	"[""French Canadian Leigh disease"",""French Canadian type COX deficiency"",""French Canadian type Leigh syndrome"",""French Canadian type cytochrome c oxidase deficiency"",""Saguenay Lac saint Jean type COX deficiency"",""Saguenay Lac saint Jean type Leigh syndrome"",""mitochondrial complex IV deficiency nuclear type 5""]"	"[{""label"":""LRPPRC"",""id"":""10128""}]"	"[""10128""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111180""}]"
DOID:0111181	"[""familial hemiplegic migraine 1"",""FHM1"",""MHP1"",""familial hemiplegic migraine1 with progressive cerebellar ataxia""]"	"[{""label"":""cac"",""id"":""32158""}]"	"[""32158""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111181""}]"
DOID:0111181	"[""familial hemiplegic migraine 1"",""FHM1"",""MHP1"",""familial hemiplegic migraine1 with progressive cerebellar ataxia""]"	"[{""label"":""CACNA1A"",""id"":""773""}]"	"[""773""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111181""}]"
DOID:0111182	"[""familial hemiplegic migraine 2"",""FHM2"",""Familial hemiplegic migraine-2"",""MHP2""]"	"[{""label"":""Atp1a2"",""id"":""98660""}]"	"[""98660""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111182""}]"
DOID:0111182	"[""familial hemiplegic migraine 2"",""FHM2"",""Familial hemiplegic migraine-2"",""MHP2""]"	"[{""label"":""ATP1A2"",""id"":""477""}]"	"[""477""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111182""}]"
DOID:0111183	"[""familial hemiplegic migraine 3"",""FHM3"",""MHP3""]"	"[{""label"":""SCN1A"",""id"":""6323""}]"	"[""6323""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111183""}]"
DOID:0111186	"[""myopathy, lactic acidosis, and sideroblastic anemia 2"",""MLASA2""]"	"[{""label"":""YARS2"",""id"":""51067""}]"	"[""51067""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111186""}]"
DOID:0111187	"[""distal myopathy with anterior tibial onset"",""DMAT"",""distal muscular dystrophy with anterior tibial onset""]"	"[{""label"":""DYSF"",""id"":""8291""}]"	"[""8291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111187""}]"
DOID:0111188	"[""myofibrillar myopathy 9"",""Edstrom myopathy"",""HIBM-ERF"",""HMERF"",""Hereditary inclusion body myopathy with early respiratory failure"",""MFM-titinopathy"",""MFM9"",""MPRM"",""Myofibrillar myopathy-titinopathy"",""autosomal dominant distal myopathy with early respiratory failure"",""hereditary myopathy with early respiratory failure"",""myofibrillar myopathy 9 with early respiratory failure"",""proximal myopathy with early respiratory muscle involvement""]"	"[{""label"":""TTN"",""id"":""7273""}]"	"[""7273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111188""}]"
DOID:0111189	"[""distal myopathy 3"",""MPD3"",""distal muscular dystrophy 3"",""distal myopathy type 3""]"	"[{""label"":""HNRNPA1"",""id"":""3178""}]"	"[""3178""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111189""}]"
DOID:0111190	"[""distal myopathy 4"",""MPD4"",""distal ABD-filaminopathy"",""distal muscular dystrophy 4"",""distal myopathy with posterior leg and anterior hand involvement""]"	"[{""label"":""FLNC"",""id"":""2318""}]"	"[""2318""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111190""}]"
DOID:0111193	"[""facioscapulohumeral muscular dystrophy 2"",""FSHD2"",""facioscapulohumeral muscular dystrophy 1B"",""facioscapulohumeral muscular dystrophy type 2""]"	"[{""label"":""SMCHD1"",""id"":""23347""}]"	"[""23347""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111193""}]"
DOID:0111194	"[""autosomal dominant adult-onset proximal spinal muscular atrophy"",""Finkel disease"",""Finkel late-adult type SMA"",""SMAFK"",""autosomal dominant adult proximal spinal muscular atrophy"",""autosomal dominant adult-onset proximal SMA"",""autosomal dominant late-onset spinal muscular atrophy, Finkel type""]"	"[{""label"":""VAPB"",""id"":""9217""}]"	"[""9217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111194""}]"
DOID:0111196	"[""X-linked distal spinal muscular atrophy 3"",""ATP7A-related distal motor neuropathy"",""DSMAX"",""SMAX3"",""X-linked dHMN3"",""X-linked dSMA3"",""X-linked distal hereditary motor neuropathy type 3"",""X-linked recessive distal spinal muscular atrophy""]"	"[{""label"":""Atp7a"",""id"":""11977""}]"	"[""11977""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111196""}]"
DOID:0111196	"[""X-linked distal spinal muscular atrophy 3"",""ATP7A-related distal motor neuropathy"",""DSMAX"",""SMAX3"",""X-linked dHMN3"",""X-linked dSMA3"",""X-linked distal hereditary motor neuropathy type 3"",""X-linked recessive distal spinal muscular atrophy""]"	"[{""label"":""ATP7A"",""id"":""538""}]"	"[""538""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111196""}]"
DOID:0111199	"[""autosomal dominant distal hereditary motor neuronopathy 7"",""DHMN7A"",""DHMNVPy"",""HMN VIIA"",""HMN7A"",""Harper-Young myopath"",""dHMN7"",""distal hereditary motor neuronopathy type 7"",""distal hereditary motor neuropathy type VIIA"",""distal spinal muscular atrophy with vocal cord paralysis"",""distal spinal muscular atrophy with vocal cord paralysis type 7A""]"	"[{""label"":""SLC5A7"",""id"":""60482""}]"	"[""60482""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111199""}]"
DOID:0111202	"[""autosomal dominant distal hereditary motor neuronopathy 14"",""DHMN7B"",""HMN VIIB"",""HMN7B"",""Harper-Young myopathy"",""distal hereditary motor neuronopathy type 7B"",""distal hereditary motor neuropathy type VIIB"",""distal spinal muscular atrophy with vocal cord paralysis type 7B""]"	"[{""label"":""DCTN1"",""id"":""1639""}]"	"[""1639""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111202""}]"
DOID:0111206	"[""autosomal dominant distal hereditary motor neuronopathy 2"",""HMN II"",""HMN IIA"",""HMN2"",""HMN2A"",""autosomal dominant adult spinal muscular atrophy IIA"",""distal hereditary motor neuronopathy type 2"",""distal hereditary motor neuronopathy type 2A"",""distal hereditary motor neuropathy type II"",""distal hereditary motor neuropathy type IIA"",""spinal Charcot-Marie-Tooth disease IIA""]"	"[{""label"":""HSPB8"",""id"":""26353""}]"	"[""26353""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111206""}]"
DOID:0111207	"[""autosomal dominant distal hereditary motor neuronopathy 3"",""HMN IIB"",""HMN2B"",""distal hereditary motor neuronopathy type 2B"",""distal hereditary motor neuropathy type IIB""]"	"[{""label"":""HSPB1"",""id"":""3315""}]"	"[""3315""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111207""}]"
DOID:0111210	"[""autosomal dominant distal hereditary motor neuronopathy 6"",""HMN IID"",""HMN2D"",""distal hereditary motor neuronopathy type 2D"",""distal hereditary motor neuropathy type IID"",""distal spinal muscular atrophy with calf predominance""]"	"[{""label"":""FBXO38"",""id"":""81545""}]"	"[""81545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111210""}]"
DOID:0111212	"[""autosomal dominant distal hereditary motor neuronopathy 9"",""DHMN9"",""HMN9"",""distal hereditary motor neuronopathy type 9"",""distal hereditary motor neuropathy type IX""]"	"[{""label"":""WARS1"",""id"":""7453""}]"	"[""7453""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111212""}]"
DOID:0111214	"[""autosomal recessive distal hereditary motor neuronopathy 5"",""DSMA5"",""autosomal recessive distal spinal muscular atrophy type 5"",""distal spinal muscular atrophy type 5"",""young adult-onset dHMN"",""young adult-onset distal hereditary motor neuropathy""]"	"[{""label"":""DNAJB2"",""id"":""3300""}]"	"[""3300""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111214""}]"
DOID:0111220	"[""centronuclear myopathy 2"",""CNM2""]"	"[{""label"":""BIN1"",""id"":""274""}]"	"[""274""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111220""}]"
DOID:0111222	"[""centronuclear myopathy 5"",""CNM5""]"	"[{""label"":""SPEG"",""id"":""10290""}]"	"[""10290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111222""}]"
DOID:0111223	"[""centronuclear myopathy 1"",""CNM1""]"	"[{""label"":""VPS1"",""id"":""853870""}]"	"[""853870""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111223""}]"
DOID:0111223	"[""centronuclear myopathy 1"",""CNM1""]"	"[{""label"":""DNM2"",""id"":""1785""},{""label"":""MTMR14"",""id"":""64419""}]"	"[""1785"",""64419""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111223""}]"
DOID:0111227	"[""frontotemporal dementia and/or amyotrophic lateral sclerosis 7"",""ALS17"",""AMYOTROPHIC LATERAL SCLEROSIS"",""AMYOTROPHIC LATERAL SCLEROSIS 17 (FORMERLY)"",""CHMP2B-RELATED"",""CHMP2B-related frontotemporal dementia"",""FRONTOTEMPORAL DEMENTIA"",""FTD3"",""FTDALS7"",""amyotrophic lateral sclerosis type 17"",""chromosome 3-linked frontotemporal dementia""]"	"[{""label"":""CHMP2B"",""id"":""25978""}]"	"[""25978""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111227""}]"
DOID:0111228	"[""Sveinsson chorioretinal atrophy"",""HPCD"",""SCRA"",""atrophia areata"",""helicoid peripapillary chorioretinal degeneration"",""peripapillary chorioretinal degeneration, Icelandic type""]"	"[{""label"":""TEAD1"",""id"":""7003""}]"	"[""7003""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111228""}]"
DOID:0111230	"[""congenital muscular dystrophy-dystroglycanopathy type A11"",""MDDGA11"",""Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11""]"	"[{""label"":""B3GALNT2"",""id"":""148789""}]"	"[""148789""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111230""}]"
DOID:0111231	"[""congenital muscular dystrophy-dystroglycanopathy type A8"",""MDDGA8"",""Walker-Warburg syndrome or muscle-eye-brain disease GTDC2-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A8""]"	"[{""label"":""POMGNT2"",""id"":""84892""}]"	"[""84892""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111231""}]"
DOID:0111232	"[""congenital muscular dystrophy-dystroglycanopathy type A9"",""MDDGA9"",""Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9""]"	"[{""label"":""DAG1"",""id"":""1605""}]"	"[""1605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111232""}]"
DOID:0111233	"[""congenital muscular dystrophy-dystroglycanopathy type A14"",""MDDGA14"",""Walker-Warburg syndrome or muscle-eye-brain disease GMPPB-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A14""]"	"[{""label"":""GMPPB"",""id"":""29925""}]"	"[""29925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111233""}]"
DOID:0111234	"[""congenital muscular dystrophy-dystroglycanopathy type A7"",""MDDGA7"",""Walker-Warburg syndrome or muscle-eye-brain disease ISPD-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A7""]"	"[{""label"":""CRPPA"",""id"":""729920""}]"	"[""729920""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111234""}]"
DOID:0111235	"[""congenital muscular dystrophy-dystroglycanopathy type A12"",""MDDGA12"",""Walker-Warburg syndrome or muscle-eye-brain disease POMK-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A12""]"	"[{""label"":""POMK"",""id"":""84197""}]"	"[""84197""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111235""}]"
DOID:0111236	"[""congenital muscular dystrophy-dystroglycanopathy type A3"",""MDDGA3"",""Walker-Warburg syndrome or muscle-eye-brain disease, POMGNT1-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A3""]"	"[{""label"":""POMGNT1"",""id"":""55624""}]"	"[""55624""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00377""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111236""}]"
DOID:0111237	"[""congenital muscular dystrophy-dystroglycanopathy type A1"",""MDDGA1"",""Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1""]"	"[{""label"":""rt"",""id"":""39297""}]"	"[""39297""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111237""}]"
DOID:0111237	"[""congenital muscular dystrophy-dystroglycanopathy type A1"",""MDDGA1"",""Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1""]"	"[{""label"":""POMT1"",""id"":""10585""}]"	"[""10585""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111237""}]"
DOID:0111238	"[""congenital muscular dystrophy-dystroglycanopathy type A13"",""MDDGA13"",""Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related"",""Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13""]"	"[{""label"":""B4GAT1"",""id"":""11041""}]"	"[""11041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111238""}]"
DOID:0111239	"[""congenital muscular dystrophy-dystroglycanopathy type A10"",""MDDGA10"",""Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10""]"	"[{""label"":""RXYLT1"",""id"":""10329""}]"	"[""10329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111239""}]"
DOID:0111240	"[""congenital muscular dystrophy-dystroglycanopathy type A2"",""MDDGA2"",""Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2""]"	"[{""label"":""POMT2"",""id"":""29954""}]"	"[""29954""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111240""}]"
DOID:0111241	"[""congenital muscular dystrophy-dystroglycanopathy type A5"",""MDDGA5"",""Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5""]"	"[{""label"":""FKRP"",""id"":""79147""}]"	"[""79147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111241""}]"
DOID:0111242	"[""congenital muscular dystrophy-dystroglycanopathy type A6"",""MDDGA6"",""Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related"",""congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6""]"	"[{""label"":""LARGE1"",""id"":""9215""}]"	"[""9215""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111242""}]"
DOID:0111243	"[""acromicric dysplasia"",""ACMICD"",""acromicric skeletal dysplasia""]"	"[{""label"":""FBN1"",""id"":""2200""}]"	"[""2200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111243""}]"
DOID:0111247	"[""hypertension and brachydactyly syndrome"",""Bilginturan brachydactyly"",""Bilginturan syndrome"",""HTNB"",""brachydactyly with hypertension"",""type E brachydactyly with short stature and hypertension""]"	"[{""label"":""PDE3A"",""id"":""5139""}]"	"[""5139""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111247""}]"
DOID:0111248	"[""cerebrocostomandibular syndrome"",""CCM syndrome"",""CCMS"",""cerebro-costo-mandibular syndrome"",""rib gap defects with micrognathia""]"	"[{""label"":""SNRPB"",""id"":""6628""}]"	"[""6628""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111248""}]"
DOID:0111249	"[""uveal coloboma-cleft lip and palate-intellectual disability"",""COB1"",""Uveal coloboma-cleft lip/palate-mental retardation syndrome"",""coloboma-microphthalmos syndrome"",""coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate"",""ocular coloboma with or without hearing impairment, cleft lip/palate, and/or mental retardation""]"	"[{""label"":""YAP1"",""id"":""10413""}]"	"[""10413""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111249""}]"
DOID:0111252	"[""vestibular schwannomatosis"",""ACN"",""BANF"",""NF2"",""NF2-related schwannomatosis"",""SWN3"",""SWNV"",""acoustic neurofibromatosis"",""bilateral acoustic neurinoma"",""bilateral acoustic neurofibromatosis"",""bilateral acoustic schwannomas"",""central neurofibromatosis"",""familial acoustic neuromas"",""neurofibromatosis 2"",""neurofibromatosis type II"",""schwannomatosis 3""]"	"[{""label"":""SMARCB1"",""id"":""6598""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""6598"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111252""}]"
DOID:0111253	"[""neurofibromatosis 1"",""NF1"",""Peripheral Neurofibromatosis"",""Recklinghausen's neurofibromatosis"",""neurofibromatosis type I"",""von Recklinghausen Disease""]"	"[{""label"":""NF1"",""id"":""4763""}]"	"[""4763""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111253""}]"
DOID:0111253	"[""neurofibromatosis 1"",""NF1"",""Peripheral Neurofibromatosis"",""Recklinghausen's neurofibromatosis"",""neurofibromatosis type I"",""von Recklinghausen Disease""]"	"[{""label"":""Nf1"",""id"":""18015""}]"	"[""18015""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111253""}]"
DOID:0111254	"[""glutaric acidemia I"",""GA1"",""glutaric academia type 1"",""glutaric aciduria 1"",""glutaric aciduria type I"",""glutaryl-coA dehydrogenase deficiency"",""glutaryl-coenzyme A dehydrogenase deficiency""]"	"[{""label"":""GCDH"",""id"":""2639""}]"	"[""2639""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111254""}]"
DOID:0111257	"[""gamma-glutamyl transpeptidase deficiency"",""GGT deficiency"",""GGT1 deficiency"",""GTG deficiency"",""gamma-glutamyl transferase deficiency"",""glutathionuria""]"	"[{""label"":""GGT1"",""id"":""2678""}]"	"[""2678""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111257""}]"
DOID:0111258	"[""pentosuria"",""L-xylulose reductase deficiency"",""L-xylulosuria"",""PNTSU"",""essential pentosuria"",""xylitol dehydrogenase deficiency""]"	"[{""label"":""DCXR"",""id"":""51181""}]"	"[""51181""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111258""}]"
DOID:0111260	"[""phosphoribosylpyrophosphate synthetase superactivity"",""PRPP synthetase superactivity"",""PRPS1 superactivity""]"	"[{""label"":""PRPS1"",""id"":""5631""}]"	"[""5631""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111260""}]"
DOID:0111261	"[""fumarase deficiency"",""FMRD"",""fumaric aciduria""]"	"[{""label"":""FH"",""id"":""2271""}]"	"[""2271""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111261""}]"
DOID:0111263	"[""combined malonic and methylmalonic acidemia"",""CMAMMA"",""combined malonic and methylmalonic aciduria""]"	"[{""label"":""ACSF3"",""id"":""197322""}]"	"[""197322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111263""}]"
DOID:0111265	"[""Boucher-Neuhauser syndrome"",""ataxia-hypogonadism-choroidal dystrophy syndrome""]"	"[{""label"":""PNPLA6"",""id"":""10908""}]"	"[""10908""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111265""}]"
DOID:0111268	"[""autosomal recessive hyaline body myopathy"",""MSMB"",""Myopathy, myosin storage, autosomal recessive"",""congenital myopathy 7B""]"	"[{""label"":""MYH7"",""id"":""4625""}]"	"[""4625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111268""}]"
DOID:0111269	"[""autosomal dominant hyaline body myopathy"",""MSMA"",""Myopathy, myosin storage, autosomal dominant"",""congenital myopathy 7A"",""myopathy with lysis of type I myofibrils""]"	"[{""label"":""MYH7"",""id"":""4625""}]"	"[""4625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111269""}]"
DOID:0111271	"[""Oliver-McFarlane syndrome"",""OMCS"",""eyelashes long mental retardation"",""long eyelashes-intellectual disability syndrome"",""trichomegaly-retina pigmentary degeneration-dwarfism syndrome""]"	"[{""label"":""PNPLA6"",""id"":""10908""}]"	"[""10908""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111271""}]"
DOID:0111272	"[""occipital horn syndrome"",""EDS IX"",""Ehlers-Danlos syndrome type 9"",""Ehlers-Danlos syndrome type IX"",""X-linked cutis laxa""]"	"[{""label"":""ATP7A"",""id"":""538""}]"	"[""538""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111272""}]"
DOID:0111274	"[""CODAS syndrome"",""cerebral, ocular, dental, auricular, and skeletal syndrome"",""cerebro-oculo-dento-auriculo-skeletal syndrome""]"	"[{""label"":""LONP1"",""id"":""9361""}]"	"[""9361""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111274""}]"
DOID:0111275	"[""speech-language disorder-1"",""CAS"",""articulatory apraxia"",""childhood apraxia of speech"",""developmental apraxia of speech"",""developmental verbal dyspraxia"",""speech and language disorder with orofacial dyspraxia"",""speech-language disorder type 1""]"	"[{""label"":""FOXP2"",""id"":""93986""}]"	"[""93986""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111275""}]"
DOID:0111278	"[""histiocytosis-lymphadenopathy plus syndrome"",""Faisalabad histiocytosis"",""H syndrome"",""HJCD"",""PHID"",""Rosai–Dorfman disease"",""SHML"",""cutaneous hyperpigmentation with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss"",""familial Rosai-Dorfman disease"",""histiocytosis and lymphadenopathy with or without cutaneous, cardiac, and/or endocrine features, joint contractures and/or deafness"",""histiocytosis with joint contractures and sensorineural deafness"",""pigmented hypertrichosis with insulin-dependent diabetes mellitus"",""sinus histiocytosis and massive lymphadenopathy""]"	"[{""label"":""SLC29A3"",""id"":""55315""}]"	"[""55315""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111278""}]"
DOID:0111279	"[""psoriasis 7"",""PSORS7""]"	"[{""label"":""IL23R"",""id"":""149233""}]"	"[""149233""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111279""}]"
DOID:0111286	"[""psoriasis 1"",""PSORS1""]"	"[{""label"":""HLA-C"",""id"":""3107""}]"	"[""3107""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111286""}]"
DOID:0111287	"[""psoriasis 13"",""PSORS13""]"	"[{""label"":""TRAF3IP2"",""id"":""10758""}]"	"[""10758""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111287""}]"
DOID:0111292	"[""obsolete idiopathic generalized epilepsy 10""]"	"[{""label"":""GABRD"",""id"":""2563""}]"	"[""2563""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111292""}]"
DOID:0111294	"[""generalized epilepsy with febrile seizures plus 2"",""GEFS+2"",""GEFSP2"",""generalised epilepsy with febrile seizures plus 2"",""generalised epilepsy with febrile seizures plus type 2"",""generalized epilepsy with febrile seizures plus type 2""]"	"[{""label"":""para"",""id"":""32619""}]"	"[""32619""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111294""}]"
DOID:0111294	"[""generalized epilepsy with febrile seizures plus 2"",""GEFS+2"",""GEFSP2"",""generalised epilepsy with febrile seizures plus 2"",""generalised epilepsy with febrile seizures plus type 2"",""generalized epilepsy with febrile seizures plus type 2""]"	"[{""label"":""SCN1A"",""id"":""6323""}]"	"[""6323""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111294""}]"
DOID:0111296	"[""generalized epilepsy with febrile seizures plus 10"",""GEFS+10"",""GEFSP10"",""generalised epilepsy with febrile seizures plus 10"",""generalised epilepsy with febrile seizures plus type 10"",""generalized epilepsy with febrile seizures plus type 10""]"	"[{""label"":""HCN1"",""id"":""348980""}]"	"[""348980""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111296""}]"
DOID:0111298	"[""familial febrile seizures 8"",""FEB8"",""familial febrile convulsions 8""]"	"[{""label"":""GABRG2"",""id"":""2566""}]"	"[""2566""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111298""}]"
DOID:0111302	"[""generalized epilepsy with febrile seizures plus 1"",""GEFS+1"",""GEFSP1"",""generalised epilepsy with febrile seizures plus 1"",""generalised epilepsy with febrile seizures plus type 1"",""generalized epilepsy with febrile seizures plus type 1""]"	"[{""label"":""SCN1B"",""id"":""6324""}]"	"[""6324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111302""}]"
DOID:0111305	"[""familial febrile seizures 4"",""FEB4"",""familial febrile convulsions 4""]"	"[{""label"":""ADGRV1"",""id"":""84059""}]"	"[""84059""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111305""}]"
DOID:0111308	"[""familial febrile seizures 11"",""FEB11"",""familial febrile convulsions 11""]"	"[{""label"":""CPA6"",""id"":""57094""}]"	"[""57094""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111308""}]"
DOID:0111310	"[""familial febrile seizures 2"",""FEB2"",""familial febrile convulsions 2""]"	"[{""label"":""HCN2"",""id"":""610""}]"	"[""610""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111310""}]"
DOID:0111312	"[""obsolete idiopathic generalized epilepsy 11""]"	"[{""label"":""CLCN2"",""id"":""1181""}]"	"[""1181""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111312""}]"
DOID:0111313	"[""obsolete idiopathic generalized epilepsy 12"",""EIG12""]"	"[{""label"":""SLC2A1"",""id"":""6513""}]"	"[""6513""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111313""}]"
DOID:0111314	"[""obsolete idiopathic generalized epilepsy 13""]"	"[{""label"":""GABRA1"",""id"":""2554""}]"	"[""2554""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111314""}]"
DOID:0111315	"[""obsolete idiopathic generalized epilepsy 14""]"	"[{""label"":""SLC12A5"",""id"":""57468""}]"	"[""57468""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111315""}]"
DOID:0111322	"[""obsolete idiopathic generalized epilepsy 8""]"	"[{""label"":""CASR"",""id"":""846""}]"	"[""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111322""}]"
DOID:0111330	"[""combined saposin deficiency"",""PSAPD"",""combined SAP deficiency"",""encephalopathy due to prosaposin deficiency""]"	"[{""label"":""PSAP"",""id"":""5660""}]"	"[""5660""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00098""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111330""}]"
DOID:0111330	"[""combined saposin deficiency"",""PSAPD"",""combined SAP deficiency"",""encephalopathy due to prosaposin deficiency""]"	"[{""label"":""Psap"",""id"":""19156""}]"	"[""19156""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111330""}]"
DOID:0111331	"[""intellectual disability-severe speech delay-mild dysmorphism syndrome"",""FOXP1 Haploinsufficiency"",""FOXP1 syndrome"",""FOXP1-Related Neurodevelopmental Disorder"",""Mental retardation with language impairment and with or without autistic features""]"	"[{""label"":""FOXP1"",""id"":""27086""}]"	"[""27086""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111331""}]"
DOID:0111332	"[""Pitt-Hopkins-like syndrome 2"",""PTHSL2""]"	"[{""label"":""NRXN1"",""id"":""9378""}]"	"[""9378""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111332""}]"
DOID:0111333	"[""early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome"",""EMARDD"",""Myopathy, areflexia, respiratory distress, and dysphagia, early-onset"",""congenital myopathy 10A""]"	"[{""label"":""MEGF10"",""id"":""84466""}]"	"[""84466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111333""}]"
DOID:0111334	"[""congenital leptin deficiency"",""LEPD"",""leptin deficiency or dysfunction"",""obesity due to congenital leptin deficiency""]"	"[{""label"":""LEP"",""id"":""3952""}]"	"[""3952""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111334""}]"
DOID:0111337	"[""Jackson-Weiss syndrome"",""JWS"",""craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome""]"	"[{""label"":""FGFR1"",""id"":""2260""},{""label"":""FGFR2"",""id"":""2263""}]"	"[""2260"",""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111337""}]"
DOID:0111338	"[""isolated elevated serum creatine phosphokinase levels"",""elevated serum CPK"",""idiopathic hyperCKemia"",""isolated hyperCKemia""]"	"[{""label"":""ANO5"",""id"":""203859""}]"	"[""203859""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111338""}]"
DOID:0111340	"[""dominant optic atrophy plus syndrome"",""DOA+"",""optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy""]"	"[{""label"":""OPA1"",""id"":""4976""}]"	"[""4976""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111340""}]"
DOID:0111341	"[""primary failure of tooth eruption"",""PFE"",""dental noneruption"",""familial posterior openbite malocclusion"",""nonsyndromic primary failure of eruption"",""primary retention of teeth"",""unerupted second primary molar""]"	"[{""label"":""PTH1R"",""id"":""5745""}]"	"[""5745""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111341""}]"
DOID:0111343	"[""lateral meningocele syndrome"",""Lehman syndrome""]"	"[{""label"":""NOTCH3"",""id"":""4854""}]"	"[""4854""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111343""}]"
DOID:0111344	"[""myeloproliferative disorder with eosinophilia"",""chronic myeloproliferative disorder with eosinophilia""]"	"[{""label"":""PDGFRB"",""id"":""5159""}]"	"[""5159""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111344""}]"
DOID:0111345	"[""transient bullous dermolysis of the newborn"",""DEB, bullous dermolysis of the newborn"",""DEB-BDN""]"	"[{""label"":""COL7A1"",""id"":""1294""}]"	"[""1294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111345""}]"
DOID:0111346	"[""epidermolysis bullosa simplex with mottled pigmentation"",""EBSMP"",""Epidermolysis bullosa simplex-MP"",""speckled hyperpigmentation with punctate palmoplantar keratoses and childhood blistering""]"	"[{""label"":""KRT5"",""id"":""3852""}]"	"[""3852""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111346""}]"
DOID:0111347	"[""epidermolysis bullosa with congenital localized absence of skin and deformity of nails"",""EBD, Bart type"",""epidermolysis bullosa dystrophica, Bart type""]"	"[{""label"":""COL7A1"",""id"":""1294""}]"	"[""1294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111347""}]"
DOID:0111348	"[""multiple epiphyseal dysplasia with myopia and deafness"",""EDMMD"",""multiple epiphyseal dysplasia, Beighton type"",""multiple epiphyseal dysplasia-myopia-deafness syndrome""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111348""}]"
DOID:0111349	"[""hereditary desmoid disease"",""FIF"",""familial infiltrative fibromatosis""]"	"[{""label"":""APC"",""id"":""324""}]"	"[""324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111349""}]"
DOID:0111351	"[""D-2-hydroxyglutaric aciduria 1"",""D2HGA1""]"	"[{""label"":""D2HGDH"",""id"":""728294""}]"	"[""728294""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111351""}]"
DOID:0111352	"[""D-2-hydroxyglutaric aciduria 2"",""D2HGA2""]"	"[{""label"":""IDH2"",""id"":""3418""}]"	"[""3418""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111352""}]"
DOID:0111353	"[""arthrogryposis, renal dysfunction, and cholestasis 1"",""ARCS1""]"	"[{""label"":""VPS33B"",""id"":""26276""}]"	"[""26276""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111353""}]"
DOID:0111354	"[""arthrogryposis, renal dysfunction, and cholestasis 2"",""ARCS2""]"	"[{""label"":""VIPAS39"",""id"":""63894""}]"	"[""63894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111354""}]"
DOID:0111358	"[""Floating-Harbor syndrome"",""FLHS""]"	"[{""label"":""SRCAP"",""id"":""10847""}]"	"[""10847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111358""}]"
DOID:0111359	"[""large congenital melanocytic nevus"",""Congenital pigmented nevus"",""GMN"",""Giant congenital melanocytic nevus"",""Giant pigmented hairy nevus"",""LCMN""]"	"[{""label"":""HRAS"",""id"":""3265""},{""label"":""NRAS"",""id"":""4893""}]"	"[""3265"",""4893""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111359""}]"
DOID:0111363	"[""Heinz body anemia""]"	"[{""label"":""HBA1"",""id"":""3039""},{""label"":""HBA2"",""id"":""3040""},{""label"":""HBB"",""id"":""3043""}]"	"[""3039"",""3040"",""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111363""}]"
DOID:0111364	"[""Alzheimer's disease 9"",""AD9"",""Alzheimer's disease 9, late onset""]"	"[{""label"":""ABCA7"",""id"":""10347""}]"	"[""10347""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111364""}]"
DOID:0111365	"[""benign familial hematuria"",""BFH"",""TMN"",""thin basement membrane nephropathy"",""thin membrane nephropathy""]"	"[{""label"":""COL4A3"",""id"":""1285""},{""label"":""COL4A4"",""id"":""1286""}]"	"[""1285"",""1286""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111365""}]"
DOID:0111366	"[""familial hepatic adenoma"",""familial liver cell adenomas""]"	"[{""label"":""HNF1A"",""id"":""6927""}]"	"[""6927""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111366""}]"
DOID:0111369	"[""hyperalphalipoproteinemia 1"",""HALP1""]"	"[{""label"":""CETP"",""id"":""1071""}]"	"[""1071""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111369""}]"
DOID:0111370	"[""apolipoprotein C-III deficiency"",""HALP2"",""hyperalphalipoproteinemia 2""]"	"[{""label"":""APOC3"",""id"":""345""}]"	"[""345""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111370""}]"
DOID:0111371	"[""isolated hyperchlorhidrosis"",""HYCHL"",""carbonic anhydrase XII deficiency""]"	"[{""label"":""CA12"",""id"":""771""}]"	"[""771""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111371""}]"
DOID:0111373	"[""familial progressive hyperpigmentation with or without hypopigmentation"",""FPHH"",""MUH"",""melanosis universalis hereditaria""]"	"[{""label"":""KITLG"",""id"":""4254""}]"	"[""4254""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111373""}]"
DOID:0111376	"[""fetal akinesia deformation sequence syndrome 3"",""FADS3""]"	"[{""label"":""DOK7"",""id"":""285489""}]"	"[""285489""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111376""}]"
DOID:0111377	"[""fetal akinesia deformation sequence syndrome 1"",""FADS1""]"	"[{""label"":""MUSK"",""id"":""4593""}]"	"[""4593""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111377""}]"
DOID:0111380	"[""solitary median maxillary central incisor"",""SMMCI"",""fused incisors"",""single central maxillary incisor"",""single median maxillary central incisor"",""single upper central incisor""]"	"[{""label"":""SHH"",""id"":""6469""}]"	"[""6469""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111380""}]"
DOID:0111381	"[""IVIC syndrome"",""Instituto Venezolano de Investigaciones Cientificas syndrome"",""OORS"",""Oculootoradial syndrome"",""oculo-oto-radial syndrome"",""radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia""]"	"[{""label"":""SALL4"",""id"":""57167""}]"	"[""57167""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111381""}]"
DOID:0111384	"[""inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2"",""IBMPFD2"",""MSP2"",""multisystem proteinopathy 2""]"	"[{""label"":""HNRNPA2B1"",""id"":""3181""}]"	"[""3181""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111384""}]"
DOID:0111385	"[""inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1"",""IBMPFD1"",""MSP1"",""multisystem proteinopathy 1""]"	"[{""label"":""VCP"",""id"":""7415""}]"	"[""7415""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111385""}]"
DOID:0111386	"[""inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3"",""IBMPFD3"",""MSP3"",""multisystem proteinopathy 3""]"	"[{""label"":""HNRNPA1"",""id"":""3178""}]"	"[""3178""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111386""}]"
DOID:0111389	"[""mucopolysaccharidosis Ih/s"",""MPS1H/S"",""MPSIH/S"",""Mucopolysaccharidosis type 1H/S""]"	"[{""label"":""IDUA"",""id"":""3425""}]"	"[""3425""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00029""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00030""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00031""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111389""}]"
DOID:0111390	"[""mucopolysaccharidosis Ih"",""Dysostosis multiplex syndrome"",""Hurler disease MPS type 1H"",""Hurler-Pfaundler syndrome"",""L-iduronidase deficiency, Hurler type"",""MPS1-H"",""Mucopolysaccharidosis type I severe form"",""dysostosis multiplex"",""gargoylism""]"	"[{""label"":""IDUA"",""id"":""3425""}]"	"[""3425""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00029""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00030""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00031""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111390""}]"
DOID:0111391	"[""mucopolysaccharidosis IVA"",""GALNS deficiency"",""MPS IVA"",""MPS4A"",""Morquio A disease"",""Morquio syndrome A""]"	"[{""label"":""GALNS"",""id"":""2588""},{""label"":""GLB1"",""id"":""2720""}]"	"[""2588"",""2720""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00039""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00040""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111391""}]"
DOID:0111392	"[""mucopolysaccharidosis type IVB"",""MPS IVB"",""MPS4B"",""Morquio disease type B"",""Morquio syndrome B"",""beta-D-galactosidase deficiency"",""mucopolysaccharidosis type IVB (Morquio)""]"	"[{""label"":""GALNS"",""id"":""2588""},{""label"":""GLB1"",""id"":""2720""}]"	"[""2588"",""2720""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00039""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00040""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111392""}]"
DOID:0111393	"[""mucopolysaccharidosis type IIIC"",""Acetyl-CoA alpha-glucosaminide acetyltransferase deficiency"",""HGSNAT deficiency"",""Heparan-alpha-glucosaminide N-acetyltransferase deficiency"",""MPS3C"",""MPSIIIC"",""Mucopolysaccharidosis type 3C"",""Sanfilippo syndrome type C"",""mucopolysaccharidosis type IIIC (Sanfilippo C)""]"	"[{""label"":""GNS"",""id"":""2799""},{""label"":""HGSNAT"",""id"":""138050""},{""label"":""SGSH"",""id"":""6448""}]"	"[""138050"",""2799"",""6448""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00034""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00036""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00037""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111393""}]"
DOID:0111394	"[""mucopolysaccharidosis type IIIB"",""MPS3B"",""MPSIIIB"",""Mucopoly-saccharidosis type 3B"",""Mucopolysaccharidosis type 3B"",""N-acetyl-alpha-glucosaminidase deficiency"",""NAGLU deficiency"",""Sanfilippo syndrome type B"",""mucopolysaccharidosis type IIIB (Sanfilippo B)""]"	"[{""label"":""GNS"",""id"":""2799""},{""label"":""NAGLU"",""id"":""4669""},{""label"":""SGSH"",""id"":""6448""}]"	"[""2799"",""4669"",""6448""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00034""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00035""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00037""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111394""}]"
DOID:0111395	"[""mucopolysaccharidosis type IIIA"",""MPS3A"",""MPSIIIA"",""Sanfilippo syndrome type A"",""heparan sulfamidase deficiency"",""mucopolysaccharidosis III-A"",""mucopolysaccharidosis type 3A"",""mucopolysaccharidosis type IIIA (Sanfilippo A)""]"	"[{""label"":""GNS"",""id"":""2799""},{""label"":""SGSH"",""id"":""6448""}]"	"[""2799"",""6448""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00034""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00037""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111395""}]"
DOID:0111397	"[""congenital dyserythropoietic anemia type Ib"",""CDA, type Ib"",""CDAN1B""]"	"[{""label"":""SEC23B"",""id"":""10483""}]"	"[""10483""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00373""}]"
DOID:0111398	"[""congenital dyserythropoietic anemia type Ia"",""CDA Ia"",""CDAN1A""]"	"[{""label"":""CDAN1"",""id"":""146059""}]"	"[""146059""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111398""}]"
DOID:0111399	"[""congenital dyserythropoietic anemia type IIIa"",""CDA III"",""CDA type 3"",""CDA type III"",""CDAN3"",""Congenital dyserythropoietic anaemia type 3"",""Congenital dyserythropoietic anemia type 3"",""anaemia with multinucleated erythroblasts"",""anemia with multinucleated erythroblasts"",""congenital dyserythropoietic anaemia type III"",""hereditary benign erythroreticulosis""]"	"[{""label"":""KIF23"",""id"":""9493""},{""label"":""SEC23B"",""id"":""10483""}]"	"[""10483"",""9493""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00373""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111399""}]"
DOID:0111401	"[""congenital dyserythropoietic anemia type II"",""CDA II"",""CDA type 2"",""CDA type II"",""CDAN2"",""Congenital dyserythropoietic anaemia type 2"",""Congenital dyserythropoietic anemia type 2"",""Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)"",""SEC23B-CDG"",""congenital dyserythropoietic anaemia type II""]"	"[{""label"":""SEC23B"",""id"":""10483""}]"	"[""10483""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00373""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111401""}]"
DOID:0111402	"[""mucopolysaccharidosis type IIID"",""GNS deficiency"",""MPS IIID"",""MPS3D"",""Mucopolysaccharidosis type 3D"",""N-acetylglucosamine-6-sulfatase deficiency"",""Sanfilippo syndrome D"",""Sanfilippo syndrome type D""]"	"[{""label"":""GNS"",""id"":""2799""},{""label"":""SGSH"",""id"":""6448""}]"	"[""2799"",""6448""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00034""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00037""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111402""}]"
DOID:0111403	"[""mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations"",""MCCCHCM""]"	"[{""label"":""MAST1"",""id"":""22983""}]"	"[""22983""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111403""}]"
DOID:0111403	"[""mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations"",""MCCCHCM""]"	"[{""label"":""Mast1"",""id"":""56527""}]"	"[""56527""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111403""}]"
DOID:0111404	"[""Jalili syndrome"",""Cone rod dystrophy-amelogenesis imperfecta syndrome"",""cone-rod dystrophy and amelogenesis imperfecta""]"	"[{""label"":""CNNM4"",""id"":""26504""}]"	"[""26504""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111404""}]"
DOID:0111405	"[""Fraser syndrome 1"",""FRASRS1""]"	"[{""label"":""FRAS1"",""id"":""80144""}]"	"[""80144""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111405""}]"
DOID:0111406	"[""Fraser syndrome 3"",""FRASRS3""]"	"[{""label"":""GRIP1"",""id"":""23426""}]"	"[""23426""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111406""}]"
DOID:0111407	"[""Fraser syndrome 2"",""FRASRS2""]"	"[{""label"":""FREM2"",""id"":""341640""}]"	"[""341640""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111407""}]"
DOID:0111410	"[""exudative vitreoretinopathy 6"",""EVR6""]"	"[{""label"":""ZNF408"",""id"":""79797""}]"	"[""79797""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111410""}]"
DOID:0111411	"[""exudative vitreoretinopathy 4"",""EVR4""]"	"[{""label"":""LRP5"",""id"":""4041""}]"	"[""4041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111411""}]"
DOID:0111412	"[""exudative vitreoretinopathy 1"",""EVR1""]"	"[{""label"":""FZD4"",""id"":""8322""}]"	"[""8322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111412""}]"
DOID:0111415	"[""trichohepatoenteric syndrome 1"",""THES1""]"	"[{""label"":""SKIC3"",""id"":""9652""}]"	"[""9652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111415""}]"
DOID:0111416	"[""trichohepatoenteric syndrome 2"",""THES2""]"	"[{""label"":""SKIC2"",""id"":""6499""}]"	"[""6499""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111416""}]"
DOID:0111418	"[""familial apolipoprotein C-II deficiency"",""C-II anapolipoproteinemia"",""familial APOC2 deficiency"",""familial apoC-II deficiency"",""hyperlipoproteinemia, type 1b"",""hyperlipoproteinemia, type Ib""]"	"[{""label"":""APOC2"",""id"":""344""}]"	"[""344""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111418""}]"
DOID:0111420	"[""familial GPIHBP1 deficiency"",""familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency"",""hyperlipoproteinemia type 1D"",""hyperlipoproteinemia type ID""]"	"[{""label"":""GPIHBP1"",""id"":""338328""}]"	"[""338328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111420""}]"
DOID:0111421	"[""familial apolipoprotein A5 deficiency"",""familial APOA5 deficiency"",""familial apolipoprotein A-V deficiency""]"	"[{""label"":""APOA5"",""id"":""116519""}]"	"[""116519""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111421""}]"
DOID:0111422	"[""familial lipase maturation factor 1 deficiency"",""LPL and HL deficiency"",""LPL and HTGL deficiency"",""combined lipase deficiency"",""familial LMF1 deficiency"",""lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency""]"	"[{""label"":""LMF1"",""id"":""64788""}]"	"[""64788""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111422""}]"
DOID:0111424	"[""branchiootorenal syndrome 2"",""BOR2""]"	"[{""label"":""SIX5"",""id"":""147912""}]"	"[""147912""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111424""}]"
DOID:0111425	"[""familial restrictive cardiomyopathy 1"",""RCM1"",""restrictive cardiomyopathy 1""]"	"[{""label"":""TNNI3"",""id"":""7137""}]"	"[""7137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111425""}]"
DOID:0111428	"[""essential tremor 1"",""ETM1"",""hereditary essential tremor 1""]"	"[{""label"":""DRD3"",""id"":""1814""}]"	"[""1814""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111428""}]"
DOID:0111431	"[""essential tremor 4"",""ETM4"",""hereditary essential tremor 4""]"	"[{""label"":""FUS"",""id"":""2521""}]"	"[""2521""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111431""}]"
DOID:0111432	"[""essential tremor 5"",""ETM5"",""hereditary essential tremor 5""]"	"[{""label"":""TENM4"",""id"":""26011""}]"	"[""26011""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111432""}]"
DOID:0111433	"[""optic atrophy 3"",""ADOAC"",""OPA3"",""autosomal dominant optic atrophy 3"",""autosomal dominant optic atrophy and cataract"",""autosomal dominant optic atrophy type 3"",""optic atrophy 3 with cataract""]"	"[{""label"":""OPA3"",""id"":""80207""}]"	"[""80207""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111433""}]"
DOID:0111434	"[""optic atrophy 10"",""OPA10"",""optic atrophy 10 with or without ataxia, mental retardation, and seizures""]"	"[{""label"":""RTN4IP1"",""id"":""84816""}]"	"[""84816""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111434""}]"
DOID:0111436	"[""optic atrophy 11"",""OPA11""]"	"[{""label"":""YME1L1"",""id"":""10730""}]"	"[""10730""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111436""}]"
DOID:0111437	"[""optic atrophy 7"",""OPA7"",""optic atrophy 7 with or without auditory neuropathy""]"	"[{""label"":""TMEM126A"",""id"":""84233""}]"	"[""84233""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111437""}]"
DOID:0111438	"[""optic atrophy 5"",""OPA5""]"	"[{""label"":""DNM1L"",""id"":""10059""}]"	"[""10059""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111438""}]"
DOID:0111441	"[""optic atrophy 1"",""OPA1""]"	"[{""label"":""OPA1"",""id"":""4976""},{""label"":""WFS1"",""id"":""7466""}]"	"[""4976"",""7466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111441""}]"
DOID:0111442	"[""optic atrophy 9"",""OPA9""]"	"[{""label"":""ACO1"",""id"":""851013""}]"	"[""851013""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111442""}]"
DOID:0111442	"[""optic atrophy 9"",""OPA9""]"	"[{""label"":""ACO2"",""id"":""50""}]"	"[""50""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111442""}]"
DOID:0111444	"[""progressive myoclonus epilepsy 4"",""AMRF"",""EPM4"",""Myoclonus-nephropathy syndrome"",""action myoclonus-renal failure syndrome""]"	"[{""label"":""SCARB2"",""id"":""950""}]"	"[""950""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111444""}]"
DOID:0111446	"[""progressive myoclonus epilepsy 3"",""CLN14 disease"",""EPM3"",""PME type 3"",""Progressive myoclonic epilepsy due to KCTD7 deficiency"",""Progressive myoclonus epilepsy type 3"",""neuronal ceroid lipofuscinosis 14""]"	"[{""label"":""WHI2"",""id"":""854208""}]"	"[""854208""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111446""}]"
DOID:0111447	"[""progressive myoclonus epilepsy 7"",""EPM7"",""MEAK"",""Myoclonus epilepsy and ataxia due to potassium channel mutation"",""PME type 7"",""Progressive myoclonic epilepsy due to KV3.1 deficiency"",""Progressive myoclonus epilepsy type 7""]"	"[{""label"":""KCNC1"",""id"":""3746""}]"	"[""3746""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111447""}]"
DOID:0111448	"[""progressive myoclonus epilepsy 1B"",""EPM1B""]"	"[{""label"":""PRICKLE1"",""id"":""144165""}]"	"[""144165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111448""}]"
DOID:0111450	"[""progressive myoclonus epilepsy 9"",""EMP9"",""PME type 9"",""progressive myoclonic epilepsy due to LMNB2 deficiency"",""progressive myoclonus epilepsy type 9""]"	"[{""label"":""LMNB2"",""id"":""84823""}]"	"[""84823""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111450""}]"
DOID:0111451	"[""progressive myoclonus epilepsy 8"",""EMP8"",""PME type 8"",""progressive myoclonic epilepsy due to CERS1 deficiency"",""progressive myoclonus epilepsy type 8""]"	"[{""label"":""CERS1"",""id"":""10715""}]"	"[""10715""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111451""}]"
DOID:0111452	"[""progressive myoclonus epilepsy 1A"",""EPM1A""]"	"[{""label"":""CSTB"",""id"":""1476""}]"	"[""1476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111452""}]"
DOID:0111453	"[""2-aminoadipic 2-oxoadipic aciduria"",""AMOXAD"",""alpha-aminoadipic aciduria""]"	"[{""label"":""Dhtkd1"",""id"":""209692""}]"	"[""209692""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111453""}]"
DOID:0111453	"[""2-aminoadipic 2-oxoadipic aciduria"",""AMOXAD"",""alpha-aminoadipic aciduria""]"	"[{""label"":""DHTKD1"",""id"":""55526""}]"	"[""55526""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111453""}]"
DOID:0111454	"[""SHORT syndrome"",""Aarskog-Ose-Pande syndrome"",""Lipodystrophy-Rieger anomaly-diabetes syndrome"",""Rieger anomaly-partial lipodystrophy syndrome"",""short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay""]"	"[{""label"":""Pik3r1"",""id"":""18708""}]"	"[""18708""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111454""}]"
DOID:0111457	"[""STING-associated vasculopathy with onset in infancy"",""SAVI""]"	"[{""label"":""STING1"",""id"":""340061""}]"	"[""340061""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111457""}]"
DOID:0111458	"[""galactose epimerase deficiency"",""GALE deficiency"",""GALE-D"",""UDP-galactose-4-epimerase deficiency"",""epimerase deficiency galactosemia"",""galactosemia III"",""galactosemia type 3"",""uridine diphosphate galactose-4-epimerase deficiency""]"	"[{""label"":""GALE"",""id"":""2582""}]"	"[""2582""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111458""}]"
DOID:0111459	"[""classic galactosemia"",""GALT deficiency"",""galactose-1-phosphate uridyltransferase deficiency"",""galactosemia type 1""]"	"[{""label"":""Galt"",""id"":""33935""}]"	"[""33935""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111459""}]"
DOID:0111459	"[""classic galactosemia"",""GALT deficiency"",""galactose-1-phosphate uridyltransferase deficiency"",""galactosemia type 1""]"	"[{""label"":""GALT"",""id"":""2592""}]"	"[""2592""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111459""}]"
DOID:0111461	"[""cardiofaciocutaneous syndrome 2"",""CFC2""]"	"[{""label"":""KRAS"",""id"":""3845""}]"	"[""3845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111461""}]"
DOID:0111462	"[""cardiofaciocutaneous syndrome 3"",""CFC3""]"	"[{""label"":""MAP2K1"",""id"":""5604""}]"	"[""5604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111462""}]"
DOID:0111463	"[""cardiofaciocutaneous syndrome 4"",""CFC4""]"	"[{""label"":""MAP2K2"",""id"":""5605""}]"	"[""5605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111463""}]"
DOID:0111464	"[""combined oxidative phosphorylation deficiency 35"",""COXPD35""]"	"[{""label"":""TRIT1"",""id"":""54802""}]"	"[""54802""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111464""}]"
DOID:0111465	"[""combined oxidative phosphorylation deficiency 21"",""COXPD21""]"	"[{""label"":""TARS2"",""id"":""80222""}]"	"[""80222""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111465""}]"
DOID:0111467	"[""combined oxidative phosphorylation deficiency 13"",""COXPD13""]"	"[{""label"":""PNPT1"",""id"":""87178""}]"	"[""87178""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111467""}]"
DOID:0111468	"[""combined oxidative phosphorylation deficiency 25"",""COXPD25""]"	"[{""label"":""MARS2"",""id"":""92935""}]"	"[""92935""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111468""}]"
DOID:0111469	"[""combined oxidative phosphorylation deficiency 16"",""COXPD16"",""infantile hypertrophic cardiomyopathy due to MRPL44 deficiency""]"	"[{""label"":""MRPL44"",""id"":""65080""}]"	"[""65080""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111469""}]"
DOID:0111471	"[""combined oxidative phosphorylation deficiency 30"",""COXPD30""]"	"[{""label"":""TRMT10C"",""id"":""54931""}]"	"[""54931""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111471""}]"
DOID:0111473	"[""combined oxidative phosphorylation deficiency 5"",""COXPD5"",""hypotonia with lactic acidemia and hyperammonemia""]"	"[{""label"":""MRPS22"",""id"":""56945""}]"	"[""56945""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111473""}]"
DOID:0111474	"[""combined oxidative phosphorylation deficiency 1"",""COXPD1"",""early fatal progressive hepatoencephalopathy"",""hepatoencephalopathy due to COXPD1"",""hepatoencephalopathy due to combined oxidative phosphorylation defect type 1""]"	"[{""label"":""GFM1"",""id"":""85476""}]"	"[""85476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111474""}]"
DOID:0111479	"[""combined oxidative phosphorylation deficiency 8"",""COXPD8""]"	"[{""label"":""AARS2"",""id"":""57505""}]"	"[""57505""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111479""}]"
DOID:0111480	"[""combined oxidative phosphorylation deficiency 10"",""COXPD10"",""infantile hypertrophic mitochondrial cardiomyopathy and lactic acidosis"",""mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency""]"	"[{""label"":""MTO1"",""id"":""25821""}]"	"[""25821""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111480""}]"
DOID:0111481	"[""combined oxidative phosphorylation deficiency 11"",""COXPD11"",""infantile encephaloneuromyopathy due to mitochondrial translation defect""]"	"[{""label"":""RMND1"",""id"":""55005""}]"	"[""55005""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111481""}]"
DOID:0111485	"[""combined oxidative phosphorylation deficiency 24"",""COXPD24""]"	"[{""label"":""NARS2"",""id"":""79731""}]"	"[""79731""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111485""}]"
DOID:0111487	"[""combined oxidative phosphorylation deficiency 7"",""COXPD7"",""severe C12ORF65-related COXPD"",""severe C12ORF65-related combined oxidative phosphorylation defect""]"	"[{""label"":""MTRFR"",""id"":""91574""}]"	"[""91574""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111487""}]"
DOID:0111492	"[""combined oxidative phosphorylation deficiency 32"",""COXPD32""]"	"[{""label"":""MRPS34"",""id"":""65993""}]"	"[""65993""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111492""}]"
DOID:0111495	"[""combined oxidative phosphorylation deficiency 33"",""COXPD33""]"	"[{""label"":""C1QBP"",""id"":""708""}]"	"[""708""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111495""}]"
DOID:0111496	"[""combined oxidative phosphorylation deficiency 17"",""COXPD17""]"	"[{""label"":""ELAC2"",""id"":""60528""}]"	"[""60528""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111496""}]"
DOID:0111498	"[""combined oxidative phosphorylation deficiency 22"",""COXPD22""]"	"[{""label"":""ATP5F1A"",""id"":""498""}]"	"[""498""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111498""}]"
DOID:0111502	"[""combined oxidative phosphorylation deficiency 6"",""COXPD6"",""Mitochondrial encephalomyopathy due to COXPD6"",""Mitochondrial encephalomyopathy due to combined oxidative phosphorylation defect 6"",""severe X-linked mitochondrial encephalomyopathy""]"	"[{""label"":""AIFM1"",""id"":""9131""}]"	"[""9131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111502""}]"
DOID:0111503	"[""Li-Fraumeni syndrome 1"",""LFS1""]"	"[{""label"":""TP53"",""id"":""7157""}]"	"[""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111503""}]"
DOID:0111504	"[""Li-Fraumeni syndrome 2"",""LFS2""]"	"[{""label"":""CHEK2"",""id"":""11200""}]"	"[""11200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111504""}]"
DOID:0111506	"[""palmoplantar keratoderma-esophageal carcinoma syndrome"",""Bennion-Patterson syndrome"",""Howell-Evans syndrome"",""TOC"",""keratosis palmaris et plantaris with esophageal cancer"",""keratosis palmoplantaris-esophageal carcinoma syndrome"",""palmoplantar hyperkeratosis-esophageal carcinoma syndrome"",""palmoplantar keratoderma with esophageal cancer"",""tylosis with esophageal cancer"",""tylosis-oesophageal carcinoma syndrome""]"	"[{""label"":""Rhbdf2"",""id"":""217344""}]"	"[""217344""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111506""}]"
DOID:0111506	"[""palmoplantar keratoderma-esophageal carcinoma syndrome"",""Bennion-Patterson syndrome"",""Howell-Evans syndrome"",""TOC"",""keratosis palmaris et plantaris with esophageal cancer"",""keratosis palmoplantaris-esophageal carcinoma syndrome"",""palmoplantar hyperkeratosis-esophageal carcinoma syndrome"",""palmoplantar keratoderma with esophageal cancer"",""tylosis with esophageal cancer"",""tylosis-oesophageal carcinoma syndrome""]"	"[{""label"":""RHBDF2"",""id"":""79651""}]"	"[""79651""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111506""}]"
DOID:0111507	"[""Lenz-Majewski hyperostotic dwarfism"",""Lenz-Majewski syndrome""]"	"[{""label"":""PTDSS1"",""id"":""9791""}]"	"[""9791""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111507""}]"
DOID:0111508	"[""Torrance type platyspondylic dysplasia"",""PLSD-T"",""PLSDT"",""lethal short-limbed platyspondylic dwarfism, Torrance type"",""platyspondylic dysplasia, Torrance-Luton type"",""platyspondylic lethal skeletal dysplasia, Torrance type"",""thanatophoric dysplasia, Torrance variant""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111508""}]"
DOID:0111510	"[""Marshall syndrome"",""MRSHS"",""deafness, myopia, cataract, saddle nose-Marshall type""]"	"[{""label"":""COL11A1"",""id"":""1301""}]"	"[""1301""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111510""}]"
DOID:0111512	"[""metachondromatosis"",""METCDS""]"	"[{""label"":""PTPN11"",""id"":""5781""}]"	"[""5781""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111512""}]"
DOID:0111513	"[""metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome"",""metaphyseal dysplasia maxillary hypoplasia brachydactyly"",""metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly""]"	"[{""label"":""RUNX2"",""id"":""860""}]"	"[""860""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111513""}]"
DOID:0111524	"[""autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5"",""PEOB5"",""autosomal recessive progressive external ophthalmoplegia 5""]"	"[{""label"":""TOP3A"",""id"":""7156""}]"	"[""7156""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111524""}]"
DOID:0111526	"[""Mullerian aplasia and hyperandrogenism"",""Mullerian duct failure and hyperandrogenism"",""WNT4 deficiency""]"	"[{""label"":""WNT4"",""id"":""54361""}]"	"[""54361""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111526""}]"
DOID:0111527	"[""spinal muscular atrophy with progressive myoclonic epilepsy"",""Jankovic-Rivera syndrome"",""SMA-PME"",""SMAPME"",""hereditary myoclonus-progressive distal muscular atrophy syndrome""]"	"[{""label"":""ASAH1"",""id"":""427""}]"	"[""427""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111527""}]"
DOID:0111530	"[""linear nevus sebaceous syndrome"",""JNP"",""Jadassohn nevus phakomatosis"",""SFM syndrome"",""Schimmelpenning Feuerstein Mims syndrome"",""Schimmelpenning syndrome"",""Solomon syndrome"",""nevus sebaceus of Jadassohn"",""nevus sebaceus syndrome"",""organoid nevus phakomatosis"",""organoid nevus syndrome""]"	"[{""label"":""HRAS"",""id"":""3265""},{""label"":""KRAS"",""id"":""3845""},{""label"":""NRAS"",""id"":""4893""}]"	"[""3265"",""3845"",""4893""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111530""}]"
DOID:0111532	"[""osteoglophonic dysplasia"",""Fairbank-Keats syndrome"",""OGD"",""osteoglophonic dwarfism""]"	"[{""label"":""FGFR1"",""id"":""2260""}]"	"[""2260""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111532""}]"
DOID:0111533	"[""gnathodiaphyseal dysplasia"",""GDD"",""Levin syndrome 2"",""gnathodiaphyseal sclerosis"",""osteogenesis imperfecta with unusual skeletal lesions"",""osteogenesis imperfecta, Levin type""]"	"[{""label"":""Ano5"",""id"":""233246""}]"	"[""233246""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111533""}]"
DOID:0111533	"[""gnathodiaphyseal dysplasia"",""GDD"",""Levin syndrome 2"",""gnathodiaphyseal sclerosis"",""osteogenesis imperfecta with unusual skeletal lesions"",""osteogenesis imperfecta, Levin type""]"	"[{""label"":""ANO5"",""id"":""203859""}]"	"[""203859""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111533""}]"
DOID:0111535	"[""progressive osseous heteroplasia"",""POH"",""ectopic ossification familial type"",""familial ectopic ossification"",""osteoma cutis""]"	"[{""label"":""GNAS"",""id"":""2778""}]"	"[""2778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111535""}]"
DOID:0111536	"[""Buschke-Ollendorff syndrome"",""BOS"",""dermatofibrosis lenticularis disseminata with osteopoikilosis"",""dermatoosteopoikilosis"",""disseminated dermatofibrosis with osteopoikilosis"",""osteopathia condensans disseminata""]"	"[{""label"":""LEMD3"",""id"":""23592""}]"	"[""23592""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111536""}]"
DOID:0111537	"[""paroxysmal extreme pain disorder"",""PEPD"",""PEXPD"",""familial rectal pain"",""submandibular, ocular and rectal pain with flushing""]"	"[{""label"":""SCN9A"",""id"":""6335""}]"	"[""6335""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111537""}]"
DOID:0111538	"[""paramyotonia congenita of Von Eulenburg"",""Eulenburg disease"",""PMC"",""Von Eulenburg paramyotonia congenita"",""myotonia congenita intermittens"",""paralysis periodica paramyotonica"",""paramyotonia congenita""]"	"[{""label"":""SCN4A"",""id"":""6329""}]"	"[""6329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111538""}]"
DOID:0111541	"[""pigmented paravenous chorioretinal atrophy"",""PPRCA""]"	"[{""label"":""CRB1"",""id"":""23418""}]"	"[""23418""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111541""}]"
DOID:0111542	"[""familial expansile osteolysis"",""FEO"",""McCabe disease"",""hereditary expansile polyostotic osteolytic dysplasia""]"	"[{""label"":""TNFRSF11A"",""id"":""8792""}]"	"[""8792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111542""}]"
DOID:0111543	"[""juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome"",""JP-HHT""]"	"[{""label"":""SMAD4"",""id"":""4089""}]"	"[""4089""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111543""}]"
DOID:0111545	"[""familial male-limited precocious puberty"",""FMPP"",""familial gonadotropin-independent male-limited sexual precocity"",""male-limited precocious puberty"",""testotoxicosis""]"	"[{""label"":""LHCGR"",""id"":""3973""}]"	"[""3973""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111545""}]"
DOID:0111546	"[""Currarino syndrome"",""Currarino triad""]"	"[{""label"":""MNX1"",""id"":""3110""}]"	"[""3110""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111546""}]"
DOID:0111547	"[""retinal arterial tortuosity"",""RATOR"",""retinal arteriolar tortuosity"",""retinal hemorrhage with vascular tortuosity"",""tortuosity of retinal arteries""]"	"[{""label"":""COL4A1"",""id"":""1282""}]"	"[""1282""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111547""}]"
DOID:0111548	"[""ring dermoid of cornea"",""RDC"",""ring dermoid syndrome""]"	"[{""label"":""PITX2"",""id"":""5308""}]"	"[""5308""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111548""}]"
DOID:0111549	"[""aplasia of lacrimal and salivary glands"",""ALSG"",""congenital absence of lacrimal puncta and salivary glands""]"	"[{""label"":""FGF10"",""id"":""2255""}]"	"[""2255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111549""}]"
DOID:0111551	"[""neurogenic scapuloperoneal syndrome Kaeser type"",""Kaeser syndrome"",""Stark-Kaeser syndrome"",""scapuloperoneal syndrome type Kaeser"",""scapuloperoneal syndrome, neurogenic, Kaeser type""]"	"[{""label"":""DES"",""id"":""1674""}]"	"[""1674""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111551""}]"
DOID:0111555	"[""Alkuraya-Kucinskas syndrome"",""ALKKUCS""]"	"[{""label"":""BLTP1"",""id"":""84162""}]"	"[""84162""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111555""}]"
DOID:0111556	"[""steatocystoma multiplex"",""multiple sebaceous cysts"",""sebocystomatosis""]"	"[{""label"":""KRT17"",""id"":""3872""}]"	"[""3872""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111556""}]"
DOID:0111558	"[""Charcot-Marie-Tooth disease type 2DD"",""ATP1A1-related CMT2"",""ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2"",""CMT2DD"",""Charcot-Marie-Tooth disease, axonal, type 2DD"",""Charcot-Marie-Tooth neuropathy, type 2DD""]"	"[{""label"":""ATP1A1"",""id"":""476""}]"	"[""476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111558""}]"
DOID:0111558	"[""Charcot-Marie-Tooth disease type 2DD"",""ATP1A1-related CMT2"",""ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2"",""CMT2DD"",""Charcot-Marie-Tooth disease, axonal, type 2DD"",""Charcot-Marie-Tooth neuropathy, type 2DD""]"	"[{""label"":""Atpalpha"",""id"":""48971""}]"	"[""48971""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111558""}]"
DOID:0111561	"[""stiff skin syndrome"",""SSKS""]"	"[{""label"":""FBN1"",""id"":""2200""}]"	"[""2200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111561""}]"
DOID:0111562	"[""overhydrated hereditary stomatocytosis"",""OHS"",""potassium sodium disorder of erythrocyte"",""stomatocytosisIOHST""]"	"[{""label"":""RHAG"",""id"":""6005""}]"	"[""6005""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111562""}]"
DOID:0111564	"[""hypoplastic or aplastic tibia with polydactyly"",""Werner mesomelic syndrome"",""absence of tibia with polydactyly"",""absent tibia-polydactyly syndrome"",""hypoplastic tibiae-postaxial polydactyly syndrome"",""tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome""]"	"[{""label"":""SHH"",""id"":""6469""}]"	"[""6469""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111564""}]"
DOID:0111566	"[""familial isolated trichomegaly"",""TCMGLY"",""long eyelashes""]"	"[{""label"":""FGF5"",""id"":""2250""}]"	"[""2250""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111566""}]"
DOID:0111571	"[""Weyers acrofacial dysostosis"",""Curry-Hall syndrome"",""WAD"",""Weyers acrodental dysostosis"",""acrofacial dysostosis, Weyers type""]"	"[{""label"":""EVC2"",""id"":""132884""}]"	"[""132884""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111571""}]"
DOID:0111574	"[""autosomal recessive woolly hair 3"",""ARWH3""]"	"[{""label"":""KRT25"",""id"":""147183""}]"	"[""147183""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111574""}]"
DOID:0111576	"[""dehydrated hereditary stomatocytosis 1"",""PSHK1"",""dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema"",""pseudohyperkalemia edinburgh"",""pseudohyperkalemia familial 1, due to red cell leak""]"	"[{""label"":""PIEZO1"",""id"":""9780""}]"	"[""9780""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111576""}]"
DOID:0111577	"[""dehydrated hereditary stomatocytosis 2"",""desiccytosis Gardos"",""xerocytosis Gardos""]"	"[{""label"":""KCNN4"",""id"":""3783""}]"	"[""3783""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111577""}]"
DOID:0111578	"[""Gillespie syndrome"",""GLSP"",""aniridia, cerebellar ataxia and mental deficiency"",""aniridia-cerebellar ataxia-intellectual disability syndrome""]"	"[{""label"":""ITPR1"",""id"":""3708""}]"	"[""3708""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111578""}]"
DOID:0111579	"[""asthma, nasal polyps, and aspirin intolerance"",""ASA triad""]"	"[{""label"":""PTGER2"",""id"":""5732""}]"	"[""5732""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111579""}]"
DOID:0111580	"[""Behr syndrome"",""Abortive cerebellar ataxia (BEHRS)"",""BEHRS"",""optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss"",""optic atrophy, infantile hereditary, Behr complicated form of""]"	"[{""label"":""OPA1"",""id"":""4976""}]"	"[""4976""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111580""}]"
DOID:0111581	"[""C syndrome"",""OTCS"",""Opitz C trigonocephaly"",""Opitz trigonocephaly C syndrome"",""Opitz trigonocephaly syndrome"",""trigonocephaly C syndrome""]"	"[{""label"":""CD96"",""id"":""10225""}]"	"[""10225""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111581""}]"
DOID:0111582	"[""hereditary arterial and articular multiple calcification syndrome"",""CALJA"",""arterial calcification and distal joint calcification"",""arterial calcification due to CD73 deficiency"",""arterial calcification due to deficiency of CD73"",""calcification of joints and arteries""]"	"[{""label"":""NT5E"",""id"":""4907""}]"	"[""4907""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111582""}]"
DOID:0111583	"[""carboxypeptidase N deficiency"",""anaphylotoxin inactivator deficiency"",""deficiency of carboxypeptidase B""]"	"[{""label"":""CPN1"",""id"":""1369""}]"	"[""1369""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111583""}]"
DOID:0111584	"[""dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome"",""Malouf syndrome"",""Najjar syndrome"",""cardiogenital syndrome"",""cardiomyopathy eith primary testicular failure"",""congestive cardiomyopathy with hypergonadotropic hypogonadism"",""dilated cardiomyopathy with hypergonadotropic hypogonadism"",""dilated cardiomyopathy with premature ovarian failure"",""genital anomaly with cardiomyopathy""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111584""}]"
DOID:0111588	"[""Greenberg dysplasia"",""GRBGD"",""Greenberg skeletal dysplasia"",""HEM dysplasia"",""Skeletal dysplasia, Greenberg type"",""autosomal recessive lethal chondrodystrophy with congenital hydrops"",""hydrops, ectopic calcification, moth-eaten skeletal dysplasia"",""hydrops-ectopic calcification-motheaten syndrome""]"	"[{""label"":""LBR"",""id"":""3930""}]"	"[""3930""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111588""}]"
DOID:0111589	"[""COACH syndrome"",""Gentile syndrome"",""JS-H"",""Joubert syndrome with congenital hepatic fibrosis"",""Joubert syndrome with hepatic defect"",""cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, ocular coloboma, and hepatic fibrosis""]"	"[{""label"":""TMEM67"",""id"":""91147""}]"	"[""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111589""}]"
DOID:0111590	"[""Cohen syndrome"",""COH1"",""Hypotonia, obesity, and prominent incisors"",""Pepper syndrome""]"	"[{""label"":""VPS13B"",""id"":""157680""}]"	"[""157680""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111590""}]"
DOID:0111592	"[""plasminogen deficiency type I"",""hypoplasminogenemia""]"	"[{""label"":""PLG"",""id"":""5340""}]"	"[""5340""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111592""}]"
DOID:0111594	"[""distal arthrogryposis type 5D"",""DA5D"",""distal arthrogryposis type 5 without ophthalmoparesis"",""distal arthrogryposis type 5 without ophthalmoplegia""]"	"[{""label"":""ECEL1"",""id"":""9427""}]"	"[""9427""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111594""}]"
DOID:0111595	"[""congenital contractural arachnodactyly"",""Beals syndrome"",""Beals-Hecht syndrome"",""CCA"",""arachnodactyly, contractural Beals type"",""contractures, multiple with arachnodactyly"",""distal arthrogryposis type 9"",""ear anomalies-contractures-dysplasia of bone with kyphoscoliosis""]"	"[{""label"":""FBN2"",""id"":""2201""}]"	"[""2201""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111595""}]"
DOID:0111598	"[""distal arthrogryposis type 1B"",""DA1B""]"	"[{""label"":""MYBPC1"",""id"":""4604""}]"	"[""4604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111598""}]"
DOID:0111607	"[""distal arthrogryposis type 3"",""DA3"",""Gordon syndrome"",""camptodactyly-cleft palate-clubfoot syndrome"",""distal arthrogryposis multiplex congenita type IIA""]"	"[{""label"":""PIEZO2"",""id"":""63895""}]"	"[""63895""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111607""}]"
DOID:0111608	"[""distal arthrogryposis type 5"",""DA5"",""DAIIB"",""arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome"",""distal arthrogryposis type IIB"",""distal arthrogryposis with ophthalmoplegia"",""oculomelic amyoplasia""]"	"[{""label"":""PIEZO2"",""id"":""63895""}]"	"[""63895""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111608""}]"
DOID:0111611	"[""autosomal recessive spinocerebellar ataxia 4"",""SCA24"",""SCAR4"",""SCASI"",""autosomal recessive cerebellar ataxia-saccadic intrusion syndrome"",""spinocerebellar ataxia 24"",""spinocerebellar ataxia with saccadic intrusions""]"	"[{""label"":""VPS13D"",""id"":""55187""}]"	"[""55187""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111611""}]"
DOID:0111614	"[""autosomal recessive spinocerebellar ataxia 22"",""SCAR22""]"	"[{""label"":""VWA3B"",""id"":""200403""}]"	"[""200403""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111614""}]"
DOID:0111618	"[""autosomal recessive spinocerebellar ataxia 8"",""ARCA1"",""Autosomal recessive cerebellar ataxia type 1"",""SCAR8"",""SYNE1-related autosomal recessive cerebellar ataxia"",""autosomal recessive ataxia, Beauce type"",""recessive ataxia of Beauce""]"	"[{""label"":""SYNE1"",""id"":""23345""}]"	"[""23345""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111618""}]"
DOID:0111620	"[""corneal dystrophy-perceptive deafness syndrome"",""CDPD"",""CDPD1"",""Harboyan syndrome"",""corneal dystrophy and perceptive deafness"",""corneal dystrophy with progressive deafness"",""corneal endothelial dystrophy and perceptive deafness""]"	"[{""label"":""SLC4A11"",""id"":""83959""}]"	"[""83959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111620""}]"
DOID:0111623	"[""ACTH-independent macronodular adrenal hyperplasia 1"",""AIMAH1""]"	"[{""label"":""GNAS"",""id"":""2778""}]"	"[""2778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111623""}]"
DOID:0111625	"[""ventriculomegaly - cystic kidney disease"",""VMCKD"",""congenital nephrosis-cerebral ventriculomegaly syndrome"",""cystic kidney disease with ventriculomegaly"",""ventriculomegaly with cystic kidney disease""]"	"[{""label"":""CRB2"",""id"":""286204""}]"	"[""286204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111625""}]"
DOID:0111626	"[""D-glyceric aciduria"",""D-glycerate kinase deficiency"",""D-glyceric acidemia"",""D-glycericacidemia"",""deficiency of glycerate kinase"",""non ketotic hyperglycinemia syndrome""]"	"[{""label"":""GLYCTK"",""id"":""132158""}]"	"[""132158""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111626""}]"
DOID:0111628	"[""high myopia-sensorineural deafness syndrome"",""DFNMYP"",""deafness and myopia"",""deafness and myopia syndrome""]"	"[{""label"":""SLITRK6"",""id"":""84189""}]"	"[""84189""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111628""}]"
DOID:0111630	"[""familial erythrocytosis 8"",""BPGM deficiency"",""DPGM deficiency"",""ECYT8"",""bisphosphoglycerate mutase deficiency"",""bisphosphoglyceromutase deficiency"",""diphosphoglycerate mutase deficiency of erythrocyte"",""hemolytic anemia due to diphosphoglycerate mutase deficiency""]"	"[{""label"":""BPGM"",""id"":""669""}]"	"[""669""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111630""}]"
DOID:0111631	"[""familial erythrocytosis 7"",""ECYT7"",""alpha-globin type erythrocytosis"",""alpha-globin type polycythemia""]"	"[{""label"":""HBA1"",""id"":""3039""},{""label"":""HBA2"",""id"":""3040""}]"	"[""3039"",""3040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111631""}]"
DOID:0111632	"[""familial erythrocytosis 6"",""ECYT6"",""beta-globin type erythrocytosis"",""beta-globin type polycythemia""]"	"[{""label"":""HBB"",""id"":""3043""}]"	"[""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111632""}]"
DOID:0111633	"[""congenital sucrase-isomaltase deficiency"",""CSID"",""SI deficiency"",""congenital sucrase-isomaltose malabsorption"",""congenital sucrose intolerance"",""disaccharide intolerance""]"	"[{""label"":""SI"",""id"":""6476""}]"	"[""6476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111633""}]"
DOID:0111634	"[""autosomal recessive nonsyndromic deafness 99"",""DFNB99"",""autosomal recessive deafness 99""]"	"[{""label"":""TMEM132E"",""id"":""124842""}]"	"[""124842""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111634""}]"
DOID:0111635	"[""autosomal recessive nonsyndromic deafness 57"",""DFNB57"",""autosomal recessive deafness 57""]"	"[{""label"":""PDZD7"",""id"":""79955""}]"	"[""79955""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111635""}]"
DOID:0111636	"[""autosomal recessive nonsyndromic deafness 113"",""DFNB113"",""autosomal recessive deafness 113""]"	"[{""label"":""CEACAM16"",""id"":""388551""}]"	"[""388551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111636""}]"
DOID:0111637	"[""autosomal recessive nonsyndromic deafness 112"",""DFNB112"",""autosomal recessive deafness 112""]"	"[{""label"":""BDP1"",""id"":""55814""}]"	"[""55814""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111637""}]"
DOID:0111638	"[""autosomal recessive nonsyndromic deafness 100"",""DFNB100"",""autosomal recessive deafness 100""]"	"[{""label"":""PPIP5K2"",""id"":""23262""}]"	"[""23262""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111638""}]"
DOID:0111640	"[""autosomal recessive nonsyndromic deafness 111"",""DFNB111"",""autosomal recessive deafness 111""]"	"[{""label"":""MPZL2"",""id"":""10205""}]"	"[""10205""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111640""}]"
DOID:0111641	"[""autosomal recessive nonsyndromic deafness 94"",""DFNB94"",""autosomal recessive deafness 94""]"	"[{""label"":""NARS2"",""id"":""79731""}]"	"[""79731""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111641""}]"
DOID:0111643	"[""autosomal recessive nonsyndromic deafness 115"",""DFNB115"",""autosomal recessive deafness 115""]"	"[{""label"":""SPNS2"",""id"":""124976""}]"	"[""124976""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111643""}]"
DOID:0111644	"[""autosomal recessive nonsyndromic deafness 110"",""DFNB110"",""autosomal recessive deafness 110""]"	"[{""label"":""COCH"",""id"":""1690""}]"	"[""1690""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111644""}]"
DOID:0111646	"[""congenital lactase deficiency"",""CLD"",""congenital alactasia"",""congenital alactasia syndrome"",""congenital lactose intolerance"",""congenital lactose malabsorption"",""disaccharide intolerance II""]"	"[{""label"":""LCT"",""id"":""3938""}]"	"[""3938""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111646""}]"
DOID:0111647	"[""Schopf-Schulz-Passarge syndrome"",""SSPS"",""eccrine tumors-ectodermal dysplasia"",""keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome"",""palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome"",""palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome""]"	"[{""label"":""WNT10A"",""id"":""80326""}]"	"[""80326""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111647""}]"
DOID:0111648	"[""ectopia lentis with ectopia of pupil"",""ectopia lentis et pupillae""]"	"[{""label"":""ADAMTSL4"",""id"":""54507""}]"	"[""54507""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111648""}]"
DOID:0111649	"[""ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome"",""EEM syndrome"",""EEMS"",""ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome""]"	"[{""label"":""CDH3"",""id"":""1001""}]"	"[""1001""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111649""}]"
DOID:0111650	"[""ectodermal dysplasia 13"",""ECTD13"",""ectodermal dysplasia 13, hair/tooth type""]"	"[{""label"":""KREMEN1"",""id"":""83999""}]"	"[""83999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111650""}]"
DOID:0111651	"[""ectodermal dysplasia 15"",""ECTD15"",""ectodermal dysplasia 15, hypohidrotic/hair type""]"	"[{""label"":""CST6"",""id"":""1474""}]"	"[""1474""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111651""}]"
DOID:0111662	"[""ectodermal dysplasia 14"",""ECTN14"",""ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis""]"	"[{""label"":""TSPEAR"",""id"":""54084""}]"	"[""54084""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111662""}]"
DOID:0111663	"[""ectodermal dysplasia 10A"",""ECTD10A"",""ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant""]"	"[{""label"":""EDAR"",""id"":""10913""}]"	"[""10913""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111663""}]"
DOID:0111664	"[""ectodermal dysplasia 1"",""CST syndrome"",""Christ-Siemens-Touraine syndrome"",""ED1"",""HED1"",""X-linked anhidrotic ectodermal dysplasia"",""XHED"",""XLHED"",""ectodermal dysplasia 1, anhidrotic"",""ectodermal dysplasia 1, hypohidrotic, X-linked"",""ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked"",""hypohidrotic ectodermal dysplasia, X-Linked""]"	"[{""label"":""EDA"",""id"":""1896""}]"	"[""1896""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111664""}]"
DOID:0111665	"[""ectodermal dysplasia 10B"",""ECTD10B"",""ectodermal dysplasia 10B, hypohidrotic/hair/nail type, autosomal recessive""]"	"[{""label"":""EDAR"",""id"":""10913""}]"	"[""10913""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111665""}]"
DOID:0111666	"[""proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome"",""EPV"",""Fowler syndrome"",""Fowler vasculopathy"",""PVHH"",""cerebral proliferative glomeruloid vasculopathy"",""encephaloclastic proliferative vasculopathy"",""hydranencephaly, Fowler type"",""hydrocephaly/hydranencephaly due to cerebral vasculopathy"",""proliferative vasculopathy and hydranencephaly/hydrocephaly""]"	"[{""label"":""HNM1"",""id"":""852803""}]"	"[""852803""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111666""}]"
DOID:0111667	"[""enterokinase deficiency"",""congenital enterokinase deficiency"",""congenital enteropathy due to enteropeptidase deficiency"",""deficiency of enteropeptidase""]"	"[{""label"":""TMPRSS15"",""id"":""5651""}]"	"[""5651""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111667""}]"
DOID:0111668	"[""Kohlschutter-Tonz syndrome"",""KTZS"",""Kohlschutter's syndrome"",""amelocerebrohypohidrotic syndrome"",""epilepsy and yellow teeth"",""epilepsy dementia amelogenesis imperfecta"",""epilepsy-dementia-amelogenesis imperfecta syndrome""]"	"[{""label"":""ROGDI"",""id"":""79641""}]"	"[""79641""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111668""}]"
DOID:0111669	"[""hyaline fibromatosis syndrome"",""HFS"",""inherited systemic hyalinosis"",""puretic syndrome"",""systemic hyalinosis""]"	"[{""label"":""ANTXR2"",""id"":""118429""}]"	"[""118429""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111669""}]"
DOID:0111670	"[""primary hyperoxaluria type 1"",""HP1"",""alanine-glyoxylate aminotransferase deficiency"",""glycolic aciduria"",""hepatic AGT deficiency"",""oxalosis I"",""peroxisomal alanine-glyoxylate aminotransferase deficiency"",""serine pyruvate aminotransferase deficiency""]"	"[{""label"":""AGXT"",""id"":""189""}]"	"[""189""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111670""}]"
DOID:0111671	"[""primary hyperoxaluria type 2"",""D-glycerate dehydrogenase deficiency"",""HP2"",""L-glyceric aciduria"",""glyoxylate reductase/hydroxypyruvate reductase deficiency"",""oxalosis II""]"	"[{""label"":""GRHPR"",""id"":""9380""}]"	"[""9380""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111671""}]"
DOID:0111671	"[""primary hyperoxaluria type 2"",""D-glycerate dehydrogenase deficiency"",""HP2"",""L-glyceric aciduria"",""glyoxylate reductase/hydroxypyruvate reductase deficiency"",""oxalosis II""]"	"[{""label"":""Grhpr"",""id"":""76238""}]"	"[""76238""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111671""}]"
DOID:0111672	"[""primary hyperoxaluria type 3"",""HP3"",""PH III"",""primary hyperoxaluria type III""]"	"[{""label"":""HOGA1"",""id"":""112817""}]"	"[""112817""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111672""}]"
DOID:0111673	"[""Saul-Wilson syndrome"",""SWILS"",""microcephalic osteodysplastic dysplasia, Saul-Wilson type""]"	"[{""label"":""COG4"",""id"":""25839""}]"	"[""25839""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111673""}]"
DOID:0111675	"[""neurooculocardiogenitourinary syndrome"",""NOCGUS""]"	"[{""label"":""WDR37"",""id"":""22884""}]"	"[""22884""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111675""}]"
DOID:0111676	"[""high molecular weight kininogen deficiency"",""Fitzgerald trait"",""HMWK deficiency"",""congenital high-molecular-weight kininogen deficiency""]"	"[{""label"":""KNG1"",""id"":""3827""}]"	"[""3827""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111676""}]"
DOID:0111677	"[""familial benign fleck retina"",""FRFB""]"	"[{""label"":""PLA2G5"",""id"":""5322""}]"	"[""5322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111677""}]"
DOID:0111678	"[""hereditary folate malabsorption"",""congenital defect of folate absorption"",""congenital folate malabsorption""]"	"[{""label"":""SLC46A1"",""id"":""113235""}]"	"[""113235""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111678""}]"
DOID:0111680	"[""essential fructosuria"",""fructokinase deficiency"",""hepatic fructokinase deficiency"",""ketohexokinase deficiency""]"	"[{""label"":""KHK"",""id"":""3795""}]"	"[""3795""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111680""}]"
DOID:0111681	"[""congenital nonspherocytic hemolytic anemia 7"",""gamma-glutamylcysteine synthetase deficiency"",""hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency""]"	"[{""label"":""GCLC"",""id"":""2729""}]"	"[""2729""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111681""}]"
DOID:0111682	"[""diffuse cystic renal dysplasia"",""CYSRD"",""renal dysplasia diffuse cystic"",""susceptibility to cystic renal dysplasia""]"	"[{""label"":""BICC1"",""id"":""80114""}]"	"[""80114""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111682""}]"
DOID:0111683	"[""neurofibromatosis-Noonan syndrome"",""NFNS"",""Noonan neurofibromatosis syndrome"",""neurofibromatosis type 1-Noonan syndrome"",""neurofibromatosis with Noonan phenotype""]"	"[{""label"":""NF1"",""id"":""4763""}]"	"[""4763""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111683""}]"
DOID:0111686	"[""hereditary mixed polyposis syndrome 2"",""HMPS2""]"	"[{""label"":""BMPR1A"",""id"":""657""}]"	"[""657""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111686""}]"
DOID:0111691	"[""familial adult myoclonic epilepsy 5"",""FAME5"",""FCMTE5"",""familial cortical myoclonic tremor and epilepsy 5""]"	"[{""label"":""CNTN2"",""id"":""6900""}]"	"[""6900""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111691""}]"
DOID:0111693	"[""familial adult myoclonic epilepsy 4"",""FAME4"",""FCMTE4"",""familial cortical myoclonic tremor and epilepsy 4""]"	"[{""label"":""YEATS2"",""id"":""55689""}]"	"[""55689""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111693""}]"
DOID:0111694	"[""familial adult myoclonic epilepsy 7"",""BAFME7"",""FAME7"",""FCMTE7"",""benign adult familial myoclonic epilepsy 7"",""familial cortical myoclonic tremor and epilepsy 7""]"	"[{""label"":""RAPGEF2"",""id"":""9693""}]"	"[""9693""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111694""}]"
DOID:0111696	"[""familial adult myoclonic epilepsy 6"",""BAFME6"",""FAME6"",""FCMTE6"",""benign adult familial myoclonic epilepsy 6"",""familial cortical myoclonic tremor and epilepsy 6""]"	"[{""label"":""TNRC6A"",""id"":""27327""}]"	"[""27327""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111696""}]"
DOID:0111698	"[""proprotein convertase 1/3 deficiency"",""PCI deficiency"",""obesity and endocrinopathy due to impaired processing of prohormones"",""obesity due to prohormone convertase I deficiency"",""obesity with impaired prohormone processing""]"	"[{""label"":""PCSK1"",""id"":""5122""}]"	"[""5122""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111698""}]"
DOID:0111699	"[""Van den Ende-Gupta syndrome"",""Marden-Walker-like syndrome"",""Marden-Walker-like syndrome without psychmotor retardation"",""VDEGS"",""blepharophimosis, arachnodactyly, and congenital contractures""]"	"[{""label"":""SCARF2"",""id"":""91179""}]"	"[""91179""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111699""}]"
DOID:0111700	"[""ankyrin-B-related cardiac arrhythmia"",""ankyrin-B syndrome""]"	"[{""label"":""ANK2"",""id"":""287""}]"	"[""287""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111700""}]"
DOID:0111700	"[""ankyrin-B-related cardiac arrhythmia"",""ankyrin-B syndrome""]"	"[{""label"":""Ank2"",""id"":""109676""}]"	"[""109676""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111700""}]"
DOID:0111705	"[""oculoectodermal syndrome"",""Toriello-Lacassie-Droste syndrome"",""aplasia cutis congenita-epibulbar dermoids syndrome""]"	"[{""label"":""KRAS"",""id"":""3845""}]"	"[""3845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111705""}]"
DOID:0111706	"[""oblique facial clefting 1"",""Tessier number 4 facial cleft""]"	"[{""label"":""SPECC1L"",""id"":""23384""}]"	"[""23384""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111706""}]"
DOID:0111707	"[""Bothnian type palmoplantar keratoderma"",""PPKB"",""diffuse palmoplantar keratoderma, Bothnian type""]"	"[{""label"":""AQP5"",""id"":""362""}]"	"[""362""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111707""}]"
DOID:0111715	"[""Schaaf-Yang syndrome"",""MAGEL2-related PWLS"",""MAGEL2-related Prader-Willi-like syndrome"",""PWLS"",""SHFYNG""]"	"[{""label"":""MAGEL2"",""id"":""54551""}]"	"[""54551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111715""}]"
DOID:0111717	"[""isolated cryptophthalmia"",""CRYPTOP"",""unilateral or bilateral isolated cryptophthalmos""]"	"[{""label"":""FREM2"",""id"":""341640""}]"	"[""341640""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111717""}]"
DOID:0111717	"[""isolated cryptophthalmia"",""CRYPTOP"",""unilateral or bilateral isolated cryptophthalmos""]"	"[{""label"":""Frem2"",""id"":""242022""}]"	"[""242022""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111717""}]"
DOID:0111722	"[""amelogenesis imperfecta type 3C"",""AI3C"",""amelogenesis imperfecta type IIIC"",""autosomal recessive amelogenesis imperfecta hypocalcification type""]"	"[{""label"":""Relt"",""id"":""320100""}]"	"[""320100""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111722""}]"
DOID:0111722	"[""amelogenesis imperfecta type 3C"",""AI3C"",""amelogenesis imperfecta type IIIC"",""autosomal recessive amelogenesis imperfecta hypocalcification type""]"	"[{""label"":""RELT"",""id"":""84957""}]"	"[""84957""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111722""}]"
DOID:0111725	"[""geleophysic dysplasia 1"",""GPHYSD1""]"	"[{""label"":""Adamtsl2"",""id"":""77794""}]"	"[""77794""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111725""}]"
DOID:0111725	"[""geleophysic dysplasia 1"",""GPHYSD1""]"	"[{""label"":""ADAMTSL2"",""id"":""9719""}]"	"[""9719""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111725""}]"
DOID:0111726	"[""geleophysic dysplasia 2"",""GPHYSD2""]"	"[{""label"":""FBN1"",""id"":""2200""}]"	"[""2200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111726""}]"
DOID:0111727	"[""geleophysic dysplasia 3"",""GPHYSD3""]"	"[{""label"":""LTBP3"",""id"":""4054""}]"	"[""4054""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111727""}]"
DOID:0111729	"[""familial episodic pain syndrome 1"",""FEPS1""]"	"[{""label"":""TRPA1"",""id"":""8989""}]"	"[""8989""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111729""}]"
DOID:0111730	"[""familial episodic pain syndrome 2"",""FEPS2""]"	"[{""label"":""SCN10A"",""id"":""6336""}]"	"[""6336""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111730""}]"
DOID:0111731	"[""familial episodic pain syndrome 3"",""FEPS3""]"	"[{""label"":""Scn11a"",""id"":""24046""}]"	"[""24046""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111731""}]"
DOID:0111731	"[""familial episodic pain syndrome 3"",""FEPS3""]"	"[{""label"":""SCN11A"",""id"":""11280""}]"	"[""11280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111731""}]"
DOID:0111732	"[""Eiken syndrome"",""Eiken skeletal dysplasia"",""bone modeling defect of hands and feet""]"	"[{""label"":""PTH1R"",""id"":""5745""}]"	"[""5745""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111732""}]"
DOID:0111735	"[""X-linked deafness 4"",""DFN6"",""DFNX4"",""X-linked progressive deafness 6"",""nonsyndromic sensorineural progressive deafness 6""]"	"[{""label"":""SMPX"",""id"":""23676""}]"	"[""23676""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111735""}]"
DOID:0111739	"[""X-linked deafness 1"",""DFN2"",""DFNX1"",""X-linked sensorineural congenital deafness 2""]"	"[{""label"":""PRPS1"",""id"":""5631""}]"	"[""5631""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111739""}]"
DOID:0111740	"[""X-linked deafness 6"",""DFNX6""]"	"[{""label"":""COL4A6"",""id"":""1288""}]"	"[""1288""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111740""}]"
DOID:0111741	"[""X-linked deafness 5"",""AUNX1"",""DFNX5"",""X-linked HSAN with deafness"",""X-linked auditory neuropathy 1 with peripheral sensory neuropathy"",""X-linked auditory neuropathy with peripheral sensory neuropathy type 1""]"	"[{""label"":""AIFM1"",""id"":""9131""}]"	"[""9131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111741""}]"
DOID:0111742	"[""cerebellar ataxia type 42"",""SCA42""]"	"[{""label"":""Cacna1g"",""id"":""12291""}]"	"[""12291""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111742""}]"
DOID:0111742	"[""cerebellar ataxia type 42"",""SCA42""]"	"[{""label"":""CACNA1G"",""id"":""8913""}]"	"[""8913""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111742""}]"
DOID:0111743	"[""cerebellar ataxia type 47"",""SCA47""]"	"[{""label"":""PUM1"",""id"":""9698""}]"	"[""9698""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111743""}]"
DOID:0111744	"[""cerebellar ataxia type 41"",""SCA41""]"	"[{""label"":""TRPC3"",""id"":""7222""}]"	"[""7222""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111744""}]"
DOID:0111745	"[""cerebellar ataxia type 43"",""SCA43""]"	"[{""label"":""MME"",""id"":""4311""}]"	"[""4311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111745""}]"
DOID:0111758	"[""Y-linked deafness 2"",""DFNY2""]"	"[{""label"":""TBL1Y"",""id"":""90665""}]"	"[""90665""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111758""}]"
DOID:0111765	"[""X-linked cardiac valvular dysplasia"",""CVD1"",""Dystrophie valvulaire associee a FLNA"",""EDS5"",""Ehlers-Danlos syndrome, type 5"",""FLNA-related X-linked myxomatous valvular dysplasia"",""FLNA-related valvular dystrophy"",""Filamin A-related X-linked myxomatous valvular dysplasia"",""XMVD""]"	"[{""label"":""FLNA"",""id"":""2316""}]"	"[""2316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111765""}]"
DOID:0111768	"[""X-linked properdin deficiency"",""CFPD"",""complement factor properdin deficiency""]"	"[{""label"":""CFP"",""id"":""5199""}]"	"[""5199""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111768""}]"
DOID:0111769	"[""46,XY sex reversal 6"",""46,XY gonadal dysgenesis, partial or complete, MAP3K1-related"",""46,XY sex reversal, partial or complete, MAP3K1-related"",""SRXY6""]"	"[{""label"":""MAP3K1"",""id"":""4214""}]"	"[""4214""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111769""}]"
DOID:0111773	"[""46,XY sex reversal 8"",""SRXY8"",""TDD"",""male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase""]"	"[{""label"":""AKR1C2"",""id"":""1646""},{""label"":""AKR1C4"",""id"":""1109""}]"	"[""1109"",""1646""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111773""}]"
DOID:0111776	"[""46,XY sex reversal 5"",""46,XY gonadal dysgenesis, complete, CBX2-related"",""46,XY sex reversal, CBX2-related"",""SRXY5"",""disorder of sex development, 46,XY, CBX2-related"",""sex reversal, XY, CBX2-related""]"	"[{""label"":""CBX2"",""id"":""84733""}]"	"[""84733""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111776""}]"
DOID:0111777	"[""46,XY sex reversal 2"",""46,XY sex reversal, DAX1-related"",""46XY sex reversal 2, dosage-sensitive"",""SRXY2"",""dosage-sensitive sex reversal""]"	"[{""label"":""NR0B1"",""id"":""190""}]"	"[""190""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111777""}]"
DOID:0111780	"[""TARP syndrome"",""Pierre Robin sequence-congenital heart defect-talipes syndrome"",""Pierre Robin syndrome-congenital heart defect-talipes syndrome"",""TARPS"",""talipes equinovarus-atrial septal defect-Robin sequence-persistence of the left superior vena cava syndrome""]"	"[{""label"":""RBM10"",""id"":""8241""}]"	"[""8241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111780""}]"
DOID:0111782	"[""otopalatodigital syndrome spectrum disorder"",""OPD spectrum disorder"",""OPSD"",""fronto-otopalatodigital osteodysplasia""]"	"[{""label"":""FLNA"",""id"":""2316""}]"	"[""2316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111782""}]"
DOID:0111783	"[""otopalatodigital syndrome type 1"",""OPD I syndrome"",""OPD syndrome 1"",""OPD1"",""Taybi syndrome"",""oto-palato-digital syndrome type 1"",""otopalatodigital syndrome type I""]"	"[{""label"":""FLNA"",""id"":""2316""}]"	"[""2316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111783""}]"
DOID:0111784	"[""otopalatodigital syndrome type 2"",""Andre syndrome"",""OPD II syndrome"",""OPD syndrome 2"",""OPD2"",""faciopalatoosseous syndrome"",""oto-palato-digital syndrome type 2"",""otopalatodigital syndrome type II""]"	"[{""label"":""FLNA"",""id"":""2316""}]"	"[""2316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111784""}]"
DOID:0111785	"[""frontometaphyseal dysplasia"",""FMD""]"	"[{""label"":""MAP3K7"",""id"":""6885""}]"	"[""6885""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111785""}]"
DOID:0111786	"[""frontometaphyseal dysplasia 1"",""FMD1""]"	"[{""label"":""FLNA"",""id"":""2316""}]"	"[""2316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111786""}]"
DOID:0111787	"[""frontometaphyseal dysplasia 2"",""FMD2""]"	"[{""label"":""MAP3K7"",""id"":""6885""}]"	"[""6885""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111787""}]"
DOID:0111788	"[""Melnick-Needles syndrome"",""MNS"",""Melnick-Needles osteodysplasty"",""osteodysplasty of Melnick and Needles""]"	"[{""label"":""FLNA"",""id"":""2316""}]"	"[""2316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111788""}]"
DOID:0111789	"[""Frank-Ter Haar syndrome"",""Borrone dermatocardioskeletal syndrome"",""FTHS"",""Ter Haar syndrome"",""autosomal recessive Melnick-Needles syndrome"",""megalocornea, multiple skeletal anomalies, and developmental delay""]"	"[{""label"":""SH3PXD2B"",""id"":""285590""}]"	"[""285590""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111789""}]"
DOID:0111795	"[""congenital nystagmus 6"",""NYS6"",""X-linked congenital nystagmus 6""]"	"[{""label"":""GPR143"",""id"":""4935""}]"	"[""4935""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111795""}]"
DOID:0111797	"[""autosomal recessive congenital nystagmus"",""autosomal recessive congenital motor nystagmus""]"	"[{""label"":""ROBO1"",""id"":""6091""}]"	"[""6091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111797""}]"
DOID:0111798	"[""X-linked nephrolithiasis type I"",""NPHL1"",""X-linked nephrolithiasis with renal failure"",""X-linked recessive urolithiasis type 1"",""XRN"",""nephrolithiasis 1"",""nephrolithiasis X-linked recessive type 1""]"	"[{""label"":""CLCN5"",""id"":""1184""}]"	"[""1184""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111798""}]"
DOID:0111799	"[""syndromic microphthalmia 1"",""Lenz dysplasia"",""Lenz microphthalmia"",""Lenz type microphthalmia"",""MCOPS1""]"	"[{""label"":""BCOR"",""id"":""54880""}]"	"[""54880""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111799""}]"
DOID:0111800	"[""syndromic microphthalmia 12"",""MCOPS12"",""microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or cardiac defects""]"	"[{""label"":""RARB"",""id"":""5915""}]"	"[""5915""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111800""}]"
DOID:0111801	"[""syndromic microphthalmia 3"",""AEG syndrome"",""MCOPS3"",""SOX2 anophthalmia syndrome"",""anophthalmia clinical with associated anomalies"",""anophthalmia esophageal genital syndrome"",""anophthalmia microphthalmia esophageal atresia"",""anophthalmia/microphthalmia-esophageal atresia syndrome"",""microphthalmia and esophageal atresia syndrome"",""syndromic microphthalmia type 3""]"	"[{""label"":""SOX2"",""id"":""6657""}]"	"[""6657""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111801""}]"
DOID:0111805	"[""syndromic microphthalmia 6"",""Bakrania-Ragge syndrome"",""MCOPS6"",""anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia"",""microphthalmia and pituitary anomalies"",""microphthalmia with brain and digit anomalies"",""syndromic microphthalmia type 6""]"	"[{""label"":""BMP4"",""id"":""652""}]"	"[""652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111805""}]"
DOID:0111806	"[""syndromic microphthalmia 5"",""MCOPS5"",""syndromic microphthalmia type 5"",""syndromic microphthalmia/anophthalmia due to OTX2 mutation""]"	"[{""label"":""OTX2"",""id"":""5015""}]"	"[""5015""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111806""}]"
DOID:0111807	"[""syndromic microphthalmia 9"",""Matthew-Wood syndrome"",""anophthalmia-pulmonary hypoplasia syndrome"",""anophthalmia/microphthalmia and pulmonary hypoplasia"",""clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations"",""pulmonary agenesis microphthalmi and diaphragmatic defect"",""spear syndrome""]"	"[{""label"":""STRA6"",""id"":""64220""}]"	"[""64220""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111807""}]"
DOID:0111808	"[""linear skin defects with multiple congenital anomalies 1"",""MCOPS7"",""MIDAS syndrome"",""Microphthalmia with linear skin defect syndrome"",""microphthalmia-dermal aplasia-sclerocornea syndrome"",""syndromic microphthalmia 7"",""syndromic microphthalmia type 7""]"	"[{""label"":""HCCS"",""id"":""3052""}]"	"[""3052""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111808""}]"
DOID:0111809	"[""syndromic microphthalmia 2"",""ANOP2"",""MAA2"",""MCOPS2"",""OFCD syndrome"",""cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome"",""microphthalmia cataracts radiculomegaly and septal heart defects"",""oculofaciocardiodental syndrome"",""syndromic microphthalmia type 2""]"	"[{""label"":""Bcor"",""id"":""71458""}]"	"[""71458""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111809""}]"
DOID:0111809	"[""syndromic microphthalmia 2"",""ANOP2"",""MAA2"",""MCOPS2"",""OFCD syndrome"",""cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome"",""microphthalmia cataracts radiculomegaly and septal heart defects"",""oculofaciocardiodental syndrome"",""syndromic microphthalmia type 2""]"	"[{""label"":""BCOR"",""id"":""54880""}]"	"[""54880""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111809""}]"
DOID:0111813	"[""syndactyly type 8"",""fusion of metacarpals 4 and 5"",""metacarpal 4-5 fusion""]"	"[{""label"":""FGF16"",""id"":""8823""}]"	"[""8823""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111813""}]"
DOID:0111814	"[""methylmalonic acidemia and homocysteinemia cblX type"",""combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX"",""mental retardation, X-linked 3"",""methylmalonic aciduria with homocystinuria, type cblX""]"	"[{""label"":""HCFC1"",""id"":""3054""}]"	"[""3054""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111814""}]"
DOID:0111814	"[""methylmalonic acidemia and homocysteinemia cblX type"",""combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX"",""mental retardation, X-linked 3"",""methylmalonic aciduria with homocystinuria, type cblX""]"	"[{""label"":""Hcfc1"",""id"":""15161""}]"	"[""15161""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111814""}]"
DOID:0111815	"[""low molecular weight proteinuria with hypercalciuric nephrocalcinosis""]"	"[{""label"":""CLCN5"",""id"":""1184""}]"	"[""1184""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111815""}]"
DOID:0111816	"[""syndactyly type 1"",""SDTY1"",""chromosome 2q35 duplication syndrome"",""syndactyly, type 1, with or without craniosynostosis""]"	"[{""label"":""IHH"",""id"":""3549""}]"	"[""3549""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111816""}]"
DOID:0111818	"[""syndactyly type 4"",""Haas type syndactyly"",""SDTY4"",""polysyndactyly, Haas type""]"	"[{""label"":""SHH"",""id"":""6469""}]"	"[""6469""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111818""}]"
DOID:0111819	"[""syndactyly type 5"",""SDTY5"",""syndactyly with associated metacarpal and metatarsal fusion""]"	"[{""label"":""HOXD13"",""id"":""3239""}]"	"[""3239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111819""}]"
DOID:0111821	"[""ichthyosis follicularis-alopecia-photophobia syndrome 1"",""IFAP syndrome 1"",""IFAP syndrome 1 with or without BRESHECK syndrome"",""ichthyosis follicularis-atrichia-photophobia syndrome 1""]"	"[{""label"":""MBTPS2"",""id"":""51360""}]"	"[""51360""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111821""}]"
DOID:0111822	"[""CHILD syndrome"",""CHILD nevus"",""congenital hemidysplasia with ichthyosiform nevus and limbs defects""]"	"[{""label"":""NSDHL"",""id"":""50814""}]"	"[""50814""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111822""}]"
DOID:0111827	"[""X-linked spinal muscular atrophy 2"",""SMAX2"",""X-linked distal arthrogryposis multiplex congenita"",""X-linked spinal muscular atrophy type 2"",""infantile-onset X-linked spinal muscular atrophy"",""spinal muscular atrophy with arthrogryposis""]"	"[{""label"":""UBA1"",""id"":""7317""}]"	"[""7317""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111827""}]"
DOID:0111834	"[""X-linked reticulate pigmentary disorder"",""Partington disease"",""X-linked reticulate pigmentary disorder with systemic manifestations""]"	"[{""label"":""POLA1"",""id"":""5422""}]"	"[""5422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111834""}]"
DOID:0111835	"[""congenital nongoitrous hypothyroidism 9"",""CHNG9""]"	"[{""label"":""IRS4"",""id"":""8471""}]"	"[""8471""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111835""}]"
DOID:0111836	"[""congenital nongoitrous hypothyroidism 7"",""CHNG7"",""TRH resistance syndrome"",""central hypothyroidism due to TRH receptor deficiency"",""resistance to thyrotropin-releasing hormone syndrome""]"	"[{""label"":""TRHR"",""id"":""7201""}]"	"[""7201""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111836""}]"
DOID:0111837	"[""congenital nongoitrous hypothyroidism 8"",""CHNG8""]"	"[{""label"":""TBL1X"",""id"":""6907""}]"	"[""6907""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111837""}]"
DOID:0111839	"[""congenital disorder of glycosylation Icc"",""congenital disorder of glycosylation type Icc""]"	"[{""label"":""MAGT1"",""id"":""84061""}]"	"[""84061""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111839""}]"
DOID:0111840	"[""Van Esch-O'Driscoll syndrome"",""MRXSVEOD"",""VEODS"",""X-linked intellectual disability, Van Esch type"",""X-linked syndromic mental retardation Van Esch-O'Driscoll type""]"	"[{""label"":""POLA1"",""id"":""5422""}]"	"[""5422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111840""}]"
DOID:0111841	"[""Shukla-Vernon syndrome"",""SHUVER""]"	"[{""label"":""BCORL1"",""id"":""63035""}]"	"[""63035""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111841""}]"
DOID:0111842	"[""Keipert syndrome"",""KPTS"",""nasodigitoacoustic syndrome""]"	"[{""label"":""GPC4"",""id"":""2239""}]"	"[""2239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111842""}]"
DOID:0111843	"[""Paganini-Miozzo syndrome"",""MRXSPM""]"	"[{""label"":""HS6ST2"",""id"":""90161""}]"	"[""90161""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111843""}]"
DOID:0111844	"[""X-linked intellectual developmental disorder 108"",""MRX108""]"	"[{""label"":""SLC9A7"",""id"":""84679""}]"	"[""84679""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111844""}]"
DOID:0111847	"[""osteogenesis imperfecta type 19"",""OI19"",""osteogenesis imperfecta type XIX""]"	"[{""label"":""MBTPS2"",""id"":""51360""}]"	"[""51360""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111847""}]"
DOID:0111849	"[""osteogenesis imperfecta type 20"",""OI20"",""osteogenesis imperfecta type XX""]"	"[{""label"":""MESD"",""id"":""23184""}]"	"[""23184""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111849""}]"
DOID:0111853	"[""primary ciliary dyskinesia 40"",""CILD40"",""primary ciliary dyskinesia 40 with or without situs inversus""]"	"[{""label"":""DNAH9"",""id"":""1770""}]"	"[""1770""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111853""}]"
DOID:0111854	"[""primary ciliary dyskinesia 39"",""CILD39"",""primary ciliary dyskinesia 39 with or without situs inversus""]"	"[{""label"":""LRRC56"",""id"":""115399""}]"	"[""115399""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111854""}]"
DOID:0111861	"[""Meester-Loeys syndrome"",""MRLS""]"	"[{""label"":""BGN"",""id"":""633""}]"	"[""633""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111861""}]"
DOID:0111862	"[""congenital bilateral absence of vas deferens"",""CAVD"",""CBAVD"",""congenital bilateral agenesis of vas deferens"",""congenital bilateral aplasia of vas deferens""]"	"[{""label"":""Cftr"",""id"":""24255""}]"	"[""24255""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111862""}]"
DOID:0111862	"[""congenital bilateral absence of vas deferens"",""CAVD"",""CBAVD"",""congenital bilateral agenesis of vas deferens"",""congenital bilateral aplasia of vas deferens""]"	"[{""label"":""CFTR"",""id"":""1080""}]"	"[""1080""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111862""}]"
DOID:0111863	"[""X-linked congenital bilateral absence of vas deferens"",""CBAVDX""]"	"[{""label"":""ADGRG2"",""id"":""10149""}]"	"[""10149""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111863""}]"
DOID:0111864	"[""autosomal recessive congenital bilateral absence of vas deferens""]"	"[{""label"":""CFTR"",""id"":""1080""}]"	"[""1080""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111864""}]"
DOID:0111865	"[""MEND syndrome"",""male EBP disorder with neurological defects""]"	"[{""label"":""EBP"",""id"":""10682""}]"	"[""10682""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111865""}]"
DOID:0111866	"[""trichothiodystrophy"",""TTD""]"	"[{""label"":""AARS1"",""id"":""16""},{""label"":""MARS1"",""id"":""4141""}]"	"[""16"",""4141""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111866""}]"
DOID:0111870	"[""nonphotosensitive trichothiodystrophy 7"",""TTD7""]"	"[{""label"":""TARS1"",""id"":""6897""}]"	"[""6897""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111870""}]"
DOID:0111872	"[""nonphotosensitive trichothiodystrophy 6"",""TTD6""]"	"[{""label"":""GTF2E2"",""id"":""2961""}]"	"[""2961""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111872""}]"
DOID:0111876	"[""linear skin defects with multiple congenital anomalies 3"",""LSDMCA3"",""linear skin defects with cardiomyopathy and other congenital anomalies""]"	"[{""label"":""NDUFB11"",""id"":""54539""}]"	"[""54539""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111876""}]"
DOID:0111882	"[""Diamond-Blackfan anemia 12"",""DBA12"",""RPL15-related Diamond-Blackfan anemia""]"	"[{""label"":""RPL15"",""id"":""6138""}]"	"[""6138""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111882""}]"
DOID:0111883	"[""Diamond-Blackfan anemia 5"",""DBA5"",""RPL35A-related Diamond-Blackfan anemia""]"	"[{""label"":""RPL35A"",""id"":""6165""}]"	"[""6165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111883""}]"
DOID:0111887	"[""Diamond-blackfan anemia 3"",""DBA3"",""RPS24-related Diamond-Blackfan anemia""]"	"[{""label"":""RPS24"",""id"":""6229""}]"	"[""6229""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111887""}]"
DOID:0111890	"[""Diamond-Blackfan anemia 4"",""DBA4"",""RPS17-related Diamond-Blackfan anemia""]"	"[{""label"":""RPS17"",""id"":""6218""}]"	"[""6218""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111890""}]"
DOID:0111892	"[""Diamond-Blackfan anemia 11"",""DBA11"",""RPL26-related Diamond-Blackfan anemia""]"	"[{""label"":""RPL26"",""id"":""6154""}]"	"[""6154""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111892""}]"
DOID:0111894	"[""Diamond-Blackfan anemia 15 with mandibulofacial dysostosis"",""DBA15""]"	"[{""label"":""RPS28"",""id"":""6234""}]"	"[""6234""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111894""}]"
DOID:0111895	"[""Diamond-Blackfan anemia 1"",""DBA1"",""RPS19-related Diamond-Blackfan anemia""]"	"[{""label"":""RPS19"",""id"":""6223""}]"	"[""6223""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111895""}]"
DOID:0111896	"[""Diamond-Blackfan anemia 18"",""DBA18"",""RPL18-related Diamond-Blackfan anemia""]"	"[{""label"":""RPL18"",""id"":""6141""}]"	"[""6141""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111896""}]"
DOID:0111898	"[""CK syndrome"",""X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome""]"	"[{""label"":""NSDHL"",""id"":""50814""}]"	"[""50814""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111898""}]"
DOID:0111899	"[""X-linked thrombophilia due to factor IX defect"",""THPH8""]"	"[{""label"":""F9"",""id"":""2158""}]"	"[""2158""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111899""}]"
DOID:0111900	"[""autosomal dominant thrombophilia due to protein S deficiency"",""THPH5""]"	"[{""label"":""PROS1"",""id"":""5627""}]"	"[""5627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111900""}]"
DOID:0111901	"[""heparin cofactor II deficiency"",""HCF 2 deficiency"",""HCF II deficiency"",""THPH10"",""thrombophilia due to heparin cofactor II deficiency""]"	"[{""label"":""SERPIND1"",""id"":""3053""}]"	"[""3053""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111901""}]"
DOID:0111902	"[""thrombophilia due to activated protein C resistance"",""APC resistance"",""PCCF deficiency"",""PROC cofactor deficiency"",""THPH2"",""activated protein C resistance"",""thrombophilia V"",""thrombophilia due to deficiency of activated protein C cofactor""]"	"[{""label"":""F5"",""id"":""2153""},{""label"":""PROC"",""id"":""5624""}]"	"[""2153"",""5624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111902""}]"
DOID:0111903	"[""thrombophilia due to HRG deficiency"",""THPH11"",""hereditary thrombophilia due to congenital HRG deficiency"",""hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency""]"	"[{""label"":""HRG"",""id"":""3273""}]"	"[""3273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111903""}]"
DOID:0111904	"[""autosomal recessive thrombophilia due to protein C deficiency"",""THPH4"",""autosomal recessive PROC deficiency"",""autosomal recessive protein C deficiency""]"	"[{""label"":""PROC"",""id"":""5624""}]"	"[""5624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111904""}]"
DOID:0111905	"[""autosomal recessive thrombophilia due to protein S deficiency"",""THPH6"",""autosomal recessive thrombophilia due to congenital protein S deficiency"",""severe hereditary thrombophilia due to congenital protein S deficiency""]"	"[{""label"":""PROS1"",""id"":""5627""}]"	"[""5627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111905""}]"
DOID:0111907	"[""thrombophilia due to thrombin defect"",""THPH1"",""prothrombin-related thrombophilia"",""thrombophilia due to factor 2 defect""]"	"[{""label"":""F13A1"",""id"":""2162""},{""label"":""F2"",""id"":""2147""},{""label"":""HABP2"",""id"":""3026""}]"	"[""2147"",""2162"",""3026""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111907""}]"
DOID:0111908	"[""thrombophilia due to thrombomodulin defect"",""THBD-related bleeding disorder"",""THBD-related coagulopathy"",""THPH12"",""thrombomodulin-related bleeding disorder"",""thrombomodulin-related coagulopathy""]"	"[{""label"":""THBD"",""id"":""7056""}]"	"[""7056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111908""}]"
DOID:0111909	"[""autosomal dominant thrombophilia due to protein C deficiency"",""THPH3"",""autosomal dominant PROC deficiency"",""autosomal dominant protein C deficiency""]"	"[{""label"":""PROC"",""id"":""5624""}]"	"[""5624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111909""}]"
DOID:0111911	"[""spermatogenic failure 34"",""SPGF34""]"	"[{""label"":""FSIP2"",""id"":""401024""}]"	"[""401024""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111911""}]"
DOID:0111913	"[""spermatogenic failure 30"",""SPGF30""]"	"[{""label"":""TDRD9"",""id"":""122402""}]"	"[""122402""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111913""}]"
DOID:0111916	"[""spermatogenic failure 28"",""SPGF28""]"	"[{""label"":""FANCM"",""id"":""57697""}]"	"[""57697""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111916""}]"
DOID:0111917	"[""spermatogenic failure 43"",""SPGF43""]"	"[{""label"":""SPEF2"",""id"":""79925""}]"	"[""79925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111917""}]"
DOID:0111918	"[""spermatogenic failure 40"",""SPGF40""]"	"[{""label"":""CFAP65"",""id"":""255101""}]"	"[""255101""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111918""}]"
DOID:0111919	"[""spermatogenic failure 38"",""SPGF38""]"	"[{""label"":""ARMC2"",""id"":""84071""}]"	"[""84071""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111919""}]"
DOID:0111922	"[""spermatogenic failure 31"",""SPGF31""]"	"[{""label"":""PMFBP1"",""id"":""83449""}]"	"[""83449""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111922""}]"
DOID:0111923	"[""spermatogenic failure 42"",""SPGF42""]"	"[{""label"":""TTC29"",""id"":""83894""}]"	"[""83894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111923""}]"
DOID:0111926	"[""spermatogenic failure 39"",""SPGF39""]"	"[{""label"":""DNAH17"",""id"":""8632""}]"	"[""8632""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111926""}]"
DOID:0111927	"[""spermatogenic failure 37"",""SPGF37""]"	"[{""label"":""TTC21A"",""id"":""199223""}]"	"[""199223""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111927""}]"
DOID:0111932	"[""severe congenital encephalopathy due to MECP2 mutation"",""neonatal severe encephalopathy due to MECP2 mutations"",""severe neonatal-onset encephalopathy with microcephaly""]"	"[{""label"":""MECP2"",""id"":""4204""}]"	"[""4204""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111932""}]"
DOID:0111933	"[""phosphoglycerate kinase 1 deficiency"",""GSD due to phosphoglycerate kinase 1 deficiency"",""PGK1 deficiency"",""glycogen storage disease due to phosphoglycerate kinase 1 deficiency"",""glycogenosis due to phosphoglycerate kinase 1 deficiency""]"	"[{""label"":""PGK1"",""id"":""5230""}]"	"[""5230""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111933""}]"
DOID:0111935	"[""immunodeficiency 16"",""IMD16"",""OX40 deficiency"",""combined immunodeficiency due to OX40 deficiency"",""combined immunodeficiency with childhood-onset Kaposi sarcoma"",""combined immunodeficiency with impaired immunity to HHV-8"",""combined immunodeficiency with impaired immunity to human herpes virus 8""]"	"[{""label"":""TNFRSF4"",""id"":""7293""}]"	"[""7293""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111935""}]"
DOID:0111936	"[""immunodeficiency 14"",""APDS"",""IMD14"",""PASLI disease"",""activated PI3K-delta syndrome"",""senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation""]"	"[{""label"":""PIK3CD"",""id"":""5293""}]"	"[""5293""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111936""}]"
DOID:0111938	"[""immunodeficiency 24"",""IMD24"",""SCID due to CTPS1 deficiency"",""severe combined immunodeficiency due to CTPS1 deficiency""]"	"[{""label"":""CTPS1"",""id"":""1503""}]"	"[""1503""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111938""}]"
DOID:0111941	"[""immunodeficiency 20"",""CD16 deficiency"",""IMD20"",""autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity"",""autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity""]"	"[{""label"":""FCGR3A"",""id"":""2214""}]"	"[""2214""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111941""}]"
DOID:0111943	"[""immunodeficiency 48"",""IMD48"",""combined immunodeficiency due to ZAP70 deficiency"",""zeta-associated-protein 70 deficiency""]"	"[{""label"":""ZAP70"",""id"":""7535""}]"	"[""7535""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111943""}]"
DOID:0111944	"[""immunodeficiency 31B"",""IMD31B"",""autosomal recessive STAT1 deficiency"",""autosomal recessive immunodeficiency 31B, mycobacterial and viral infections"",""predisposition to severe viral infection due to STAT1 deficiency"",""susceptibility to viral and mycobacterial infections due to STAT1 deficiency""]"	"[{""label"":""STAT1"",""id"":""6772""}]"	"[""6772""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111944""}]"
DOID:0111945	"[""immunodeficiency 31A"",""IMD31A"",""MSMD due to partial STAT1 deficiency"",""MSMD due to partial signal transducer and activator of transcription 1 deficiency"",""Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency"",""Mendelian susceptibility to mycobacterial diseases due to partial signal transducer and activator of transcription 1 deficiency"",""autosomal dominant immunodeficiency 31A, mycobacteriosis""]"	"[{""label"":""STAT1"",""id"":""6772""}]"	"[""6772""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111945""}]"
DOID:0111946	"[""immunodeficiency 31C"",""CANDF7"",""IMD31C"",""autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome"",""autosomal dominant chronic mucocutaneous familial candidiasis"",""autosomal dominant immunodeficiency 31C"",""familial candidiasis 7""]"	"[{""label"":""STAT1"",""id"":""6772""}]"	"[""6772""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111946""}]"
DOID:0111947	"[""immunodeficiency 21"",""DCML"",""GATA2 deficiency"",""IMD21"",""MonoMAC"",""combined immunodeficiency with susceptibility to mycobacterial, viral and fungal infections"",""dendritic cell, monocyte, B and NK lymphoid deficiency"",""monocyte-B-natural killer-dendritic cell deficiency syndrome"",""monocytopenia and mycobacterial infection syndrome"",""monocytopenia with susceptibility to infections""]"	"[{""label"":""GATA2"",""id"":""2624""}]"	"[""2624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111947""}]"
DOID:0111948	"[""immunodeficiency 46"",""CID due to TFRC deficiency"",""IMD46"",""TFRC-related combined immunodeficiency"",""combined immunodeficiency due to TFRC deficiency""]"	"[{""label"":""TFRC"",""id"":""7037""}]"	"[""7037""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111948""}]"
DOID:0111950	"[""immunodeficiency 29"",""IL12B deficiency"",""IMD29"",""MSMD due to complete IL12B deficiency"",""MSMD due to complete interleukin 12B deficiency"",""Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency"",""Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency"",""immunodeficiency 29, mycobacteriosis""]"	"[{""label"":""IL12B"",""id"":""3593""}]"	"[""3593""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111950""}]"
DOID:0111952	"[""immunodeficiency 57"",""IMD57"",""immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome"",""immunodeficiency 57 with autoinflammation""]"	"[{""label"":""RIPK1"",""id"":""8737""}]"	"[""8737""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111952""}]"
DOID:0111953	"[""immunodeficiency 23"",""CID due to PGM3 deficiency"",""IMD23"",""PGM3-CDG"",""PGM3-related congenital disorder of glycosylation"",""combined immunodeficiency due to PGM3 deficiency""]"	"[{""label"":""PGM3"",""id"":""5238""}]"	"[""5238""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111953""}]"
DOID:0111954	"[""immunodeficiency 60"",""BACH2-related immunodeficiency and autoimmunity"",""BRIDA"",""IMD60""]"	"[{""label"":""BACH2"",""id"":""60468""}]"	"[""60468""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111954""}]"
DOID:0111955	"[""immunodeficiency 27A"",""IMD27A"",""autosomal recessive IFNGR1 deficiency"",""autosomal recessive MSMD due to partial IFNgammaR1 deficiency"",""autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency"",""autosomal recessive immunodeficiency 27A, mycobacteriosis"",""autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency"",""autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency""]"	"[{""label"":""IFNGR1"",""id"":""3459""}]"	"[""3459""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111955""}]"
DOID:0111956	"[""immunodeficiency 27B"",""IMD27B"",""autosomal dominant IFNGR1 deficiency"",""autosomal dominant MSMD due to partial IFNgammaR1 deficiency"",""autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency"",""autosomal dominant immunodeficiency 27B, mycobacteriosis"",""autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency"",""autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency""]"	"[{""label"":""IFNGR1"",""id"":""3459""}]"	"[""3459""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111956""}]"
DOID:0111957	"[""immunodeficiency 11A"",""CARD11 deficiency"",""IMD11A"",""SCID due to CARD11 deficiency"",""severe combined immunodeficiency due to CARD11 deficiency""]"	"[{""label"":""CARD11"",""id"":""84433""}]"	"[""84433""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111957""}]"
DOID:0111958	"[""immunodeficiency 11B"",""IMD11B"",""atopic dermatitis, elevated IgE, and eosinophilia"",""immunodeficiency 11B with atopic dermatitis""]"	"[{""label"":""CARD11"",""id"":""84433""}]"	"[""84433""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111958""}]"
DOID:0111959	"[""immunodeficiency 15B"",""IMD15B""]"	"[{""label"":""IKBKB"",""id"":""3551""}]"	"[""3551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111959""}]"
DOID:0111960	"[""immunodeficiency 15A"",""IMD15A""]"	"[{""label"":""IKBKB"",""id"":""3551""}]"	"[""3551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111960""}]"
DOID:0111960	"[""immunodeficiency 15A"",""IMD15A""]"	"[{""label"":""Ikbkb"",""id"":""16150""}]"	"[""16150""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111960""}]"
DOID:0111961	"[""immunodeficiency 26"",""IMD26"",""SCID due to DNA-PKcs deficiency"",""immunodeficiency 26, with or without neurologic abnormalities"",""severe combined immunodeficiency due to DNA-PKcs deficiency""]"	"[{""label"":""PRKDC"",""id"":""5591""}]"	"[""5591""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111961""}]"
DOID:0111967	"[""immunodeficiency 54"",""IMD54"",""NKCD"",""familial isolated natural killer cell deficiency"",""primary immunodeficiency due to MCM4 deficiency"",""primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency""]"	"[{""label"":""MCM4"",""id"":""4173""}]"	"[""4173""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111967""}]"
DOID:0111968	"[""immunodeficiency 41"",""CD25 deficiency"",""IL2RA deficiency"",""IMD41"",""immunodeficiency 41 with lymphoproliferation and autoimmunity"",""immunodeficiency due to CD25 deficiency"",""interleukin-2 receptor alpha chain deficiency""]"	"[{""label"":""IL2RA"",""id"":""3559""}]"	"[""3559""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111968""}]"
DOID:0111969	"[""immunodeficiency 39"",""IMD39""]"	"[{""label"":""IRF7"",""id"":""3665""}]"	"[""3665""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111969""}]"
DOID:0111970	"[""immunodeficiency 10"",""CID due to STIM1 deficiency"",""IMD10"",""STIM1 deficiency"",""combined immunodeficiency due to STIM1 deficiency"",""immune dysfunction with T-cell inactivation due to calcium entry defect 2""]"	"[{""label"":""STIM1"",""id"":""6786""}]"	"[""6786""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111970""}]"
DOID:0111972	"[""immunodeficiency 19"",""CD3-delta deficiency"",""IMD19"",""SCID T cell-negative, B cell-positive, NK cell-positive"",""severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive""]"	"[{""label"":""CD3D"",""id"":""915""}]"	"[""915""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111972""}]"
DOID:0111973	"[""immunodeficiency 17"",""CD3-gamma deficiency"",""IMD17"",""SCID-like immunodeficiency, T cell-partial, B cell-positive, NK cell-positive"",""immunodeficiency 17, CD3 gamma deficient""]"	"[{""label"":""CD3G"",""id"":""917""}]"	"[""917""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111973""}]"
DOID:0111974	"[""immunodeficiency 59"",""IMD59"",""granulocytopenia with immunoglobin abnormality"",""immunodeficiency 59 and hypoglycemia""]"	"[{""label"":""HYOU1"",""id"":""10525""}]"	"[""10525""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111974""}]"
DOID:0111975	"[""immunodeficiency 44"",""IMD44""]"	"[{""label"":""STAT2"",""id"":""6773""}]"	"[""6773""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111975""}]"
DOID:0111976	"[""immunodeficiency 9"",""CID due to ORAI1 deficiency"",""IMD9"",""combined immunodeficiency due to ORAI1 deficiency"",""immune dysfunction with T-cell inactivation due to calcium entry defect 1""]"	"[{""label"":""ORAI1"",""id"":""84876""}]"	"[""84876""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111976""}]"
DOID:0111979	"[""immunodeficiency 49"",""IMD49"",""SCID, T-cell negative, B-cell positive, NK cell positive, with intellectual disability, spasticity, and craniofacial abnormalities"",""severe combined immunodeficiency, T-cell negative, B-cell positive, NK cell positive, with intellectual disability, spasticity, and craniofacial abnormalities""]"	"[{""label"":""BCL11B"",""id"":""64919""}]"	"[""64919""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111979""}]"
DOID:0111981	"[""immunodeficiency 43"",""B2M deficiency"",""IMD43"",""beta-2-microglobulin deficiency"",""hypercatabolic hypoproteinemia""]"	"[{""label"":""B2M"",""id"":""567""}]"	"[""567""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111981""}]"
DOID:0111982	"[""immunodeficiency 56"",""IL21R immunodeficiency"",""IMD56"",""combined immunodeficiency due to IL21R deficiency""]"	"[{""label"":""IL21R"",""id"":""50615""}]"	"[""50615""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111982""}]"
DOID:0111983	"[""immunodeficiency 52"",""IMD52"",""severe combined immunodeficiency due to LAT deficiency""]"	"[{""label"":""LAT"",""id"":""27040""}]"	"[""27040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111983""}]"
DOID:0111984	"[""immunodeficiency 58"",""IMD58"",""severe combined immunodeficiency due to CARMIL2 deficiency""]"	"[{""label"":""CARMIL2"",""id"":""146206""}]"	"[""146206""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111984""}]"
DOID:0111988	"[""immunodeficiency 12"",""IMD12"",""combined immunodeficiency due to MALT1 deficiency""]"	"[{""label"":""MALT1"",""id"":""10892""}]"	"[""10892""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111988""}]"
DOID:0111989	"[""immunodeficiency 35"",""IMD35"",""TYK2 deficiency"",""autosomal recessiv HIES with atypical mycobacteriosis"",""autosomal recessive hyper-IgE syndrome with atypical mycobacteriosis"",""susceptibility to infection due to TYK2 deficiency"",""tyrosine kinase 2 deficiency""]"	"[{""label"":""TYK2"",""id"":""7297""}]"	"[""7297""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111989""}]"
DOID:0111990	"[""immunodeficiency 30"",""IMD30"",""MSMD due to complete IL12RB1 deficiency"",""MSMD due to complete interleukin 12 receptor beta 1 deficiency"",""Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency"",""Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency""]"	"[{""label"":""IL12RB1"",""id"":""3594""}]"	"[""3594""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111990""}]"
DOID:0111992	"[""immunodeficiency 53"",""IMD53""]"	"[{""label"":""RELB"",""id"":""5971""}]"	"[""5971""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111992""}]"
DOID:0111994	"[""immunodeficiency 45"",""IMD45""]"	"[{""label"":""IFNAR2"",""id"":""3455""}]"	"[""3455""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111994""}]"
DOID:0111995	"[""immunodeficiency 28"",""IFNGR2 deficiency"",""IMD28"",""MSMD due to complete IFNgammaR2 deficiency"",""MSMD due to complete interferon gamma receptor 2 deficiency"",""Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency"",""Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency"",""immunodeficiency 28, mycobacteriosis""]"	"[{""label"":""IFNGR2"",""id"":""3460""}]"	"[""3460""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111995""}]"
DOID:0111996	"[""immunodeficiency 51"",""CANDF5"",""IMD51"",""familial candidiasis 5""]"	"[{""label"":""IL17RA"",""id"":""23765""}]"	"[""23765""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111996""}]"
DOID:0111997	"[""immunodeficiency 63"",""IL2RB deficiency"",""IMD63"",""immunodeficiency 63 with lymphoproliferation and autoimmunity""]"	"[{""label"":""IL2RB"",""id"":""3560""}]"	"[""3560""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111997""}]"
DOID:0111998	"[""immunodeficiency 66"",""IMD66""]"	"[{""label"":""MRTFA"",""id"":""57591""}]"	"[""57591""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111998""}]"
DOID:0111999	"[""immunodeficiency 61"",""IMD61""]"	"[{""label"":""SH3KBP1"",""id"":""30011""}]"	"[""30011""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0111999""}]"
DOID:0112000	"[""immunodeficiency 34"",""AMCBX2"",""IMD34"",""X-linked MSMD due to CYBB deficiency"",""X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency"",""familial atypical mycobacteriosis X-linked 2"",""immunodeficiency 34, mycobacteriosis, X-linked""]"	"[{""label"":""CYBB"",""id"":""1536""}]"	"[""1536""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112000""}]"
DOID:0112001	"[""immunodeficiency 50"",""CID due to Moesin deficiency"",""IMD50"",""MSN-related combined immunodeficiency"",""X-linked Moesin-associated immunodeficiency"",""combined immunodeficiency due to Moesin deficiency"",""immunodeficiency 50 X linked recessive""]"	"[{""label"":""MSN"",""id"":""4478""}]"	"[""4478""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112001""}]"
DOID:0112002	"[""immunodeficiency 47"",""CDG IIs"",""CDG2S"",""CDGIIs"",""IMD47"",""congenital disorder of glycosylation type IIs"",""immunodeficiency and hepatopathy with or without neurologic features""]"	"[{""label"":""ATP6AP1"",""id"":""537""}]"	"[""537""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112002""}]"
DOID:0112004	"[""immunodeficiency 71"",""IMD71"",""PLTEID"",""immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia"",""platelet abnormalities with eosinophilia and immune-mediated inflammatory disease""]"	"[{""label"":""ARPC1B"",""id"":""10095""}]"	"[""10095""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112004""}]"
DOID:0112006	"[""immunodeficiency 69"",""IMD69""]"	"[{""label"":""IFNG"",""id"":""3458""}]"	"[""3458""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112006""}]"
DOID:0112007	"[""growth hormone secreting pituitary adenoma 2"",""GH-secreting pituitary adenoma 2"",""PITA2"",""X-linked acromegaly"",""acromegaly due to pituitary adenoma 2""]"	"[{""label"":""GPR101"",""id"":""83550""}]"	"[""83550""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112007""}]"
DOID:0112008	"[""pituitary adenoma 5"",""PITA5"",""pituitary adenoma 5, multiple types""]"	"[{""label"":""CDH23"",""id"":""64072""}]"	"[""64072""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112008""}]"
DOID:0112010	"[""pituitary adenoma 3"",""PITA3"",""pituitary adenoma 3, multiple types""]"	"[{""label"":""GNAS"",""id"":""2778""}]"	"[""2778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112010""}]"
DOID:0112012	"[""X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques"",""OLMSX"",""X-linked Olmsted syndrome""]"	"[{""label"":""MBTPS2"",""id"":""51360""}]"	"[""51360""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112012""}]"
DOID:0112018	"[""non-syndromic X-linked intellectual disability 104"",""MRX104"",""X-linked mental retardation 104""]"	"[{""label"":""FRMPD4"",""id"":""9758""}]"	"[""9758""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112018""}]"
DOID:0112019	"[""non-syndromic X-linked intellectual disability 19"",""MRX19"",""X-linked mental retardation 19""]"	"[{""label"":""RPS6KA3"",""id"":""6197""}]"	"[""6197""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112019""}]"
DOID:0112021	"[""non-syndromic X-linked intellectual disability ARX-related"",""ARX-related intellectual disability"",""MRXARX"",""X-linked mental retardation 29"",""X-linked mental retardation 29 and others"",""X-linked mental retardation 32"",""X-linked mental retardation 33"",""X-linked mental retardation 38"",""X-linked mental retardation 43"",""X-linked mental retardation 52"",""X-linked mental retardation 54"",""X-linked mental retardation 76"",""X-linked mental retardation 87"",""X-linked mental retardation with or without seizures ARX-related""]"	"[{""label"":""ARX"",""id"":""170302""}]"	"[""170302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112021""}]"
DOID:0112022	"[""non-syndromic X-linked intellectual disability 21"",""MRX21"",""MRX34"",""X-linked mental retardation 21"",""X-linked mental retardation 21/34"",""X-linked mental retardation 34""]"	"[{""label"":""IL1RAPL1"",""id"":""11141""}]"	"[""11141""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112022""}]"
DOID:0112024	"[""non-syndromic X-linked intellectual disability 58"",""MRX58"",""X-linked mental retardation 58""]"	"[{""label"":""TSPAN7"",""id"":""7102""}]"	"[""7102""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112024""}]"
DOID:0112025	"[""female-restricted syndromic X-linked intellectual disability 99"",""MRXS99F"",""X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability"",""female-restricted syndromic X-linked mental retardation 99""]"	"[{""label"":""USP9X"",""id"":""8239""}]"	"[""8239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112025""}]"
DOID:0112026	"[""non-syndromic X-linked intellectual disability 99"",""MRX99"",""X-linked mental retardation 99""]"	"[{""label"":""USP9X"",""id"":""8239""}]"	"[""8239""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112026""}]"
DOID:0112029	"[""non-syndromic X-linked intellectual disability 50"",""MRX50"",""X-linked intellectual developmental disorder 50"",""X-linked mental retardation 50"",""XLID50""]"	"[{""label"":""SYN1"",""id"":""6853""}]"	"[""6853""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112029""}]"
DOID:0112034	"[""non-syndromic X-linked intellectual disability 9"",""MRX44"",""MRX9"",""X-linked mental retardation 44"",""X-linked mental retardation 9""]"	"[{""label"":""FTSJ1"",""id"":""24140""}]"	"[""24140""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112034""}]"
DOID:0112035	"[""non-syndromic X-linked intellectual disability 96"",""MRX96"",""X-linked mental retardation 96""]"	"[{""label"":""SYP"",""id"":""6855""}]"	"[""6855""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112035""}]"
DOID:0112038	"[""non-syndromic X-linked intellectual disability 1"",""MRX1"",""MRX18"",""MRX78"",""X-linked mental retardation 1"",""X-linked mental retardation 1/78"",""X-linked mental retardation 18"",""X-linked mental retardation 78""]"	"[{""label"":""IQSEC2"",""id"":""23096""}]"	"[""23096""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112038""}]"
DOID:0112040	"[""non-syndromic X-linked intellectual disability 100"",""MRX100"",""X-linked mental retardation 100""]"	"[{""label"":""KIF4A"",""id"":""24137""}]"	"[""24137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112040""}]"
DOID:0112045	"[""non-syndromic X-linked intellectual disability 93"",""MRX93"",""X-linked mental retardation 93"",""X-linked mental retardation with macrocephaly""]"	"[{""label"":""BRWD3"",""id"":""254065""}]"	"[""254065""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112045""}]"
DOID:0112050	"[""non-syndromic X-linked intellectual disability 63"",""ACSL4-related intellectual disability"",""MRX63"",""MRX68"",""X-linked mental retardation 63"",""X-linked mental retardation 68""]"	"[{""label"":""ACSL4"",""id"":""2182""}]"	"[""2182""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112050""}]"
DOID:0112051	"[""non-syndromic X-linked intellectual disability 30"",""MRX30"",""MRX47"",""X-linked mental retardation 30"",""X-linked mental retardation 30/47"",""X-linked mental retardation 47""]"	"[{""label"":""Pak3"",""id"":""18481""}]"	"[""18481""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112051""}]"
DOID:0112051	"[""non-syndromic X-linked intellectual disability 30"",""MRX30"",""MRX47"",""X-linked mental retardation 30"",""X-linked mental retardation 30/47"",""X-linked mental retardation 47""]"	"[{""label"":""PAK3"",""id"":""5063""}]"	"[""5063""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112051""}]"
DOID:0112056	"[""X-linked intellectual disability-short stature-overweight syndrome"",""MRX12"",""MRX35"",""X-linked mental retardation 12"",""X-linked mental retardation 35""]"	"[{""label"":""THOC2"",""id"":""57187""}]"	"[""57187""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112056""}]"
DOID:0112056	"[""X-linked intellectual disability-short stature-overweight syndrome"",""MRX12"",""MRX35"",""X-linked mental retardation 12"",""X-linked mental retardation 35""]"	"[{""label"":""Thoc2"",""id"":""331401""}]"	"[""331401""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112056""}]"
DOID:0112061	"[""immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia"",""IMD73B""]"	"[{""label"":""RAC2"",""id"":""5880""}]"	"[""5880""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112061""}]"
DOID:0112062	"[""immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia"",""IMD73C""]"	"[{""label"":""RAC2"",""id"":""5880""}]"	"[""5880""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112062""}]"
DOID:0112063	"[""X-Linked immunodeficiency 74"",""IMD74"",""TLR7 deficiency"",""X-linked immunodeficiency 74,COVID-19-related"",""respiratory insufficiency due to SARS-CoV-2 viral infection""]"	"[{""label"":""TLR7"",""id"":""51284""}]"	"[""51284""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112063""}]"
DOID:0112064	"[""immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis"",""IMD73A"",""neutrophil immunodeficiency syndrome""]"	"[{""label"":""RAC2"",""id"":""5880""}]"	"[""5880""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112064""}]"
DOID:0112066	"[""nuclear type mitochondrial complex I deficiency 6"",""MC1DN6""]"	"[{""label"":""NDUFS2"",""id"":""4720""}]"	"[""4720""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112066""}]"
DOID:0112068	"[""nuclear type mitochondrial complex I deficiency 5"",""MC1DN5""]"	"[{""label"":""NDUFS1"",""id"":""4719""}]"	"[""4719""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112068""}]"
DOID:0112072	"[""nuclear type mitochondrial complex I deficiency 20"",""ACAD9 deficiency"",""Acyl-CoA dehydrogenase 9 deficiency"",""MC1DN20"",""mitochondrial complex 1 deficiency due to ACAD9 deficiency""]"	"[{""label"":""Acad9"",""id"":""229211""}]"	"[""229211""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112072""}]"
DOID:0112072	"[""nuclear type mitochondrial complex I deficiency 20"",""ACAD9 deficiency"",""Acyl-CoA dehydrogenase 9 deficiency"",""MC1DN20"",""mitochondrial complex 1 deficiency due to ACAD9 deficiency""]"	"[{""label"":""ACAD9"",""id"":""28976""}]"	"[""28976""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112072""}]"
DOID:0112075	"[""nuclear type mitochondrial complex I deficiency 10"",""MC1DN10""]"	"[{""label"":""NDUFAF2"",""id"":""91942""}]"	"[""91942""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112075""}]"
DOID:0112080	"[""nuclear type mitochondrial complex I deficiency 32"",""MC1DN32""]"	"[{""label"":""NDUFB8"",""id"":""4714""}]"	"[""4714""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112080""}]"
DOID:0112081	"[""nuclear type mitochondrial complex I deficiency 8"",""MC1DN8""]"	"[{""label"":""NDUFS3"",""id"":""4722""}]"	"[""4722""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112081""}]"
DOID:0112091	"[""nuclear type mitochondrial complex I deficiency 34"",""MC1DN34""]"	"[{""label"":""NDUFAF8"",""id"":""284184""}]"	"[""284184""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112091""}]"
DOID:0112098	"[""nuclear type mitochondrial complex I deficiency 30"",""MC1DN30""]"	"[{""label"":""NDUFB11"",""id"":""54539""}]"	"[""54539""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112098""}]"
DOID:0112102	"[""Sotos syndrome 2"",""SOTOS2""]"	"[{""label"":""NFIX"",""id"":""4784""}]"	"[""4784""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112102""}]"
DOID:0112102	"[""Sotos syndrome 2"",""SOTOS2""]"	"[{""label"":""Nfix"",""id"":""18032""}]"	"[""18032""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112102""}]"
DOID:0112103	"[""Sotos syndrome 1"",""SOTOS1""]"	"[{""label"":""NSD1"",""id"":""64324""}]"	"[""64324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112103""}]"
DOID:0112104	"[""Sotos syndrome 3"",""SOTOS3""]"	"[{""label"":""APC2"",""id"":""10297""}]"	"[""10297""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112104""}]"
DOID:0112105	"[""X-linked parkinsonism-spasticity syndrome"",""X-linked Parkinsonism with spasticity"",""XPDS""]"	"[{""label"":""ATP6AP2"",""id"":""10159""}]"	"[""10159""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112105""}]"
DOID:0112106	"[""chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia"",""X-linked dominant chondrodysplasia, Chassaing-Lacombe type"",""X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome""]"	"[{""label"":""HDAC6"",""id"":""10013""}]"	"[""10013""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112106""}]"
DOID:0112108	"[""myofibrillar myopathy 10"",""MFM10""]"	"[{""label"":""SVIL"",""id"":""6840""}]"	"[""6840""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112108""}]"
DOID:0112115	"[""combined oxidative phosphorylation deficiency 46"",""COXPD46""]"	"[{""label"":""MRPS23"",""id"":""51649""}]"	"[""51649""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112115""}]"
DOID:0112121	"[""nephrogenic syndrome of inappropriate antidiuresis"",""NSIAD""]"	"[{""label"":""AVPR2"",""id"":""554""}]"	"[""554""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112121""}]"
DOID:0112122	"[""X-linked epilepsy with variable learning disabilities and behavior disorders"",""X-linked epilepsy-learning disabilities-behavior disorders syndrome""]"	"[{""label"":""SYN1"",""id"":""6853""}]"	"[""6853""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112122""}]"
DOID:0112125	"[""alpha-thalassemia myelodysplasia syndrome"",""ATMDS"",""acquired HbH disease"",""acquired hemoglobin H disease"",""alpha-thalassemia-myelodysplastic syndrome""]"	"[{""label"":""ATRX"",""id"":""546""}]"	"[""546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112125""}]"
DOID:0112127	"[""HRPT-related hyperuricemia"",""HPRT deficiency, grade I"",""HPRT partial deficiency"",""HPRT-related gout"",""HPRT-related hyperuricemia"",""HPRT1 partial deficiency"",""Kelley-Seegmiller syndrome"",""hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency"",""hypoxanthine guanine phosphoribosyltransferase deficiency, grade I"",""hypoxanthine guanine phosphoribosyltransferase partial deficiency""]"	"[{""label"":""HPRT1"",""id"":""3251""}]"	"[""3251""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112127""}]"
DOID:0112129	"[""severe congenital neutropenia 7"",""SCN7"",""autosomal recessive severe congenital neutropenia due to CSF3R deficiency""]"	"[{""label"":""CSF3R"",""id"":""1441""}]"	"[""1441""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112129""}]"
DOID:0112133	"[""severe congenital neutropenia 3"",""Kostmann disease"",""Kostmann syndrome"",""SCN3"",""infantile agranulocytosis""]"	"[{""label"":""HAX1"",""id"":""10456""}]"	"[""10456""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112133""}]"
DOID:0112135	"[""severe congenital neutropenia 8"",""SCN8"",""SDSL"",""Shwachman-Diamond syndrome-like"",""autosomal dominant severe congenital neutropenia 8 with or without pancreatic dysfunction and/or neurological abnormalities""]"	"[{""label"":""SRP54"",""id"":""6729""}]"	"[""6729""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112135""}]"
DOID:0112136	"[""severe congenital neutropenia 4"",""Dursun syndrome"",""SCN4"",""autosomal recessive severe congenital neutropenia due to G6PC3 deficiency"",""severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome""]"	"[{""label"":""G6PC3"",""id"":""92579""}]"	"[""92579""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112136""}]"
DOID:0112137	"[""combined oxidative phosphorylation deficiency 51"",""COXPD51""]"	"[{""label"":""PTCD3"",""id"":""55037""}]"	"[""55037""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112137""}]"
DOID:0112140	"[""retinitis pigmentosa 83"",""RP83""]"	"[{""label"":""ARL3"",""id"":""403""}]"	"[""403""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112140""}]"
DOID:0112141	"[""retinitis pigmentosa 84"",""RP84""]"	"[{""label"":""DHX38"",""id"":""9785""}]"	"[""9785""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112141""}]"
DOID:0112142	"[""retinitis pigmentosa 85"",""RP85""]"	"[{""label"":""AHR"",""id"":""196""}]"	"[""196""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112142""}]"
DOID:0112143	"[""retinitis pigmentosa 86"",""RP86""]"	"[{""label"":""KIAA1549"",""id"":""57670""}]"	"[""57670""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112143""}]"
DOID:0112145	"[""retinitis pigmentosa 88"",""RP88""]"	"[{""label"":""RP1L1"",""id"":""94137""}]"	"[""94137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112145""}]"
DOID:0112147	"[""retinitis pigmentosa 90"",""RP90""]"	"[{""label"":""IDH3A"",""id"":""3419""}]"	"[""3419""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112147""}]"
DOID:0112148	"[""Uruguay faciocardiomusculoskeletal syndrome"",""FCMSU""]"	"[{""label"":""FHL1"",""id"":""2273""}]"	"[""2273""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112148""}]"
DOID:0112149	"[""terminal osseous dysplasia"",""ODPD"",""ODPF syndrome"",""TOD"",""TODPD"",""digital osseous dysplasia with facial pigmentary defects and multiple frenula"",""terminal osseous dysplasia-pigmentary defects syndrome""]"	"[{""label"":""FLNA"",""id"":""2316""}]"	"[""2316""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112149""}]"
DOID:0112150	"[""X-linked spondyloepimetaphyseal dysplasia"",""SEMD X-linked"",""SEMDX""]"	"[{""label"":""BGN"",""id"":""633""}]"	"[""633""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112150""}]"
DOID:0112151	"[""corpus callosum agenesis-abnormal genitalia syndrome"",""ACC with abnormal genitalia"",""Proud syndrome"",""Proud-Levine-Carpenter syndrome"",""corpus callosum agenesis with abnormal genitalia"",""microcephaly-corpus callosum agenesis-abnormal genitalia syndrome""]"	"[{""label"":""ARX"",""id"":""170302""}]"	"[""170302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112151""}]"
DOID:0112152	"[""CHIME syndrome"",""PIGL-CDG"",""Zunich neuroectodermal syndrome"",""Zunich-Kaye syndrome"",""coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome"",""congenital disorder of glycosylation due to PIGL deficiency"",""neuroectodermal dysplasia, CHIME type"",""neuroectodermal syndrome, Zunich type""]"	"[{""label"":""PIGL"",""id"":""9487""}]"	"[""9487""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112152""}]"
DOID:0112155	"[""inflammatory bowel disease 29"",""IBD29""]"	"[{""label"":""INAVA"",""id"":""55765""}]"	"[""55765""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112155""}]"
DOID:0112158	"[""De Sanctis-Cacchione syndrome"",""xeroderma pigmentosum with neurologic manifestation""]"	"[{""label"":""ERCC6"",""id"":""2074""}]"	"[""2074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112158""}]"
DOID:0112159	"[""autosomal dominant nonsyndromic deafness 78"",""DFNA78""]"	"[{""label"":""SLC12A2"",""id"":""6558""}]"	"[""6558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112159""}]"
DOID:0112160	"[""autosomal dominant nonsyndromic deafness 79"",""DFNA79""]"	"[{""label"":""SCD5"",""id"":""79966""}]"	"[""79966""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112160""}]"
DOID:0112162	"[""autosomal recessive nonsyndromic deafness 116"",""DFNB116""]"	"[{""label"":""CLDN9"",""id"":""9080""}]"	"[""9080""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112162""}]"
DOID:0112163	"[""spermatogenic failure 45"",""SPGF45""]"	"[{""label"":""DNAH2"",""id"":""146754""}]"	"[""146754""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112163""}]"
DOID:0112164	"[""spermatogenic failure 46"",""SPGF46""]"	"[{""label"":""DNAH8"",""id"":""1769""}]"	"[""1769""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112164""}]"
DOID:0112166	"[""autosomal dominant nonsyndromic deafness 75"",""DFNA75""]"	"[{""label"":""TRRAP"",""id"":""8295""}]"	"[""8295""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112166""}]"
DOID:0112167	"[""autosomal dominant nonsyndromic deafness 76"",""DFNA76""]"	"[{""label"":""PLS1"",""id"":""5357""}]"	"[""5357""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112167""}]"
DOID:0112168	"[""autosomal dominant nonsyndromic deafness 77"",""DFNA77""]"	"[{""label"":""ABCC1"",""id"":""4363""}]"	"[""4363""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112168""}]"
DOID:0112170	"[""Noonan syndrome 12"",""NS12""]"	"[{""label"":""RRAS2"",""id"":""22800""}]"	"[""22800""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112170""}]"
DOID:0112171	"[""wrinkly skin syndrome"",""WSS""]"	"[{""label"":""ATP6V0A2"",""id"":""23545""}]"	"[""23545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112171""}]"
DOID:0112173	"[""combined deficiency of vitamin K-dependent clotting factors 1"",""VKCFD1""]"	"[{""label"":""GGCX"",""id"":""2677""}]"	"[""2677""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112173""}]"
DOID:0112175	"[""spermatogenic failure 47"",""SPGF47""]"	"[{""label"":""DZIP1"",""id"":""22873""}]"	"[""22873""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112175""}]"
DOID:0112180	"[""urocanase deficiency"",""UROCD"",""encephalopathy due to urocanase deficiency"",""high urine urocanic acid levels"",""urocanate hydratase deficiency"",""urocanic aciduria""]"	"[{""label"":""UROC1"",""id"":""131669""}]"	"[""131669""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112180""}]"
DOID:0112181	"[""Schinzel type phocomelia"",""AARRS"",""Al Awadi-Raas-Rothschild syndrome"",""Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome"",""LPHAS"",""Schinzel phocomelia syndrome"",""absence of ulna and fibula with severe limb deficiency"",""aplasia/hypoplasia of limbs and pelvis"",""congenital absence of ulna and fibula"",""limb/pelvis-hypoplasia/aplasia syndrome"",""severe limb deficit""]"	"[{""label"":""WNT7A"",""id"":""7476""}]"	"[""7476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112181""}]"
DOID:0112182	"[""mismatch repair cancer syndrome"",""BTP1 syndrome"",""BTPS1"",""CMMR-D syndrome"",""CMMRDS"",""MMR deficiency"",""Turcot syndrome"",""brain tumor-polyposis syndrome 1"",""childhood cancer syndrome"",""constitutional mismatch repair deficiency syndrome""]"	"[{""label"":""MLH1"",""id"":""4292""},{""label"":""MSH2"",""id"":""4436""},{""label"":""MSH6"",""id"":""2956""},{""label"":""POLE"",""id"":""5426""},{""label"":""RNASET2"",""id"":""8635""},{""label"":""SLC22A9"",""id"":""114571""},{""label"":""TGFBR2"",""id"":""7048""},{""label"":""TP53"",""id"":""7157""}]"	"[""114571"",""2956"",""4292"",""4436"",""5426"",""7048"",""7157"",""8635""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112182""}]"
DOID:0112184	"[""thyroid dyshormonogenesis 5"",""TDH5"",""genetic defect in thyroid hormonogenesis 5""]"	"[{""label"":""DUOXA2"",""id"":""405753""}]"	"[""405753""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112184""}]"
DOID:0112185	"[""thyroid dyshormonogenesis 1"",""TDH1"",""genetic defect in thyroid hormonogenesis 1"",""iodide accumulation, transport, or trapping defect""]"	"[{""label"":""SLC5A5"",""id"":""6528""}]"	"[""6528""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112185""}]"
DOID:0112186	"[""thyroid dyshormonogenesis 2A"",""TDH2A"",""genetic defect in thyroid hormonogenesis 2A"",""iodide peroxidase deficiency"",""thyroid peroxidase deficiency""]"	"[{""label"":""TPO"",""id"":""7173""}]"	"[""7173""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112186""}]"
DOID:0112187	"[""thyroid dyshormonogenesis 3"",""TDH3"",""genetic defect in thyroid hormonogenesis 3""]"	"[{""label"":""TG"",""id"":""7038""}]"	"[""7038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112187""}]"
DOID:0112189	"[""thyroid dyshormonogenesis 6"",""TDH6"",""genetic defect in thyroid hormonogenesis 6""]"	"[{""label"":""DUOX2"",""id"":""50506""}]"	"[""50506""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112189""}]"
DOID:0112192	"[""tetraamelia syndrome 1"",""TETAMS1"",""tetra-amelia syndrome 1""]"	"[{""label"":""WNT3"",""id"":""7473""}]"	"[""7473""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112192""}]"
DOID:0112193	"[""tetraamelia syndrome 2"",""TETAMS2"",""tetra-amelia with pulmonary hypoplasia"",""tetraamelia with pulmonary hypoplasia""]"	"[{""label"":""RSPO2"",""id"":""340419""}]"	"[""340419""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112193""}]"
DOID:0112194	"[""Filippi syndrome"",""Scott craniodigital syndrome with mental retardation"",""type 1 syndactyly-microcephaly-intellectual disability syndrome""]"	"[{""label"":""CKAP2L"",""id"":""150468""}]"	"[""150468""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112194""}]"
DOID:0112195	"[""spondyloperipheral dysplasia"",""spondyloperipheral dysplasia-short ulna syndrome""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112195""}]"
DOID:0112196	"[""spondylometaepiphyseal dysplasia, short limb-hand type"",""SMED short limb-abnormal calcification type"",""SMED short limb-hand type"",""SMED type 2"",""SMED, type II"",""SMED-SL"",""SMED-SL/AC"",""spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome"",""spondylometaepiphyseal dysplasia short limb-hand type""]"	"[{""label"":""DDR2"",""id"":""4921""}]"	"[""4921""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112196""}]"
DOID:0112198	"[""spondyloepimetaphyseal dysplasia with joint laxity type 1"",""SEMDJL1"",""spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures""]"	"[{""label"":""B3GALT6"",""id"":""126792""}]"	"[""126792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112198""}]"
DOID:0112199	"[""spondyloepimetaphyseal dysplasia with joint laxity type 2"",""SEMD-MD"",""SEMDJL2"",""spondyloepimetaphyseal dysplasia with joint laxicity, Hall type"",""spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type"",""spondyloepimetaphyseal dysplasia with multiple dislocations, Hall type""]"	"[{""label"":""KIF22"",""id"":""3835""}]"	"[""3835""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112199""}]"
DOID:0112202	"[""developmental and epileptic encephalopathy""]"	"[{""label"":""DEPDC5"",""id"":""9681""},{""label"":""KCNH5"",""id"":""27133""},{""label"":""SLC32A1"",""id"":""140679""},{""label"":""SV2A"",""id"":""9900""}]"	"[""140679"",""27133"",""9681"",""9900""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112202""}]"
DOID:0112202	"[""developmental and epileptic encephalopathy""]"	"[{""label"":""VPS1"",""id"":""853870""}]"	"[""853870""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112202""}]"
DOID:0112204	"[""developmental and epileptic encephalopathy 68"",""DEE68"",""early infantile epileptic encephalopathy 68""]"	"[{""label"":""TRAK1"",""id"":""22906""}]"	"[""22906""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112204""}]"
DOID:0112205	"[""developmental and epileptic encephalopathy 69"",""DEE69"",""early infantile epileptic encephalopathy 69""]"	"[{""label"":""CACNA1E"",""id"":""777""}]"	"[""777""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112205""}]"
DOID:0112207	"[""developmental and epileptic encephalopathy 71"",""DEE71"",""early infantile epileptic encephalopathy 71"",""glutaminase deficiency with neonatal epileptic encephalopathy""]"	"[{""label"":""GLS"",""id"":""2744""}]"	"[""2744""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112207""}]"
DOID:0112209	"[""developmental and epileptic encephalopathy 73"",""DEE73"",""early infantile epileptic encephalopathy 73""]"	"[{""label"":""RNF13"",""id"":""11342""}]"	"[""11342""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112209""}]"
DOID:0112210	"[""developmental and epileptic encephalopathy 74"",""DEE74"",""early infantile epileptic encephalopathy 74""]"	"[{""label"":""GABRG2"",""id"":""2566""}]"	"[""2566""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112210""}]"
DOID:0112213	"[""multiple congenital anomalies-hypotonia-seizures syndrome 4"",""DEE77"",""GPIBD19"",""MCAHS4"",""developmental and epileptic encephalopathy 77"",""early infantile epileptic encephalopathy 77"",""glycosylphosphatidylinositol biosynthesis defect 19""]"	"[{""label"":""PIGQ"",""id"":""9091""}]"	"[""9091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112213""}]"
DOID:0112214	"[""developmental and epileptic encephalopathy 78"",""DEE78"",""early infantile epileptic encephalopathy 78""]"	"[{""label"":""GABRA2"",""id"":""2555""}]"	"[""2555""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112214""}]"
DOID:0112215	"[""developmental and epileptic encephalopathy 79"",""DEE79"",""early infantile epileptic encephalopathy 79""]"	"[{""label"":""GABRA5"",""id"":""2558""}]"	"[""2558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112215""}]"
DOID:0112216	"[""developmental and epileptic encephalopathy 80"",""DEE80"",""GPIBD20"",""early infantile epileptic encephalopathy 80"",""glycosylphosphatidylinositol biosynthesis defect 20""]"	"[{""label"":""PIGB"",""id"":""9488""}]"	"[""9488""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112216""}]"
DOID:0112217	"[""developmental and epileptic encephalopathy 81"",""DEE81"",""early infantile epileptic encephalopathy 81""]"	"[{""label"":""DMXL2"",""id"":""23312""}]"	"[""23312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112217""}]"
DOID:0112218	"[""developmental and epileptic encephalopathy 83"",""DEE83"",""early infantile epileptic encephalopathy 83""]"	"[{""label"":""UGP2"",""id"":""7360""}]"	"[""7360""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112218""}]"
DOID:0112219	"[""developmental and epileptic encephalopathy 84"",""DEE84"",""Jamuar syndrome"",""early infantile epileptic encephalopathy 84""]"	"[{""label"":""UGDH"",""id"":""7358""}]"	"[""7358""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112219""}]"
DOID:0112222	"[""developmental and epileptic encephalopathy 88"",""DEE88"",""early infantile epileptic encephalopathy 88""]"	"[{""label"":""MDH1"",""id"":""4190""}]"	"[""4190""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112222""}]"
DOID:0112223	"[""developmental and epileptic encephalopathy 89"",""DEE89"",""early infantile epileptic encephalopathy 89""]"	"[{""label"":""GAD1"",""id"":""2571""}]"	"[""2571""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112223""}]"
DOID:0112224	"[""chondrodysplasia with joint dislocations gPAPP type"",""gPAPP deficiency""]"	"[{""label"":""BPNT2"",""id"":""54928""}]"	"[""54928""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112224""}]"
DOID:0112224	"[""chondrodysplasia with joint dislocations gPAPP type"",""gPAPP deficiency""]"	"[{""label"":""Bpnt2"",""id"":""242291""}]"	"[""242291""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112224""}]"
DOID:0112228	"[""lissencephaly 9 with complex brainstem malformation"",""LIS9"",""posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome""]"	"[{""label"":""MACF1"",""id"":""23499""}]"	"[""23499""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112228""}]"
DOID:0112230	"[""lissencephaly 5"",""LIS5""]"	"[{""label"":""LAMB1"",""id"":""3912""}]"	"[""3912""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112230""}]"
DOID:0112231	"[""lissencephaly 7 with cerebellar hypoplasia"",""LIS7""]"	"[{""label"":""CDK5"",""id"":""1020""}]"	"[""1020""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112231""}]"
DOID:0112232	"[""lissencephaly 3"",""LIS3""]"	"[{""label"":""TUBA1A"",""id"":""7846""}]"	"[""7846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112232""}]"
DOID:0112233	"[""lissencephaly 8"",""LIS8""]"	"[{""label"":""TMTC3"",""id"":""160418""}]"	"[""160418""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112233""}]"
DOID:0112236	"[""lissencephaly 6"",""LIS6""]"	"[{""label"":""KATNB1"",""id"":""10300""}]"	"[""10300""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112236""}]"
DOID:0112237	"[""lissencephaly 1"",""LIS1"",""PAFAH1B1-related lissencephaly""]"	"[{""label"":""PAFAH1B1"",""id"":""5048""}]"	"[""5048""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112237""}]"
DOID:0112238	"[""X-linked lissencephaly 2"",""X-linked lissencephaly with abnormal genitalia"",""X-linked lissencephaly with ambiguous genitalia"",""X-linked lissencephaly-corpus callosum agenesis-genital anomalies syndrome"",""XLAG"",""XLAG (X-linked lissencephaly with abnormal genitalia) syndrome"",""XLIS2""]"	"[{""label"":""ARX"",""id"":""170302""}]"	"[""170302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112238""}]"
DOID:0112240	"[""Leber congenital amaurosis with early-onset deafness"",""LCAEOD""]"	"[{""label"":""TUBB4B"",""id"":""10383""}]"	"[""10383""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112240""}]"
DOID:0112242	"[""congenital symmetric circumferential skin creases 1"",""CSCSC1""]"	"[{""label"":""TUBB"",""id"":""203068""}]"	"[""203068""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112242""}]"
DOID:0112243	"[""congenital symmetric circumferential skin creases 2"",""CSCSC2""]"	"[{""label"":""MAPRE2"",""id"":""10982""}]"	"[""10982""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112243""}]"
DOID:0112245	"[""focal segmental glomerulosclerosis 3"",""FSGS3""]"	"[{""label"":""CD2AP"",""id"":""23607""}]"	"[""23607""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112245""}]"
DOID:0112245	"[""focal segmental glomerulosclerosis 3"",""FSGS3""]"	"[{""label"":""Cd2ap"",""id"":""12488""}]"	"[""12488""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112245""}]"
DOID:0112247	"[""congenital heart defects, dysmorphic facial features, and intellectual developmental disorder"",""CDK13-Related CHDFIDD"",""CDK13-Related Disorder"",""CHDFIDD""]"	"[{""label"":""Cdk13"",""id"":""69562""}]"	"[""69562""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112247""}]"
DOID:0112247	"[""congenital heart defects, dysmorphic facial features, and intellectual developmental disorder"",""CDK13-Related CHDFIDD"",""CDK13-Related Disorder"",""CHDFIDD""]"	"[{""label"":""CDK13"",""id"":""8621""}]"	"[""8621""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112247""}]"
DOID:0112248	"[""17-beta hydroxysteroid dehydrogenase 3 deficiency"",""17-KSR deficiency"",""17-beta-hydroxysteroid dehydrogenase 3 deficiency"",""17-ketoreductase deficiency"",""17-ketosteroidreductase deficiency"",""46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency"",""male pseudohermaphroditism with gynecomastia"",""neutral 17-beta-hydroxysteroid oxidoreductase deficiency""]"	"[{""label"":""HSD17B3"",""id"":""3293""}]"	"[""3293""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112248""}]"
DOID:0112249	"[""GAPO syndrome"",""growth delay-alopecia-pseudoanodontia-optic atrophy syndrome""]"	"[{""label"":""ANTXR1"",""id"":""84168""}]"	"[""84168""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112249""}]"
DOID:0112250	"[""Gaucher's disease type IIIC"",""GD3C"",""Gaucher disease type 3C"",""Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome"",""Gaucher-like disease"",""cardiovascular Gaucher disease""]"	"[{""label"":""GBA1"",""id"":""2629""}]"	"[""2629""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00071""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112250""}]"
DOID:0112251	"[""Ghosal hematodiaphyseal syndrome"",""Ghosal hematodiaphyseal dysplasia"",""Ghosal syndrome"",""diaphyseal dysplasia-anemia syndrome""]"	"[{""label"":""TBXAS1"",""id"":""6916""}]"	"[""6916""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112251""}]"
DOID:0112259	"[""Leydig cell hypoplasia"",""46,XY DSD due to LH resistance or LHB deficiency"",""46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency"",""46,XY disorder of sex development due to LH resistance or LHB deficiency"",""46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency""]"	"[{""label"":""LHCGR"",""id"":""3973""}]"	"[""3973""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112259""}]"
DOID:0112262	"[""leucine-sensitive hypoglycemia of infancy"",""LIH"",""leucine-induced hypoglycemia""]"	"[{""label"":""ABCC8"",""id"":""6833""}]"	"[""6833""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112262""}]"
DOID:0112263	"[""hypoinsulinemic hypoglycemia with hemihypertrophy"",""HIHGHH"",""hypoinsulinemic hypoglycemia and body hemihypertrophy""]"	"[{""label"":""AKT2"",""id"":""208""}]"	"[""208""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112263""}]"
DOID:0112266	"[""nephrotic syndrome type 23"",""NPHS23""]"	"[{""label"":""KIRREL1"",""id"":""55243""}]"	"[""55243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112266""}]"
DOID:0112271	"[""spermatogenic failure 49"",""SPGF98""]"	"[{""label"":""CFAP58"",""id"":""159686""}]"	"[""159686""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112271""}]"
DOID:0112274	"[""X-linked spermatogenic failure 3"",""SPGFX3""]"	"[{""label"":""CFAP47"",""id"":""286464""}]"	"[""286464""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112274""}]"
DOID:0112275	"[""developmental and epileptic encephalopathy 93"",""DEE93"",""IECEE3"",""infantile or early childhood epileptic encephalopathy 3""]"	"[{""label"":""ATP6V1A"",""id"":""523""}]"	"[""523""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112275""}]"
DOID:0112276	"[""neurodevelopmental disorder with involuntary movements"",""NEDIM""]"	"[{""label"":""Gnao1"",""id"":""14681""}]"	"[""14681""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112276""}]"
DOID:0112277	"[""immunodeficiency 79"",""IMD79""]"	"[{""label"":""CD4"",""id"":""920""}]"	"[""920""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112277""}]"
DOID:0112281	"[""spondyloepiphyseal dysplasia Stanescu type"",""SED Stanescu type"",""SEDSTN""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112281""}]"
DOID:0112282	"[""spondyloepiphyseal dysplasia Kimberley type"",""SEDK""]"	"[{""label"":""ACAN"",""id"":""176""}]"	"[""176""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112282""}]"
DOID:0112283	"[""spondyloepiphyseal dysplasia Kondo-Fu type"",""SED with elevated blood lysosomal enzymes"",""SEDKF""]"	"[{""label"":""MBTPS1"",""id"":""8720""}]"	"[""8720""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112283""}]"
DOID:0112295	"[""spondylometaphyseal dysplasia""]"	"[{""label"":""ACP5"",""id"":""54""}]"	"[""54""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112295""}]"
DOID:0112297	"[""spondylometaphyseal dysplasia corner fracture type"",""SMDCF"",""spondylometaphyseal dysplasia Sutcliffe type""]"	"[{""label"":""FN1"",""id"":""2335""}]"	"[""2335""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112297""}]"
DOID:0112300	"[""spondylometaphyseal dysplasia with cone-rod dystrophy"",""SMD-CRD"",""SMDCRD"",""spondylometaphyseal dysplasia-cone-rod dystrophy syndrome""]"	"[{""label"":""PCYT1A"",""id"":""5130""}]"	"[""5130""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112300""}]"
DOID:0112303	"[""spondylometaphyseal dysplasia with corneal dystrophy"",""SMDCD""]"	"[{""label"":""PLCB3"",""id"":""5331""}]"	"[""5331""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112303""}]"
DOID:0112306	"[""Mahvash Disease"",""GCGR-related hyperglucagonemia"",""nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumor""]"	"[{""label"":""Gcgr"",""id"":""14527""}]"	"[""14527""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112306""}]"
DOID:0112306	"[""Mahvash Disease"",""GCGR-related hyperglucagonemia"",""nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumor""]"	"[{""label"":""GCGR"",""id"":""2642""}]"	"[""2642""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112306""}]"
DOID:0112307	"[""sarcosinemia"",""SARCOS"",""SARD deficiency"",""SARDH deficiency"",""demethylation defect of N-methylglycine"",""sarcosine dehydrogenase complex deficiency""]"	"[{""label"":""SARDH"",""id"":""1757""}]"	"[""1757""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112307""}]"
DOID:0112310	"[""central precocious puberty 1"",""CPPB1""]"	"[{""label"":""KISS1R"",""id"":""84634""}]"	"[""84634""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112310""}]"
DOID:0112312	"[""male infertility due to globozoospermia"",""globozoospermia syndrome""]"	"[{""label"":""Hsp90b1"",""id"":""22027""}]"	"[""22027""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112312""}]"
DOID:0112313	"[""brain small vessel disease""]"	"[{""label"":""FGA"",""id"":""2243""},{""label"":""FGG"",""id"":""2266""},{""label"":""NR1D1"",""id"":""9572""}]"	"[""2243"",""2266"",""9572""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112313""}]"
DOID:0112314	"[""brain small vessel disease 2"",""BSVD2"",""porencephaly 2""]"	"[{""label"":""COL4A2"",""id"":""1284""}]"	"[""1284""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112314""}]"
DOID:0112315	"[""brain small vessel disease 3"",""BSVD3""]"	"[{""label"":""COLGALT1"",""id"":""79709""}]"	"[""79709""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112315""}]"
DOID:0112318	"[""Schindler disease type 1"",""NAGA deficiency type 1"",""alpha-N-acetylgalactosaminidase deficiency type 1""]"	"[{""label"":""NAGA"",""id"":""4668""}]"	"[""4668""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00020""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112318""}]"
DOID:0112319	"[""Kanzaki disease"",""NAGA deficiency type 2"",""adult-onset alpha-N-acetylgalactosaminidase deficiency"",""alpha-N-acetylgalactosaminidase deficiency type 2""]"	"[{""label"":""NAGA"",""id"":""4668""}]"	"[""4668""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00021""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112319""}]"
DOID:0112321	"[""alacrima, achalasia, and impaired intellectual development syndrome"",""AAMR"",""alacrima, achalasia, and mental retardation syndrome""]"	"[{""label"":""GMPPA"",""id"":""29926""}]"	"[""29926""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112321""}]"
DOID:0112329	"[""pontocerebellar hypoplasia type 2F"",""PCH2F""]"	"[{""label"":""TSEN15"",""id"":""116461""}]"	"[""116461""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112329""}]"
DOID:0112330	"[""pontocerebellar hypoplasia type 1E"",""PCH1E""]"	"[{""label"":""SLC25A46"",""id"":""91137""}]"	"[""91137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112330""}]"
DOID:0112332	"[""pontocerebellar hypoplasia type 13"",""PCH13""]"	"[{""label"":""VPS51"",""id"":""738""}]"	"[""738""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112332""}]"
DOID:0112333	"[""pontocerebellar hypoplasia type 16"",""PCH16""]"	"[{""label"":""MINPP1"",""id"":""9562""}]"	"[""9562""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112333""}]"
DOID:0112334	"[""pontocerebellar hypoplasia type 1C"",""PCH1C""]"	"[{""label"":""EXOSC8"",""id"":""11340""}]"	"[""11340""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112334""}]"
DOID:0112336	"[""spermatogenic failure 56"",""SPGF56""]"	"[{""label"":""DNAH10"",""id"":""196385""}]"	"[""196385""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112336""}]"
DOID:0112337	"[""spermatogenic failure 55"",""SPGF55""]"	"[{""label"":""SPAG17"",""id"":""200162""}]"	"[""200162""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112337""}]"
DOID:0112338	"[""spermatogenic failure 57"",""SPGF57""]"	"[{""label"":""PNLDC1"",""id"":""154197""}]"	"[""154197""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112338""}]"
DOID:0112341	"[""hereditary spastic paraplegia 80"",""SPG80"",""spastic paraplegia 80 autosomal dominant""]"	"[{""label"":""UBAP1"",""id"":""51271""}]"	"[""51271""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112341""}]"
DOID:0112343	"[""hereditary spastic paraplegia 82"",""SPG82"",""spastic paraplegia 82 autosomal recessive""]"	"[{""label"":""PCYT2"",""id"":""5833""}]"	"[""5833""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112343""}]"
DOID:0112346	"[""hereditary spastic paraplegia 83"",""SPG83"",""spastic paraplegia 83 autosomal recessive""]"	"[{""label"":""HPDL"",""id"":""84842""}]"	"[""84842""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112346""}]"
DOID:0112347	"[""hereditary spastic paraplegia 84"",""SPG84"",""spastic paraplegia 84 autosomal recessive""]"	"[{""label"":""PI4KA"",""id"":""5297""}]"	"[""5297""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112347""}]"
DOID:0112348	"[""hereditary spastic paraplegia 78"",""SPG78"",""spastic paraplegia 78 autosomal recessive""]"	"[{""label"":""ATP13A2"",""id"":""23400""}]"	"[""23400""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112348""}]"
DOID:0112349	"[""hereditary spastic paraplegia 81"",""SPG81"",""autosomal recessive complex SPG due to Kennedy pathway dysfunction"",""autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction"",""spastic paraplegia 81 autosomal recessive""]"	"[{""label"":""SELENOI"",""id"":""85465""}]"	"[""85465""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112349""}]"
DOID:0112350	"[""spermatogenic failure 61"",""SPGF61""]"	"[{""label"":""STAG3"",""id"":""10734""}]"	"[""10734""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112350""}]"
DOID:0112352	"[""spermatogenic failure 58"",""SPGF58""]"	"[{""label"":""IFT74"",""id"":""80173""}]"	"[""80173""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112352""}]"
DOID:0112353	"[""spermatogenic failure 64"",""SPGF64""]"	"[{""label"":""FBXO43"",""id"":""286151""}]"	"[""286151""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112353""}]"
DOID:0112354	"[""spermatogenic failure 65"",""SPGF65""]"	"[{""label"":""DNHD1"",""id"":""144132""}]"	"[""144132""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112354""}]"
DOID:0112358	"[""short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2"",""SSFSC2""]"	"[{""label"":""SCUBE3"",""id"":""222663""}]"	"[""222663""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112358""}]"
DOID:0112359	"[""congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay"",""CAKUTHED""]"	"[{""label"":""SON"",""id"":""6651""}]"	"[""6651""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112359""}]"
DOID:0112361	"[""spondylocostal dysostosis 3"",""SCDO3"",""autosomal recessive spondylocostal dysostosis 3""]"	"[{""label"":""LFNG"",""id"":""3955""}]"	"[""3955""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00405""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112361""}]"
DOID:0112363	"[""spondylocostal dysostosis 5"",""SCDO5""]"	"[{""label"":""TBX6"",""id"":""6911""}]"	"[""6911""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112363""}]"
DOID:0112367	"[""Coffin-Siris syndrome 8"",""CSS8""]"	"[{""label"":""SMARCC2"",""id"":""6601""}]"	"[""6601""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112367""}]"
DOID:0112368	"[""Coffin-Siris syndrome 5"",""CSS5""]"	"[{""label"":""SMARCE1"",""id"":""6605""}]"	"[""6605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112368""}]"
DOID:0112370	"[""Coffin-Siris syndrome 12"",""CSS12""]"	"[{""label"":""BICRA"",""id"":""29998""}]"	"[""29998""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112370""}]"
DOID:0112372	"[""Coffin-Siris syndrome 11"",""CSS11""]"	"[{""label"":""SMARCD1"",""id"":""6602""}]"	"[""6602""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112372""}]"
DOID:0112373	"[""autosomal dominant auditory neuropathy 3"",""AUNA3""]"	"[{""label"":""TMEM43"",""id"":""79188""}]"	"[""79188""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112373""}]"
DOID:0112374	"[""muscular dystrophy-dystroglycanopathy"",""MDDG""]"	"[{""label"":""Dg"",""id"":""36773""},{""label"":""rt"",""id"":""39297""},{""label"":""tw"",""id"":""31024""}]"	"[""31024"",""36773"",""39297""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112374""}]"
DOID:0112374	"[""muscular dystrophy-dystroglycanopathy"",""MDDG""]"	"[{""label"":""GMPPB"",""id"":""29925""}]"	"[""29925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112374""}]"
DOID:0112376	"[""muscular dystrophy-dystroglycanopathy type B15"",""MDDGB15"",""congenital muscular dystrophy DPM3-related""]"	"[{""label"":""DPM3"",""id"":""54344""}]"	"[""54344""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112376""}]"
DOID:0112377	"[""muscular dystrophy-dystroglycanopathy type B14"",""MDDGB14"",""congenital muscular dystrophy GMPPB-related""]"	"[{""label"":""GMPPB"",""id"":""29925""}]"	"[""29925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112377""}]"
DOID:0112378	"[""muscular dystrophy-dystroglycanopathy type B3"",""MDDGB3"",""congenital muscular dystrophy POMGNT1-related""]"	"[{""label"":""POMGNT1"",""id"":""55624""}]"	"[""55624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112378""}]"
DOID:0112379	"[""muscular dystrophy-dystroglycanopathy type B4"",""MDDGB4"",""congenital muscular dystrophy FKTN-related""]"	"[{""label"":""FKTN"",""id"":""2218""}]"	"[""2218""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112379""}]"
DOID:0112380	"[""muscular dystrophy-dystroglycanopathy type B2"",""MDDGB2"",""congenital muscular dystrophy POMT2-related""]"	"[{""label"":""POMT2"",""id"":""29954""}]"	"[""29954""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112380""}]"
DOID:0112381	"[""muscular dystrophy-dystroglycanopathy type C12"",""LGMD due to POMK deficiency"",""Limb-girdle muscular dystrophy due to POMK deficiency"",""MDDGC12"",""muscular dystrophy-dystroglycanopathy, limb-girdle, POMK-related""]"	"[{""label"":""POMK"",""id"":""84197""}]"	"[""84197""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112381""}]"
DOID:0112382	"[""muscular dystrophy-dystroglycanopathy type C8"",""LGMDR24"",""MDDGC2"",""autosomal recessive limb-girdle muscular dystrophy 24"",""muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 8"",""muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related""]"	"[{""label"":""POMGNT2"",""id"":""84892""}]"	"[""84892""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112382""}]"
DOID:0112383	"[""KINSSHIP syndrome"",""AFF3-related mesomelic dysplasia"",""KINS"",""Steichen-Gersdorf type mesomelic dysplasia""]"	"[{""label"":""AFF3"",""id"":""3899""}]"	"[""3899""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:0112383""}]"
DOID:10003	"[""sensorineural hearing loss"",""High Frequency Hearing Loss"",""High frequency deafness"",""Perceptive deafness"",""Perceptive hearing loss"",""Perceptive hearing loss or deafness"",""Sensorineural Deafness"",""Sensory hearing loss"",""central hearing loss"",""high-frequency hearing loss""]"	"[{""label"":""Ednrb"",""id"":""50672""}]"	"[""50672""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10003""}]"
DOID:10003	"[""sensorineural hearing loss"",""High Frequency Hearing Loss"",""High frequency deafness"",""Perceptive deafness"",""Perceptive hearing loss"",""Perceptive hearing loss or deafness"",""Sensorineural Deafness"",""Sensory hearing loss"",""central hearing loss"",""high-frequency hearing loss""]"	"[{""label"":""Rh5"",""id"":""34615""},{""label"":""Rh6"",""id"":""41889""}]"	"[""34615"",""41889""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10003""}]"
DOID:10003	"[""sensorineural hearing loss"",""High Frequency Hearing Loss"",""High frequency deafness"",""Perceptive deafness"",""Perceptive hearing loss"",""Perceptive hearing loss or deafness"",""Sensorineural Deafness"",""Sensory hearing loss"",""central hearing loss"",""high-frequency hearing loss""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""DIAPH1"",""id"":""1729""},{""label"":""EYA4"",""id"":""2070""},{""label"":""F2"",""id"":""2147""},{""label"":""F5"",""id"":""2153""},{""label"":""GATA3"",""id"":""2625""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL2"",""id"":""3558""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MYH14"",""id"":""79784""},{""label"":""MYH9"",""id"":""4627""},{""label"":""MYO15A"",""id"":""51168""},{""label"":""MYO1A"",""id"":""4640""},{""label"":""MYO6"",""id"":""4646""},{""label"":""MYO7A"",""id"":""4647""},{""label"":""STRC"",""id"":""161497""},{""label"":""TECTA"",""id"":""7007""},{""label"":""TMPRSS3"",""id"":""64699""},{""label"":""TNF"",""id"":""7124""},{""label"":""WFS1"",""id"":""7466""},{""label"":""WHRN"",""id"":""25861""}]"	"[""161497"",""1729"",""2070"",""2147"",""2153"",""25861"",""2625"",""3106"",""3123"",""3458"",""348"",""3558"",""3673"",""4153"",""4627"",""4640"",""4646"",""4647"",""51168"",""64699"",""7007"",""7124"",""7466"",""79784""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10003""}]"
DOID:10003	"[""sensorineural hearing loss"",""High Frequency Hearing Loss"",""High frequency deafness"",""Perceptive deafness"",""Perceptive hearing loss"",""Perceptive hearing loss or deafness"",""Sensorineural Deafness"",""Sensory hearing loss"",""central hearing loss"",""high-frequency hearing loss""]"	"[{""label"":""Slc7a14"",""id"":""241919""}]"	"[""241919""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10003""}]"
DOID:10003	"[""sensorineural hearing loss"",""High Frequency Hearing Loss"",""High frequency deafness"",""Perceptive deafness"",""Perceptive hearing loss"",""Perceptive hearing loss or deafness"",""Sensorineural Deafness"",""Sensory hearing loss"",""central hearing loss"",""high-frequency hearing loss""]"	"[{""label"":""slc44a4"",""id"":""393385""}]"	"[""393385""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10003""}]"
DOID:10016	"[""multiple endocrine neoplasia type 2B"",""MEN type IIB"",""MEN2B"",""Multiple endocrine neoplasia, type 3"",""Wagenmann-Froboese syndrome"",""mucosal neuroma syndrome""]"	"[{""label"":""RET"",""id"":""5979""}]"	"[""5979""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10016""}]"
DOID:10016	"[""multiple endocrine neoplasia type 2B"",""MEN type IIB"",""MEN2B"",""Multiple endocrine neoplasia, type 3"",""Wagenmann-Froboese syndrome"",""mucosal neuroma syndrome""]"	"[{""label"":""Ret"",""id"":""19713""}]"	"[""19713""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10016""}]"
DOID:10024	"[""migraine with aura"",""classic migraine""]"	"[{""label"":""ATP1A2"",""id"":""477""},{""label"":""CACNA1A"",""id"":""773""},{""label"":""DBH"",""id"":""1621""},{""label"":""DRD2"",""id"":""1813""}]"	"[""1621"",""1813"",""477"",""773""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10024""}]"
DOID:1003	"[""pelvic inflammatory disease"",""PID""]"	"[{""label"":""Il4"",""id"":""287287""}]"	"[""287287""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1003""}]"
DOID:10112	"[""sleeping sickness"",""African sleeping sickness"",""African trypanosomiasis""]"	"[{""label"":""GPI10"",""id"":""852735""}]"	"[""852735""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10112""}]"
DOID:10123	"[""pigmentation disease""]"	"[{""label"":""ASIP"",""id"":""434""},{""label"":""HERC2"",""id"":""8924""},{""label"":""IRF4"",""id"":""3662""},{""label"":""KITLG"",""id"":""4254""},{""label"":""MC1R"",""id"":""4157""},{""label"":""MMP9"",""id"":""4318""},{""label"":""OCA2"",""id"":""4948""},{""label"":""SLC24A4"",""id"":""123041""},{""label"":""SLC45A2"",""id"":""51151""},{""label"":""TPCN2"",""id"":""219931""},{""label"":""TYR"",""id"":""7299""},{""label"":""TYRP1"",""id"":""7306""}]"	"[""123041"",""219931"",""3662"",""4157"",""4254"",""4318"",""434"",""4948"",""51151"",""7299"",""7306"",""8924""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10123""}]"
DOID:10126	"[""keratoconus"",""conical cornea""]"	"[{""label"":""HGF"",""id"":""3082""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""}]"	"[""3082"",""3552"",""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10126""}]"
DOID:10140	"[""dry eye syndrome"",""Tear film insufficiency"",""dry eye disease""]"	"[{""label"":""IL6"",""id"":""3569""},{""label"":""MUC1"",""id"":""4582""},{""label"":""MUC5AC"",""id"":""4586""}]"	"[""3569"",""4582"",""4586""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10140""}]"
DOID:10140	"[""dry eye syndrome"",""Tear film insufficiency"",""dry eye disease""]"	"[{""label"":""Aqp5"",""id"":""11830""},{""label"":""Muc5ac"",""id"":""17833""},{""label"":""Pltp"",""id"":""18830""},{""label"":""Sod1"",""id"":""20655""}]"	"[""11830"",""17833"",""18830"",""20655""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10140""}]"
DOID:10155	"[""intestinal cancer"",""malignant intestinal tumors"",""malignant neoplasm of intestine""]"	"[{""label"":""Egfr"",""id"":""37455""},{""label"":""N"",""id"":""31293""},{""label"":""spi"",""id"":""35253""}]"	"[""31293"",""35253"",""37455""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10155""}]"
DOID:10159	"[""osteonecrosis"",""Avascular necrosis of bone"",""aseptic necrosis"",""bone necrosis""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ANXA2"",""id"":""302""},{""label"":""CAT"",""id"":""847""},{""label"":""COL2A1"",""id"":""1280""},{""label"":""F2"",""id"":""2147""},{""label"":""F5"",""id"":""2153""},{""label"":""IL23R"",""id"":""149233""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PLAT"",""id"":""5327""},{""label"":""TFPI"",""id"":""7035""}]"	"[""1280"",""149233"",""2147"",""2153"",""302"",""4846"",""5243"",""5327"",""7035"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10159""}]"
DOID:1019	"[""osteomyelitis""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1019""}]"
DOID:10211	"[""cholelithiasis""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""CYP17A1"",""id"":""1586""},{""label"":""UGT1A1"",""id"":""54658""}]"	"[""1586"",""348"",""54658""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10211""}]"
DOID:10223	"[""dermatomyositis"",""Polymyositis with skin involvement"",""dermatopolymyositis""]"	"[{""label"":""MBL2"",""id"":""4153""},{""label"":""PMS1"",""id"":""5378""},{""label"":""STAT4"",""id"":""6775""}]"	"[""4153"",""5378"",""6775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10223""}]"
DOID:10223	"[""dermatomyositis"",""Polymyositis with skin involvement"",""dermatopolymyositis""]"	"[{""label"":""Angptl2"",""id"":""26360""}]"	"[""26360""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10223""}]"
DOID:10230	"[""aortic atherosclerosis"",""Atherosclerosis of aorta""]"	"[{""label"":""EDN1"",""id"":""1906""}]"	"[""1906""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10230""}]"
DOID:10230	"[""aortic atherosclerosis"",""Atherosclerosis of aorta""]"	"[{""label"":""Ldlr"",""id"":""300438""}]"	"[""300438""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10230""}]"
DOID:1024	"[""leprosy""]"	"[{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""LTA"",""id"":""4049""},{""label"":""NOD2"",""id"":""64127""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""TLR1"",""id"":""7096""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TNF"",""id"":""7124""}]"	"[""3123"",""4049"",""64127"",""6556"",""7096"",""7097"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1024""}]"
DOID:10247	"[""pleurisy""]"	"[{""label"":""Bdkrb1"",""id"":""81509""},{""label"":""Bdkrb2"",""id"":""25245""},{""label"":""Ccl11"",""id"":""29397""},{""label"":""Esr1"",""id"":""24890""},{""label"":""Ptafr"",""id"":""58949""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Tnf"",""id"":""24835""}]"	"[""24835"",""24890"",""25245"",""29397"",""29527"",""58949"",""81509""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10247""}]"
DOID:10247	"[""pleurisy""]"	"[{""label"":""CSF3"",""id"":""1440""},{""label"":""IL15"",""id"":""3600""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""SERPINE1"",""id"":""5054""}]"	"[""1440"",""3557"",""3600"",""5054""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10247""}]"
DOID:10273	"[""heart conduction disease"",""heart rhythm disease""]"	"[{""label"":""Slc6a2"",""id"":""20538""}]"	"[""20538""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10273""}]"
DOID:10273	"[""heart conduction disease"",""heart rhythm disease""]"	"[{""label"":""Nep4"",""id"":""42449""},{""label"":""Ork1"",""id"":""32020""}]"	"[""32020"",""42449""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10273""}]"
DOID:10283	"[""prostate cancer"",""NGP - new growth of prostate"",""hereditary prostate cancer"",""malignant tumor of the prostate"",""prostate cancer, familial"",""prostate neoplasm"",""prostatic cancer"",""prostatic neoplasm"",""tumor of the prostate""]"	"[{""label"":""Acp3"",""id"":""56318""},{""label"":""Ctnnb1"",""id"":""12387""},{""label"":""Kras"",""id"":""16653""},{""label"":""Tgfbr2"",""id"":""21813""}]"	"[""12387"",""16653"",""21813"",""56318""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10283""}]"
DOID:10283	"[""prostate cancer"",""NGP - new growth of prostate"",""hereditary prostate cancer"",""malignant tumor of the prostate"",""prostate cancer, familial"",""prostate neoplasm"",""prostatic cancer"",""prostatic neoplasm"",""tumor of the prostate""]"	"[{""label"":""CHD1"",""id"":""856911""}]"	"[""856911""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10283""}]"
DOID:10283	"[""prostate cancer"",""NGP - new growth of prostate"",""hereditary prostate cancer"",""malignant tumor of the prostate"",""prostate cancer, familial"",""prostate neoplasm"",""prostatic cancer"",""prostatic neoplasm"",""tumor of the prostate""]"	"[{""label"":""CadN"",""id"":""35070""},{""label"":""Ostgamma"",""id"":""34137""},{""label"":""Semp1"",""id"":""34914""},{""label"":""shg"",""id"":""37386""}]"	"[""34137"",""34914"",""35070"",""37386""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10283""}]"
DOID:10283	"[""prostate cancer"",""NGP - new growth of prostate"",""hereditary prostate cancer"",""malignant tumor of the prostate"",""prostate cancer, familial"",""prostate neoplasm"",""prostatic cancer"",""prostatic neoplasm"",""tumor of the prostate""]"	"[{""label"":""Fgfr2"",""id"":""25022""},{""label"":""Pdgfrb"",""id"":""24629""}]"	"[""24629"",""25022""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10283""}]"
DOID:10283	"[""prostate cancer"",""NGP - new growth of prostate"",""hereditary prostate cancer"",""malignant tumor of the prostate"",""prostate cancer, familial"",""prostate neoplasm"",""prostatic cancer"",""prostatic neoplasm"",""tumor of the prostate""]"	"[{""label"":""ACP3"",""id"":""55""},{""label"":""ACSL3"",""id"":""2181""},{""label"":""AGAP2"",""id"":""116986""},{""label"":""AKT1"",""id"":""207""},{""label"":""AKT2"",""id"":""208""},{""label"":""AKT3"",""id"":""10000""},{""label"":""APC"",""id"":""324""},{""label"":""AR"",""id"":""367""},{""label"":""BMP2"",""id"":""650""},{""label"":""BMP7"",""id"":""655""},{""label"":""BRCA1"",""id"":""672""},{""label"":""BRCA2"",""id"":""675""},{""label"":""CADM1"",""id"":""23705""},{""label"":""CD44"",""id"":""960""},{""label"":""CD55"",""id"":""1604""},{""label"":""CDC25A"",""id"":""993""},{""label"":""CDH13"",""id"":""1012""},{""label"":""CDH1"",""id"":""999""},{""label"":""CHD1"",""id"":""1105""},{""label"":""CHEK2"",""id"":""11200""},{""label"":""CHGA"",""id"":""1113""},{""label"":""CHUK"",""id"":""1147""},{""label"":""COMT"",""id"":""1312""},{""label"":""CXCR4"",""id"":""7852""},{""label"":""CYP17A1"",""id"":""1586""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""EGFR"",""id"":""1956""},{""label"":""EIF3H"",""id"":""8667""},{""label"":""ENO2"",""id"":""2026""},{""label"":""EPHB1"",""id"":""2047""},{""label"":""ERBB2"",""id"":""2064""},{""label"":""ESR1"",""id"":""2099""},{""label"":""FAS"",""id"":""355""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""FLT3"",""id"":""2322""},{""label"":""GRB2"",""id"":""2885""},{""label"":""HIF1A"",""id"":""3091""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IGFBP3"",""id"":""3486""},{""label"":""IKBKB"",""id"":""3551""},{""label"":""IL16"",""id"":""3603""},{""label"":""JAK1"",""id"":""3716""},{""label"":""JUP"",""id"":""3728""},{""label"":""KLK10"",""id"":""5655""},{""label"":""KLK4"",""id"":""9622""},{""label"":""MAP3K7"",""id"":""6885""},{""label"":""MSR1"",""id"":""4481""},{""label"":""MTOR"",""id"":""2475""},{""label"":""MXI1"",""id"":""4601""},{""label"":""MYC"",""id"":""4609""},{""label"":""NAT2"",""id"":""10""},{""label"":""NBN"",""id"":""4683""},{""label"":""NFKB1"",""id"":""4790""},{""label"":""NOS3"",""id"":""4846""},{""label"":""OGG1"",""id"":""4968""},{""label"":""PDPK1"",""id"":""5170""},{""label"":""PEBP1"",""id"":""5037""},{""label"":""PIK3CB"",""id"":""5291""},{""label"":""PTEN"",""id"":""5728""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""RB1"",""id"":""5925""},{""label"":""RNASEL"",""id"":""6041""},{""label"":""SRC"",""id"":""6714""},{""label"":""SRD5A1"",""id"":""6715""},{""label"":""SRD5A2"",""id"":""6716""},{""label"":""SREBF2"",""id"":""6721""},{""label"":""STAT3"",""id"":""6774""},{""label"":""SULT2A1"",""id"":""6822""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TMEFF2"",""id"":""23671""},{""label"":""TNF"",""id"":""7124""},{""label"":""TP53"",""id"":""7157""},{""label"":""TSG101"",""id"":""7251""},{""label"":""VDAC1"",""id"":""7416""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""XIAP"",""id"":""331""},{""label"":""XRCC1"",""id"":""7515""},{""label"":""ZFHX3"",""id"":""463""}]"	"[""10"",""10000"",""1012"",""1105"",""1113"",""11200"",""1147"",""116986"",""1312"",""1543"",""1586"",""1604"",""1956"",""2026"",""2047"",""2064"",""207"",""208"",""2099"",""2181"",""2264"",""2322"",""23671"",""23705"",""2475"",""2885"",""3091"",""3123"",""324"",""331"",""3383"",""3486"",""355"",""3551"",""3603"",""367"",""3716"",""3728"",""4481"",""4601"",""4609"",""463"",""4683"",""4790"",""4846"",""4968"",""5037"",""5170"",""5291"",""55"",""5655"",""5728"",""5743"",""5925"",""6041"",""650"",""655"",""6714"",""6715"",""6716"",""672"",""6721"",""675"",""6774"",""6822"",""6885"",""7097"",""7124"",""7157"",""7251"",""7416"",""7422"",""7515"",""7852"",""8667"",""960"",""9622"",""993"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10283""}]"
DOID:10286	"[""prostate carcinoma"",""cancer of prostate"",""carcinoma of prostate""]"	"[{""label"":""AKT2"",""id"":""208""},{""label"":""ATF4"",""id"":""468""},{""label"":""AZGP1"",""id"":""563""},{""label"":""CDK13"",""id"":""8621""},{""label"":""EIF3H"",""id"":""8667""},{""label"":""INHA"",""id"":""3623""},{""label"":""PRKCA"",""id"":""5578""},{""label"":""SKP2"",""id"":""6502""},{""label"":""SPP1"",""id"":""6696""},{""label"":""STAT3"",""id"":""6774""},{""label"":""STAT6"",""id"":""6778""}]"	"[""208"",""3623"",""468"",""5578"",""563"",""6502"",""6696"",""6774"",""6778"",""8621"",""8667""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10286""}]"
DOID:10300	"[""Raynaud disease"",""Raynaud's disease"",""Raynaud's syndrome""]"	"[{""label"":""HNRNPK"",""id"":""3190""}]"	"[""3190""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10300""}]"
DOID:10303	"[""sialadenitis"",""Sialoadenitis""]"	"[{""label"":""Cd4"",""id"":""24932""}]"	"[""24932""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10303""}]"
DOID:10316	"[""pneumoconiosis""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10316""}]"
DOID:10322	"[""berylliosis"",""beryllium poisoning""]"	"[{""label"":""BTNL2"",""id"":""56244""},{""label"":""CCR5"",""id"":""1234""},{""label"":""TGFB1"",""id"":""7040""}]"	"[""1234"",""56244"",""7040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10322""}]"
DOID:10325	"[""silicosis"",""Pneumoconiosis due to silicates"",""Silica pneumoconiosis"",""Silicotic fibrosis of lung"",""silicotuberculosis""]"	"[{""label"":""Il1rn"",""id"":""60582""},{""label"":""Prkcb"",""id"":""25023""}]"	"[""25023"",""60582""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10325""}]"
DOID:10325	"[""silicosis"",""Pneumoconiosis due to silicates"",""Silica pneumoconiosis"",""Silicotic fibrosis of lung"",""silicotuberculosis""]"	"[{""label"":""C3"",""id"":""718""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""TNF"",""id"":""7124""}]"	"[""3119"",""3557"",""7124"",""718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10325""}]"
DOID:1037	"[""lymphoid leukemia"",""lymphoblastic leukaemia"",""lymphoblastic leukemia"",""lymphocytic leukaemia""]"	"[{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR2B"",""id"":""2213""}]"	"[""2212"",""2213""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1037""}]"
DOID:104	"[""bacterial infectious disease""]"	"[{""label"":""Sdc4"",""id"":""24771""}]"	"[""24771""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:104""}]"
DOID:104	"[""bacterial infectious disease""]"	"[{""label"":""DOCK8"",""id"":""81704""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""MBL2"",""id"":""4153""}]"	"[""3119"",""3123"",""4153"",""81704""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:104""}]"
DOID:1040	"[""chronic lymphocytic leukemia"",""B-cell chronic lymphocytic leukaemia"",""B-cell chronic lymphocytic leukemia"",""CLL"",""chronic lymphatic leukaemia"",""chronic lymphatic leukemia"",""chronic lymphocytic leukaemia"",""lymphoplasmacytic leukaemia"",""lymphoplasmacytic leukemia""]"	"[{""label"":""CD79B"",""id"":""974""},{""label"":""CD86"",""id"":""942""},{""label"":""IRF4"",""id"":""3662""},{""label"":""PON1"",""id"":""5444""}]"	"[""3662"",""5444"",""942"",""974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1040""}]"
DOID:10457	"[""Legionnaires' disease"",""Infection by Legionella pneumophilia"",""Legionella"",""Legionella pneumonia"",""Legionnaire's disease""]"	"[{""label"":""TLR5"",""id"":""7100""}]"	"[""7100""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10457""}]"
DOID:10459	"[""common cold"",""Acute viral rhinopharyngitis"",""Nasopharyngitis - acute"",""Nasopharyngitis, acute"",""acute coryza"",""acute nasopharyngitis"",""acute rhinitis"",""rhino-sinusitis""]"	"[{""label"":""CX3CL1"",""id"":""6376""},{""label"":""IFNA2"",""id"":""3440""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RN"",""id"":""3557""}]"	"[""3440"",""3557"",""3586"",""6376""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10459""}]"
DOID:10485	"[""esophageal atresia"",""Congenital atresia of esophagus"",""Congenital imperforate esophagus"",""Imperforate esophagus"",""Oesophageal atresia""]"	"[{""label"":""EFTUD2"",""id"":""9343""}]"	"[""9343""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10485""}]"
DOID:10486	"[""intestinal atresia""]"	"[{""label"":""Fgf10"",""id"":""14165""},{""label"":""Fgfr2"",""id"":""14183""}]"	"[""14165"",""14183""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10486""}]"
DOID:10487	"[""Hirschsprung's disease"",""Hirschsprung disease"",""aganglionic megacolon"",""congenital megacolon"",""macrocolon"",""pelvirectal achalasia"",""total intestinal aganglionosis""]"	"[{""label"":""ret"",""id"":""30512""}]"	"[""30512""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10487""}]"
DOID:10487	"[""Hirschsprung's disease"",""Hirschsprung disease"",""aganglionic megacolon"",""congenital megacolon"",""macrocolon"",""pelvirectal achalasia"",""total intestinal aganglionosis""]"	"[{""label"":""Ednrb"",""id"":""13618""},{""label"":""Erbb2"",""id"":""13866""},{""label"":""Gdnf"",""id"":""14573""},{""label"":""Gfra1"",""id"":""14585""},{""label"":""Ihh"",""id"":""16147""},{""label"":""Itgb1"",""id"":""16412""},{""label"":""Ret"",""id"":""19713""}]"	"[""13618"",""13866"",""14573"",""14585"",""16147"",""16412"",""19713""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10487""}]"
DOID:10487	"[""Hirschsprung's disease"",""Hirschsprung disease"",""aganglionic megacolon"",""congenital megacolon"",""macrocolon"",""pelvirectal achalasia"",""total intestinal aganglionosis""]"	"[{""label"":""Ednrb"",""id"":""50672""}]"	"[""50672""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10487""}]"
DOID:10487	"[""Hirschsprung's disease"",""Hirschsprung disease"",""aganglionic megacolon"",""congenital megacolon"",""macrocolon"",""pelvirectal achalasia"",""total intestinal aganglionosis""]"	"[{""label"":""EDNRB"",""id"":""1910""},{""label"":""GDNF"",""id"":""2668""},{""label"":""RET"",""id"":""5979""},{""label"":""SHH"",""id"":""6469""},{""label"":""STX1A"",""id"":""6804""},{""label"":""WNT8B"",""id"":""7479""}]"	"[""1910"",""2668"",""5979"",""6469"",""6804"",""7479""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10487""}]"
DOID:10533	"[""viral pneumonia""]"	"[{""label"":""TLR9"",""id"":""54106""}]"	"[""54106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10533""}]"
DOID:10534	"[""stomach cancer"",""gastric cancer"",""gastric neoplasm""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ACVR1B"",""id"":""91""},{""label"":""APC"",""id"":""324""},{""label"":""ARID1A"",""id"":""8289""},{""label"":""ATP4B"",""id"":""496""},{""label"":""BCOR"",""id"":""54880""},{""label"":""BRCA1"",""id"":""672""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CXCR4"",""id"":""7852""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""DDR2"",""id"":""4921""},{""label"":""EEF2"",""id"":""1938""},{""label"":""ERBB2"",""id"":""2064""},{""label"":""ERCC5"",""id"":""2073""},{""label"":""ERCC6"",""id"":""2074""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FGFR2"",""id"":""2263""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""FOSL1"",""id"":""8061""},{""label"":""FOXA1"",""id"":""3169""},{""label"":""FUT11"",""id"":""170384""},{""label"":""GPX1"",""id"":""2876""},{""label"":""GPX3"",""id"":""2878""},{""label"":""GSE1"",""id"":""23199""},{""label"":""HDAC2"",""id"":""3066""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL5"",""id"":""3567""},{""label"":""IL6"",""id"":""3569""},{""label"":""IL6R"",""id"":""3570""},{""label"":""IL7R"",""id"":""3575""},{""label"":""JAK1"",""id"":""3716""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""KDR"",""id"":""3791""},{""label"":""KMT2C"",""id"":""58508""},{""label"":""KRAS"",""id"":""3845""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""MAP3K1"",""id"":""4214""},{""label"":""MUTYH"",""id"":""4595""},{""label"":""NTRK3"",""id"":""4916""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PTCH1"",""id"":""5727""},{""label"":""PTPN11"",""id"":""5781""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TEP1"",""id"":""7011""},{""label"":""TET2"",""id"":""54790""},{""label"":""TMEM260"",""id"":""54916""},{""label"":""TP53"",""id"":""7157""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1136"",""1543"",""1571"",""1636"",""170384"",""1938"",""2064"",""2073"",""2074"",""2146"",""2263"",""2264"",""23199"",""2876"",""2878"",""3066"",""3117"",""3169"",""324"",""3557"",""3567"",""3569"",""3570"",""3575"",""3586"",""3716"",""3791"",""3845"",""4214"",""4595"",""4916"",""4921"",""496"",""5290"",""53353"",""54790"",""54880"",""54916"",""5727"",""5781"",""58508"",""6648"",""672"",""7011"",""7157"",""7403"",""7515"",""7852"",""8061"",""8289"",""91""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10534""}]"
DOID:10534	"[""stomach cancer"",""gastric cancer"",""gastric neoplasm""]"	"[{""label"":""Il6st"",""id"":""16195""}]"	"[""16195""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10534""}]"
DOID:1056	"[""oculocerebrorenal syndrome"",""Lowe syndrome"",""lowe oculocerebrorenal syndrome"",""oculocerebrorenal syndrome of Lowe""]"	"[{""label"":""OCRL"",""id"":""4952""}]"	"[""4952""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1056""}]"
DOID:10573	"[""osteomalacia""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10573""}]"
DOID:10579	"[""leukodystrophy""]"	"[{""label"":""AARS1"",""id"":""16""}]"	"[""16""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10579""}]"
DOID:10579	"[""leukodystrophy""]"	"[{""label"":""Clcn2"",""id"":""12724""}]"	"[""12724""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10579""}]"
DOID:10581	"[""metachromatic leukodystrophy"",""MLD"",""Scholz cerebral sclerosis"",""arylsulfatase A deficiency"",""deficiency of cerebroside-sulfatase"",""sulfatide lipoidosis""]"	"[{""label"":""Arsa"",""id"":""11883""},{""label"":""Psap"",""id"":""19156""}]"	"[""11883"",""19156""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10581""}]"
DOID:10581	"[""metachromatic leukodystrophy"",""MLD"",""Scholz cerebral sclerosis"",""arylsulfatase A deficiency"",""deficiency of cerebroside-sulfatase"",""sulfatide lipoidosis""]"	"[{""label"":""ARSA"",""id"":""410""},{""label"":""PSAP"",""id"":""5660""}]"	"[""410"",""5660""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00080""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00081""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00082""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00083""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00084""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10581""}]"
DOID:10584	"[""retinitis pigmentosa"",""pericentral pigmentary retinopathy""]"	"[{""label"":""Ccdc66"",""id"":""320234""},{""label"":""Crb2"",""id"":""241324""},{""label"":""Slc6a6"",""id"":""21366""}]"	"[""21366"",""241324"",""320234""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10584""}]"
DOID:10584	"[""retinitis pigmentosa"",""pericentral pigmentary retinopathy""]"	"[{""label"":""eys"",""id"":""557044""},{""label"":""rho"",""id"":""30295""}]"	"[""30295"",""557044""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10584""}]"
DOID:10584	"[""retinitis pigmentosa"",""pericentral pigmentary retinopathy""]"	"[{""label"":""Fgfr2"",""id"":""25022""}]"	"[""25022""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10584""}]"
DOID:10584	"[""retinitis pigmentosa"",""pericentral pigmentary retinopathy""]"	"[{""label"":""ABCA4"",""id"":""24""},{""label"":""CA4"",""id"":""762""},{""label"":""CAT"",""id"":""847""},{""label"":""CC2D2A"",""id"":""57545""},{""label"":""CNGA1"",""id"":""1259""},{""label"":""CNGB1"",""id"":""1258""},{""label"":""CRB1"",""id"":""23418""},{""label"":""GUCY2D"",""id"":""3000""},{""label"":""HK1"",""id"":""3098""},{""label"":""HKDC1"",""id"":""80201""},{""label"":""IMPG1"",""id"":""3617""},{""label"":""MFRP"",""id"":""83552""},{""label"":""POMGNT1"",""id"":""55624""},{""label"":""PRPF3"",""id"":""9129""},{""label"":""PRPF8"",""id"":""10594""},{""label"":""PRPH2"",""id"":""5961""},{""label"":""PRPS1"",""id"":""5631""},{""label"":""RGR"",""id"":""5995""},{""label"":""RHO"",""id"":""6010""},{""label"":""RLBP1"",""id"":""6017""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""SNRNP200"",""id"":""23020""},{""label"":""SOD1"",""id"":""6647""},{""label"":""USH2A"",""id"":""7399""}]"	"[""10594"",""1258"",""1259"",""23020"",""23418"",""24"",""3000"",""3098"",""3617"",""5176"",""55624"",""5631"",""57545"",""5961"",""5995"",""6010"",""6017"",""6647"",""7399"",""762"",""80201"",""83552"",""847"",""9129""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10584""}]"
DOID:10584	"[""retinitis pigmentosa"",""pericentral pigmentary retinopathy""]"	"[{""label"":""crb"",""id"":""42896""},{""label"":""ninaE"",""id"":""42367""}]"	"[""42367"",""42896""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10584""}]"
DOID:10587	"[""Krabbe disease"",""Diffuse globoid body sclerosis"",""GLOBOID CELL LEUKOENCEPHALOPATHY"",""Galactosylceramide beta-galactosidase deficiency"",""Krabbe's disease"",""Krabbe's leukodystrophy"",""beta galactocerebrosidase deficiency"",""globoid cell leukodystrophy""]"	"[{""label"":""GALC"",""id"":""2581""}]"	"[""2581""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00073""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00074""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00075""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10587""}]"
DOID:10587	"[""Krabbe disease"",""Diffuse globoid body sclerosis"",""GLOBOID CELL LEUKOENCEPHALOPATHY"",""Galactosylceramide beta-galactosidase deficiency"",""Krabbe's disease"",""Krabbe's leukodystrophy"",""beta galactocerebrosidase deficiency"",""globoid cell leukodystrophy""]"	"[{""label"":""Galc"",""id"":""14420""},{""label"":""Psap"",""id"":""19156""}]"	"[""14420"",""19156""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10587""}]"
DOID:10588	"[""adrenoleukodystrophy"",""ALD"",""Bronze Schilder disease"",""Encephalitis periaxialis concentrica"",""Encephalitis periaxialis, Schilder's"",""Siemerling-Creutzfeldt Disease"",""X-linked adrenoleukodystrophy"",""diffuse sclerosis"",""sudanophilic cerebral sclerosis""]"	"[{""label"":""PXA1"",""id"":""855956""},{""label"":""PXA2"",""id"":""853647""}]"	"[""853647"",""855956""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10588""}]"
DOID:10588	"[""adrenoleukodystrophy"",""ALD"",""Bronze Schilder disease"",""Encephalitis periaxialis concentrica"",""Encephalitis periaxialis, Schilder's"",""Siemerling-Creutzfeldt Disease"",""X-linked adrenoleukodystrophy"",""diffuse sclerosis"",""sudanophilic cerebral sclerosis""]"	"[{""label"":""ABCD1"",""id"":""215""}]"	"[""215""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10588""}]"
DOID:10588	"[""adrenoleukodystrophy"",""ALD"",""Bronze Schilder disease"",""Encephalitis periaxialis concentrica"",""Encephalitis periaxialis, Schilder's"",""Siemerling-Creutzfeldt Disease"",""X-linked adrenoleukodystrophy"",""diffuse sclerosis"",""sudanophilic cerebral sclerosis""]"	"[{""label"":""Abcd1"",""id"":""11666""}]"	"[""11666""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10588""}]"
DOID:1059	"[""intellectual disability""]"	"[{""label"":""SEC12"",""id"":""855760""}]"	"[""855760""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1059""}]"
DOID:1059	"[""intellectual disability""]"	"[{""label"":""drl"",""id"":""44355""},{""label"":""if"",""id"":""32661""},{""label"":""sfl"",""id"":""38736""}]"	"[""32661"",""38736"",""44355""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1059""}]"
DOID:1059	"[""intellectual disability""]"	"[{""label"":""Cul4b"",""id"":""72584""},{""label"":""Gprasp2"",""id"":""245607""},{""label"":""Hivep2"",""id"":""15273""}]"	"[""15273"",""245607"",""72584""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1059""}]"
DOID:1059	"[""intellectual disability""]"	"[{""label"":""mef-2"",""id"":""172732""}]"	"[""172732""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1059""}]"
DOID:1059	"[""intellectual disability""]"	"[{""label"":""ACSL4"",""id"":""2182""},{""label"":""AGTR2"",""id"":""186""},{""label"":""ARHGEF6"",""id"":""9459""},{""label"":""ARID1B"",""id"":""57492""},{""label"":""CASR"",""id"":""846""},{""label"":""CC2D1A"",""id"":""54862""},{""label"":""CC2D2A"",""id"":""57545""},{""label"":""CDK13"",""id"":""8621""},{""label"":""CDKL5"",""id"":""6792""},{""label"":""CHKB"",""id"":""1120""},{""label"":""DMD"",""id"":""1756""},{""label"":""DRD4"",""id"":""1815""},{""label"":""DYRK1A"",""id"":""1859""},{""label"":""EIF4A3"",""id"":""9775""},{""label"":""GPI"",""id"":""2821""},{""label"":""HPN"",""id"":""3249""},{""label"":""IL1RAPL1"",""id"":""11141""},{""label"":""IMPA1"",""id"":""3612""},{""label"":""KRAS"",""id"":""3845""},{""label"":""NONO"",""id"":""4841""},{""label"":""PRSS12"",""id"":""8492""},{""label"":""RPGRIP1L"",""id"":""23322""},{""label"":""RPS6KA3"",""id"":""6197""},{""label"":""SARS1"",""id"":""6301""},{""label"":""SLC6A8"",""id"":""6535""},{""label"":""SMC3"",""id"":""9126""},{""label"":""TSC1"",""id"":""7248""},{""label"":""WDR62"",""id"":""284403""}]"	"[""11141"",""1120"",""1756"",""1815"",""1859"",""186"",""2182"",""23322"",""2821"",""284403"",""3249"",""3612"",""3845"",""4841"",""54862"",""57492"",""57545"",""6197"",""6301"",""6535"",""6792"",""7248"",""846"",""8492"",""8621"",""9126"",""9459"",""9775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1059""}]"
DOID:10591	"[""pre-eclampsia"",""gestational hypertension"",""hypertension induced by pregnancy"",""pre-eclamptic toxaemia"",""preeclampsia"",""preeclampsia/eclampsia"",""pregnancy associated hypertension"",""pregnancy toxemia"",""proteinuric hypertension of pregnancy"",""toxaemia of pregnancy""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGT"",""id"":""183""},{""label"":""CD46"",""id"":""4179""},{""label"":""CLU"",""id"":""1191""},{""label"":""CORIN"",""id"":""10699""},{""label"":""CYP11B2"",""id"":""1585""},{""label"":""F2"",""id"":""2147""},{""label"":""F5"",""id"":""2153""},{""label"":""FAS"",""id"":""355""},{""label"":""FASLG"",""id"":""356""},{""label"":""FLT1"",""id"":""2321""},{""label"":""HLA-A"",""id"":""3105""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""HP"",""id"":""3240""},{""label"":""HSD11B1"",""id"":""3290""},{""label"":""ITGAM"",""id"":""3684""},{""label"":""PPARG"",""id"":""5468""},{""label"":""PROC"",""id"":""5624""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF1B"",""id"":""7133""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""10699"",""1191"",""1585"",""1636"",""183"",""2147"",""2153"",""2321"",""3105"",""3119"",""3240"",""3290"",""355"",""356"",""3684"",""4179"",""5468"",""5624"",""6927"",""7124"",""7133"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10591""}]"
DOID:10591	"[""pre-eclampsia"",""gestational hypertension"",""hypertension induced by pregnancy"",""pre-eclamptic toxaemia"",""preeclampsia"",""preeclampsia/eclampsia"",""pregnancy associated hypertension"",""pregnancy toxemia"",""proteinuric hypertension of pregnancy"",""toxaemia of pregnancy""]"	"[{""label"":""Comt"",""id"":""12846""},{""label"":""Notch2"",""id"":""18129""},{""label"":""Ptgs1"",""id"":""19224""}]"	"[""12846"",""18129"",""19224""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10591""}]"
DOID:10591	"[""pre-eclampsia"",""gestational hypertension"",""hypertension induced by pregnancy"",""pre-eclamptic toxaemia"",""preeclampsia"",""preeclampsia/eclampsia"",""pregnancy associated hypertension"",""pregnancy toxemia"",""proteinuric hypertension of pregnancy"",""toxaemia of pregnancy""]"	"[{""label"":""C3"",""id"":""24232""},{""label"":""Cd40lg"",""id"":""84349""},{""label"":""Icam1"",""id"":""25464""}]"	"[""24232"",""25464"",""84349""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10591""}]"
DOID:10595	"[""Charcot-Marie-Tooth disease"",""CMT - Charcot-Marie-Tooth disease""]"	"[{""label"":""CSG2"",""id"":""852324""}]"	"[""852324""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10595""}]"
DOID:10595	"[""Charcot-Marie-Tooth disease"",""CMT - Charcot-Marie-Tooth disease""]"	"[{""label"":""FIG4"",""id"":""33658""}]"	"[""33658""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10595""}]"
DOID:10595	"[""Charcot-Marie-Tooth disease"",""CMT - Charcot-Marie-Tooth disease""]"	"[{""label"":""CADM3"",""id"":""57863""},{""label"":""FBLN5"",""id"":""10516""},{""label"":""ITPR3"",""id"":""3710""},{""label"":""JAG1"",""id"":""182""},{""label"":""MPZ"",""id"":""4359""},{""label"":""NEFL"",""id"":""4747""},{""label"":""NRG1"",""id"":""3084""},{""label"":""PMP22"",""id"":""5376""},{""label"":""POLR3B"",""id"":""55703""},{""label"":""SLC12A6"",""id"":""9990""}]"	"[""10516"",""182"",""3084"",""3710"",""4359"",""4747"",""5376"",""55703"",""57863"",""9990""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10595""}]"
DOID:106	"[""pleural tuberculosis"",""Pearly disease"",""Tuberculosis of pleura"",""Tuberculous pleurisy"",""Tuberculous pleuritis"",""tuberculous pleurisy in primary progressive tuberculosis""]"	"[{""label"":""CCR2"",""id"":""729230""},{""label"":""IL1RN"",""id"":""3557""}]"	"[""3557"",""729230""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:106""}]"
DOID:1060	"[""Hartnup disease"",""Neutral 1 amino acid transport defect"",""deficiency of tryptophan oxygenase"",""neutral amino acid transport defect""]"	"[{""label"":""Slc6a19"",""id"":""74338""}]"	"[""74338""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1060""}]"
DOID:1060	"[""Hartnup disease"",""Neutral 1 amino acid transport defect"",""deficiency of tryptophan oxygenase"",""neutral amino acid transport defect""]"	"[{""label"":""SLC6A19"",""id"":""340024""}]"	"[""340024""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1060""}]"
DOID:10603	"[""glucose intolerance"",""Glucose malabsorption"",""Malabsorption of glucose""]"	"[{""label"":""APOC3"",""id"":""345""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""HSPD1"",""id"":""3329""},{""label"":""PON1"",""id"":""5444""}]"	"[""3117"",""3329"",""345"",""5444"",""6927""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10603""}]"
DOID:10603	"[""glucose intolerance"",""Glucose malabsorption"",""Malabsorption of glucose""]"	"[{""label"":""Lep"",""id"":""25608""},{""label"":""Lepr"",""id"":""24536""}]"	"[""24536"",""25608""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10603""}]"
DOID:10605	"[""short bowel syndrome"",""acquired short bowel syndrome"",""short gut syndrome""]"	"[{""label"":""Lep"",""id"":""25608""}]"	"[""25608""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10605""}]"
DOID:10605	"[""short bowel syndrome"",""acquired short bowel syndrome"",""short gut syndrome""]"	"[{""label"":""CLMP"",""id"":""79827""}]"	"[""79827""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10605""}]"
DOID:10608	"[""celiac disease"",""celiac sprue"",""coeliac disease"",""idiopathic steatorrhea""]"	"[{""label"":""CD14"",""id"":""929""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""F2"",""id"":""2147""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""ICOS"",""id"":""29851""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL6"",""id"":""3569""}]"	"[""149233"",""1493"",""2147"",""29851"",""3117"",""3119"",""3123"",""3569"",""929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10608""}]"
DOID:10609	"[""rickets"",""active rickets""]"	"[{""label"":""CYP27B1"",""id"":""1594""}]"	"[""1594""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10609""}]"
DOID:10609	"[""rickets"",""active rickets""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10609""}]"
DOID:10609	"[""rickets"",""active rickets""]"	"[{""label"":""Fam20c"",""id"":""80752""}]"	"[""80752""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10609""}]"
DOID:10611	"[""protein-losing enteropathy"",""Enteropathy, exudative"",""Exudative enteropathy""]"	"[{""label"":""CD55"",""id"":""1604""}]"	"[""1604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10611""}]"
DOID:1062	"[""Fanconi syndrome"",""Congenital Fanconi syndrome"",""De Toni-Fanconi syndrome"",""Fanconi-de Toni syndrome"",""Fanconi-de-Toni syndrome"",""Infantile nephropathic cystinosis"",""Lignac-Fanconi syndrome"",""adult Fanconi Anemia"",""adult Fanconi syndrome"",""deToni Fanconi syndrome""]"	"[{""label"":""SLC34A1"",""id"":""6569""}]"	"[""6569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1062""}]"
DOID:1062	"[""Fanconi syndrome"",""Congenital Fanconi syndrome"",""De Toni-Fanconi syndrome"",""Fanconi-de Toni syndrome"",""Fanconi-de-Toni syndrome"",""Infantile nephropathic cystinosis"",""Lignac-Fanconi syndrome"",""adult Fanconi Anemia"",""adult Fanconi syndrome"",""deToni Fanconi syndrome""]"	"[{""label"":""Lrp2"",""id"":""14725""}]"	"[""14725""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1062""}]"
DOID:10629	"[""microphthalmia"",""microphthalmos"",""simple microphthalmos""]"	"[{""label"":""crim1"",""id"":""404210""},{""label"":""gdf6a"",""id"":""566470""}]"	"[""404210"",""566470""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10629""}]"
DOID:10629	"[""microphthalmia"",""microphthalmos"",""simple microphthalmos""]"	"[{""label"":""HCCS"",""id"":""3052""},{""label"":""LRP5"",""id"":""4041""},{""label"":""MFRP"",""id"":""83552""}]"	"[""3052"",""4041"",""83552""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10629""}]"
DOID:10629	"[""microphthalmia"",""microphthalmos"",""simple microphthalmos""]"	"[{""label"":""Hccs"",""id"":""15159""}]"	"[""15159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10629""}]"
DOID:10632	"[""Wolfram syndrome"",""WFS""]"	"[{""label"":""WFS1"",""id"":""7466""}]"	"[""7466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10632""}]"
DOID:1064	"[""cystinosis"",""cystine storage disease""]"	"[{""label"":""ctns-1"",""id"":""174308""}]"	"[""174308""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1064""}]"
DOID:1064	"[""cystinosis"",""cystine storage disease""]"	"[{""label"":""CTNS"",""id"":""1497""}]"	"[""1497""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1064""}]"
DOID:1064	"[""cystinosis"",""cystine storage disease""]"	"[{""label"":""Ctns"",""id"":""83429""}]"	"[""83429""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1064""}]"
DOID:1064	"[""cystinosis"",""cystine storage disease""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1064""}]"
DOID:10646	"[""schizotypal personality disorder""]"	"[{""label"":""AGER"",""id"":""177""}]"	"[""177""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10646""}]"
DOID:10652	"[""Alzheimer's disease"",""Alzheimer disease"",""Alzheimers dementia""]"	"[{""label"":""App"",""id"":""11820""},{""label"":""Lrp1"",""id"":""16971""},{""label"":""Mme"",""id"":""17380""}]"	"[""11820"",""16971"",""17380""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10652""}]"
DOID:10652	"[""Alzheimer's disease"",""Alzheimer disease"",""Alzheimers dementia""]"	"[{""label"":""Appl"",""id"":""31002""},{""label"":""Nct"",""id"":""42964""},{""label"":""Psn"",""id"":""40260""},{""label"":""amrt"",""id"":""32342""},{""label"":""amx"",""id"":""43869""},{""label"":""bisc"",""id"":""37443""}]"	"[""31002"",""32342"",""37443"",""40260"",""42964"",""43869""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10652""}]"
DOID:10652	"[""Alzheimer's disease"",""Alzheimer disease"",""Alzheimers dementia""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""App"",""id"":""54226""},{""label"":""Bdnf"",""id"":""24225""},{""label"":""Ccr5"",""id"":""117029""},{""label"":""Gapdh"",""id"":""24383""},{""label"":""Gsk3b"",""id"":""84027""},{""label"":""Hspd1"",""id"":""63868""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Igf1r"",""id"":""25718""},{""label"":""Lep"",""id"":""25608""},{""label"":""Map2"",""id"":""25595""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Ptgs2"",""id"":""29527""}]"	"[""117029"",""24225"",""24310"",""24383"",""25595"",""25608"",""25718"",""29527"",""29595"",""54226"",""63868"",""83516"",""84027""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10652""}]"
DOID:10652	"[""Alzheimer's disease"",""Alzheimer disease"",""Alzheimers dementia""]"	"[{""label"":""apl-1"",""id"":""180783""},{""label"":""lin-12"",""id"":""176282""}]"	"[""176282"",""180783""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10652""}]"
DOID:10652	"[""Alzheimer's disease"",""Alzheimer disease"",""Alzheimers dementia""]"	"[{""label"":""HRR25"",""id"":""855897""}]"	"[""855897""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10652""}]"
DOID:10652	"[""Alzheimer's disease"",""Alzheimer disease"",""Alzheimers dementia""]"	"[{""label"":""A2M"",""id"":""2""},{""label"":""ABAT"",""id"":""18""},{""label"":""ABCA1"",""id"":""19""},{""label"":""ACHE"",""id"":""43""},{""label"":""ADAM17"",""id"":""6868""},{""label"":""ADRA1A"",""id"":""148""},{""label"":""ADRB3"",""id"":""155""},{""label"":""AGER"",""id"":""177""},{""label"":""AGTR1"",""id"":""185""},{""label"":""ALDH2"",""id"":""217""},{""label"":""APBB1"",""id"":""322""},{""label"":""APOA1"",""id"":""335""},{""label"":""APOA4"",""id"":""337""},{""label"":""APOE"",""id"":""348""},{""label"":""APP"",""id"":""351""},{""label"":""BACE1"",""id"":""23621""},{""label"":""BACE2"",""id"":""25825""},{""label"":""BCHE"",""id"":""590""},{""label"":""BDNF"",""id"":""627""},{""label"":""C2"",""id"":""717""},{""label"":""C3"",""id"":""718""},{""label"":""CASP7"",""id"":""840""},{""label"":""CDK5"",""id"":""1020""},{""label"":""CHAT"",""id"":""1103""},{""label"":""CLOCK"",""id"":""9575""},{""label"":""CTSD"",""id"":""1509""},{""label"":""CYP19A1"",""id"":""1588""},{""label"":""CYP46A1"",""id"":""10858""},{""label"":""DLST"",""id"":""1743""},{""label"":""ECE1"",""id"":""1889""},{""label"":""EIF2AK2"",""id"":""5610""},{""label"":""EIF2S1"",""id"":""1965""},{""label"":""ENO1"",""id"":""2023""},{""label"":""EPO"",""id"":""2056""},{""label"":""ESR1"",""id"":""2099""},{""label"":""FAS"",""id"":""355""},{""label"":""GAPDH"",""id"":""2597""},{""label"":""GAPDHS"",""id"":""26330""},{""label"":""GCG"",""id"":""2641""},{""label"":""GLUL"",""id"":""2752""},{""label"":""GRIN2B"",""id"":""2904""},{""label"":""GRN"",""id"":""2896""},{""label"":""GSK3B"",""id"":""2932""},{""label"":""GSTO1"",""id"":""9446""},{""label"":""GSTO2"",""id"":""119391""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IGFBP3"",""id"":""3486""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL4"",""id"":""3565""},{""label"":""IL6R"",""id"":""3570""},{""label"":""IREB2"",""id"":""3658""},{""label"":""IRS1"",""id"":""3667""},{""label"":""KCNMA1"",""id"":""3778""},{""label"":""KLK6"",""id"":""5653""},{""label"":""LDLR"",""id"":""3949""},{""label"":""LIPC"",""id"":""3990""},{""label"":""LPL"",""id"":""4023""},{""label"":""LRP1"",""id"":""4035""},{""label"":""LRP8"",""id"":""7804""},{""label"":""LRPAP1"",""id"":""4043""},{""label"":""MAOA"",""id"":""4128""},{""label"":""MAPT"",""id"":""4137""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MCM2"",""id"":""4171""},{""label"":""MME"",""id"":""4311""},{""label"":""NCSTN"",""id"":""23385""},{""label"":""NECTIN2"",""id"":""5819""},{""label"":""NEFM"",""id"":""4741""},{""label"":""NFE2L2"",""id"":""4780""},{""label"":""NGFR"",""id"":""4804""},{""label"":""NOS1"",""id"":""4842""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NTF3"",""id"":""4908""},{""label"":""NTRK1"",""id"":""4914""},{""label"":""NTRK2"",""id"":""4915""},{""label"":""PARP1"",""id"":""142""},{""label"":""PCK1"",""id"":""5105""},{""label"":""PLAU"",""id"":""5328""},{""label"":""PON1"",""id"":""5444""},{""label"":""PON2"",""id"":""5445""},{""label"":""PON3"",""id"":""5446""},{""label"":""PPARA"",""id"":""5465""},{""label"":""PPARG"",""id"":""5468""},{""label"":""SERPINE2"",""id"":""5270""},{""label"":""SNCA"",""id"":""6622""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SORL1"",""id"":""6653""},{""label"":""STAT3"",""id"":""6774""},{""label"":""TFAM"",""id"":""7019""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""},{""label"":""TPH1"",""id"":""7166""},{""label"":""TTR"",""id"":""7276""},{""label"":""UQCRC1"",""id"":""7384""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""VLDLR"",""id"":""7436""},{""label"":""XRN1"",""id"":""54464""}]"	"[""1020"",""10858"",""1103"",""119391"",""142"",""148"",""1509"",""155"",""1588"",""1743"",""177"",""18"",""185"",""1889"",""19"",""1965"",""2"",""2023"",""2056"",""2099"",""217"",""23385"",""23621"",""25825"",""2597"",""26330"",""2641"",""2752"",""2896"",""2904"",""2932"",""3077"",""3123"",""3156"",""322"",""3303"",""3304"",""335"",""337"",""3383"",""348"",""3486"",""351"",""355"",""3552"",""3558"",""3565"",""3570"",""3586"",""3658"",""3667"",""3778"",""3949"",""3990"",""4023"",""4035"",""4043"",""4128"",""4137"",""4153"",""4171"",""43"",""4311"",""4741"",""4780"",""4804"",""4842"",""4846"",""4908"",""4914"",""4915"",""5105"",""5270"",""5328"",""5444"",""5445"",""5446"",""54464"",""5465"",""5468"",""5610"",""5653"",""5819"",""590"",""627"",""6622"",""6648"",""6653"",""6774"",""6868"",""7019"",""7099"",""7124"",""7166"",""717"",""718"",""7276"",""7384"",""7422"",""7436"",""7804"",""840"",""9446"",""9575""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10652""}]"
DOID:1067	"[""open-angle glaucoma"",""Wide-angle glaucoma"",""glaucoma simplex"",""open angle glaucoma"",""pigmentary glaucoma""]"	"[{""label"":""Myoc"",""id"":""17926""}]"	"[""17926""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1067""}]"
DOID:1067	"[""open-angle glaucoma"",""Wide-angle glaucoma"",""glaucoma simplex"",""open angle glaucoma"",""pigmentary glaucoma""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""APOE"",""id"":""348""},{""label"":""GMDS"",""id"":""2762""},{""label"":""MYOC"",""id"":""4653""},{""label"":""OPTN"",""id"":""10133""},{""label"":""PON1"",""id"":""5444""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TNF"",""id"":""7124""}]"	"[""10133"",""154"",""2762"",""348"",""4653"",""5444"",""6890"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1067""}]"
DOID:1068	"[""juvenile glaucoma"",""Glaucoma of childhood""]"	"[{""label"":""MYOC"",""id"":""4653""}]"	"[""4653""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1068""}]"
DOID:1070	"[""primary open angle glaucoma"",""chronic simple glaucoma""]"	"[{""label"":""Gucy1a1"",""id"":""60596""}]"	"[""60596""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1070""}]"
DOID:1070	"[""primary open angle glaucoma"",""chronic simple glaucoma""]"	"[{""label"":""ACVR1"",""id"":""90""},{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""ADRB2"",""id"":""154""},{""label"":""APOE"",""id"":""348""},{""label"":""COL6A3"",""id"":""1293""},{""label"":""CYP1B1"",""id"":""1545""},{""label"":""LAMB2"",""id"":""3913""},{""label"":""LOXL1"",""id"":""4016""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MYOC"",""id"":""4653""},{""label"":""NOS3"",""id"":""4846""},{""label"":""OGG1"",""id"":""4968""},{""label"":""OPTN"",""id"":""10133""},{""label"":""PON1"",""id"":""5444""},{""label"":""SOD2"",""id"":""6648""},{""label"":""THBS1"",""id"":""7057""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""},{""label"":""TP53"",""id"":""7157""},{""label"":""WDR36"",""id"":""134430""}]"	"[""10133"",""1293"",""134430"",""154"",""1545"",""348"",""3913"",""4016"",""4312"",""4653"",""4846"",""4968"",""5444"",""6648"",""7057"",""7099"",""7124"",""7157"",""90"",""9370""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1070""}]"
DOID:1073	"[""renal hypertension""]"	"[{""label"":""Mmp2"",""id"":""81686""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Nos3"",""id"":""24600""}]"	"[""24600"",""81686"",""81687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1073""}]"
DOID:1073	"[""renal hypertension""]"	"[{""label"":""CYP2C8"",""id"":""1558""},{""label"":""CYP2J2"",""id"":""1573""},{""label"":""HSPA8"",""id"":""3312""},{""label"":""NPPA"",""id"":""4878""}]"	"[""1558"",""1573"",""3312"",""4878""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1073""}]"
DOID:1074	"[""kidney failure"",""renal failure""]"	"[{""label"":""Kl"",""id"":""83504""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Tbxa2r"",""id"":""24816""}]"	"[""24816"",""83504"",""83516""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1074""}]"
DOID:1074	"[""kidney failure"",""renal failure""]"	"[{""label"":""DRD1"",""id"":""1812""},{""label"":""GFER"",""id"":""2671""}]"	"[""1812"",""2671""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1074""}]"
DOID:10754	"[""otitis media""]"	"[{""label"":""Bpifa1"",""id"":""18843""},{""label"":""Dnah5"",""id"":""110082""},{""label"":""Enpp1"",""id"":""18605""},{""label"":""Eya4"",""id"":""14051""},{""label"":""Fgfr1"",""id"":""14182""},{""label"":""Idua"",""id"":""15932""},{""label"":""Lmna"",""id"":""16905""},{""label"":""Naglu"",""id"":""27419""},{""label"":""Phex"",""id"":""18675""},{""label"":""Sall4"",""id"":""99377""},{""label"":""Sh3pxd2b"",""id"":""268396""}]"	"[""110082"",""14051"",""14182"",""15932"",""16905"",""18605"",""18675"",""18843"",""268396"",""27419"",""99377""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10754""}]"
DOID:10754	"[""otitis media""]"	"[{""label"":""A2ML1"",""id"":""144568""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL6"",""id"":""3569""},{""label"":""MBL2"",""id"":""4153""}]"	"[""144568"",""3569"",""3586"",""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10754""}]"
DOID:10762	"[""portal hypertension""]"	"[{""label"":""Angpt2"",""id"":""89805""},{""label"":""Avp"",""id"":""24221""},{""label"":""Bdkrb2"",""id"":""25245""},{""label"":""Ednra"",""id"":""24326""},{""label"":""Ednrb"",""id"":""50672""},{""label"":""Nos1"",""id"":""24598""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Pik3r1"",""id"":""25513""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Tnf"",""id"":""24835""}]"	"[""24221"",""24326"",""24598"",""24600"",""24835"",""25245"",""25513"",""29527"",""50672"",""89805""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10762""}]"
DOID:10762	"[""portal hypertension""]"	"[{""label"":""REN"",""id"":""5972""},{""label"":""TMEM67"",""id"":""91147""},{""label"":""VASH1"",""id"":""22846""}]"	"[""22846"",""5972"",""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10762""}]"
DOID:10763	"[""hypertension"",""HTN"",""hyperpiesia"",""vascular hypertensive disorder""]"	"[{""label"":""ABCC8"",""id"":""6833""},{""label"":""ABO"",""id"":""28""},{""label"":""ACE2"",""id"":""59272""},{""label"":""ACE"",""id"":""1636""},{""label"":""ADD1"",""id"":""118""},{""label"":""ADD2"",""id"":""119""},{""label"":""ADRA1A"",""id"":""148""},{""label"":""ADRB1"",""id"":""153""},{""label"":""ADRB2"",""id"":""154""},{""label"":""ADRB3"",""id"":""155""},{""label"":""AGT"",""id"":""183""},{""label"":""AGTR1"",""id"":""185""},{""label"":""ALDH2"",""id"":""217""},{""label"":""ANGPT1"",""id"":""284""},{""label"":""ATP1A2"",""id"":""477""},{""label"":""AVPR1A"",""id"":""552""},{""label"":""BDKRB1"",""id"":""623""},{""label"":""BDKRB2"",""id"":""624""},{""label"":""BRCA1"",""id"":""672""},{""label"":""CACNB2"",""id"":""783""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CD14"",""id"":""929""},{""label"":""CHGA"",""id"":""1113""},{""label"":""CLCNKB"",""id"":""1188""},{""label"":""CLU"",""id"":""1191""},{""label"":""COL6A3"",""id"":""1293""},{""label"":""COMT"",""id"":""1312""},{""label"":""CORIN"",""id"":""10699""},{""label"":""CYP11B2"",""id"":""1585""},{""label"":""CYP2C9"",""id"":""1559""},{""label"":""CYP2J2"",""id"":""1573""},{""label"":""CYP2R1"",""id"":""120227""},{""label"":""CYP4A11"",""id"":""1579""},{""label"":""DBH"",""id"":""1621""},{""label"":""DRD1"",""id"":""1812""},{""label"":""DRD2"",""id"":""1813""},{""label"":""ECE1"",""id"":""1889""},{""label"":""EDN1"",""id"":""1906""},{""label"":""EDN2"",""id"":""1907""},{""label"":""EDNRA"",""id"":""1909""},{""label"":""EPHX2"",""id"":""2053""},{""label"":""F11R"",""id"":""50848""},{""label"":""F7"",""id"":""2155""},{""label"":""FTO"",""id"":""79068""},{""label"":""GCK"",""id"":""2645""},{""label"":""GLCE"",""id"":""26035""},{""label"":""GNAS"",""id"":""2778""},{""label"":""GPX3"",""id"":""2878""},{""label"":""HGF"",""id"":""3082""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HP"",""id"":""3240""},{""label"":""HSD11B1"",""id"":""3290""},{""label"":""HSD11B2"",""id"":""3291""},{""label"":""HSD3B1"",""id"":""3283""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL6"",""id"":""3569""},{""label"":""INPPL1"",""id"":""3636""},{""label"":""INVS"",""id"":""27130""},{""label"":""ITGA9"",""id"":""3680""},{""label"":""KCNMB1"",""id"":""3779""},{""label"":""KDR"",""id"":""3791""},{""label"":""KLK1"",""id"":""3816""},{""label"":""LEP"",""id"":""3952""},{""label"":""LEPR"",""id"":""3953""},{""label"":""LOX"",""id"":""4015""},{""label"":""LPL"",""id"":""4023""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP2"",""id"":""4313""},{""label"":""MMP9"",""id"":""4318""},{""label"":""MOV10"",""id"":""4343""},{""label"":""MTR"",""id"":""4548""},{""label"":""NOS2"",""id"":""4843""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NPHP3"",""id"":""27031""},{""label"":""NPPB"",""id"":""4879""},{""label"":""NPPC"",""id"":""4880""},{""label"":""NPR3"",""id"":""4883""},{""label"":""OGG1"",""id"":""4968""},{""label"":""PON1"",""id"":""5444""},{""label"":""PPARG"",""id"":""5468""},{""label"":""PRLHR"",""id"":""2834""},{""label"":""PTGIS"",""id"":""5740""},{""label"":""PTPRD"",""id"":""5789""},{""label"":""RAMP2"",""id"":""10266""},{""label"":""REN"",""id"":""5972""},{""label"":""SLC6A2"",""id"":""6530""},{""label"":""SLC8A1"",""id"":""6546""},{""label"":""SOD1"",""id"":""6647""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TNF"",""id"":""7124""},{""label"":""TRHR"",""id"":""7201""},{""label"":""UCP2"",""id"":""7351""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""WNK1"",""id"":""65125""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10266"",""10699"",""1113"",""118"",""1188"",""119"",""1191"",""120227"",""1234"",""1293"",""1312"",""148"",""153"",""154"",""155"",""1559"",""1573"",""1579"",""1585"",""1621"",""1636"",""1812"",""1813"",""183"",""185"",""1889"",""1906"",""1907"",""1909"",""2053"",""2155"",""217"",""26035"",""2645"",""27031"",""27130"",""2778"",""28"",""2834"",""284"",""2878"",""3082"",""3117"",""3240"",""3283"",""3290"",""3291"",""3356"",""3557"",""3569"",""3636"",""3680"",""3779"",""3791"",""3816"",""3952"",""3953"",""4015"",""4023"",""4312"",""4313"",""4318"",""4343"",""4548"",""477"",""4843"",""4846"",""4879"",""4880"",""4883"",""4968"",""50848"",""5444"",""5468"",""552"",""5740"",""5789"",""59272"",""5972"",""623"",""624"",""65125"",""6530"",""6546"",""6647"",""6648"",""672"",""6833"",""7124"",""7201"",""7351"",""7422"",""7515"",""783"",""79068"",""929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10763""}]"
DOID:10763	"[""hypertension"",""HTN"",""hyperpiesia"",""vascular hypertensive disorder""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Add1"",""id"":""24170""},{""label"":""Adora1"",""id"":""29290""},{""label"":""Agt"",""id"":""24179""},{""label"":""Agtr1a"",""id"":""24180""},{""label"":""Agtr2"",""id"":""24182""},{""label"":""Akt1"",""id"":""24185""},{""label"":""Atf2"",""id"":""81647""},{""label"":""Avpr2"",""id"":""25108""},{""label"":""Bdkrb1"",""id"":""81509""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Cnr1"",""id"":""25248""},{""label"":""Comt"",""id"":""24267""},{""label"":""Creb1"",""id"":""81646""},{""label"":""Crhr1"",""id"":""58959""},{""label"":""Drd3"",""id"":""29238""},{""label"":""Ednra"",""id"":""24326""},{""label"":""Ednrb"",""id"":""50672""},{""label"":""Esr2"",""id"":""25149""},{""label"":""Glp1r"",""id"":""25051""},{""label"":""Hrh3"",""id"":""85268""},{""label"":""Il1rn"",""id"":""60582""},{""label"":""Ins2"",""id"":""24506""},{""label"":""Kcnmb1"",""id"":""29747""},{""label"":""Kcnq1"",""id"":""84020""},{""label"":""Kl"",""id"":""83504""},{""label"":""Klk1b3"",""id"":""24594""},{""label"":""Lep"",""id"":""25608""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Lipg"",""id"":""291437""},{""label"":""Lrp2"",""id"":""29216""},{""label"":""Mas1"",""id"":""25153""},{""label"":""Mme"",""id"":""24590""},{""label"":""Ngfr"",""id"":""24596""},{""label"":""Nos1"",""id"":""24598""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Nox4"",""id"":""85431""},{""label"":""Npr1"",""id"":""24603""},{""label"":""Pik3r1"",""id"":""25513""},{""label"":""Plcd1"",""id"":""24655""},{""label"":""Ppara"",""id"":""25747""},{""label"":""Pparg"",""id"":""25664""},{""label"":""Prkcb"",""id"":""25023""},{""label"":""Prkcd"",""id"":""170538""},{""label"":""Prkce"",""id"":""29340""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Ren"",""id"":""24715""},{""label"":""S1pr1"",""id"":""29733""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Slc5a2"",""id"":""64522""},{""label"":""Sod2"",""id"":""24787""},{""label"":""Sod3"",""id"":""25352""},{""label"":""Tacr3"",""id"":""24808""},{""label"":""Tgfb1"",""id"":""59086""},{""label"":""Tnf"",""id"":""24835""},{""label"":""Trhr"",""id"":""25570""},{""label"":""Ucp2"",""id"":""54315""},{""label"":""Uts2r"",""id"":""57305""},{""label"":""Vcam1"",""id"":""25361""}]"	"[""170538"",""24170"",""24179"",""24180"",""24182"",""24185"",""24267"",""24310"",""24326"",""24506"",""24536"",""24590"",""24594"",""24596"",""24598"",""24600"",""24603"",""24617"",""24655"",""24715"",""24770"",""24787"",""24808"",""24835"",""25023"",""25051"",""25108"",""25149"",""25153"",""25248"",""25352"",""25361"",""25513"",""25570"",""25608"",""25664"",""25747"",""291437"",""29216"",""29238"",""29290"",""29340"",""29527"",""29733"",""29747"",""50672"",""54315"",""57305"",""58959"",""59086"",""60582"",""64522"",""81509"",""81646"",""81647"",""83504"",""84020"",""85268"",""85431""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10763""}]"
DOID:10772	"[""thrombotic thrombocytopenic purpura"",""Moschcowitz's syndrome""]"	"[{""label"":""ADAMTS13"",""id"":""11093""},{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""11093"",""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10772""}]"
DOID:10783	"[""methemoglobinemia""]"	"[{""label"":""CYB5R3"",""id"":""1727""}]"	"[""1727""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10783""}]"
DOID:10808	"[""gastric ulcer"",""acute gastric ulcer with haemorrhage and perforation"",""acute gastric ulcer with hemorrhage AND with perforation but without obstruction"",""acute gastric ulcer with hemorrhage and obstruction"",""acute gastric ulcer with hemorrhage and perforation"",""acute gastric ulcer with hemorrhage and perforation, with obstruction"",""acute gastric ulcer with hemorrhage and perforation, without mention of obstruction"",""acute gastric ulcer with hemorrhage, with obstruction"",""acute gastric ulcer with hemorrhage, with perforation AND with obstruction"",""acute gastric ulcer with perforation"",""acute gastric ulcer with perforation AND obstruction"",""acute gastric ulcer with perforation, with obstruction"",""acute gastric ulcer without hemorrhage and without perforation"",""acute gastric ulcer without hemorrhage, without perforation AND without obstruction"",""acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction"",""bleeding acute gastric ulcer"",""chronic gastric ulcer without hemorrhage AND without perforation"",""chronic gastric ulcer without hemorrhage AND without perforation but with obstruction"",""chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction""]"	"[{""label"":""Agt"",""id"":""24179""},{""label"":""Bad"",""id"":""64639""},{""label"":""Cftr"",""id"":""24255""},{""label"":""Hrh3"",""id"":""85268""},{""label"":""Oxtr"",""id"":""25342""},{""label"":""Ptger1"",""id"":""25637""},{""label"":""Ptgs2"",""id"":""29527""}]"	"[""24179"",""24255"",""25342"",""25637"",""29527"",""64639"",""85268""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10808""}]"
DOID:10811	"[""nasal cavity cancer"",""malignant neoplasm of nasal cavities"",""malignant tumor of the nasal cavity""]"	"[{""label"":""SOX2"",""id"":""6657""},{""label"":""TP53"",""id"":""7157""}]"	"[""6657"",""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10811""}]"
DOID:10825	"[""essential hypertension"",""idiopathic hypertension"",""primary hypertension""]"	"[{""label"":""Nos3"",""id"":""18127""}]"	"[""18127""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10825""}]"
DOID:10825	"[""essential hypertension"",""idiopathic hypertension"",""primary hypertension""]"	"[{""label"":""ADD1"",""id"":""118""},{""label"":""AGTR1"",""id"":""185""},{""label"":""ATP1B1"",""id"":""481""},{""label"":""ATP2A2"",""id"":""488""},{""label"":""CAT"",""id"":""847""},{""label"":""CYP3A5"",""id"":""1577""},{""label"":""ECE1"",""id"":""1889""},{""label"":""FTO"",""id"":""79068""},{""label"":""HSD11B1"",""id"":""3290""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NPR2"",""id"":""4882""},{""label"":""PTGIS"",""id"":""5740""},{""label"":""PTPN1"",""id"":""5770""},{""label"":""REN"",""id"":""5972""},{""label"":""SLC12A3"",""id"":""6559""}]"	"[""118"",""1577"",""185"",""1889"",""3290"",""481"",""4846"",""488"",""4882"",""5740"",""5770"",""5972"",""6559"",""79068"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10825""}]"
DOID:10871	"[""age related macular degeneration"",""Age Related Maculopathies"",""Age Related Maculopathy"",""Senile macular degeneration"",""Senile macular retinal degeneration"",""age-related macular degeneration""]"	"[{""label"":""Ccl2"",""id"":""20296""},{""label"":""Cd46"",""id"":""17221""},{""label"":""Ppargc1a"",""id"":""19017""}]"	"[""17221"",""19017"",""20296""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10871""}]"
DOID:10871	"[""age related macular degeneration"",""Age Related Maculopathies"",""Age Related Maculopathy"",""Senile macular degeneration"",""Senile macular retinal degeneration"",""age-related macular degeneration""]"	"[{""label"":""FBLN5"",""id"":""10516""}]"	"[""10516""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10871""}]"
DOID:10873	"[""Kuhnt-Junius degeneration"",""Exudative senile macular degeneration of retina"",""Neovascular age-related macular degeneration"",""Senile macular degeneration, wet"",""Wet senile macular retinal degeneration""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""C3"",""id"":""718""},{""label"":""CFI"",""id"":""3426""},{""label"":""ELN"",""id"":""2006""},{""label"":""FLT1"",""id"":""2321""},{""label"":""KDR"",""id"":""3791""},{""label"":""LOXL1"",""id"":""4016""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PON1"",""id"":""5444""},{""label"":""SOD2"",""id"":""6648""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""2006"",""2321"",""3426"",""348"",""3791"",""4016"",""4846"",""5444"",""6648"",""718"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10873""}]"
DOID:10881	"[""hand, foot and mouth disease"",""HFMD"",""Vesicular stomatitis and exanthem""]"	"[{""label"":""REN"",""id"":""5972""}]"	"[""5972""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10881""}]"
DOID:10887	"[""lepromatous leprosy"",""type L leprosy""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""MBL2"",""id"":""4153""}]"	"[""3117"",""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10887""}]"
DOID:10892	"[""hypospadias"",""familial hypospadias""]"	"[{""label"":""AR"",""id"":""367""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""HSD3B2"",""id"":""3284""},{""label"":""MAMLD1"",""id"":""10046""},{""label"":""SRD5A2"",""id"":""6716""}]"	"[""10046"",""1543"",""3284"",""367"",""6716""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10892""}]"
DOID:10907	"[""microcephaly"",""Microcephalus"",""microencephaly""]"	"[{""label"":""Tubb5"",""id"":""22154""}]"	"[""22154""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10907""}]"
DOID:10907	"[""microcephaly"",""Microcephalus"",""microencephaly""]"	"[{""label"":""mfsd2aa"",""id"":""492810""}]"	"[""492810""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10907""}]"
DOID:10907	"[""microcephaly"",""Microcephalus"",""microencephaly""]"	"[{""label"":""CDK5RAP2"",""id"":""55755""},{""label"":""EFTUD2"",""id"":""9343""},{""label"":""NSD1"",""id"":""64324""},{""label"":""SLC25A19"",""id"":""60386""},{""label"":""TUBA1A"",""id"":""7846""}]"	"[""55755"",""60386"",""64324"",""7846"",""9343""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10907""}]"
DOID:10907	"[""microcephaly"",""Microcephalus"",""microencephaly""]"	"[{""label"":""Sas-4"",""id"":""40859""}]"	"[""40859""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10907""}]"
DOID:10908	"[""hydrocephalus"",""hydrocephalus, X-linked"",""hydrocephalus, nonsyndromic, autosomal recessive""]"	"[{""label"":""Add1"",""id"":""11518""},{""label"":""Celsr2"",""id"":""53883""},{""label"":""Mboat7"",""id"":""77582""},{""label"":""Pomk"",""id"":""74653""},{""label"":""Trim71"",""id"":""636931""}]"	"[""11518"",""53883"",""636931"",""74653"",""77582""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10908""}]"
DOID:10908	"[""hydrocephalus"",""hydrocephalus, X-linked"",""hydrocephalus, nonsyndromic, autosomal recessive""]"	"[{""label"":""Itgb1"",""id"":""24511""},{""label"":""L1cam"",""id"":""50687""}]"	"[""24511"",""50687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10908""}]"
DOID:10908	"[""hydrocephalus"",""hydrocephalus, X-linked"",""hydrocephalus, nonsyndromic, autosomal recessive""]"	"[{""label"":""CCDC88C"",""id"":""440193""},{""label"":""L1CAM"",""id"":""3897""},{""label"":""MPDZ"",""id"":""8777""},{""label"":""SMARCC1"",""id"":""6599""}]"	"[""3897"",""440193"",""6599"",""8777""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10908""}]"
DOID:10914	"[""amnestic disorder"",""Amnestic syndrome"",""Korsakoff's psychosis or syndrome"",""amnesia""]"	"[{""label"":""Creb1"",""id"":""81646""},{""label"":""Drd3"",""id"":""29238""},{""label"":""Hrh3"",""id"":""85268""},{""label"":""Htr7"",""id"":""65032""}]"	"[""29238"",""65032"",""81646"",""85268""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10914""}]"
DOID:10923	"[""sickle cell anemia"",""Hb SC disease"",""Hb-S/Hb-C disease"",""Hb-SS disease without crisis"",""HbSS disease"",""Hemoglobin S disease without crisis"",""Sickle-cell/Hb-C disease without crisis"",""drepanocytosis"",""haemoglobin SC disease"",""hemoglobin SC disease"",""homozygous sickle cell disease"",""sickle cell anaemia""]"	"[{""label"":""Spta1"",""id"":""20739""}]"	"[""20739""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10923""}]"
DOID:10923	"[""sickle cell anemia"",""Hb SC disease"",""Hb-S/Hb-C disease"",""Hb-SS disease without crisis"",""HbSS disease"",""Hemoglobin S disease without crisis"",""Sickle-cell/Hb-C disease without crisis"",""drepanocytosis"",""haemoglobin SC disease"",""hemoglobin SC disease"",""homozygous sickle cell disease"",""sickle cell anaemia""]"	"[{""label"":""APOB"",""id"":""338""},{""label"":""BCL11A"",""id"":""53335""},{""label"":""C3"",""id"":""718""},{""label"":""CFB"",""id"":""629""},{""label"":""CYP2C19"",""id"":""1557""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HBB"",""id"":""3043""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""NOS3"",""id"":""4846""}]"	"[""1557"",""2876"",""3043"",""3119"",""338"",""4846"",""53335"",""629"",""718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10923""}]"
DOID:10930	"[""borderline personality disorder""]"	"[{""label"":""TPH1"",""id"":""7166""}]"	"[""7166""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10930""}]"
DOID:10933	"[""obsessive-compulsive disorder"",""Anancastic neurosis"",""obsessive compulsive disorder""]"	"[{""label"":""BDNF"",""id"":""627""},{""label"":""COMT"",""id"":""1312""},{""label"":""HRAS"",""id"":""3265""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""SLC6A4"",""id"":""6532""}]"	"[""1312"",""3265"",""3356"",""627"",""6532""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10933""}]"
DOID:10933	"[""obsessive-compulsive disorder"",""Anancastic neurosis"",""obsessive compulsive disorder""]"	"[{""label"":""Creb1"",""id"":""81646""}]"	"[""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10933""}]"
DOID:10937	"[""impulse control disorder""]"	"[{""label"":""PRL"",""id"":""5617""}]"	"[""5617""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10937""}]"
DOID:10939	"[""antisocial personality disorder"",""Asocial personality"",""Dissocial personality disorder"",""Psychopath.personality"",""Psychopathic personality"",""Psychopathic personality disorder"",""sociopathic personality""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""DRD4"",""id"":""1815""},{""label"":""HTR1B"",""id"":""3351""}]"	"[""1815"",""3351"",""5243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10939""}]"
DOID:1094	"[""attention deficit hyperactivity disorder"",""ADHD"",""attention deficit disorder"",""hyperkinetic disorder""]"	"[{""label"":""Cirl"",""id"":""35846""},{""label"":""DAT"",""id"":""36849""}]"	"[""35846"",""36849""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1094""}]"
DOID:1094	"[""attention deficit hyperactivity disorder"",""ADHD"",""attention deficit disorder"",""hyperkinetic disorder""]"	"[{""label"":""Grin2b"",""id"":""24410""}]"	"[""24410""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1094""}]"
DOID:1094	"[""attention deficit hyperactivity disorder"",""ADHD"",""attention deficit disorder"",""hyperkinetic disorder""]"	"[{""label"":""Adgrl3"",""id"":""319387""},{""label"":""Brinp1"",""id"":""56710""},{""label"":""Cdh2"",""id"":""12558""},{""label"":""Chrnb2"",""id"":""11444""},{""label"":""Csnk1d"",""id"":""104318""},{""label"":""Git1"",""id"":""216963""},{""label"":""Per1"",""id"":""18626""},{""label"":""Ptchd1"",""id"":""211612""},{""label"":""Slc6a3"",""id"":""13162""},{""label"":""Snap25"",""id"":""20614""},{""label"":""Tacr1"",""id"":""21336""}]"	"[""104318"",""11444"",""12558"",""13162"",""18626"",""20614"",""211612"",""21336"",""216963"",""319387"",""56710""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1094""}]"
DOID:1094	"[""attention deficit hyperactivity disorder"",""ADHD"",""attention deficit disorder"",""hyperkinetic disorder""]"	"[{""label"":""ADRA2A"",""id"":""150""},{""label"":""AR"",""id"":""367""},{""label"":""BAIAP2"",""id"":""10458""},{""label"":""CALY"",""id"":""50632""},{""label"":""COMT"",""id"":""1312""},{""label"":""DBH"",""id"":""1621""},{""label"":""DOCK3"",""id"":""1795""},{""label"":""DRD4"",""id"":""1815""},{""label"":""DRD5"",""id"":""1816""},{""label"":""FOXP2"",""id"":""93986""},{""label"":""GIT1"",""id"":""28964""},{""label"":""GRM8"",""id"":""2918""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""HTR1B"",""id"":""3351""},{""label"":""SLC6A3"",""id"":""6531""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""TPH1"",""id"":""7166""},{""label"":""UST"",""id"":""10090""}]"	"[""10090"",""10458"",""1312"",""150"",""1621"",""1795"",""1815"",""1816"",""28964"",""2918"",""3156"",""3351"",""367"",""50632"",""6531"",""6532"",""7166"",""93986""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1094""}]"
DOID:10941	"[""intracranial aneurysm"",""brain aneurysm""]"	"[{""label"":""COL1A2"",""id"":""1278""},{""label"":""COL22A1"",""id"":""169044""},{""label"":""ENG"",""id"":""2022""},{""label"":""IL6"",""id"":""3569""},{""label"":""KMT2D"",""id"":""8085""},{""label"":""MMP2"",""id"":""4313""},{""label"":""MMP9"",""id"":""4318""},{""label"":""PKD1"",""id"":""5310""},{""label"":""PKD2"",""id"":""5311""},{""label"":""VCAN"",""id"":""1462""}]"	"[""1278"",""1462"",""169044"",""2022"",""3569"",""4313"",""4318"",""5310"",""5311"",""8085""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10941""}]"
DOID:10941	"[""intracranial aneurysm"",""brain aneurysm""]"	"[{""label"":""Ccl2"",""id"":""24770""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Tnf"",""id"":""24835""}]"	"[""24770"",""24835"",""81687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10941""}]"
DOID:10952	"[""nephritis""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PARP1"",""id"":""142""},{""label"":""SNRPD1"",""id"":""6632""}]"	"[""142"",""1636"",""4846"",""6632""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10952""}]"
DOID:10952	"[""nephritis""]"	"[{""label"":""Agtr1a"",""id"":""24180""},{""label"":""Cxcr2"",""id"":""29385""},{""label"":""Icam1"",""id"":""25464""}]"	"[""24180"",""25464"",""29385""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10952""}]"
DOID:10964	"[""cholesteatoma of middle ear"",""Cholesteatoma of middle ear and mastoid"",""Cholesteatoma of middle ear and/or mastoid"",""Cholesteatoma of the middle ear"",""Epidermosis of ear"",""Epidermosis of middle ear"",""middle ear cholesteatoma""]"	"[{""label"":""IL2"",""id"":""3558""}]"	"[""3558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10964""}]"
DOID:10966	"[""lipoid nephrosis"",""Minimal Change Glomerulonephritis"",""Minimal change disease"",""Nephrotic syndrome with lesion of minimal change glomerulonephritis"",""Nephrotic syndrome with lesion of minimal change nephrotic syndrome""]"	"[{""label"":""Il13"",""id"":""116553""}]"	"[""116553""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10966""}]"
DOID:10966	"[""lipoid nephrosis"",""Minimal Change Glomerulonephritis"",""Minimal change disease"",""Nephrotic syndrome with lesion of minimal change glomerulonephritis"",""Nephrotic syndrome with lesion of minimal change nephrotic syndrome""]"	"[{""label"":""STAT6"",""id"":""6778""}]"	"[""6778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10966""}]"
DOID:10976	"[""membranous glomerulonephritis"",""membranous nephropathy""]"	"[{""label"":""CFB"",""id"":""629""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""MME"",""id"":""4311""}]"	"[""3117"",""4311"",""629""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10976""}]"
DOID:10976	"[""membranous glomerulonephritis"",""membranous nephropathy""]"	"[{""label"":""C3"",""id"":""24232""},{""label"":""Lrpap1"",""id"":""116565""}]"	"[""116565"",""24232""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10976""}]"
DOID:1098	"[""hemolytic disease of the fetus"",""EF - Erythroblastosis foetalis"",""Haemolytic disease due to rhesus isoimmunisation"",""Hemolytic disease of the fetus and newborn"",""alloimmune HDFN"",""erythroblastosis fetalis"",""fetal erythroblastosis"",""rhesus isoimmunisation of the newborn""]"	"[{""label"":""FCGR2A"",""id"":""2212""}]"	"[""2212""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1098""}]"
DOID:10983	"[""Alport syndrome"",""Hereditary Nephritis""]"	"[{""label"":""COL4A3"",""id"":""1285""},{""label"":""COL4A5"",""id"":""1287""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""1285"",""1287"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:10983""}]"
DOID:1099	"[""alpha thalassemia"",""Alpha thalassaemia"",""alpha-Thalassemia""]"	"[{""label"":""GPX1"",""id"":""2876""},{""label"":""HBA1"",""id"":""3039""},{""label"":""HBA2"",""id"":""3040""},{""label"":""HBB"",""id"":""3043""}]"	"[""2876"",""3039"",""3040"",""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1099""}]"
DOID:110	"[""lens disease""]"	"[{""label"":""Adamtsl4"",""id"":""229595""}]"	"[""229595""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:110""}]"
DOID:11044	"[""gastroschisis""]"	"[{""label"":""Lrp1"",""id"":""16971""}]"	"[""16971""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11044""}]"
DOID:11044	"[""gastroschisis""]"	"[{""label"":""ADD1"",""id"":""118""}]"	"[""118""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11044""}]"
DOID:11049	"[""meconium aspiration syndrome"",""Neonatal aspiration of meconium"",""meconium aspiration""]"	"[{""label"":""Agtr2"",""id"":""24182""}]"	"[""24182""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11049""}]"
DOID:11049	"[""meconium aspiration syndrome"",""Neonatal aspiration of meconium"",""meconium aspiration""]"	"[{""label"":""Atf2"",""id"":""11909""}]"	"[""11909""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11049""}]"
DOID:11054	"[""urinary bladder cancer"",""bladder cancer"",""tumor of the bladder""]"	"[{""label"":""AMACR"",""id"":""23600""},{""label"":""APEX1"",""id"":""328""},{""label"":""BRCA1"",""id"":""672""},{""label"":""CASP9"",""id"":""842""},{""label"":""CDC25A"",""id"":""993""},{""label"":""CDH13"",""id"":""1012""},{""label"":""CHEK2"",""id"":""11200""},{""label"":""CXCR2"",""id"":""3579""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2C9"",""id"":""1559""},{""label"":""ERBB2"",""id"":""2064""},{""label"":""FAS"",""id"":""355""},{""label"":""FASLG"",""id"":""356""},{""label"":""FGFR2"",""id"":""2263""},{""label"":""FGFR3"",""id"":""2261""},{""label"":""HRAS"",""id"":""3265""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL2"",""id"":""3558""},{""label"":""KDR"",""id"":""3791""},{""label"":""KRAS"",""id"":""3845""},{""label"":""MAP2K4"",""id"":""6416""},{""label"":""MGMT"",""id"":""4255""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MRE11"",""id"":""4361""},{""label"":""MSH2"",""id"":""4436""},{""label"":""MTR"",""id"":""4548""},{""label"":""MUC5B"",""id"":""727897""},{""label"":""MYC"",""id"":""4609""},{""label"":""NAT2"",""id"":""10""},{""label"":""PLAU"",""id"":""5328""},{""label"":""PLK1"",""id"":""5347""},{""label"":""PTEN"",""id"":""5728""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""RB1"",""id"":""5925""},{""label"":""RUNX3"",""id"":""864""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""TERT"",""id"":""7015""},{""label"":""TGFBR1"",""id"":""7046""},{""label"":""TIMP3"",""id"":""7078""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TMEFF2"",""id"":""23671""},{""label"":""TNFRSF10A"",""id"":""8797""},{""label"":""WIF1"",""id"":""11197""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10"",""1012"",""11197"",""11200"",""1543"",""1559"",""2064"",""2261"",""2263"",""23600"",""23671"",""3265"",""328"",""3303"",""355"",""3557"",""3558"",""356"",""3579"",""3791"",""3845"",""4255"",""4312"",""4361"",""4436"",""4548"",""4609"",""5054"",""5328"",""5347"",""5728"",""5743"",""5925"",""6416"",""6556"",""672"",""7015"",""7046"",""7078"",""7097"",""727897"",""7515"",""842"",""864"",""8797"",""993""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11054""}]"
DOID:11054	"[""urinary bladder cancer"",""bladder cancer"",""tumor of the bladder""]"	"[{""label"":""Ctnnb1"",""id"":""12387""},{""label"":""Ncstn"",""id"":""59287""}]"	"[""12387"",""59287""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11054""}]"
DOID:11054	"[""urinary bladder cancer"",""bladder cancer"",""tumor of the bladder""]"	"[{""label"":""Hk1"",""id"":""25058""}]"	"[""25058""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11054""}]"
DOID:1107	"[""esophageal carcinoma"",""cancer of esophagus"",""cancer of oesophagus"",""carcinoma of esophagus"",""carcinoma of oesophagus""]"	"[{""label"":""AKT1"",""id"":""207""},{""label"":""STAT3"",""id"":""6774""}]"	"[""207"",""6774""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1107""}]"
DOID:11105	"[""fundus albipunctatus"",""Pigmentary retinal dystrophy"",""retinitis punctata albescens""]"	"[{""label"":""Mfrp"",""id"":""259172""}]"	"[""259172""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11105""}]"
DOID:11105	"[""fundus albipunctatus"",""Pigmentary retinal dystrophy"",""retinitis punctata albescens""]"	"[{""label"":""PRPH2"",""id"":""5961""},{""label"":""RDH5"",""id"":""5959""},{""label"":""RHO"",""id"":""6010""},{""label"":""RLBP1"",""id"":""6017""}]"	"[""5959"",""5961"",""6010"",""6017""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11105""}]"
DOID:11111	"[""hydronephrosis""]"	"[{""label"":""AGT"",""id"":""183""}]"	"[""183""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11111""}]"
DOID:11119	"[""Gilles de la Tourette syndrome"",""Guinon's disease"",""Psychogenic tics"",""Tourette syndrome"",""motor-verbal tic disorder""]"	"[{""label"":""BAIAP2"",""id"":""10458""},{""label"":""DRD4"",""id"":""1815""},{""label"":""HCN4"",""id"":""10021""},{""label"":""SLITRK1"",""id"":""114798""}]"	"[""10021"",""10458"",""114798"",""1815""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11119""}]"
DOID:11119	"[""Gilles de la Tourette syndrome"",""Guinon's disease"",""Psychogenic tics"",""Tourette syndrome"",""motor-verbal tic disorder""]"	"[{""label"":""Met"",""id"":""17295""},{""label"":""Slc6a3"",""id"":""13162""},{""label"":""Slitrk1"",""id"":""76965""}]"	"[""13162"",""17295"",""76965""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11119""}]"
DOID:11123	"[""IgA vasculitis"",""Allergic purpura"",""Autoimmune purpura"",""HSP"",""Henoch Schoenlein purpura"",""Henoch Scholein purpura"",""Henoch Schonlein purpura"",""Henoch Schönlein purpura"",""Henoch-Schoenlein purpura"",""Henoch-Scholein purpura"",""Henoch-Schonlein purpura"",""Henoch-Schönlein purpura"",""IgAV"",""Purpura, autoimmune"",""immunoglobulin A vasculitis""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGT"",""id"":""183""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CD86"",""id"":""942""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MEFV"",""id"":""4210""},{""label"":""PON1"",""id"":""5444""}]"	"[""1636"",""183"",""3117"",""3557"",""4210"",""5444"",""6347"",""942""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11123""}]"
DOID:11132	"[""prostatic hypertrophy""]"	"[{""label"":""PDGFB"",""id"":""5155""},{""label"":""PDGFD"",""id"":""80310""},{""label"":""SRD5A1"",""id"":""6715""}]"	"[""5155"",""6715"",""80310""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11132""}]"
DOID:11132	"[""prostatic hypertrophy""]"	"[{""label"":""Esr1"",""id"":""24890""},{""label"":""Myc"",""id"":""24577""}]"	"[""24577"",""24890""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11132""}]"
DOID:1115	"[""sarcoma"",""connective and soft tissue neoplasm"",""tumor of soft tissue and skeleton""]"	"[{""label"":""HSPB1"",""id"":""3315""},{""label"":""KNL1"",""id"":""57082""},{""label"":""MDM2"",""id"":""4193""},{""label"":""PDHX"",""id"":""8050""},{""label"":""PTPRB"",""id"":""5787""},{""label"":""SREBF2"",""id"":""6721""},{""label"":""TP53"",""id"":""7157""}]"	"[""3315"",""4193"",""57082"",""5787"",""6721"",""7157"",""8050""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1115""}]"
DOID:1115	"[""sarcoma"",""connective and soft tissue neoplasm"",""tumor of soft tissue and skeleton""]"	"[{""label"":""Tp53"",""id"":""24842""}]"	"[""24842""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1115""}]"
DOID:11151	"[""cholecystolithiasis""]"	"[{""label"":""PLA2G2A"",""id"":""5320""},{""label"":""UGT1A1"",""id"":""54658""}]"	"[""5320"",""54658""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11151""}]"
DOID:11162	"[""respiratory failure"",""acute and chronic respiratory failure"",""acute respiratory Failure"",""acute-on-chronic respiratory failure"",""chronic respiratory failure"",""respiratory insufficiency/failure""]"	"[{""label"":""MBL2"",""id"":""4153""},{""label"":""NUP188"",""id"":""23511""},{""label"":""SFTPB"",""id"":""6439""}]"	"[""23511"",""4153"",""6439""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11162""}]"
DOID:11165	"[""common wart""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11165""}]"
DOID:11166	"[""Human papillomavirus infectious disease"",""HPV""]"	"[{""label"":""ADAR"",""id"":""103""},{""label"":""FGFR3"",""id"":""2261""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""103"",""2261"",""3115"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11166""}]"
DOID:11193	"[""syndactyly"",""symphalangism"",""symphalangy"",""webbing of digits""]"	"[{""label"":""GLI3"",""id"":""2737""}]"	"[""2737""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11193""}]"
DOID:11198	"[""DiGeorge syndrome"",""22q11.2 deletion syndrome"",""DiGeorge sequence"",""DiGeorge's syndrome"",""Pharyngeal pouch syndrome""]"	"[{""label"":""DVL1"",""id"":""1855""},{""label"":""UFD1"",""id"":""7353""}]"	"[""1855"",""7353""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11198""}]"
DOID:11198	"[""DiGeorge syndrome"",""22q11.2 deletion syndrome"",""DiGeorge sequence"",""DiGeorge's syndrome"",""Pharyngeal pouch syndrome""]"	"[{""label"":""Chrd"",""id"":""12667""},{""label"":""Crkl"",""id"":""12929""},{""label"":""Fgf8"",""id"":""14179""},{""label"":""Ndst1"",""id"":""15531""},{""label"":""Plxnd1"",""id"":""67784""},{""label"":""Tgfbr2"",""id"":""21813""},{""label"":""Vegfa"",""id"":""22339""}]"	"[""12667"",""12929"",""14179"",""15531"",""21813"",""22339"",""67784""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11198""}]"
DOID:11199	"[""hypoparathyroidism""]"	"[{""label"":""GATA3"",""id"":""2625""},{""label"":""TBCE"",""id"":""6905""}]"	"[""2625"",""6905""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11199""}]"
DOID:11204	"[""allergic conjunctivitis""]"	"[{""label"":""IL13"",""id"":""3596""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL4R"",""id"":""3566""},{""label"":""TNC"",""id"":""3371""}]"	"[""3371"",""3557"",""3566"",""3596""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11204""}]"
DOID:11204	"[""allergic conjunctivitis""]"	"[{""label"":""Ifng"",""id"":""25712""}]"	"[""25712""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11204""}]"
DOID:11206	"[""opioid abuse""]"	"[{""label"":""Ncam1"",""id"":""24586""}]"	"[""24586""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11206""}]"
DOID:11206	"[""opioid abuse""]"	"[{""label"":""DRD4"",""id"":""1815""},{""label"":""OPRD1"",""id"":""4985""},{""label"":""OPRK1"",""id"":""4986""},{""label"":""OPRM1"",""id"":""4988""}]"	"[""1815"",""4985"",""4986"",""4988""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11206""}]"
DOID:11211	"[""buphthalmos"",""primary congenital glaucoma 3A"",""simple buphthalmos""]"	"[{""label"":""CYP1B1"",""id"":""1545""}]"	"[""1545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11211""}]"
DOID:11211	"[""buphthalmos"",""primary congenital glaucoma 3A"",""simple buphthalmos""]"	"[{""label"":""Tyr"",""id"":""22173""}]"	"[""22173""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11211""}]"
DOID:11212	"[""hydrophthalmos""]"	"[{""label"":""CYP1B1"",""id"":""1545""}]"	"[""1545""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11212""}]"
DOID:1123	"[""spondyloarthropathy"",""spondarthropathy"",""spondylarthrosis""]"	"[{""label"":""Enpp1"",""id"":""18605""},{""label"":""Tnf"",""id"":""21926""}]"	"[""18605"",""21926""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1123""}]"
DOID:1123	"[""spondyloarthropathy"",""spondarthropathy"",""spondylarthrosis""]"	"[{""label"":""COL2A1"",""id"":""1280""},{""label"":""HLA-B"",""id"":""3106""}]"	"[""1280"",""3106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1123""}]"
DOID:11240	"[""appendiceal neoplasm"",""appendix neoplasm"",""neoplasm of appendix""]"	"[{""label"":""DAXX"",""id"":""1616""}]"	"[""1616""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11240""}]"
DOID:11247	"[""disseminated intravascular coagulation"",""DIC"",""Defibrination syndrome"",""Diffuse or disseminated intravascular coagulation""]"	"[{""label"":""F13A1"",""id"":""2162""},{""label"":""F3"",""id"":""2152""},{""label"":""SERPINC1"",""id"":""462""},{""label"":""TFPI"",""id"":""7035""},{""label"":""THBD"",""id"":""7056""}]"	"[""2152"",""2162"",""462"",""7035"",""7056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11247""}]"
DOID:11247	"[""disseminated intravascular coagulation"",""DIC"",""Defibrination syndrome"",""Diffuse or disseminated intravascular coagulation""]"	"[{""label"":""Plat"",""id"":""25692""},{""label"":""Serpine1"",""id"":""24617""}]"	"[""24617"",""25692""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11247""}]"
DOID:11252	"[""microcytic anemia""]"	"[{""label"":""TMPRSS6"",""id"":""164656""}]"	"[""164656""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11252""}]"
DOID:11252	"[""microcytic anemia""]"	"[{""label"":""VPS1"",""id"":""853870""}]"	"[""853870""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11252""}]"
DOID:11252	"[""microcytic anemia""]"	"[{""label"":""Dnm2"",""id"":""13430""}]"	"[""13430""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11252""}]"
DOID:11257	"[""social phobia""]"	"[{""label"":""CNTNAP2"",""id"":""26047""}]"	"[""26047""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11257""}]"
DOID:11265	"[""trachoma"",""active stage trachoma"",""trachoma dubium""]"	"[{""label"":""HLA-B"",""id"":""3106""},{""label"":""IL10"",""id"":""3586""},{""label"":""TNF"",""id"":""7124""}]"	"[""3106"",""3586"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11265""}]"
DOID:11266	"[""Hantavirus hemorrhagic fever with renal syndrome"",""HFRS"",""Hemorrhagic fever, Russian"",""Hemorrhagic nephrosonephritis"",""Puumala virus nephropathy""]"	"[{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HLA-DRB5"",""id"":""3127""}]"	"[""3123"",""3127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11266""}]"
DOID:11294	"[""arteriovenous malformation"",""Arteriovenous hemangioma"",""Cirsoid aneurysm"",""Racemose Angioma"",""Racemose aneurysm"",""Racemose hemangioma""]"	"[{""label"":""ENG"",""id"":""2022""},{""label"":""GLMN"",""id"":""11146""},{""label"":""RASA1"",""id"":""5921""},{""label"":""TEK"",""id"":""7010""}]"	"[""11146"",""2022"",""5921"",""7010""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11294""}]"
DOID:11335	"[""sarcoidosis"",""Boeck sarcoid"",""lymphogranulomatosis""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGTR1"",""id"":""185""},{""label"":""BTNL2"",""id"":""56244""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CD14"",""id"":""929""},{""label"":""CFH"",""id"":""3075""},{""label"":""CMA1"",""id"":""1215""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL23R"",""id"":""149233""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SLC11A1"",""id"":""6556""}]"	"[""1215"",""1234"",""149233"",""1493"",""1636"",""185"",""3075"",""3106"",""3119"",""3123"",""56244"",""5743"",""6556"",""729230"",""929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11335""}]"
DOID:11336	"[""rhinoscleroma""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3117"",""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11336""}]"
DOID:11342	"[""arcus senilis"",""Arcus of cornea"",""corneal arcus""]"	"[{""label"":""KERA"",""id"":""11081""}]"	"[""11081""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11342""}]"
DOID:11372	"[""megacolon"",""Dilatation of colon""]"	"[{""label"":""Ednrb"",""id"":""50672""}]"	"[""50672""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11372""}]"
DOID:11382	"[""corneal neovascularization""]"	"[{""label"":""IL1RN"",""id"":""3557""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""TNFAIP6"",""id"":""7130""}]"	"[""3557"",""5176"",""7130""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11382""}]"
DOID:11383	"[""cryptorchidism"",""Cryptorchism"",""Undescended testicle"",""Undescended testis"",""undescended testicles""]"	"[{""label"":""AR"",""id"":""367""},{""label"":""HOXD13"",""id"":""3239""},{""label"":""RXFP2"",""id"":""122042""}]"	"[""122042"",""3239"",""367""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11383""}]"
DOID:11383	"[""cryptorchidism"",""Cryptorchism"",""Undescended testicle"",""Undescended testis"",""undescended testicles""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11383""}]"
DOID:11394	"[""adult respiratory distress syndrome"",""ARDS"",""Non-cardiogenic pulmonary edema"",""Shock lung"",""acute respiratory distress syndrome"",""adult RDS""]"	"[{""label"":""AMBP"",""id"":""259""},{""label"":""LEP"",""id"":""3952""},{""label"":""LTA"",""id"":""4049""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MYLK"",""id"":""4638""},{""label"":""PLAU"",""id"":""5328""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPC"",""id"":""6440""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""259"",""3952"",""4049"",""4153"",""4638"",""5328"",""6439"",""6440"",""7124"",""7133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11394""}]"
DOID:11394	"[""adult respiratory distress syndrome"",""ARDS"",""Non-cardiogenic pulmonary edema"",""Shock lung"",""acute respiratory distress syndrome"",""adult RDS""]"	"[{""label"":""C3ar1"",""id"":""84007""},{""label"":""C5ar1"",""id"":""113959""},{""label"":""Il1rn"",""id"":""60582""},{""label"":""Serpina3n"",""id"":""24795""},{""label"":""Tbxa2r"",""id"":""24816""}]"	"[""113959"",""24795"",""24816"",""60582"",""84007""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11394""}]"
DOID:11396	"[""pulmonary edema""]"	"[{""label"":""Vegfa"",""id"":""83785""}]"	"[""83785""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11396""}]"
DOID:11396	"[""pulmonary edema""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""AGT"",""id"":""183""},{""label"":""IL13"",""id"":""3596""},{""label"":""SFTPA1"",""id"":""653509""}]"	"[""154"",""183"",""3596"",""653509""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11396""}]"
DOID:114	"[""heart disease""]"	"[{""label"":""Pgi"",""id"":""35886""}]"	"[""35886""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:114""}]"
DOID:114	"[""heart disease""]"	"[{""label"":""Fbn1"",""id"":""14118""},{""label"":""Ryr2"",""id"":""20191""}]"	"[""14118"",""20191""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:114""}]"
DOID:114	"[""heart disease""]"	"[{""label"":""Gsk3b"",""id"":""84027""},{""label"":""Pln"",""id"":""64672""},{""label"":""Ppargc1a"",""id"":""83516""}]"	"[""64672"",""83516"",""84027""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:114""}]"
DOID:114	"[""heart disease""]"	"[{""label"":""GLUL"",""id"":""2752""},{""label"":""MTR"",""id"":""4548""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""SOD3"",""id"":""6649""}]"	"[""2752"",""4548"",""6532"",""6649""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:114""}]"
DOID:11400	"[""pyelonephritis""]"	"[{""label"":""CXCR1"",""id"":""3577""},{""label"":""TLR1"",""id"":""7096""}]"	"[""3577"",""7096""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11400""}]"
DOID:11446	"[""sciatic neuropathy""]"	"[{""label"":""HGF"",""id"":""3082""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""LRP1"",""id"":""4035""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""SOD1"",""id"":""6647""}]"	"[""3082"",""3557"",""4035"",""5176"",""6647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11446""}]"
DOID:11446	"[""sciatic neuropathy""]"	"[{""label"":""Agt"",""id"":""24179""},{""label"":""Bdkrb1"",""id"":""81509""},{""label"":""Bdnf"",""id"":""24225""},{""label"":""Cnr2"",""id"":""57302""},{""label"":""Creb1"",""id"":""81646""},{""label"":""Gsk3b"",""id"":""84027""},{""label"":""Hmgb1"",""id"":""25459""},{""label"":""Hrh3"",""id"":""85268""},{""label"":""Il10"",""id"":""25325""},{""label"":""Mag"",""id"":""29409""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Scn10a"",""id"":""29571""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Tlr4"",""id"":""29260""}]"	"[""24179"",""24225"",""24617"",""25325"",""25459"",""29260"",""29409"",""29571"",""57302"",""81509"",""81646"",""83516"",""84027"",""85268""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11446""}]"
DOID:11450	"[""allergic cutaneous vasculitis"",""Allergic Cutaneous Angiitis"",""Autoimmune Hypersensitivity angiitis""]"	"[{""label"":""CSF3"",""id"":""1440""}]"	"[""1440""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11450""}]"
DOID:11476	"[""osteoporosis""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Igf2"",""id"":""24483""},{""label"":""Lep"",""id"":""25608""},{""label"":""Myc"",""id"":""24577""},{""label"":""Ptger4"",""id"":""84023""}]"	"[""24310"",""24483"",""24577"",""25608"",""84023""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11476""}]"
DOID:11476	"[""osteoporosis""]"	"[{""label"":""Ifngr1"",""id"":""15979""},{""label"":""Pls3"",""id"":""102866""},{""label"":""Tnfrsf11b"",""id"":""18383""},{""label"":""Tnfsf11"",""id"":""21943""}]"	"[""102866"",""15979"",""18383"",""21943""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11476""}]"
DOID:11476	"[""osteoporosis""]"	"[{""label"":""BMP2"",""id"":""650""},{""label"":""CALCA"",""id"":""796""},{""label"":""CALCR"",""id"":""799""},{""label"":""COL1A1"",""id"":""1277""},{""label"":""COL1A2"",""id"":""1278""},{""label"":""CXCR4"",""id"":""7852""},{""label"":""CYP17A1"",""id"":""1586""},{""label"":""CYP19A1"",""id"":""1588""},{""label"":""ESR1"",""id"":""2099""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""LEP"",""id"":""3952""},{""label"":""LEPR"",""id"":""3953""},{""label"":""LRP5"",""id"":""4041""},{""label"":""NRIP1"",""id"":""8204""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TNFRSF11A"",""id"":""8792""},{""label"":""TNFRSF1B"",""id"":""7133""},{""label"":""TNFSF11"",""id"":""8600""}]"	"[""1277"",""1278"",""1586"",""1588"",""2099"",""3480"",""3552"",""3557"",""3952"",""3953"",""4041"",""650"",""6648"",""7133"",""7852"",""796"",""799"",""8204"",""8600"",""8792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11476""}]"
DOID:1148	"[""polydactyly"",""postaxial polydactyly""]"	"[{""label"":""GLI3"",""id"":""2737""},{""label"":""SHH"",""id"":""6469""}]"	"[""2737"",""6469""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1148""}]"
DOID:11512	"[""Budd-Chiari syndrome"",""hepatic vein thrombosis""]"	"[{""label"":""F5"",""id"":""2153""}]"	"[""2153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11512""}]"
DOID:11555	"[""Fuchs' endothelial dystrophy"",""FCED"",""Fuchs' corneal dystrophy"",""Fuchs' endothelial corneal dystrophy""]"	"[{""label"":""AGBL1"",""id"":""123624""},{""label"":""COL8A2"",""id"":""1296""},{""label"":""LOXHD1"",""id"":""125336""},{""label"":""SLC4A11"",""id"":""83959""},{""label"":""TCF4"",""id"":""6925""},{""label"":""ZEB1"",""id"":""6935""}]"	"[""123624"",""125336"",""1296"",""6925"",""6935"",""83959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11555""}]"
DOID:11555	"[""Fuchs' endothelial dystrophy"",""FCED"",""Fuchs' corneal dystrophy"",""Fuchs' endothelial corneal dystrophy""]"	"[{""label"":""Col8a2"",""id"":""329941""}]"	"[""329941""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11555""}]"
DOID:11563	"[""retinal vasculitis""]"	"[{""label"":""HLA-B"",""id"":""3106""}]"	"[""3106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11563""}]"
DOID:11569	"[""neurocirculatory asthenia"",""Cardiovascular malfunction arising from mental factors"",""Cardiovascular neurosis"",""Da Costa's syndrome"",""Krishaber's disease""]"	"[{""label"":""SLC6A2"",""id"":""6530""}]"	"[""6530""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11569""}]"
DOID:11573	"[""listeriosis"",""Infection by Listeria monocytogenes"",""Listeria infection""]"	"[{""label"":""IL1RN"",""id"":""3557""}]"	"[""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11573""}]"
DOID:11589	"[""Riley-Day syndrome"",""HSAN III"",""familial autonomic nervous dysfunction"",""familial dysautonomia""]"	"[{""label"":""ELP1"",""id"":""8518""}]"	"[""8518""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11589""}]"
DOID:11589	"[""Riley-Day syndrome"",""HSAN III"",""familial autonomic nervous dysfunction"",""familial dysautonomia""]"	"[{""label"":""Elp1"",""id"":""230233""}]"	"[""230233""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11589""}]"
DOID:11612	"[""polycystic ovary syndrome"",""Multicystic ovaries"",""PCOS"",""Polycystic Ovarian disease"",""Polycystic ovaries"",""Stein-Leventhal synd."",""Stein-Leventhal syndrome"",""polycystic ovary""]"	"[{""label"":""Akt2"",""id"":""11652""}]"	"[""11652""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11612""}]"
DOID:11612	"[""polycystic ovary syndrome"",""Multicystic ovaries"",""PCOS"",""Polycystic Ovarian disease"",""Polycystic ovaries"",""Stein-Leventhal synd."",""Stein-Leventhal syndrome"",""polycystic ovary""]"	"[{""label"":""CAPN10"",""id"":""11132""},{""label"":""CYP19A1"",""id"":""1588""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""FST"",""id"":""10468""}]"	"[""10468"",""11132"",""1543"",""1588""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11612""}]"
DOID:11613	"[""hyperandrogenism"",""hyperandrogenization syndrome""]"	"[{""label"":""IL6ST"",""id"":""3572""}]"	"[""3572""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11613""}]"
DOID:11613	"[""hyperandrogenism"",""hyperandrogenization syndrome""]"	"[{""label"":""Prl3c1"",""id"":""27372""}]"	"[""27372""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11613""}]"
DOID:11633	"[""thyroid hormone resistance syndrome"",""Generalized thyroid hormone resistance"",""Refetoff syndrome"",""Thyroid hormone responsiveness defect"",""thyroid hormone resistance""]"	"[{""label"":""Ncoa1"",""id"":""17977""}]"	"[""17977""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11633""}]"
DOID:11650	"[""bronchopulmonary dysplasia"",""Bronchopulmonary dysplasia of newborn"",""Chronic lung disease of prematurity"",""Neonatal chronic lung disease"",""Perinatal bronchopulmonary dysplasia"",""Respiratory insufficiency"",""neonatal chronic respiratory disease""]"	"[{""label"":""DAG1"",""id"":""1605""},{""label"":""FLT1"",""id"":""2321""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MBL2"",""id"":""4153""},{""label"":""SFTPA1"",""id"":""653509""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""TNF"",""id"":""7124""}]"	"[""1605"",""2321"",""3557"",""4153"",""6439"",""6441"",""653509"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11650""}]"
DOID:11656	"[""cicatricial pemphigoid"",""Cicatricial pemphigoid with ocular involvement"",""Ocular pemphigoid"",""benign mucous membrane pemphigoid"",""benign mucous membrane pemphigoid with ocular involvement"",""ocular pemphigus""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11656""}]"
DOID:11664	"[""nephrosclerosis"",""renal sclerosis""]"	"[{""label"":""ADRB1"",""id"":""153""}]"	"[""153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11664""}]"
DOID:11678	"[""onchocerciasis"",""Infection by Onchocerca volvulus"",""Onchocerca volvulus infection"",""volvulosis""]"	"[{""label"":""HLA-DPA1"",""id"":""3113""},{""label"":""HLA-DQA1"",""id"":""3117""}]"	"[""3113"",""3117""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11678""}]"
DOID:1168	"[""familial hyperlipidemia"",""familial hyperlipoproteinemia"",""hyperlipemia""]"	"[{""label"":""Kl"",""id"":""83504""},{""label"":""Lcat"",""id"":""24530""},{""label"":""Ldlr"",""id"":""300438""},{""label"":""Lpl"",""id"":""24539""},{""label"":""Rgn"",""id"":""25106""},{""label"":""Sdc1"",""id"":""25216""},{""label"":""Tgfb1"",""id"":""59086""}]"	"[""24530"",""24539"",""25106"",""25216"",""300438"",""59086"",""83504""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1168""}]"
DOID:1168	"[""familial hyperlipidemia"",""familial hyperlipoproteinemia"",""hyperlipemia""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ABCG8"",""id"":""64241""},{""label"":""APOB"",""id"":""338""},{""label"":""APOC2"",""id"":""344""},{""label"":""CCL2"",""id"":""6347""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""LPL"",""id"":""4023""}]"	"[""3304"",""338"",""344"",""4023"",""5243"",""6347"",""64241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1168""}]"
DOID:11695	"[""portal vein thrombosis""]"	"[{""label"":""IGF1R"",""id"":""3480""},{""label"":""SERPINE1"",""id"":""5054""}]"	"[""3480"",""5054""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11695""}]"
DOID:11702	"[""dysgammaglobulinemia""]"	"[{""label"":""CD40LG"",""id"":""959""},{""label"":""UNG"",""id"":""7374""}]"	"[""7374"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11702""}]"
DOID:1171	"[""hyperlipoproteinemia type V"",""Fredrickson type V lipaemia"",""familial hyperlipoproteinemia type V"",""familial type 5 hyperlipoproteinemia""]"	"[{""label"":""APOA5"",""id"":""116519""}]"	"[""116519""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1171""}]"
DOID:11712	"[""lipoatrophic diabetes mellitus"",""lipoatrophic diabetes""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11712""}]"
DOID:11713	"[""diabetic angiopathy"",""Diabetic vascular disorder"",""diabetic peripheral angiopathy""]"	"[{""label"":""EPO"",""id"":""2056""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""PLAT"",""id"":""5327""},{""label"":""PON1"",""id"":""5444""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TNF"",""id"":""7124""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""2056"",""3123"",""3557"",""5054"",""5327"",""5444"",""6648"",""7124"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11713""}]"
DOID:11713	"[""diabetic angiopathy"",""Diabetic vascular disorder"",""diabetic peripheral angiopathy""]"	"[{""label"":""Bdkrb1"",""id"":""81509""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Icam1"",""id"":""25464""}]"	"[""24770"",""25464"",""81509""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11713""}]"
DOID:11714	"[""gestational diabetes"",""GDM"",""Gestational diabetes mellitus"",""Maternal gestational diabetes mellitus""]"	"[{""label"":""CDKAL1"",""id"":""54901""},{""label"":""GAD2"",""id"":""2572""},{""label"":""GCK"",""id"":""2645""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""IL6"",""id"":""3569""},{""label"":""INSR"",""id"":""3643""}]"	"[""2572"",""2645"",""3569"",""3643"",""54901"",""6927""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11714""}]"
DOID:11714	"[""gestational diabetes"",""GDM"",""Gestational diabetes mellitus"",""Maternal gestational diabetes mellitus""]"	"[{""label"":""Met"",""id"":""17295""}]"	"[""17295""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11714""}]"
DOID:11716	"[""prediabetes syndrome"",""Prediabetes"",""impaired glucose tolerance"",""prediabetic state""]"	"[{""label"":""CCR2"",""id"":""729230""},{""label"":""GCG"",""id"":""2641""},{""label"":""IL6"",""id"":""3569""},{""label"":""PTPRN2"",""id"":""5799""},{""label"":""UCP3"",""id"":""7352""}]"	"[""2641"",""3569"",""5799"",""729230"",""7352""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11716""}]"
DOID:11717	"[""neonatal diabetes mellitus"",""diabetes mellitus syndrome in newborn infant"",""neonatal diabetes""]"	"[{""label"":""GLK1"",""id"":""850317""}]"	"[""850317""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11717""}]"
DOID:11717	"[""neonatal diabetes mellitus"",""diabetes mellitus syndrome in newborn infant"",""neonatal diabetes""]"	"[{""label"":""Ins2"",""id"":""16334""}]"	"[""16334""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11717""}]"
DOID:11719	"[""oculopharyngeal muscular dystrophy"",""Muscular dystrophy, oculopharyngeal""]"	"[{""label"":""PABPN1"",""id"":""8106""}]"	"[""8106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11719""}]"
DOID:1172	"[""hyperlipoproteinemia type IV"",""Endogenous hyperlipidaemia"",""Fredrickson type IV Lipidemia"",""Fredrickson type IV hyperlipoproteinemia"",""Fredrickson type IV lipidaemia"",""VLDL hyperlipoproteinemia"",""familial hypertriglyceridemia""]"	"[{""label"":""APOA5"",""id"":""116519""}]"	"[""116519""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1172""}]"
DOID:11720	"[""distal myopathy"",""distal muscular dystrophy""]"	"[{""label"":""LDB3"",""id"":""11155""}]"	"[""11155""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11720""}]"
DOID:11720	"[""distal myopathy"",""distal muscular dystrophy""]"	"[{""label"":""Dysf"",""id"":""26903""}]"	"[""26903""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11720""}]"
DOID:11721	"[""glycogen storage disease VII"",""Glycogen storage disease 7"",""Glycogen storage disease, type VII"",""Muscle phosphofructokinase deficiency"",""glycogen storage disease type VII"",""phosphofructokinase myopathy""]"	"[{""label"":""Pfkm"",""id"":""18642""}]"	"[""18642""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11721""}]"
DOID:11721	"[""glycogen storage disease VII"",""Glycogen storage disease 7"",""Glycogen storage disease, type VII"",""Muscle phosphofructokinase deficiency"",""glycogen storage disease type VII"",""phosphofructokinase myopathy""]"	"[{""label"":""PFKM"",""id"":""5213""}]"	"[""5213""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11721""}]"
DOID:11723	"[""Duchenne muscular dystrophy"",""Muscular dystrophy, Duchenne""]"	"[{""label"":""Ctss"",""id"":""13040""},{""label"":""Dmd"",""id"":""13405""}]"	"[""13040"",""13405""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11723""}]"
DOID:11723	"[""Duchenne muscular dystrophy"",""Muscular dystrophy, Duchenne""]"	"[{""label"":""DAG1"",""id"":""1605""},{""label"":""DMD"",""id"":""1756""},{""label"":""ITGA7"",""id"":""3679""}]"	"[""1605"",""1756"",""3679""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00384""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11723""}]"
DOID:11724	"[""limb-girdle muscular dystrophy"",""Erb's muscular dystrophy"",""Leyden-Mbius muscular dystrophy"",""limb girdle muscular dystrophy""]"	"[{""label"":""Sgcg"",""id"":""24053""}]"	"[""24053""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11724""}]"
DOID:11724	"[""limb-girdle muscular dystrophy"",""Erb's muscular dystrophy"",""Leyden-Mbius muscular dystrophy"",""limb girdle muscular dystrophy""]"	"[{""label"":""GLR1"",""id"":""856014""}]"	"[""856014""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11724""}]"
DOID:11724	"[""limb-girdle muscular dystrophy"",""Erb's muscular dystrophy"",""Leyden-Mbius muscular dystrophy"",""limb girdle muscular dystrophy""]"	"[{""label"":""FKRP"",""id"":""79147""}]"	"[""79147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11724""}]"
DOID:11725	"[""Cornelia de Lange syndrome"",""Brachmann de Lange syndrome"",""De Lange syndrome""]"	"[{""label"":""NIPBL"",""id"":""25836""}]"	"[""25836""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11725""}]"
DOID:11726	"[""Emery-Dreifuss muscular dystrophy"",""EDMD""]"	"[{""label"":""Lmna"",""id"":""16905""},{""label"":""Syne1"",""id"":""64009""}]"	"[""16905"",""64009""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11726""}]"
DOID:11726	"[""Emery-Dreifuss muscular dystrophy"",""EDMD""]"	"[{""label"":""EMD"",""id"":""2010""},{""label"":""LMNA"",""id"":""4000""}]"	"[""2010"",""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11726""}]"
DOID:11726	"[""Emery-Dreifuss muscular dystrophy"",""EDMD""]"	"[{""label"":""Msp300"",""id"":""3771968""}]"	"[""3771968""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11726""}]"
DOID:11727	"[""facioscapulohumeral muscular dystrophy"",""Landouzy Dejerine muscular dystrophy"",""Landouzy-Dejerine muscular dystrophy"",""Muscular dystrophy, Landouzy-Dejerine""]"	"[{""label"":""Fat1"",""id"":""14107""},{""label"":""Large1"",""id"":""16795""}]"	"[""14107"",""16795""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11727""}]"
DOID:11758	"[""iron deficiency anemia""]"	"[{""label"":""GPX1"",""id"":""2876""},{""label"":""HFE"",""id"":""3077""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""PON1"",""id"":""5444""},{""label"":""TF"",""id"":""7018""},{""label"":""TNF"",""id"":""7124""}]"	"[""2876"",""3077"",""3673"",""5444"",""7018"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11758""}]"
DOID:11759	"[""hypochromic anemia"",""ANEMIA HYPOCHROMIC""]"	"[{""label"":""Slc11a2"",""id"":""25715""}]"	"[""25715""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11759""}]"
DOID:11759	"[""hypochromic anemia"",""ANEMIA HYPOCHROMIC""]"	"[{""label"":""SLC11A2"",""id"":""4891""}]"	"[""4891""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11759""}]"
DOID:11829	"[""degenerative myopia"",""degenerative progressive high myopia"",""pathological myopia"",""progressive high (degenerative) myopia"",""progressive high myopia""]"	"[{""label"":""Lrp2"",""id"":""14725""}]"	"[""14725""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11829""}]"
DOID:11829	"[""degenerative myopia"",""degenerative progressive high myopia"",""pathological myopia"",""progressive high (degenerative) myopia"",""progressive high myopia""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11829""}]"
DOID:11830	"[""myopia"",""near vision"",""near-sightedness"",""short-sightedness""]"	"[{""label"":""COL2A1"",""id"":""1280""},{""label"":""CPSF1"",""id"":""29894""},{""label"":""HGF"",""id"":""3082""},{""label"":""LAMA2"",""id"":""3908""},{""label"":""LOXL3"",""id"":""84695""},{""label"":""LRPAP1"",""id"":""4043""},{""label"":""MMP2"",""id"":""4313""},{""label"":""P4HA2"",""id"":""8974""},{""label"":""PRIMPOL"",""id"":""201973""},{""label"":""SLC39A5"",""id"":""283375""},{""label"":""ZNF644"",""id"":""84146""}]"	"[""1280"",""201973"",""283375"",""29894"",""3082"",""3908"",""4043"",""4313"",""84146"",""84695"",""8974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11830""}]"
DOID:11830	"[""myopia"",""near vision"",""near-sightedness"",""short-sightedness""]"	"[{""label"":""Adora2a"",""id"":""11540""}]"	"[""11540""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11830""}]"
DOID:11832	"[""visual epilepsy"",""epilepsy, visual""]"	"[{""label"":""Grik5"",""id"":""24407""},{""label"":""Grm8"",""id"":""60590""},{""label"":""Hrh3"",""id"":""85268""},{""label"":""Nfe2l2"",""id"":""83619""},{""label"":""Npy5r"",""id"":""25340""},{""label"":""Pdgfb"",""id"":""24628""},{""label"":""Scn2b"",""id"":""25349""},{""label"":""Spp1"",""id"":""25353""},{""label"":""Tnf"",""id"":""24835""},{""label"":""Tnfrsf1a"",""id"":""25625""},{""label"":""Tnfrsf1b"",""id"":""156767""},{""label"":""Vdac1"",""id"":""83529""},{""label"":""Vdac2"",""id"":""83531""}]"	"[""156767"",""24407"",""24628"",""24835"",""25340"",""25349"",""25353"",""25625"",""60590"",""83529"",""83531"",""83619"",""85268""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11832""}]"
DOID:11832	"[""visual epilepsy"",""epilepsy, visual""]"	"[{""label"":""L2HGDH"",""id"":""79944""},{""label"":""TNF"",""id"":""7124""},{""label"":""TUBA1A"",""id"":""7846""}]"	"[""7124"",""7846"",""79944""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11832""}]"
DOID:11836	"[""clubfoot"",""Congenital equinovarus"",""Equinovarus deformity of foot"",""congenital clubfoot"",""congenital talipes equinovarus""]"	"[{""label"":""Fras1"",""id"":""231470""},{""label"":""Grip1"",""id"":""74053""},{""label"":""Ret"",""id"":""19713""}]"	"[""19713"",""231470"",""74053""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11836""}]"
DOID:11836	"[""clubfoot"",""Congenital equinovarus"",""Equinovarus deformity of foot"",""congenital clubfoot"",""congenital talipes equinovarus""]"	"[{""label"":""CYP1A1"",""id"":""1543""},{""label"":""FLNB"",""id"":""2317""},{""label"":""HOXD13"",""id"":""3239""},{""label"":""PITX1"",""id"":""5307""}]"	"[""1543"",""2317"",""3239"",""5307""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11836""}]"
DOID:1184	"[""nephrotic syndrome""]"	"[{""label"":""syg-1"",""id"":""180555""},{""label"":""syg-2"",""id"":""181561""}]"	"[""180555"",""181561""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1184""}]"
DOID:1184	"[""nephrotic syndrome""]"	"[{""label"":""Fat1"",""id"":""14107""},{""label"":""Nphs1"",""id"":""54631""}]"	"[""14107"",""54631""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1184""}]"
DOID:1184	"[""nephrotic syndrome""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Scnn1a"",""id"":""25122""},{""label"":""Scnn1b"",""id"":""24767""}]"	"[""24310"",""24767"",""25122"",""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1184""}]"
DOID:1184	"[""nephrotic syndrome""]"	"[{""label"":""ALB"",""id"":""213""},{""label"":""EPO"",""id"":""2056""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""PLCE1"",""id"":""51196""}]"	"[""2056"",""213"",""3557"",""51196""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1184""}]"
DOID:1184	"[""nephrotic syndrome""]"	"[{""label"":""kirre"",""id"":""31292""}]"	"[""31292""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1184""}]"
DOID:11847	"[""coronary thrombosis"",""Coronary artery thrombosis""]"	"[{""label"":""GP6"",""id"":""51206""}]"	"[""51206""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11847""}]"
DOID:11870	"[""Pick's disease"",""Dementia in Pick's disease"",""LOBAR ATROPHY OF BRAIN"",""PICK DISEASE OF BRAIN"",""Pick disease""]"	"[{""label"":""MAP2K6"",""id"":""5608""},{""label"":""MAPT"",""id"":""4137""}]"	"[""4137"",""5608""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11870""}]"
DOID:1192	"[""peripheral nervous system neoplasm"",""neoplasm of peripheral nerve"",""nerve sheath neoplasm"",""tumor of PNS""]"	"[{""label"":""PTEN"",""id"":""5728""}]"	"[""5728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1192""}]"
DOID:11934	"[""head and neck cancer"",""head and neck neoplasm"",""head and neck tumours"",""head/neck neoplasm"",""tumor of head and neck""]"	"[{""label"":""CYP1A1"",""id"":""1543""},{""label"":""KDM4C"",""id"":""23081""}]"	"[""1543"",""23081""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11934""}]"
DOID:11949	"[""Creutzfeldt-Jakob disease"",""CJD"",""Creutzfeldt Jacob syndrome"",""Creutzfeldt Jakob disease"",""Creutzfeldt-Jacob disease"",""Jakob-Creutzfeldt disease"",""Subacute spongiform encephalopathy"",""Transmissible virus dementia""]"	"[{""label"":""Prnp"",""id"":""19122""}]"	"[""19122""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11949""}]"
DOID:11949	"[""Creutzfeldt-Jakob disease"",""CJD"",""Creutzfeldt Jacob syndrome"",""Creutzfeldt Jakob disease"",""Creutzfeldt-Jacob disease"",""Jakob-Creutzfeldt disease"",""Subacute spongiform encephalopathy"",""Transmissible virus dementia""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""PRNP"",""id"":""5621""},{""label"":""STX1A"",""id"":""6804""}]"	"[""3119"",""5621"",""6804""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11949""}]"
DOID:11963	"[""esophagitis"",""acute esophagitis""]"	"[{""label"":""IL4R"",""id"":""3566""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""TNF"",""id"":""7124""}]"	"[""3566"",""5743"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11963""}]"
DOID:11981	"[""morbid obesity"",""Severe obesity""]"	"[{""label"":""AGER"",""id"":""177""},{""label"":""CTNNBL1"",""id"":""56259""},{""label"":""GHRL"",""id"":""51738""},{""label"":""MC4R"",""id"":""4160""},{""label"":""MCHR1"",""id"":""2847""},{""label"":""NPY2R"",""id"":""4887""},{""label"":""NTRK2"",""id"":""4915""}]"	"[""177"",""2847"",""4160"",""4887"",""4915"",""51738"",""56259""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11981""}]"
DOID:11983	"[""Prader-Willi syndrome"",""Prader Willi syndrome""]"	"[{""label"":""Htr2c"",""id"":""15560""}]"	"[""15560""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11983""}]"
DOID:11984	"[""hypertrophic cardiomyopathy"",""hypertrophic obstructive cardiomyopathy""]"	"[{""label"":""Htr2b"",""id"":""15559""},{""label"":""Pkd1"",""id"":""18763""},{""label"":""Ptpn11"",""id"":""19247""}]"	"[""15559"",""18763"",""19247""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11984""}]"
DOID:11984	"[""hypertrophic cardiomyopathy"",""hypertrophic obstructive cardiomyopathy""]"	"[{""label"":""AGT"",""id"":""183""},{""label"":""CACNB2"",""id"":""783""},{""label"":""CMA1"",""id"":""1215""},{""label"":""CS"",""id"":""1431""},{""label"":""CTSL"",""id"":""1514""},{""label"":""LAMP2"",""id"":""3920""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MYBPC3"",""id"":""4607""},{""label"":""MYH7"",""id"":""4625""},{""label"":""NDUFS2"",""id"":""4720""},{""label"":""TNNI3"",""id"":""7137""},{""label"":""VCL"",""id"":""7414""}]"	"[""1215"",""1431"",""1514"",""183"",""3920"",""4312"",""4607"",""4625"",""4720"",""7137"",""7414"",""783""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11984""}]"
DOID:11984	"[""hypertrophic cardiomyopathy"",""hypertrophic obstructive cardiomyopathy""]"	"[{""label"":""Stim"",""id"":""32556""}]"	"[""32556""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11984""}]"
DOID:11984	"[""hypertrophic cardiomyopathy"",""hypertrophic obstructive cardiomyopathy""]"	"[{""label"":""Lamp2"",""id"":""24944""}]"	"[""24944""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:11984""}]"
DOID:12010	"[""anterior ischemic optic neuropathy"",""Ischemic optic neuropathy""]"	"[{""label"":""CSF3"",""id"":""1440""},{""label"":""NOS3"",""id"":""4846""}]"	"[""1440"",""4846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12010""}]"
DOID:12029	"[""sympathetic ophthalmia"",""Sympathetic uveitis""]"	"[{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12029""}]"
DOID:12030	"[""panuveitis"",""Diffuse uveitis""]"	"[{""label"":""CFH"",""id"":""3075""},{""label"":""IL10"",""id"":""3586""}]"	"[""3075"",""3586""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12030""}]"
DOID:1205	"[""allergic disease"",""allergic hypersensitivity disease"",""hypersensitivity"",""hypersensitivity reaction type I disease""]"	"[{""label"":""Akr1b1"",""id"":""24192""}]"	"[""24192""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1205""}]"
DOID:1205	"[""allergic disease"",""allergic hypersensitivity disease"",""hypersensitivity"",""hypersensitivity reaction type I disease""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGT"",""id"":""183""},{""label"":""CD14"",""id"":""929""},{""label"":""CYSLTR1"",""id"":""10800""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRA"",""id"":""3122""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL13"",""id"":""3596""},{""label"":""LTA"",""id"":""4049""},{""label"":""MIF"",""id"":""4282""},{""label"":""TAP1"",""id"":""6890""}]"	"[""10800"",""1636"",""183"",""2214"",""3117"",""3119"",""3122"",""3123"",""3596"",""4049"",""4282"",""6890"",""929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1205""}]"
DOID:1206	"[""Rett syndrome"",""Rett's disorder"",""cerebroatrophic hyperammonemia""]"	"[{""label"":""Mecp2"",""id"":""29386""}]"	"[""29386""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1206""}]"
DOID:1206	"[""Rett syndrome"",""Rett's disorder"",""cerebroatrophic hyperammonemia""]"	"[{""label"":""Mecp2"",""id"":""17257""}]"	"[""17257""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1206""}]"
DOID:1206	"[""Rett syndrome"",""Rett's disorder"",""cerebroatrophic hyperammonemia""]"	"[{""label"":""CDKL5"",""id"":""6792""},{""label"":""MECP2"",""id"":""4204""}]"	"[""4204"",""6792""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1206""}]"
DOID:12098	"[""trigeminal neuralgia"",""Trifacial neuralgia"",""trifocal neuralgia""]"	"[{""label"":""Cdk5"",""id"":""140908""}]"	"[""140908""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12098""}]"
DOID:12098	"[""trigeminal neuralgia"",""Trifacial neuralgia"",""trifocal neuralgia""]"	"[{""label"":""Gabrg1"",""id"":""14405""}]"	"[""14405""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12098""}]"
DOID:1210	"[""optic neuritis""]"	"[{""label"":""AQP4"",""id"":""361""},{""label"":""CAT"",""id"":""847""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""MOG"",""id"":""4340""},{""label"":""SOD2"",""id"":""6648""}]"	"[""3119"",""3123"",""361"",""4340"",""6648"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1210""}]"
DOID:12117	"[""pulmonary alveolar microlithiasis""]"	"[{""label"":""SLC34A2"",""id"":""10568""}]"	"[""10568""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12117""}]"
DOID:12119	"[""hemosiderosis"",""haemosiderosis""]"	"[{""label"":""CP"",""id"":""1356""}]"	"[""1356""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12119""}]"
DOID:12120	"[""pulmonary alveolar proteinosis""]"	"[{""label"":""Abca3"",""id"":""27410""},{""label"":""Csf2"",""id"":""12981""},{""label"":""Csf2ra"",""id"":""12982""},{""label"":""Csf2rb"",""id"":""12983""}]"	"[""12981"",""12982"",""12983"",""27410""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12120""}]"
DOID:12120	"[""pulmonary alveolar proteinosis""]"	"[{""label"":""ABCA3"",""id"":""21""},{""label"":""CSF2"",""id"":""1437""},{""label"":""CSF2RA"",""id"":""1438""},{""label"":""CSF2RB"",""id"":""1439""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPC"",""id"":""6440""}]"	"[""1437"",""1438"",""1439"",""21"",""6439"",""6440""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12120""}]"
DOID:12129	"[""bulimia nervosa"",""hyperorexia nervosa""]"	"[{""label"":""COMT"",""id"":""1312""}]"	"[""1312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12129""}]"
DOID:12132	"[""granulomatosis with polyangiitis"",""Necrotizing respiratory granulomatosis"",""Wegener granulomatosis, formerly""]"	"[{""label"":""CCR5"",""id"":""1234""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""FCAR"",""id"":""2204""},{""label"":""IL10"",""id"":""3586""},{""label"":""VTN"",""id"":""7448""}]"	"[""1234"",""1493"",""2204"",""3586"",""7448""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12132""}]"
DOID:12134	"[""factor VIII deficiency"",""Congenital factor VIII disorder"",""Hemophilia A"",""Subhemophilia"",""classic hemophilia"",""classic hemophilia A""]"	"[{""label"":""F8"",""id"":""14069""}]"	"[""14069""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12134""}]"
DOID:12134	"[""factor VIII deficiency"",""Congenital factor VIII disorder"",""Hemophilia A"",""Subhemophilia"",""classic hemophilia"",""classic hemophilia A""]"	"[{""label"":""F2"",""id"":""2147""},{""label"":""F8"",""id"":""2157""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL10"",""id"":""3586""},{""label"":""PLAT"",""id"":""5327""},{""label"":""TFPI"",""id"":""7035""},{""label"":""TGFB1"",""id"":""7040""}]"	"[""2147"",""2157"",""2212"",""3117"",""3458"",""3586"",""5327"",""7035"",""7040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12134""}]"
DOID:1214	"[""tympanosclerosis""]"	"[{""label"":""TLR4"",""id"":""7099""}]"	"[""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1214""}]"
DOID:1214	"[""tympanosclerosis""]"	"[{""label"":""Enpp1"",""id"":""18605""}]"	"[""18605""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1214""}]"
DOID:12140	"[""Chagas disease"",""Chagas' disease"",""chagas' disease with digestive system involvement"",""chagas' disease with nervous system involvement"",""chagas' disease with other organ involvement""]"	"[{""label"":""CHRM2"",""id"":""1129""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HSPA4"",""id"":""3308""},{""label"":""SOAT1"",""id"":""6646""}]"	"[""1129"",""3123"",""3308"",""6646""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12140""}]"
DOID:12140	"[""Chagas disease"",""Chagas' disease"",""chagas' disease with digestive system involvement"",""chagas' disease with nervous system involvement"",""chagas' disease with other organ involvement""]"	"[{""label"":""Ifng"",""id"":""25712""}]"	"[""25712""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12140""}]"
DOID:12143	"[""neurogenic bladder"",""Neuropathic bladder"",""neurogenic dysfunction of the urinary bladder"",""neurogenic urinary bladder disorder""]"	"[{""label"":""Ngf"",""id"":""310738""}]"	"[""310738""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12143""}]"
DOID:12148	"[""alveolar echinococcosis"",""Multilocular hydatid"",""alveolococcosis"",""small fox tapeworm""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12148""}]"
DOID:12176	"[""goiter"",""goitre""]"	"[{""label"":""TG"",""id"":""7038""}]"	"[""7038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12176""}]"
DOID:12177	"[""common variable immunodeficiency"",""CVID"",""acquired agammaglobulinemia"",""acquired hypogammaglobulinemia"",""common variable agammaglobulinemia"",""sporadic hypogammaglobulinemia""]"	"[{""label"":""DCLRE1C"",""id"":""64421""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IL21R"",""id"":""50615""},{""label"":""MBL2"",""id"":""4153""}]"	"[""3119"",""4153"",""50615"",""64421""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12177""}]"
DOID:12177	"[""common variable immunodeficiency"",""CVID"",""acquired agammaglobulinemia"",""acquired hypogammaglobulinemia"",""common variable agammaglobulinemia"",""sporadic hypogammaglobulinemia""]"	"[{""label"":""Icos"",""id"":""54167""}]"	"[""54167""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12177""}]"
DOID:12185	"[""otosclerosis""]"	"[{""label"":""AGT"",""id"":""183""},{""label"":""BMP2"",""id"":""650""},{""label"":""BMP4"",""id"":""652""},{""label"":""COL1A1"",""id"":""1277""},{""label"":""HLA-B"",""id"":""3106""}]"	"[""1277"",""183"",""3106"",""650"",""652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12185""}]"
DOID:12205	"[""dengue disease"",""Dengue Fever"",""breakbone fever"",""classic dengue""]"	"[{""label"":""CD209"",""id"":""30835""},{""label"":""F2"",""id"":""2147""},{""label"":""FCGR2A"",""id"":""2212""}]"	"[""2147"",""2212"",""30835""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12205""}]"
DOID:12206	"[""dengue hemorrhagic fever"",""DHF""]"	"[{""label"":""CD209"",""id"":""30835""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""IFNL1"",""id"":""282618""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""SLC6A4"",""id"":""6532""}]"	"[""2212"",""282618"",""30835"",""3813"",""6532""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12206""}]"
DOID:12217	"[""Lewy body dementia"",""Dementia with Lewy bodies"",""Diffuse Lewy body disease"",""Lewy body disease"",""Senile dementia of the Lewy body type""]"	"[{""label"":""GBA1"",""id"":""2629""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""KLK6"",""id"":""5653""},{""label"":""NOS2"",""id"":""4843""},{""label"":""SNCA"",""id"":""6622""},{""label"":""SNCB"",""id"":""6620""},{""label"":""SNCG"",""id"":""6623""}]"	"[""2629"",""3480"",""4843"",""5653"",""6620"",""6622"",""6623""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12217""}]"
DOID:1222	"[""cartilage disease"",""Cartilage disorder"",""Chondropathy""]"	"[{""label"":""BMP4"",""id"":""652""}]"	"[""652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1222""}]"
DOID:12236	"[""primary biliary cholangitis"",""biliary liver cirrhosis"",""cholestatic cirrhosis"",""chronic nonsuppurative destructive cholangitis"",""primary biliary cirrhosis""]"	"[{""label"":""ABCB4"",""id"":""5244""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""IL12A"",""id"":""3592""},{""label"":""LBR"",""id"":""3930""},{""label"":""NUP62"",""id"":""23636""},{""label"":""STAT4"",""id"":""6775""},{""label"":""UTP4"",""id"":""84916""}]"	"[""1493"",""23636"",""3117"",""3592"",""3930"",""5244"",""6775"",""84916""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12236""}]"
DOID:12236	"[""primary biliary cholangitis"",""biliary liver cirrhosis"",""cholestatic cirrhosis"",""chronic nonsuppurative destructive cholangitis"",""primary biliary cirrhosis""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12236""}]"
DOID:12241	"[""beta thalassemia""]"	"[{""label"":""BCL11A"",""id"":""53335""},{""label"":""COL1A1"",""id"":""1277""},{""label"":""HBB"",""id"":""3043""},{""label"":""HBS1L"",""id"":""10767""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""TNF"",""id"":""7124""}]"	"[""10767"",""1277"",""3043"",""3077"",""3119"",""53335"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12241""}]"
DOID:12253	"[""testicular lymphoma"",""lymphoma of the testis"",""malignant lymphoma of testis""]"	"[{""label"":""MYD88"",""id"":""4615""}]"	"[""4615""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12253""}]"
DOID:12259	"[""hemophilia B"",""Congenital factor IX deficiency"",""Congenital factor IX disorder"",""deficiency, functional factor IX"",""factor IX deficiency""]"	"[{""label"":""F9"",""id"":""14071""}]"	"[""14071""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12259""}]"
DOID:12259	"[""hemophilia B"",""Congenital factor IX deficiency"",""Congenital factor IX disorder"",""deficiency, functional factor IX"",""factor IX deficiency""]"	"[{""label"":""F2"",""id"":""2147""},{""label"":""F9"",""id"":""2158""}]"	"[""2147"",""2158""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12259""}]"
DOID:1227	"[""neutropenia""]"	"[{""label"":""AP3B1"",""id"":""8546""},{""label"":""C5"",""id"":""727""},{""label"":""CSF2"",""id"":""1437""},{""label"":""CSF3"",""id"":""1440""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""STAT2"",""id"":""6773""},{""label"":""TNF"",""id"":""7124""}]"	"[""1437"",""1440"",""2212"",""6773"",""7124"",""727"",""8546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1227""}]"
DOID:1227	"[""neutropenia""]"	"[{""label"":""C5ar1"",""id"":""113959""},{""label"":""Ptafr"",""id"":""58949""}]"	"[""113959"",""58949""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1227""}]"
DOID:12270	"[""coloboma"",""coloboma of eye"",""coloboma of macula"",""congenital ocular coloboma""]"	"[{""label"":""SALL2"",""id"":""6297""},{""label"":""TMEM67"",""id"":""91147""}]"	"[""6297"",""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12270""}]"
DOID:12271	"[""aniridia"",""Aplasia of iris"",""isolated aniridia""]"	"[{""label"":""ELP4"",""id"":""26610""}]"	"[""26610""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12271""}]"
DOID:1229	"[""paranoid schizophrenia"",""Paranoid type schizophrenia"",""Paraphrenia - late"",""Paraphrenic schizophrenia"",""chronic paranoid schizophrenia"",""paranoid type schizophrenia subchronic state""]"	"[{""label"":""HSPA1A"",""id"":""3303""},{""label"":""KCNN3"",""id"":""3782""}]"	"[""3303"",""3782""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1229""}]"
DOID:12297	"[""Vogt-Koyanagi-Harada disease"",""Harada's disease"",""Vogt-Koyanagi syndrome"",""uveomeningoencephalitic syndrome""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""STAT4"",""id"":""6775""}]"	"[""3117"",""3119"",""3123"",""6775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12297""}]"
DOID:12306	"[""vitiligo""]"	"[{""label"":""C4A"",""id"":""720""},{""label"":""CAT"",""id"":""847""},{""label"":""COMT"",""id"":""1312""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""ESR1"",""id"":""2099""},{""label"":""HGF"",""id"":""3082""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""IFNG"",""id"":""3458""},{""label"":""MBL2"",""id"":""4153""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TYR"",""id"":""7299""}]"	"[""1312"",""1493"",""2099"",""3082"",""3117"",""3119"",""3123"",""3303"",""3458"",""4153"",""6648"",""7097"",""7099"",""720"",""7299"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12306""}]"
DOID:12308	"[""Dubin-Johnson syndrome"",""Dubin Johnson syndrome"",""chronic idiopathic jaundice""]"	"[{""label"":""ABCC2"",""id"":""1244""}]"	"[""1244""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12308""}]"
DOID:12308	"[""Dubin-Johnson syndrome"",""Dubin Johnson syndrome"",""chronic idiopathic jaundice""]"	"[{""label"":""Abcc2"",""id"":""25303""}]"	"[""25303""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12308""}]"
DOID:12336	"[""male infertility""]"	"[{""label"":""Bscl2"",""id"":""14705""},{""label"":""Csnk2a2"",""id"":""13000""}]"	"[""13000"",""14705""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12336""}]"
DOID:12347	"[""osteogenesis imperfecta"",""Lobstein's syndrome"",""Osteopsathyrosis"",""Vrolik's disease"",""brittle bone disease""]"	"[{""label"":""Col1a1"",""id"":""12842""},{""label"":""Col1a2"",""id"":""12843""},{""label"":""Smad4"",""id"":""17128""}]"	"[""12842"",""12843"",""17128""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12347""}]"
DOID:12347	"[""osteogenesis imperfecta"",""Lobstein's syndrome"",""Osteopsathyrosis"",""Vrolik's disease"",""brittle bone disease""]"	"[{""label"":""CCDC134"",""id"":""79879""},{""label"":""COL1A1"",""id"":""1277""},{""label"":""COL1A2"",""id"":""1278""},{""label"":""PHLDB1"",""id"":""23187""}]"	"[""1277"",""1278"",""23187"",""79879""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12347""}]"
DOID:12361	"[""Graves' disease"",""Grave's disease"",""Graves disease"",""exophthalmic goiter""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""BTNL2"",""id"":""56244""},{""label"":""C4A"",""id"":""720""},{""label"":""C4B"",""id"":""721""},{""label"":""CD40"",""id"":""958""},{""label"":""CD40LG"",""id"":""959""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""DNMT1"",""id"":""1786""},{""label"":""GC"",""id"":""2638""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HLA-DRB3"",""id"":""3125""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL17A"",""id"":""3605""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL3"",""id"":""3562""},{""label"":""IL6"",""id"":""3569""},{""label"":""LTA"",""id"":""4049""},{""label"":""OGG1"",""id"":""4968""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""TG"",""id"":""7038""},{""label"":""TNF"",""id"":""7124""},{""label"":""TP53"",""id"":""7157""},{""label"":""TSHR"",""id"":""7253""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""149233"",""1493"",""154"",""1543"",""1786"",""2638"",""3106"",""3117"",""3119"",""3123"",""3125"",""3383"",""3458"",""3558"",""3562"",""3569"",""3586"",""3596"",""3605"",""4049"",""4968"",""5054"",""56244"",""7038"",""7124"",""7157"",""720"",""721"",""7253"",""7422"",""958"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12361""}]"
DOID:12365	"[""malaria"",""induced malaria""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ACKR1"",""id"":""2532""},{""label"":""APOE"",""id"":""348""},{""label"":""CBS"",""id"":""875""},{""label"":""CD36"",""id"":""948""},{""label"":""CR1"",""id"":""1378""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR2B"",""id"":""2213""},{""label"":""G6PD"",""id"":""2539""},{""label"":""GYPA"",""id"":""2993""},{""label"":""GYPB"",""id"":""2994""},{""label"":""GYPC"",""id"":""2995""},{""label"":""HBB"",""id"":""3043""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""KIR3DL1"",""id"":""3811""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""NCR3"",""id"":""259197""},{""label"":""NOS2"",""id"":""4843""},{""label"":""PKLR"",""id"":""5313""},{""label"":""SLC19A1"",""id"":""6573""},{""label"":""TNF"",""id"":""7124""},{""label"":""TREM1"",""id"":""54210""}]"	"[""1378"",""2212"",""2213"",""2532"",""2539"",""259197"",""2993"",""2994"",""2995"",""3043"",""3383"",""348"",""3811"",""3813"",""4843"",""5243"",""5313"",""54210"",""6573"",""7124"",""875"",""948""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12365""}]"
DOID:12365	"[""malaria"",""induced malaria""]"	"[{""label"":""Aqp4"",""id"":""11829""},{""label"":""Fcgr2b"",""id"":""14130""},{""label"":""Icam1"",""id"":""15894""},{""label"":""Ifng"",""id"":""15978""}]"	"[""11829"",""14130"",""15894"",""15978""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12365""}]"
DOID:12377	"[""spinal muscular atrophy""]"	"[{""label"":""AR"",""id"":""367""},{""label"":""DPP6"",""id"":""1804""},{""label"":""HEXB"",""id"":""3074""},{""label"":""VAPB"",""id"":""9217""}]"	"[""1804"",""3074"",""367"",""9217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12377""}]"
DOID:12387	"[""nephrogenic diabetes insipidus""]"	"[{""label"":""Aqp2"",""id"":""11827""},{""label"":""Aqp3"",""id"":""11828""},{""label"":""Avpr2"",""id"":""12000""},{""label"":""Clcnka"",""id"":""12733""},{""label"":""Grn"",""id"":""14824""}]"	"[""11827"",""11828"",""12000"",""12733"",""14824""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12387""}]"
DOID:12387	"[""nephrogenic diabetes insipidus""]"	"[{""label"":""Slc4a4"",""id"":""84484""},{""label"":""Stim1"",""id"":""361618""}]"	"[""361618"",""84484""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12387""}]"
DOID:12387	"[""nephrogenic diabetes insipidus""]"	"[{""label"":""AQP2"",""id"":""359""},{""label"":""AVPR2"",""id"":""554""}]"	"[""359"",""554""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12387""}]"
DOID:12388	"[""neurohypophyseal diabetes insipidus"",""Pituitary diabetes insipidus"",""Vasopressin deficiency"",""vasopressin defective diabetes insipidus""]"	"[{""label"":""AVP"",""id"":""551""}]"	"[""551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12388""}]"
DOID:12388	"[""neurohypophyseal diabetes insipidus"",""Pituitary diabetes insipidus"",""Vasopressin deficiency"",""vasopressin defective diabetes insipidus""]"	"[{""label"":""Avp"",""id"":""11998""}]"	"[""11998""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12388""}]"
DOID:12399	"[""pathological gambling"",""Compulsive gambling""]"	"[{""label"":""COMT"",""id"":""1312""},{""label"":""DRD4"",""id"":""1815""},{""label"":""HTR2A"",""id"":""3356""}]"	"[""1312"",""1815"",""3356""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12399""}]"
DOID:1240	"[""leukemia""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""ACE"",""id"":""1636""},{""label"":""ACSL6"",""id"":""23305""},{""label"":""AKR1C3"",""id"":""8644""},{""label"":""BCR"",""id"":""613""},{""label"":""FADD"",""id"":""8772""},{""label"":""GPX1"",""id"":""2876""},{""label"":""NAT2"",""id"":""10""},{""label"":""PDGFRA"",""id"":""5156""}]"	"[""10"",""1636"",""23305"",""28"",""2876"",""5156"",""613"",""8644"",""8772""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1240""}]"
DOID:12401	"[""intermittent explosive disorder"",""explosive personality disorder""]"	"[{""label"":""COMT"",""id"":""1312""}]"	"[""1312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12401""}]"
DOID:12449	"[""aplastic anemia""]"	"[{""label"":""DKC1"",""id"":""1736""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IFNG"",""id"":""3458""},{""label"":""NBN"",""id"":""4683""},{""label"":""PRF1"",""id"":""5551""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""THPO"",""id"":""7066""},{""label"":""TNF"",""id"":""7124""}]"	"[""1736"",""3117"",""3119"",""3458"",""4683"",""5551"",""7040"",""7066"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12449""}]"
DOID:12449	"[""aplastic anemia""]"	"[{""label"":""Ifng"",""id"":""15978""},{""label"":""Rasa3"",""id"":""19414""}]"	"[""15978"",""19414""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12449""}]"
DOID:1245	"[""vulva cancer"",""Ca vulva"",""Vulvar tumor"",""malignant Vulvar tumor"",""malignant neoplasm of vulva"",""malignant tumor of vulva"",""neoplasm of vulva"",""vulval cancer"",""vulval neoplasm"",""vulvar neoplasm""]"	"[{""label"":""HLA-A"",""id"":""3105""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""NOS3"",""id"":""4846""}]"	"[""3105"",""3119"",""3123"",""4846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1245""}]"
DOID:12466	"[""secondary hyperparathyroidism""]"	"[{""label"":""Ptgs2"",""id"":""29527""}]"	"[""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12466""}]"
DOID:12466	"[""secondary hyperparathyroidism""]"	"[{""label"":""CASR"",""id"":""846""}]"	"[""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12466""}]"
DOID:12531	"[""von Willebrand's disease"",""vascular hemophilia"",""vascular pseudohemophilia"",""von Willebrand disease"",""von Willebrand disorder"",""von Willebrand's-Jurgens' disease"",""von Willebrand-Jrgens disease""]"	"[{""label"":""Vwf"",""id"":""22371""}]"	"[""22371""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12531""}]"
DOID:12531	"[""von Willebrand's disease"",""vascular hemophilia"",""vascular pseudohemophilia"",""von Willebrand disease"",""von Willebrand disorder"",""von Willebrand's-Jurgens' disease"",""von Willebrand-Jrgens disease""]"	"[{""label"":""F3"",""id"":""2152""},{""label"":""VWF"",""id"":""7450""}]"	"[""2152"",""7450""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12531""}]"
DOID:12549	"[""hepatitis A"",""Viral hepatitis, type A""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1636"",""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12549""}]"
DOID:12554	"[""hemolytic-uremic syndrome"",""haemolytic-uraemic syndrome"",""hemolytic uremic syndrome""]"	"[{""label"":""C1GALT1C1"",""id"":""29071""},{""label"":""CD36"",""id"":""948""},{""label"":""CD46"",""id"":""4179""},{""label"":""CFH"",""id"":""3075""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MBL2"",""id"":""4153""},{""label"":""PLA2G7"",""id"":""7941""}]"	"[""29071"",""3075"",""3557"",""4153"",""4179"",""7941"",""948""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12554""}]"
DOID:12554	"[""hemolytic-uremic syndrome"",""haemolytic-uraemic syndrome"",""hemolytic uremic syndrome""]"	"[{""label"":""Cfh"",""id"":""12628""}]"	"[""12628""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12554""}]"
DOID:12557	"[""Duane retraction syndrome"",""Duane's syndrome"",""Stilling-Turk-Duane syndrome""]"	"[{""label"":""SALL4"",""id"":""57167""}]"	"[""57167""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12557""}]"
DOID:12558	"[""chronic progressive external ophthalmoplegia"",""progressive external ophthalmoplegia""]"	"[{""label"":""RRM1"",""id"":""6240""}]"	"[""6240""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12558""}]"
DOID:12559	"[""idiopathic juvenile osteoporosis"",""Idiopathic osteoporosis"",""juvenile osteoporosis""]"	"[{""label"":""LRP5"",""id"":""4041""}]"	"[""4041""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12559""}]"
DOID:12574	"[""posterior uveitis"",""Uveitis, posterior""]"	"[{""label"":""CCR2"",""id"":""729230""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CFH"",""id"":""3075""}]"	"[""1234"",""3075"",""729230""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12574""}]"
DOID:12577	"[""urethral obstruction"",""Obstruction of urethra""]"	"[{""label"":""CYP19A1"",""id"":""1588""}]"	"[""1588""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12577""}]"
DOID:12583	"[""velocardiofacial syndrome"",""Shprintzen syndrome"",""VCF-Velocardiofacial syndrome""]"	"[{""label"":""Chrd"",""id"":""12667""},{""label"":""Crkl"",""id"":""12929""},{""label"":""Ednra"",""id"":""13617""},{""label"":""Trappc10"",""id"":""216131""}]"	"[""12667"",""12929"",""13617"",""216131""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12583""}]"
DOID:12662	"[""paracoccidioidomycosis"",""Mucocutaneous-lymphangitic paracoccidioidomycosis"",""paracoccidioidal mycosis""]"	"[{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""TNF"",""id"":""7124""}]"	"[""3123"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12662""}]"
DOID:12678	"[""hypercalcemia""]"	"[{""label"":""CASR"",""id"":""846""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""SLC34A1"",""id"":""6569""}]"	"[""1591"",""6569"",""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12678""}]"
DOID:12678	"[""hypercalcemia""]"	"[{""label"":""Pth1r"",""id"":""56813""}]"	"[""56813""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12678""}]"
DOID:12689	"[""acoustic neuroma"",""Vestibular Neurilemmoma"",""Vestibular schwannoma""]"	"[{""label"":""CYP2E1"",""id"":""1571""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""1571"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12689""}]"
DOID:127	"[""leiomyoma"",""leiomyomatous neoplasm"",""leiomyomatous tumor""]"	"[{""label"":""AR"",""id"":""367""},{""label"":""COMT"",""id"":""1312""},{""label"":""HMGA2"",""id"":""8091""},{""label"":""KAT6B"",""id"":""23522""},{""label"":""PTK2"",""id"":""5747""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1312"",""23522"",""367"",""5747"",""7515"",""8091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:127""}]"
DOID:127	"[""leiomyoma"",""leiomyomatous neoplasm"",""leiomyomatous tumor""]"	"[{""label"":""Myc"",""id"":""24577""},{""label"":""Tgfbr1"",""id"":""29591""}]"	"[""24577"",""29591""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:127""}]"
DOID:1270	"[""hereditary hemorrhagic telangiectasia"",""Osler hemorrhagic telangiectasia syndrome"",""Osler-Weber-Rendu disease"",""Rendu-Osler-Weber disease""]"	"[{""label"":""ACVRL1"",""id"":""94""},{""label"":""ENG"",""id"":""2022""},{""label"":""GDF2"",""id"":""2658""},{""label"":""SMAD4"",""id"":""4089""}]"	"[""2022"",""2658"",""4089"",""94""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1270""}]"
DOID:1270	"[""hereditary hemorrhagic telangiectasia"",""Osler hemorrhagic telangiectasia syndrome"",""Osler-Weber-Rendu disease"",""Rendu-Osler-Weber disease""]"	"[{""label"":""Acvrl1"",""id"":""11482""},{""label"":""Eng"",""id"":""13805""}]"	"[""11482"",""13805""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1270""}]"
DOID:12700	"[""hyperprolactinemia"",""Chiari-Frommel syndrome"",""Pregnancy-related A-G syndrome"",""hyperprolactinaemia""]"	"[{""label"":""PGR"",""id"":""5241""},{""label"":""PRLR"",""id"":""5618""}]"	"[""5241"",""5618""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12700""}]"
DOID:12700	"[""hyperprolactinemia"",""Chiari-Frommel syndrome"",""Pregnancy-related A-G syndrome"",""hyperprolactinaemia""]"	"[{""label"":""Gdnf"",""id"":""25453""}]"	"[""25453""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12700""}]"
DOID:12704	"[""ataxia telangiectasia"",""Boder-Sedgwick syndrome"",""Louis Bar syndrome""]"	"[{""label"":""ATM"",""id"":""472""},{""label"":""BAX"",""id"":""581""},{""label"":""HDAC4"",""id"":""9759""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL2"",""id"":""3558""}]"	"[""3458"",""3558"",""472"",""581"",""9759""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12704""}]"
DOID:12705	"[""Friedreich ataxia"",""Friedreich's ataxia"",""Friedreich's tabes""]"	"[{""label"":""AGTR1"",""id"":""185""}]"	"[""185""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12705""}]"
DOID:12712	"[""nephronophthisis"",""medullary cystic disease"",""medullary cystic kidney""]"	"[{""label"":""NPHP3"",""id"":""27031""},{""label"":""RPGRIP1L"",""id"":""23322""},{""label"":""TMEM67"",""id"":""91147""}]"	"[""23322"",""27031"",""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12712""}]"
DOID:12712	"[""nephronophthisis"",""medullary cystic disease"",""medullary cystic kidney""]"	"[{""label"":""Wwtr1"",""id"":""97064""}]"	"[""97064""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12712""}]"
DOID:12714	"[""Ellis-Van Creveld syndrome"",""Chondroectodermal dysplasia"",""mesoectodermal dysplasia""]"	"[{""label"":""Evc2"",""id"":""68525""},{""label"":""Evc"",""id"":""59056""}]"	"[""59056"",""68525""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12714""}]"
DOID:12714	"[""Ellis-Van Creveld syndrome"",""Chondroectodermal dysplasia"",""mesoectodermal dysplasia""]"	"[{""label"":""EVC2"",""id"":""132884""},{""label"":""WDR35"",""id"":""57539""}]"	"[""132884"",""57539""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12714""}]"
DOID:12716	"[""newborn respiratory distress syndrome"",""HMD - Hyaline membrane disease"",""Neonatal respiratory Distress syndrome"",""hyaline membrane disease"",""pulmonary hyaline membrane disease"",""pulmonary hypoperfusion syndrome of newborn"",""respiratory distress syndrome of newborn""]"	"[{""label"":""Ndst1"",""id"":""15531""},{""label"":""Vegfa"",""id"":""22339""}]"	"[""15531"",""22339""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12716""}]"
DOID:12716	"[""newborn respiratory distress syndrome"",""HMD - Hyaline membrane disease"",""Neonatal respiratory Distress syndrome"",""hyaline membrane disease"",""pulmonary hyaline membrane disease"",""pulmonary hypoperfusion syndrome of newborn"",""respiratory distress syndrome of newborn""]"	"[{""label"":""CAT"",""id"":""847""},{""label"":""NPSR1"",""id"":""387129""},{""label"":""SFTPA1"",""id"":""653509""},{""label"":""SFTPA2"",""id"":""729238""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""SOD1"",""id"":""6647""}]"	"[""387129"",""6439"",""6441"",""653509"",""6647"",""729238"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12716""}]"
DOID:1272	"[""telangiectasis"",""telangiectasia""]"	"[{""label"":""NOS3"",""id"":""4846""}]"	"[""4846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1272""}]"
DOID:12720	"[""cerebral atherosclerosis""]"	"[{""label"":""KALRN"",""id"":""8997""}]"	"[""8997""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12720""}]"
DOID:12721	"[""multiple epiphyseal dysplasia"",""polyepiphyseal dysplasia""]"	"[{""label"":""Comp"",""id"":""12845""}]"	"[""12845""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12721""}]"
DOID:1273	"[""respiratory syncytial virus infectious disease"",""RSV"",""respiratory syncytial virus""]"	"[{""label"":""ACE2"",""id"":""59272""},{""label"":""CCR5"",""id"":""1234""},{""label"":""IL9"",""id"":""3578""},{""label"":""SFTPA1"",""id"":""653509""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPC"",""id"":""6440""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""TLR4"",""id"":""7099""}]"	"[""1234"",""3578"",""59272"",""6439"",""6440"",""6441"",""653509"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1273""}]"
DOID:12732	"[""intermediate uveitis"",""chronic cyclitis"",""peripheral uveoretinitis""]"	"[{""label"":""CCR2"",""id"":""729230""},{""label"":""TNF"",""id"":""7124""}]"	"[""7124"",""729230""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12732""}]"
DOID:12783	"[""migraine without aura"",""common migraine""]"	"[{""label"":""LDLR"",""id"":""3949""},{""label"":""TNF"",""id"":""7124""}]"	"[""3949"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12783""}]"
DOID:12798	"[""mucopolysaccharidosis""]"	"[{""label"":""ARSK"",""id"":""153642""},{""label"":""HYAL1"",""id"":""3373""}]"	"[""153642"",""3373""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12798""}]"
DOID:12798	"[""mucopolysaccharidosis""]"	"[{""label"":""Arsg"",""id"":""74008""},{""label"":""Arsk"",""id"":""77041""}]"	"[""74008"",""77041""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12798""}]"
DOID:12798	"[""mucopolysaccharidosis""]"	"[{""label"":""K09E4.4"",""id"":""175063""}]"	"[""175063""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12798""}]"
DOID:12799	"[""mucopolysaccharidosis II"",""Hunter syndrome"",""Hunter's syndrome"",""MPS II - Hunter syndrome"",""Mucopolysaccharidosis, MPS-II"",""deficiency of iduronate-2-sulphatase""]"	"[{""label"":""Ids"",""id"":""15931""}]"	"[""15931""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12799""}]"
DOID:12799	"[""mucopolysaccharidosis II"",""Hunter syndrome"",""Hunter's syndrome"",""MPS II - Hunter syndrome"",""Mucopolysaccharidosis, MPS-II"",""deficiency of iduronate-2-sulphatase""]"	"[{""label"":""IDS"",""id"":""3423""}]"	"[""3423""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00032""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12799""}]"
DOID:12800	"[""mucopolysaccharidosis VI"",""MPS VI - Maroteaux-Lamy syndrome"",""Maroteaux - Lamy syndrome"",""Maroteaux-Lamy syndrome"",""arylsulfatase B deficiency"",""deficiency of N-acetylgalactosamine-4-sulfatase""]"	"[{""label"":""ARSB"",""id"":""411""}]"	"[""411""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00041""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00042""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00043""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00044""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12800""}]"
DOID:12800	"[""mucopolysaccharidosis VI"",""MPS VI - Maroteaux-Lamy syndrome"",""Maroteaux - Lamy syndrome"",""Maroteaux-Lamy syndrome"",""arylsulfatase B deficiency"",""deficiency of N-acetylgalactosamine-4-sulfatase""]"	"[{""label"":""Arsb"",""id"":""25227""}]"	"[""25227""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12800""}]"
DOID:12800	"[""mucopolysaccharidosis VI"",""MPS VI - Maroteaux-Lamy syndrome"",""Maroteaux - Lamy syndrome"",""Maroteaux-Lamy syndrome"",""arylsulfatase B deficiency"",""deficiency of N-acetylgalactosamine-4-sulfatase""]"	"[{""label"":""Arsb"",""id"":""11881""}]"	"[""11881""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12800""}]"
DOID:12801	"[""mucopolysaccharidosis III"",""Mucopolysaccharidosis, MPS-III"",""N-sulphoglucosamine sulphohydrolase deficiency"",""Sanfilippo's syndrome"",""heparan sulfate sulfatase deficiency""]"	"[{""label"":""Gns"",""id"":""75612""},{""label"":""Hgsnat"",""id"":""52120""},{""label"":""Naglu"",""id"":""27419""},{""label"":""Sgsh"",""id"":""27029""}]"	"[""27029"",""27419"",""52120"",""75612""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12801""}]"
DOID:12801	"[""mucopolysaccharidosis III"",""Mucopolysaccharidosis, MPS-III"",""N-sulphoglucosamine sulphohydrolase deficiency"",""Sanfilippo's syndrome"",""heparan sulfate sulfatase deficiency""]"	"[{""label"":""GNS"",""id"":""2799""},{""label"":""NAGLU"",""id"":""4669""},{""label"":""SGSH"",""id"":""6448""}]"	"[""2799"",""4669"",""6448""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00034""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00037""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12801""}]"
DOID:12802	"[""mucopolysaccharidosis I"",""Hurler syndrome"",""Hurler-Scheie syndrome"",""Lipochondrodystrophy"",""MPS I - Hurler syndrome"",""Mucopolysaccharidosis, MPS-I"",""Mucopolysaccharidosis, type 1"",""iduronidase deficiency disease""]"	"[{""label"":""Idua"",""id"":""34544""}]"	"[""34544""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12802""}]"
DOID:12802	"[""mucopolysaccharidosis I"",""Hurler syndrome"",""Hurler-Scheie syndrome"",""Lipochondrodystrophy"",""MPS I - Hurler syndrome"",""Mucopolysaccharidosis, MPS-I"",""Mucopolysaccharidosis, type 1"",""iduronidase deficiency disease""]"	"[{""label"":""IDUA"",""id"":""3425""}]"	"[""3425""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00029""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00030""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00031""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12802""}]"
DOID:12802	"[""mucopolysaccharidosis I"",""Hurler syndrome"",""Hurler-Scheie syndrome"",""Lipochondrodystrophy"",""MPS I - Hurler syndrome"",""Mucopolysaccharidosis, MPS-I"",""Mucopolysaccharidosis, type 1"",""iduronidase deficiency disease""]"	"[{""label"":""Idua"",""id"":""15932""}]"	"[""15932""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12802""}]"
DOID:12803	"[""mucopolysaccharidosis type VII"",""MPS VII - Sly syndrome"",""Sly syndrome"",""beta-glucuronidase deficiency"",""deficiency of beta-glucuronidase"",""mucopolysaccharidosis VII""]"	"[{""label"":""Gusb"",""id"":""110006""}]"	"[""110006""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12803""}]"
DOID:12803	"[""mucopolysaccharidosis type VII"",""MPS VII - Sly syndrome"",""Sly syndrome"",""beta-glucuronidase deficiency"",""deficiency of beta-glucuronidase"",""mucopolysaccharidosis VII""]"	"[{""label"":""GUSB"",""id"":""2990""}]"	"[""2990""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00045""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12803""}]"
DOID:12804	"[""mucopolysaccharidosis IV"",""Mucopolysaccharidosis, MPS-IV"",""deficiency of N-acetylgalactosamine-6-sulphatase"",""deficiency of chondroitinsulphatase"",""galactosamine-6-sulfatase deficiency""]"	"[{""label"":""Galns"",""id"":""50917""}]"	"[""50917""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12804""}]"
DOID:12804	"[""mucopolysaccharidosis IV"",""Mucopolysaccharidosis, MPS-IV"",""deficiency of N-acetylgalactosamine-6-sulphatase"",""deficiency of chondroitinsulphatase"",""galactosamine-6-sulfatase deficiency""]"	"[{""label"":""GALNS"",""id"":""2588""},{""label"":""GLB1"",""id"":""2720""}]"	"[""2588"",""2720""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00039""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00040""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12804""}]"
DOID:1283	"[""enterocele"",""vaginal enterocele""]"	"[{""label"":""ALDH18A1"",""id"":""5832""}]"	"[""5832""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1283""}]"
DOID:12835	"[""quadriplegia"",""tetraplegia""]"	"[{""label"":""IL6"",""id"":""3569""}]"	"[""3569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12835""}]"
DOID:12842	"[""Guillain-Barre syndrome"",""Infectious neuronitis"",""Post-infectious polyneuritis"",""Postinfectious polyneuritis"",""acute infective polyneuritis"",""acute inflammatory demyelinating polyradiculopathy"",""acute postinfectious polyneuropathy""]"	"[{""label"":""Cd86"",""id"":""12524""}]"	"[""12524""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12842""}]"
DOID:12842	"[""Guillain-Barre syndrome"",""Infectious neuronitis"",""Post-infectious polyneuritis"",""Postinfectious polyneuritis"",""acute infective polyneuritis"",""acute inflammatory demyelinating polyradiculopathy"",""acute postinfectious polyneuropathy""]"	"[{""label"":""PMP22"",""id"":""5376""}]"	"[""5376""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12842""}]"
DOID:12849	"[""autistic disorder"",""Kanner's syndrome"",""autism"",""autistic disorder of childhood onset"",""childhood autism"",""infantile autism""]"	"[{""label"":""C4B"",""id"":""721""},{""label"":""CNTNAP2"",""id"":""26047""},{""label"":""EIF4E"",""id"":""1977""},{""label"":""EN2"",""id"":""2020""},{""label"":""FOXP2"",""id"":""93986""},{""label"":""GABRA2"",""id"":""2555""},{""label"":""GABRA4"",""id"":""2557""},{""label"":""GABRB1"",""id"":""2560""},{""label"":""GABRB2"",""id"":""2561""},{""label"":""GABRR2"",""id"":""2570""},{""label"":""GLO1"",""id"":""2739""},{""label"":""GRM8"",""id"":""2918""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HRAS"",""id"":""3265""},{""label"":""HSPD1"",""id"":""3329""},{""label"":""KCNQ3"",""id"":""3786""},{""label"":""KDM4C"",""id"":""23081""},{""label"":""KMT2E"",""id"":""55904""},{""label"":""LAMB1"",""id"":""3912""},{""label"":""MECP2"",""id"":""4204""},{""label"":""MET"",""id"":""4233""},{""label"":""MTR"",""id"":""4548""},{""label"":""NF1"",""id"":""4763""},{""label"":""NLGN1"",""id"":""22871""},{""label"":""NLGN3"",""id"":""54413""},{""label"":""NLGN4X"",""id"":""57502""},{""label"":""NTRK2"",""id"":""4915""},{""label"":""PIK3CG"",""id"":""5294""},{""label"":""PTCHD1"",""id"":""139411""},{""label"":""RELN"",""id"":""5649""},{""label"":""SETDB1"",""id"":""9869""},{""label"":""SHANK2"",""id"":""22941""},{""label"":""SLC25A12"",""id"":""8604""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""SLC9A9"",""id"":""285195""}]"	"[""139411"",""1977"",""2020"",""22871"",""22941"",""23081"",""2555"",""2557"",""2560"",""2561"",""2570"",""26047"",""2739"",""285195"",""2918"",""3123"",""3265"",""3329"",""3786"",""3912"",""4204"",""4233"",""4548"",""4763"",""4915"",""5294"",""54413"",""55904"",""5649"",""57502"",""6532"",""721"",""8604"",""93986"",""9869""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12849""}]"
DOID:12849	"[""autistic disorder"",""Kanner's syndrome"",""autism"",""autistic disorder of childhood onset"",""childhood autism"",""infantile autism""]"	"[{""label"":""Ank2"",""id"":""109676""}]"	"[""109676""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12849""}]"
DOID:12858	"[""Huntington's disease"",""HD"",""Huntington disease"",""Huntington's chorea""]"	"[{""label"":""Cnr2"",""id"":""57302""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Qprt"",""id"":""293504""}]"	"[""293504"",""29527"",""57302"",""83516""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12858""}]"
DOID:12858	"[""Huntington's disease"",""HD"",""Huntington disease"",""Huntington's chorea""]"	"[{""label"":""ABAT"",""id"":""18""},{""label"":""BDNF"",""id"":""627""},{""label"":""EIF2AK2"",""id"":""5610""},{""label"":""GLUL"",""id"":""2752""},{""label"":""GRIK2"",""id"":""2898""},{""label"":""GRIN2A"",""id"":""2903""},{""label"":""GRIN2B"",""id"":""2904""},{""label"":""HSF1"",""id"":""3297""},{""label"":""HTT"",""id"":""3064""},{""label"":""IL6"",""id"":""3569""},{""label"":""IL6R"",""id"":""3570""},{""label"":""NOG"",""id"":""9241""},{""label"":""NPY2R"",""id"":""4887""},{""label"":""NRF1"",""id"":""4899""},{""label"":""PPARGC1A"",""id"":""10891""},{""label"":""PRKAA1"",""id"":""5562""},{""label"":""SIRT1"",""id"":""23411""},{""label"":""TFAM"",""id"":""7019""}]"	"[""10891"",""18"",""23411"",""2752"",""2898"",""2903"",""2904"",""3064"",""3297"",""3569"",""3570"",""4887"",""4899"",""5562"",""5610"",""627"",""7019"",""9241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12858""}]"
DOID:12858	"[""Huntington's disease"",""HD"",""Huntington disease"",""Huntington's chorea""]"	"[{""label"":""atg-18"",""id"":""179246""}]"	"[""179246""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12858""}]"
DOID:12859	"[""choreatic disease"",""chorea"",""hereditary chorea""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""NKX2-1"",""id"":""7080""},{""label"":""VPS13A"",""id"":""23230""}]"	"[""23230"",""3117"",""3119"",""3123"",""7080""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12859""}]"
DOID:1287	"[""cardiovascular system disease"",""disease of subdivision of hemolymphoid system""]"	"[{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""AGER"",""id"":""177""},{""label"":""CFH"",""id"":""3075""},{""label"":""ENPP1"",""id"":""5167""},{""label"":""FGB"",""id"":""2244""},{""label"":""FTO"",""id"":""79068""},{""label"":""GIPR"",""id"":""2696""},{""label"":""GPX1"",""id"":""2876""},{""label"":""GYS1"",""id"":""2997""},{""label"":""LIPG"",""id"":""9388""},{""label"":""MPO"",""id"":""4353""},{""label"":""PPARG"",""id"":""5468""},{""label"":""PPARGC1A"",""id"":""10891""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""TLR9"",""id"":""54106""},{""label"":""UBR1"",""id"":""197131""}]"	"[""10891"",""177"",""197131"",""2244"",""2696"",""2876"",""2997"",""3075"",""4353"",""5167"",""54106"",""5468"",""5743"",""79068"",""9370"",""9388""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1287""}]"
DOID:1287	"[""cardiovascular system disease"",""disease of subdivision of hemolymphoid system""]"	"[{""label"":""enpl-1"",""id"":""178014""}]"	"[""178014""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1287""}]"
DOID:1289	"[""neurodegenerative disease"",""degenerative disease""]"	"[{""label"":""AttC"",""id"":""36484""},{""label"":""Dro"",""id"":""36635""},{""label"":""Drs"",""id"":""38419""},{""label"":""FIG4"",""id"":""33658""},{""label"":""Gga"",""id"":""31902""},{""label"":""Nup50"",""id"":""35784""},{""label"":""Sarm"",""id"":""38895""},{""label"":""Tpi"",""id"":""43582""},{""label"":""drpr"",""id"":""38218""},{""label"":""ft"",""id"":""33627""},{""label"":""ptc"",""id"":""35851""},{""label"":""st"",""id"":""39836""}]"	"[""31902"",""33627"",""33658"",""35784"",""35851"",""36484"",""36635"",""38218"",""38419"",""38895"",""39836"",""43582""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1289""}]"
DOID:1289	"[""neurodegenerative disease"",""degenerative disease""]"	"[{""label"":""deg-1"",""id"":""181035""},{""label"":""glr-1"",""id"":""176204""},{""label"":""glt-3"",""id"":""177882""},{""label"":""mec-4"",""id"":""181728""},{""label"":""pkc-2"",""id"":""181166""},{""label"":""poml-1"",""id"":""187297""}]"	"[""176204"",""177882"",""181035"",""181166"",""181728"",""187297""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1289""}]"
DOID:1289	"[""neurodegenerative disease"",""degenerative disease""]"	"[{""label"":""EPO"",""id"":""2056""},{""label"":""FUS"",""id"":""2521""}]"	"[""2056"",""2521""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1289""}]"
DOID:1289	"[""neurodegenerative disease"",""degenerative disease""]"	"[{""label"":""ACO1"",""id"":""851013""},{""label"":""HRR25"",""id"":""855897""}]"	"[""851013"",""855897""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1289""}]"
DOID:12894	"[""Sjogren's syndrome"",""Sicca syndrome"",""Sjogren syndrome"",""xerodermosteosis""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""CAST"",""id"":""831""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HNRNPH1"",""id"":""3187""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL6"",""id"":""3569""},{""label"":""LTA"",""id"":""4049""},{""label"":""MMP9"",""id"":""4318""},{""label"":""STAT4"",""id"":""6775""},{""label"":""TNF"",""id"":""7124""},{""label"":""VIM"",""id"":""7431""}]"	"[""1234"",""1493"",""1543"",""3117"",""3119"",""3123"",""3187"",""348"",""3557"",""3569"",""3586"",""4049"",""4318"",""6775"",""7124"",""7431"",""831""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12894""}]"
DOID:12894	"[""Sjogren's syndrome"",""Sicca syndrome"",""Sjogren syndrome"",""xerodermosteosis""]"	"[{""label"":""Ccr7"",""id"":""12775""},{""label"":""Fas"",""id"":""14102""},{""label"":""Il2"",""id"":""16183""},{""label"":""Il2ra"",""id"":""16184""},{""label"":""Il4"",""id"":""16189""},{""label"":""Muc19"",""id"":""239611""},{""label"":""St14"",""id"":""19143""},{""label"":""Tgfb1"",""id"":""21803""},{""label"":""Thbs1"",""id"":""21825""},{""label"":""Tnfsf13b"",""id"":""24099""}]"	"[""12775"",""14102"",""16183"",""16184"",""16189"",""19143"",""21803"",""21825"",""239611"",""24099""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12894""}]"
DOID:12918	"[""thromboangiitis obliterans"",""Buerger's disease"",""Presenile gangrene""]"	"[{""label"":""HLA-A"",""id"":""3105""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3105"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12918""}]"
DOID:12930	"[""dilated cardiomyopathy"",""primary dilated cardiomyopathy""]"	"[{""label"":""Delta"",""id"":""42313""},{""label"":""Psn"",""id"":""40260""},{""label"":""Ser"",""id"":""43275""},{""label"":""Stim"",""id"":""32556""}]"	"[""32556"",""40260"",""42313"",""43275""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12930""}]"
DOID:12930	"[""dilated cardiomyopathy"",""primary dilated cardiomyopathy""]"	"[{""label"":""Cap2"",""id"":""67252""},{""label"":""Ctsl"",""id"":""13039""},{""label"":""Dag1"",""id"":""13138""},{""label"":""Dnm1l"",""id"":""74006""},{""label"":""Erbb2"",""id"":""13866""},{""label"":""Esrrb"",""id"":""26380""},{""label"":""Med1"",""id"":""19014""},{""label"":""Mrgprd"",""id"":""211578""},{""label"":""Myh6"",""id"":""17888""},{""label"":""Nr2f2"",""id"":""11819""},{""label"":""Pdcd1"",""id"":""18566""},{""label"":""Pdlim5"",""id"":""56376""},{""label"":""Phc1"",""id"":""13619""},{""label"":""Ppp3ca"",""id"":""19055""},{""label"":""Ptger4"",""id"":""19219""},{""label"":""Ptpn11"",""id"":""19247""},{""label"":""Rtf1"",""id"":""76246""},{""label"":""Rxra"",""id"":""20181""},{""label"":""Snai1"",""id"":""20613""},{""label"":""Sod2"",""id"":""20656""},{""label"":""Srf"",""id"":""20807""},{""label"":""Tbx20"",""id"":""57246""},{""label"":""Timp3"",""id"":""21859""},{""label"":""Tnf"",""id"":""21926""}]"	"[""11819"",""13039"",""13138"",""13619"",""13866"",""17888"",""18566"",""19014"",""19055"",""19219"",""19247"",""20181"",""20613"",""20656"",""20807"",""211578"",""21859"",""21926"",""26380"",""56376"",""57246"",""67252"",""74006"",""76246""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12930""}]"
DOID:12930	"[""dilated cardiomyopathy"",""primary dilated cardiomyopathy""]"	"[{""label"":""Adrb1"",""id"":""24925""},{""label"":""Agtr1a"",""id"":""24180""},{""label"":""Cxcr3"",""id"":""84475""},{""label"":""Ltbp2"",""id"":""59106""},{""label"":""Ppargc1a"",""id"":""83516""}]"	"[""24180"",""24925"",""59106"",""83516"",""84475""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12930""}]"
DOID:12930	"[""dilated cardiomyopathy"",""primary dilated cardiomyopathy""]"	"[{""label"":""ABCC9"",""id"":""10060""},{""label"":""ACTC1"",""id"":""70""},{""label"":""APOE"",""id"":""348""},{""label"":""CAP2"",""id"":""10486""},{""label"":""CDK8"",""id"":""1024""},{""label"":""CS"",""id"":""1431""},{""label"":""DES"",""id"":""1674""},{""label"":""DMD"",""id"":""1756""},{""label"":""DSG2"",""id"":""1829""},{""label"":""DSP"",""id"":""1832""},{""label"":""EMD"",""id"":""2010""},{""label"":""EYA4"",""id"":""2070""},{""label"":""FKRP"",""id"":""79147""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""LDB3"",""id"":""11155""},{""label"":""LEPR"",""id"":""3953""},{""label"":""LMNA"",""id"":""4000""},{""label"":""MEF2A"",""id"":""4205""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MYH7"",""id"":""4625""},{""label"":""NEBL"",""id"":""10529""},{""label"":""NFATC4"",""id"":""4776""},{""label"":""PRKCA"",""id"":""5578""},{""label"":""RBM20"",""id"":""282996""},{""label"":""RBPJ"",""id"":""3516""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SP4"",""id"":""6671""},{""label"":""TNNI3"",""id"":""7137""},{""label"":""TTN"",""id"":""7273""},{""label"":""VCL"",""id"":""7414""},{""label"":""VEZF1"",""id"":""7716""}]"	"[""10060"",""1024"",""10486"",""10529"",""11155"",""1431"",""1674"",""1756"",""1829"",""1832"",""2010"",""2070"",""282996"",""2876"",""3077"",""3119"",""348"",""3516"",""3953"",""4000"",""4205"",""4312"",""4625"",""4776"",""5578"",""6648"",""6671"",""70"",""7137"",""7273"",""7414"",""7716"",""79147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12930""}]"
DOID:12932	"[""endomyocardial fibrosis"",""African endomyocardial fibrosis"",""Becker's disease"",""Endomyocardial sclerosis"",""obscure African cardiomyopathy""]"	"[{""label"":""Uts2r"",""id"":""57305""}]"	"[""57305""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12932""}]"
DOID:12960	"[""acrocephalosyndactylia"",""Apert syndrome""]"	"[{""label"":""Fgfr2"",""id"":""14183""}]"	"[""14183""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12960""}]"
DOID:12960	"[""acrocephalosyndactylia"",""Apert syndrome""]"	"[{""label"":""FGFR1"",""id"":""2260""},{""label"":""FGFR2"",""id"":""2263""},{""label"":""TWIST1"",""id"":""7291""}]"	"[""2260"",""2263"",""7291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12960""}]"
DOID:12971	"[""hereditary spherocytosis"",""Congenital spherocytic hemolytic anemia"",""Minkowski Chauffard syndrome"",""spherocytic anemia""]"	"[{""label"":""ANK1"",""id"":""286""},{""label"":""EPB42"",""id"":""2038""},{""label"":""SLC4A1"",""id"":""6521""},{""label"":""SPTA1"",""id"":""6708""},{""label"":""SPTB"",""id"":""6710""}]"	"[""2038"",""286"",""6521"",""6708"",""6710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12971""}]"
DOID:12978	"[""Plasmodium vivax malaria"",""Malaria by Plasmodium vivax"",""Vivax Malaria""]"	"[{""label"":""ACKR1"",""id"":""2532""}]"	"[""2532""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12978""}]"
DOID:12986	"[""leukostasis""]"	"[{""label"":""SERPINF1"",""id"":""5176""}]"	"[""5176""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12986""}]"
DOID:12986	"[""leukostasis""]"	"[{""label"":""Ace"",""id"":""24310""}]"	"[""24310""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12986""}]"
DOID:12987	"[""agranulocytosis"",""Granulocytopenic disorder"",""Granulopenia"",""granulocytopenia""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12987""}]"
DOID:12995	"[""conduct disorder""]"	"[{""label"":""AR"",""id"":""367""},{""label"":""DRD4"",""id"":""1815""},{""label"":""HTR1B"",""id"":""3351""}]"	"[""1815"",""3351"",""367""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:12995""}]"
DOID:13001	"[""carotid stenosis"",""Carotid artery stenosis"",""Stenosis, carotid artery""]"	"[{""label"":""Tlr4"",""id"":""29260""},{""label"":""Vcam1"",""id"":""25361""}]"	"[""25361"",""29260""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13001""}]"
DOID:13001	"[""carotid stenosis"",""Carotid artery stenosis"",""Stenosis, carotid artery""]"	"[{""label"":""F2"",""id"":""2147""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""MT2A"",""id"":""4502""},{""label"":""PTGIS"",""id"":""5740""}]"	"[""2147"",""4312"",""4314"",""4502"",""5740""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13001""}]"
DOID:13025	"[""retinopathy of prematurity"",""Retrolental fibroplasia"",""premature retinopathy""]"	"[{""label"":""Angpt2"",""id"":""89805""}]"	"[""89805""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13025""}]"
DOID:13025	"[""retinopathy of prematurity"",""Retrolental fibroplasia"",""premature retinopathy""]"	"[{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IHH"",""id"":""3549""},{""label"":""NOS3"",""id"":""4846""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SOD1"",""id"":""6647""}]"	"[""3106"",""3123"",""3549"",""4846"",""5054"",""6647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13025""}]"
DOID:13042	"[""persistent fetal circulation syndrome"",""Fetal circulation"",""Persistent fetal circulation"",""Persistent foetal circulation"",""congenital alveolar capillary dysplasia with misalignment of pulmonary veins"",""persistent foetal circulation syndrome"",""persistent pulmonary hypertension of the newborn""]"	"[{""label"":""CPS1"",""id"":""1373""},{""label"":""ITGAM"",""id"":""3684""}]"	"[""1373"",""3684""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13042""}]"
DOID:13042	"[""persistent fetal circulation syndrome"",""Fetal circulation"",""Persistent fetal circulation"",""Persistent foetal circulation"",""congenital alveolar capillary dysplasia with misalignment of pulmonary veins"",""persistent foetal circulation syndrome"",""persistent pulmonary hypertension of the newborn""]"	"[{""label"":""Nos3"",""id"":""18127""}]"	"[""18127""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13042""}]"
DOID:1307	"[""dementia""]"	"[{""label"":""Bace1"",""id"":""29392""}]"	"[""29392""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1307""}]"
DOID:1307	"[""dementia""]"	"[{""label"":""GRN"",""id"":""2896""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""LRP8"",""id"":""7804""},{""label"":""LRPAP1"",""id"":""4043""},{""label"":""MAPT"",""id"":""4137""},{""label"":""NOS2"",""id"":""4843""},{""label"":""NOTCH4"",""id"":""4855""},{""label"":""NRG1"",""id"":""3084""},{""label"":""PON1"",""id"":""5444""},{""label"":""VCP"",""id"":""7415""},{""label"":""VLDLR"",""id"":""7436""}]"	"[""2896"",""3084"",""3156"",""3480"",""4043"",""4137"",""4843"",""4855"",""5444"",""7415"",""7436"",""7804""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1307""}]"
DOID:13078	"[""eumycotic mycetoma"",""Madura foot"",""Maduromycosis, mycotic"",""Mycotic mycetoma"",""eumycetoma"",""maduromycosis""]"	"[{""label"":""COMT"",""id"":""1312""}]"	"[""1312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13078""}]"
DOID:13088	"[""periventricular leukomalacia""]"	"[{""label"":""Tnf"",""id"":""24835""}]"	"[""24835""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13088""}]"
DOID:13096	"[""Sneddon syndrome"",""Idiopathic livedo reticularis with systemic involvement""]"	"[{""label"":""ADA2"",""id"":""51816""}]"	"[""51816""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13096""}]"
DOID:13099	"[""Moyamoya disease"",""progressive intracranial arterial occlusion""]"	"[{""label"":""ACTA2"",""id"":""59""},{""label"":""ANO1"",""id"":""55107""},{""label"":""HLA-A"",""id"":""3105""},{""label"":""RNF213"",""id"":""57674""}]"	"[""3105"",""55107"",""57674"",""59""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13099""}]"
DOID:13100	"[""intracranial vasospasm""]"	"[{""label"":""RYR1"",""id"":""6261""}]"	"[""6261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13100""}]"
DOID:1312	"[""focal segmental glomerulosclerosis"",""FGS"",""FSGS"",""focal glomerular sclerosis"",""focal glomerulosclerosis""]"	"[{""label"":""ACTN4"",""id"":""81""},{""label"":""CD2AP"",""id"":""23607""},{""label"":""TRPC6"",""id"":""7225""}]"	"[""23607"",""7225"",""81""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1312""}]"
DOID:1312	"[""focal segmental glomerulosclerosis"",""FGS"",""FSGS"",""focal glomerular sclerosis"",""focal glomerulosclerosis""]"	"[{""label"":""Myo9a"",""id"":""270163""},{""label"":""Srgap1"",""id"":""117600""}]"	"[""117600"",""270163""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1312""}]"
DOID:13129	"[""severe pre-eclampsia"",""Severe pre-eclampsia, with delivery"",""antepartum severe pre-eclampsia"",""postpartum severe pre-eclampsia"",""severe preeclampsia""]"	"[{""label"":""APEX1"",""id"":""328""}]"	"[""328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13129""}]"
DOID:13133	"[""HELLP syndrome""]"	"[{""label"":""FAS"",""id"":""355""},{""label"":""FASLG"",""id"":""356""}]"	"[""355"",""356""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13133""}]"
DOID:13139	"[""crescentic glomerulonephritis""]"	"[{""label"":""Ccl2"",""id"":""24770""},{""label"":""Fcgr2a"",""id"":""116591""},{""label"":""Mmp12"",""id"":""117033""}]"	"[""116591"",""117033"",""24770""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13139""}]"
DOID:13139	"[""crescentic glomerulonephritis""]"	"[{""label"":""IL1RN"",""id"":""3557""}]"	"[""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13139""}]"
DOID:13141	"[""uveitis""]"	"[{""label"":""Aoc3"",""id"":""29473""},{""label"":""Icam1"",""id"":""25464""},{""label"":""Sncb"",""id"":""113893""},{""label"":""Tnfrsf1a"",""id"":""25625""},{""label"":""Vip"",""id"":""117064""}]"	"[""113893"",""117064"",""25464"",""25625"",""29473""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13141""}]"
DOID:13141	"[""uveitis""]"	"[{""label"":""GC"",""id"":""2638""},{""label"":""HLA-A"",""id"":""3105""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HSPA1L"",""id"":""3305""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL6"",""id"":""3569""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF1A"",""id"":""7132""}]"	"[""149233"",""2638"",""3105"",""3106"",""3123"",""3305"",""3569"",""3586"",""3596"",""5176"",""7040"",""7124"",""7132""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13141""}]"
DOID:13166	"[""allergic bronchopulmonary aspergillosis"",""pulmonary aspergillus disease""]"	"[{""label"":""CFTR"",""id"":""1080""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""MBL2"",""id"":""4153""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNFRSF1A"",""id"":""7132""}]"	"[""1080"",""3119"",""3123"",""4153"",""54106"",""7132""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13166""}]"
DOID:13189	"[""gout"",""Articular gout"",""Gouty arthropathy"",""gouty arthritis""]"	"[{""label"":""ABCG2"",""id"":""9429""},{""label"":""ADRB3"",""id"":""155""},{""label"":""HP"",""id"":""3240""},{""label"":""PRPS1"",""id"":""5631""},{""label"":""SLC17A3"",""id"":""10786""}]"	"[""10786"",""155"",""3240"",""5631"",""9429""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13189""}]"
DOID:1319	"[""brain cancer"",""BT - Brain tumour"",""adult brain tumor"",""adult malignant brain neoplasm"",""brain neoplasm"",""brain neoplasm, adult"",""malignant brain tumour"",""malignant primary brain neoplasm"",""malignant primary brain tumor"",""malignant tumor of Brain"",""malignant tumor of adult brain"",""neoplasm of brain"",""primary brain neoplasm"",""primary brain tumor"",""primary malignant neoplasm of brain"",""tumor of the Brain""]"	"[{""label"":""N"",""id"":""31293""}]"	"[""31293""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1319""}]"
DOID:1319	"[""brain cancer"",""BT - Brain tumour"",""adult brain tumor"",""adult malignant brain neoplasm"",""brain neoplasm"",""brain neoplasm, adult"",""malignant brain tumour"",""malignant primary brain neoplasm"",""malignant primary brain tumor"",""malignant tumor of Brain"",""malignant tumor of adult brain"",""neoplasm of brain"",""primary brain neoplasm"",""primary brain tumor"",""primary malignant neoplasm of brain"",""tumor of the Brain""]"	"[{""label"":""TERT"",""id"":""7015""}]"	"[""7015""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1319""}]"
DOID:13207	"[""proliferative diabetic retinopathy"",""PDR""]"	"[{""label"":""BCOR"",""id"":""54880""},{""label"":""CCL2"",""id"":""6347""},{""label"":""PPARG"",""id"":""5468""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""SRSF6"",""id"":""6431""}]"	"[""5054"",""5176"",""5468"",""54880"",""6347"",""6431""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13207""}]"
DOID:13207	"[""proliferative diabetic retinopathy"",""PDR""]"	"[{""label"":""Vegfa"",""id"":""83785""}]"	"[""83785""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13207""}]"
DOID:13208	"[""background diabetic retinopathy"",""Non proliferative diabetic retinopathy"",""Non-Proliferative Diabetic Retinopathy""]"	"[{""label"":""A2M"",""id"":""2""}]"	"[""2""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13208""}]"
DOID:13223	"[""uterine fibroid"",""Plexiform leiomyoma"",""UTERUS FIBROMA"",""leiomyoma of Corpus Uteri"",""uterine leiomyoma""]"	"[{""label"":""COL4A1"",""id"":""1282""},{""label"":""COL4A2"",""id"":""1284""},{""label"":""COL6A3"",""id"":""1293""},{""label"":""IRS1"",""id"":""3667""},{""label"":""TNRC6B"",""id"":""23112""}]"	"[""1282"",""1284"",""1293"",""23112"",""3667""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13223""}]"
DOID:1324	"[""lung cancer""]"	"[{""label"":""Ptgs2"",""id"":""29527""}]"	"[""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1324""}]"
DOID:1324	"[""lung cancer""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ALX4"",""id"":""60529""},{""label"":""ATR"",""id"":""545""},{""label"":""CALR"",""id"":""811""},{""label"":""CCDC116"",""id"":""164592""},{""label"":""CFTR"",""id"":""1080""},{""label"":""CHD4"",""id"":""1108""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CHRNA7"",""id"":""1139""},{""label"":""CHRNB4"",""id"":""1143""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""COMT"",""id"":""1312""},{""label"":""CSF1R"",""id"":""1436""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""DAGLA"",""id"":""747""},{""label"":""DVL3"",""id"":""1857""},{""label"":""EGFR"",""id"":""1956""},{""label"":""ERBB2"",""id"":""2064""},{""label"":""ERCC6"",""id"":""2074""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FASLG"",""id"":""356""},{""label"":""FOXA1"",""id"":""3169""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HS3ST2"",""id"":""9956""},{""label"":""IDH2"",""id"":""3418""},{""label"":""IL1R2"",""id"":""7850""},{""label"":""IRS4"",""id"":""8471""},{""label"":""KRAS"",""id"":""3845""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""MAP2K4"",""id"":""6416""},{""label"":""MAT2A"",""id"":""4144""},{""label"":""MBD4"",""id"":""8930""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MLH1"",""id"":""4292""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MPO"",""id"":""4353""},{""label"":""MPZL3"",""id"":""196264""},{""label"":""MSH2"",""id"":""4436""},{""label"":""MYD88"",""id"":""4615""},{""label"":""NAT2"",""id"":""10""},{""label"":""NCOA6"",""id"":""23054""},{""label"":""NOD2"",""id"":""64127""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""POLE"",""id"":""5426""},{""label"":""RAC1"",""id"":""5879""},{""label"":""RBM10"",""id"":""8241""},{""label"":""RECQL"",""id"":""5965""},{""label"":""RICTOR"",""id"":""253260""},{""label"":""RNASET2"",""id"":""8635""},{""label"":""SETDB1"",""id"":""9869""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SOX30"",""id"":""11063""},{""label"":""SOX9"",""id"":""6662""},{""label"":""STIM1"",""id"":""6786""},{""label"":""TRPC4"",""id"":""7223""},{""label"":""TRPC7"",""id"":""57113""},{""label"":""XRCC1"",""id"":""7515""},{""label"":""XRN2"",""id"":""22803""}]"	"[""10"",""1080"",""11063"",""1108"",""1136"",""1138"",""1139"",""1143"",""1312"",""1436"",""1543"",""1591"",""1636"",""164592"",""1857"",""1956"",""196264"",""2064"",""2074"",""2146"",""22803"",""23054"",""253260"",""2876"",""3169"",""3418"",""356"",""3845"",""4144"",""4153"",""4292"",""4312"",""4353"",""4436"",""4615"",""5290"",""53353"",""5426"",""545"",""57113"",""5879"",""5965"",""60529"",""64127"",""6416"",""6648"",""6662"",""6786"",""7223"",""747"",""7515"",""7850"",""81037"",""811"",""8241"",""8471"",""8635"",""8930"",""9869"",""9956""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1324""}]"
DOID:1324	"[""lung cancer""]"	"[{""label"":""Fgf9"",""id"":""14180""},{""label"":""Kras"",""id"":""16653""},{""label"":""Robo1"",""id"":""19876""}]"	"[""14180"",""16653"",""19876""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1324""}]"
DOID:1324	"[""lung cancer""]"	"[{""label"":""MLP1"",""id"":""853970""},{""label"":""MLP2"",""id"":""854657""}]"	"[""853970"",""854657""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1324""}]"
DOID:13241	"[""Behcet's disease"",""Adamantiades-Behcet disease"",""Behcet syndrome"",""Behet's syndrome"",""triple symptom complex""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ACE"",""id"":""1636""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""DHCR7"",""id"":""1717""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL21R"",""id"":""50615""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL4"",""id"":""3565""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""MBL2"",""id"":""4153""},{""label"":""NAT2"",""id"":""10""},{""label"":""NOD2"",""id"":""64127""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PROZ"",""id"":""8858""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""STAT3"",""id"":""6774""},{""label"":""STAT4"",""id"":""6775""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""},{""label"":""VIM"",""id"":""7431""},{""label"":""VWF"",""id"":""7450""}]"	"[""10"",""1234"",""149233"",""1493"",""1543"",""1636"",""1717"",""2214"",""3106"",""3119"",""3123"",""3383"",""3558"",""3565"",""3586"",""3673"",""4153"",""4846"",""50615"",""5243"",""6347"",""64127"",""6556"",""6774"",""6775"",""7040"",""7097"",""7099"",""7124"",""7431"",""7450"",""8858""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13241""}]"
DOID:13250	"[""diarrhea""]"	"[{""label"":""Mme"",""id"":""24590""}]"	"[""24590""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13250""}]"
DOID:13250	"[""diarrhea""]"	"[{""label"":""SLC26A3"",""id"":""1811""}]"	"[""1811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13250""}]"
DOID:13252	"[""mesenteric vascular occlusion""]"	"[{""label"":""Icam1"",""id"":""25464""}]"	"[""25464""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13252""}]"
DOID:13258	"[""typhoid fever"",""Typhoid""]"	"[{""label"":""CFTR"",""id"":""1080""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""LTA"",""id"":""4049""},{""label"":""TNF"",""id"":""7124""}]"	"[""1080"",""3119"",""3123"",""4049"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13258""}]"
DOID:13268	"[""porphyria"",""Hematoporphyria"",""Porphyrinopathy"",""disorder of porphyrin and hem metabolism"",""disorder of porphyrin metabolism""]"	"[{""label"":""EPO"",""id"":""2056""}]"	"[""2056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13268""}]"
DOID:13269	"[""hereditary coproporphyria"",""Coproporphyrinogen oxidase deficiency"",""hereditary coproporphyria porphyria""]"	"[{""label"":""CPOX"",""id"":""1371""}]"	"[""1371""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13269""}]"
DOID:13269	"[""hereditary coproporphyria"",""Coproporphyrinogen oxidase deficiency"",""hereditary coproporphyria porphyria""]"	"[{""label"":""Cpox"",""id"":""12892""}]"	"[""12892""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13269""}]"
DOID:13270	"[""erythropoietic protoporphyria"",""EPP"",""Protoporphyria""]"	"[{""label"":""CLPX"",""id"":""10845""}]"	"[""10845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13270""}]"
DOID:13270	"[""erythropoietic protoporphyria"",""EPP"",""Protoporphyria""]"	"[{""label"":""Abcg2"",""id"":""26357""}]"	"[""26357""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13270""}]"
DOID:13271	"[""cutaneous porphyria"",""Erythropoietic porphyria""]"	"[{""label"":""UROS"",""id"":""7390""}]"	"[""7390""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13271""}]"
DOID:13300	"[""Scheuermann's disease"",""Juvenile osteochondritis of the spine"",""Juvenile osteochondrosis of Scheurermann"",""Juvenile osteochondrosis of spine"",""Scheuermann's kyphosis"",""Sherman's Disease""]"	"[{""label"":""Nfix"",""id"":""18032""}]"	"[""18032""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13300""}]"
DOID:13316	"[""exocrine pancreatic insufficiency"",""EPI""]"	"[{""label"":""CFTR"",""id"":""1080""}]"	"[""1080""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13316""}]"
DOID:13317	"[""hyperinsulinemic hypoglycemia"",""Islet cell hyperplasia"",""nesidioblastosis"",""persistent hyperinsulinemia hypoglycemia of infancy""]"	"[{""label"":""Abcc8"",""id"":""20927""},{""label"":""Gck"",""id"":""103988""}]"	"[""103988"",""20927""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13317""}]"
DOID:13317	"[""hyperinsulinemic hypoglycemia"",""Islet cell hyperplasia"",""nesidioblastosis"",""persistent hyperinsulinemia hypoglycemia of infancy""]"	"[{""label"":""GLK1"",""id"":""850317""}]"	"[""850317""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13317""}]"
DOID:13336	"[""congenital toxoplasmosis"",""Toxoplasmosis - congen.""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""}]"	"[""3117""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13336""}]"
DOID:13359	"[""Ehlers-Danlos syndrome"",""Cutis hyperelastica"",""elastic skin""]"	"[{""label"":""Col1a1"",""id"":""12842""},{""label"":""Dcn"",""id"":""13179""},{""label"":""Plod1"",""id"":""18822""}]"	"[""12842"",""13179"",""18822""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13359""}]"
DOID:13359	"[""Ehlers-Danlos syndrome"",""Cutis hyperelastica"",""elastic skin""]"	"[{""label"":""b3galt6"",""id"":""572324""},{""label"":""b4galt7"",""id"":""445022""}]"	"[""445022"",""572324""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13359""}]"
DOID:13359	"[""Ehlers-Danlos syndrome"",""Cutis hyperelastica"",""elastic skin""]"	"[{""label"":""sqv-3"",""id"":""176382""}]"	"[""176382""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13359""}]"
DOID:13359	"[""Ehlers-Danlos syndrome"",""Cutis hyperelastica"",""elastic skin""]"	"[{""label"":""ADAMTS2"",""id"":""9509""},{""label"":""B4GALT7"",""id"":""11285""},{""label"":""COL1A2"",""id"":""1278""},{""label"":""COL3A1"",""id"":""1281""},{""label"":""COL5A1"",""id"":""1289""},{""label"":""COL5A2"",""id"":""1290""},{""label"":""LOX"",""id"":""4015""},{""label"":""TNXB"",""id"":""7148""}]"	"[""11285"",""1278"",""1281"",""1289"",""1290"",""4015"",""7148"",""9509""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13359""}]"
DOID:13365	"[""reading disorder""]"	"[{""label"":""CNTNAP2"",""id"":""26047""}]"	"[""26047""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13365""}]"
DOID:13366	"[""Stiff-Person syndrome"",""Stiff-man syndrome"",""stiff man syndrome""]"	"[{""label"":""Trak1"",""id"":""67095""}]"	"[""67095""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13366""}]"
DOID:13366	"[""Stiff-Person syndrome"",""Stiff-man syndrome"",""stiff man syndrome""]"	"[{""label"":""HSD17B4"",""id"":""3295""}]"	"[""3295""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13366""}]"
DOID:13372	"[""alpha 1-antitrypsin deficiency"",""AAT deficiency""]"	"[{""label"":""SERPINA1"",""id"":""5265""}]"	"[""5265""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13372""}]"
DOID:13374	"[""fibrodysplasia ossificans progressiva"",""Stone Man Syndrome"",""myositis ossificans progressiva"",""progressive myositis ossificans"",""progressive ossifying myositis""]"	"[{""label"":""Acvr1"",""id"":""11477""},{""label"":""Bmp4"",""id"":""12159""}]"	"[""11477"",""12159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13374""}]"
DOID:13374	"[""fibrodysplasia ossificans progressiva"",""Stone Man Syndrome"",""myositis ossificans progressiva"",""progressive myositis ossificans"",""progressive ossifying myositis""]"	"[{""label"":""ACVR1"",""id"":""90""}]"	"[""90""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13374""}]"
DOID:13375	"[""temporal arteritis"",""Horton's disease"",""giant cell arteritis""]"	"[{""label"":""CCL2"",""id"":""6347""},{""label"":""ELN"",""id"":""2006""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL17A"",""id"":""3605""},{""label"":""IL21R"",""id"":""50615""},{""label"":""IL4"",""id"":""3565""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MFGE8"",""id"":""4240""},{""label"":""MMP2"",""id"":""4313""},{""label"":""MMP9"",""id"":""4318""},{""label"":""TLR4"",""id"":""7099""}]"	"[""2006"",""2212"",""2214"",""3123"",""3458"",""3565"",""3605"",""4153"",""4240"",""4313"",""4318"",""50615"",""6347"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13375""}]"
DOID:13378	"[""Kawasaki disease"",""Kawasaki's disease"",""MLNS"",""acute febrile MCLS"",""acute febrile mucocutaneous lymph node syndrome"",""mucocutaneous lymph node syndrome""]"	"[{""label"":""BTNL2"",""id"":""56244""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CD40"",""id"":""958""},{""label"":""CD40LG"",""id"":""959""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""HSPA1L"",""id"":""3305""},{""label"":""MBL2"",""id"":""4153""},{""label"":""TNF"",""id"":""7124""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""1234"",""3303"",""3305"",""4153"",""56244"",""7124"",""729230"",""7422"",""958"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13378""}]"
DOID:1338	"[""congenital dyserythropoietic anemia"",""congenital dyshaematopoietic anaemia""]"	"[{""label"":""CDAN1"",""id"":""146059""},{""label"":""RACGAP1"",""id"":""29127""},{""label"":""SEC23B"",""id"":""10483""}]"	"[""10483"",""146059"",""29127""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00373""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1338""}]"
DOID:1338	"[""congenital dyserythropoietic anemia"",""congenital dyshaematopoietic anaemia""]"	"[{""label"":""Man2a1"",""id"":""17158""}]"	"[""17158""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1338""}]"
DOID:13381	"[""pernicious anemia"",""ANEMIA PERNICIOUS"",""Addison's anaemia"",""Biermer's anaemia"",""Biermer's anemia"",""pernicious anaemia""]"	"[{""label"":""CBLIF"",""id"":""2694""}]"	"[""2694""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13381""}]"
DOID:13382	"[""megaloblastic anemia"",""Grasbeck-Imerslund syndrome"",""Imerslund-Grasbeck syndrome"",""MGA1 Norwegian type"",""RH-MGA1"",""megaloblastic anaemia"",""recessive hereditary megaloblastic anaemia 1"",""recessive hereditary megaloblastic anemia 1""]"	"[{""label"":""AMN"",""id"":""81693""},{""label"":""SLC19A2"",""id"":""10560""}]"	"[""10560"",""81693""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13382""}]"
DOID:1339	"[""Diamond-Blackfan anemia"",""Blackfan - Diamond syndrome"",""chronic constitutional pure red cell anaemia""]"	"[{""label"":""HEATR3"",""id"":""55027""},{""label"":""RPS19"",""id"":""6223""}]"	"[""55027"",""6223""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1339""}]"
DOID:1339	"[""Diamond-Blackfan anemia"",""Blackfan - Diamond syndrome"",""chronic constitutional pure red cell anaemia""]"	"[{""label"":""Flvcr1"",""id"":""226844""}]"	"[""226844""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1339""}]"
DOID:13399	"[""color blindness"",""BLINDNESS COLOR"",""Colour blindness"",""Colour vision deficiency""]"	"[{""label"":""BDNF"",""id"":""627""},{""label"":""CNGA3"",""id"":""1261""}]"	"[""1261"",""627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13399""}]"
DOID:1340	"[""pure red-cell aplasia"",""Red cell hypoplasia"",""primary red cell aplasia"",""pure red cell aplasia""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1340""}]"
DOID:13404	"[""uveoparotid fever"",""Heerfordt's syndrome""]"	"[{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13404""}]"
DOID:13406	"[""pulmonary sarcoidosis"",""lung Sarcoidosis""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CFTR"",""id"":""1080""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""LTA"",""id"":""4049""},{""label"":""NOD2"",""id"":""64127""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TNF"",""id"":""7124""}]"	"[""1080"",""1234"",""28"",""3123"",""4049"",""64127"",""7040"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13406""}]"
DOID:13452	"[""scleritis""]"	"[{""label"":""TNF"",""id"":""7124""}]"	"[""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13452""}]"
DOID:13481	"[""thanatophoric dysplasia""]"	"[{""label"":""FGFR3"",""id"":""2261""}]"	"[""2261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13481""}]"
DOID:13481	"[""thanatophoric dysplasia""]"	"[{""label"":""Hspg2"",""id"":""15530""}]"	"[""15530""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13481""}]"
DOID:13482	"[""Proteus syndrome"",""Wiedemann's syndrome""]"	"[{""label"":""AKT1"",""id"":""207""}]"	"[""207""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13482""}]"
DOID:13482	"[""Proteus syndrome"",""Wiedemann's syndrome""]"	"[{""label"":""Akt1"",""id"":""11651""}]"	"[""11651""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13482""}]"
DOID:1350	"[""paranasal sinus benign neoplasm"",""neoplasm of accessory sinus"",""tumor of Accessory sinus""]"	"[{""label"":""TP53"",""id"":""7157""}]"	"[""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1350""}]"
DOID:13515	"[""tuberous sclerosis"",""Bourneville's disease"",""Epiloia"",""Tuberose sclerosis"",""Tuberous sclerosis complex"",""Tuberous sclerosis syndrome"",""cerebral sclerosis""]"	"[{""label"":""TSC1"",""id"":""7248""},{""label"":""TSC2"",""id"":""7249""}]"	"[""7248"",""7249""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13515""}]"
DOID:13515	"[""tuberous sclerosis"",""Bourneville's disease"",""Epiloia"",""Tuberose sclerosis"",""Tuberous sclerosis complex"",""Tuberous sclerosis syndrome"",""cerebral sclerosis""]"	"[{""label"":""Tsc1"",""id"":""64930""}]"	"[""64930""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13515""}]"
DOID:13533	"[""osteopetrosis"",""Albers-Schonberg disease"",""marble bone""]"	"[{""label"":""PLEKHM1"",""id"":""9842""},{""label"":""SLC4A2"",""id"":""6522""}]"	"[""6522"",""9842""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13533""}]"
DOID:13533	"[""osteopetrosis"",""Albers-Schonberg disease"",""marble bone""]"	"[{""label"":""Csf1"",""id"":""12977""},{""label"":""Mitf"",""id"":""17342""}]"	"[""12977"",""17342""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13533""}]"
DOID:13543	"[""hyperparathyroidism""]"	"[{""label"":""Casr"",""id"":""12374""}]"	"[""12374""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13543""}]"
DOID:13543	"[""hyperparathyroidism""]"	"[{""label"":""CASR"",""id"":""846""},{""label"":""CDC73"",""id"":""79577""},{""label"":""TRPV6"",""id"":""55503""}]"	"[""55503"",""79577"",""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13543""}]"
DOID:13544	"[""low tension glaucoma"",""Normal tension glaucoma""]"	"[{""label"":""Slc1a1"",""id"":""20510""},{""label"":""Slc1a3"",""id"":""20512""},{""label"":""Sod1"",""id"":""20655""}]"	"[""20510"",""20512"",""20655""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13544""}]"
DOID:13544	"[""low tension glaucoma"",""Normal tension glaucoma""]"	"[{""label"":""ADRB1"",""id"":""153""},{""label"":""APOE"",""id"":""348""},{""label"":""MYOC"",""id"":""4653""},{""label"":""OPTN"",""id"":""10133""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""},{""label"":""TP53"",""id"":""7157""}]"	"[""10133"",""153"",""348"",""4653"",""7099"",""7124"",""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13544""}]"
DOID:13544	"[""low tension glaucoma"",""Normal tension glaucoma""]"	"[{""label"":""Hspd1"",""id"":""63868""}]"	"[""63868""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13544""}]"
DOID:13550	"[""angle-closure glaucoma"",""ACG - Angle-closure glaucoma"",""Angle Closure Glaucoma"",""Closed angle glaucoma"",""Narrow cleft glaucoma"",""primary open-angle glaucoma with narrow angles""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""CAT"",""id"":""847""},{""label"":""HGF"",""id"":""3082""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NOS3"",""id"":""4846""}]"	"[""3082"",""348"",""4318"",""4846"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13550""}]"
DOID:13550	"[""angle-closure glaucoma"",""ACG - Angle-closure glaucoma"",""Angle Closure Glaucoma"",""Closed angle glaucoma"",""Narrow cleft glaucoma"",""primary open-angle glaucoma with narrow angles""]"	"[{""label"":""Tfap2b"",""id"":""21419""}]"	"[""21419""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13550""}]"
DOID:13560	"[""subserous uterine fibroid"",""subserous leiomyoma of uterus""]"	"[{""label"":""TNRC6B"",""id"":""23112""}]"	"[""23112""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13560""}]"
DOID:13564	"[""aspergillosis"",""Infection due to Aspergillus""]"	"[{""label"":""AGER"",""id"":""177""},{""label"":""CD209"",""id"":""30835""},{""label"":""CLEC1A"",""id"":""51267""},{""label"":""CLEC7A"",""id"":""64581""},{""label"":""IL15"",""id"":""3600""},{""label"":""TLR1"",""id"":""7096""},{""label"":""TLR6"",""id"":""10333""}]"	"[""10333"",""177"",""30835"",""3600"",""51267"",""64581"",""7096""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13564""}]"
DOID:13580	"[""cholestasis"",""Obstruction of bile duct"",""bile occlusion""]"	"[{""label"":""Abcb4"",""id"":""18670""}]"	"[""18670""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13580""}]"
DOID:13580	"[""cholestasis"",""Obstruction of bile duct"",""bile occlusion""]"	"[{""label"":""ABCB4"",""id"":""5244""},{""label"":""UTP4"",""id"":""84916""},{""label"":""VPS33B"",""id"":""26276""}]"	"[""26276"",""5244"",""84916""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13580""}]"
DOID:13580	"[""cholestasis"",""Obstruction of bile duct"",""bile occlusion""]"	"[{""label"":""Abcb11"",""id"":""83569""},{""label"":""Abcc2"",""id"":""25303""},{""label"":""Col1a1"",""id"":""29393""},{""label"":""Lamp2"",""id"":""24944""}]"	"[""24944"",""25303"",""29393"",""83569""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13580""}]"
DOID:13603	"[""obstructive jaundice"",""Cholestatic Jaundice"",""Cholestatic jaundice syndrome"",""Obstructive hyperbilirubinemia""]"	"[{""label"":""Ccl2"",""id"":""24770""}]"	"[""24770""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13603""}]"
DOID:13608	"[""biliary atresia"",""Atresia of bile duct"",""Congenital biliary atresia"",""biliary atresia, congenital""]"	"[{""label"":""ICAM1"",""id"":""3383""},{""label"":""SPP1"",""id"":""6696""}]"	"[""3383"",""6696""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13608""}]"
DOID:13619	"[""extrahepatic cholestasis"",""extrahepatic biliary Stasis"",""extrahepatic obstructive biliary disease""]"	"[{""label"":""Pdgfrb"",""id"":""24629""}]"	"[""24629""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13619""}]"
DOID:13628	"[""favism""]"	"[{""label"":""G6PD"",""id"":""2539""}]"	"[""2539""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13628""}]"
DOID:13628	"[""favism""]"	"[{""label"":""G6pdx"",""id"":""14381""}]"	"[""14381""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13628""}]"
DOID:13636	"[""Fanconi anemia"",""Fanconi anaemia"",""Fanconi pancytopenia"",""Fanconi panmyelopathy"",""Fanconi's anaemia"",""Fanconi's anemia""]"	"[{""label"":""BRCA2"",""id"":""675""},{""label"":""FANCD2"",""id"":""2177""},{""label"":""FANCG"",""id"":""2189""},{""label"":""FANCI"",""id"":""55215""}]"	"[""2177"",""2189"",""55215"",""675""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13636""}]"
DOID:13641	"[""exfoliation syndrome"",""Pseudoexfoliation glaucoma"",""Pseudoexfoliation syndrome""]"	"[{""label"":""ACVR1"",""id"":""90""},{""label"":""APOE"",""id"":""348""},{""label"":""CLU"",""id"":""1191""},{""label"":""LOXL1"",""id"":""4016""},{""label"":""TLR4"",""id"":""7099""}]"	"[""1191"",""348"",""4016"",""7099"",""90""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13641""}]"
DOID:13714	"[""anodontia"",""Complete absence of teeth"",""Developmental absence of tooth"",""Total anodontia of permanent and deciduous teeth""]"	"[{""label"":""DKK1"",""id"":""22943""},{""label"":""GLI3"",""id"":""2737""},{""label"":""MMP13"",""id"":""4322""},{""label"":""MMP9"",""id"":""4318""}]"	"[""22943"",""2737"",""4318"",""4322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13714""}]"
DOID:13774	"[""Addison's disease"",""Addison disease"",""Addison disease, chronic adrenal insufficiency"",""HYPOADRENOCORTICISM, FAMILIAL"",""primary adrenocortical insufficiency"",""primary hypoadrenalism""]"	"[{""label"":""CIITA"",""id"":""4261""},{""label"":""CLEC16A"",""id"":""23274""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""23274"",""3119"",""3123"",""4261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13774""}]"
DOID:13777	"[""epidermodysplasia verruciformis""]"	"[{""label"":""IL7"",""id"":""3574""},{""label"":""TMC6"",""id"":""11322""},{""label"":""TMC8"",""id"":""147138""}]"	"[""11322"",""147138"",""3574""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13777""}]"
DOID:1380	"[""endometrial cancer"",""endometrial Ca"",""endometrial neoplasm"",""malignant endometrial neoplasm"",""malignant neoplasm of endometrium"",""neoplasm of endometrium"",""primary malignant neoplasm of endometrium"",""tumor of Endometrium""]"	"[{""label"":""MCM4"",""id"":""856130""}]"	"[""856130""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1380""}]"
DOID:1380	"[""endometrial cancer"",""endometrial Ca"",""endometrial neoplasm"",""malignant endometrial neoplasm"",""malignant neoplasm of endometrium"",""neoplasm of endometrium"",""primary malignant neoplasm of endometrium"",""tumor of Endometrium""]"	"[{""label"":""ADRB3"",""id"":""155""},{""label"":""AKT2"",""id"":""208""},{""label"":""APC"",""id"":""324""},{""label"":""APEX1"",""id"":""328""},{""label"":""AR"",""id"":""367""},{""label"":""ATM"",""id"":""472""},{""label"":""BAD"",""id"":""572""},{""label"":""BRCA2"",""id"":""675""},{""label"":""BST2"",""id"":""684""},{""label"":""CDH1"",""id"":""999""},{""label"":""COMT"",""id"":""1312""},{""label"":""CYP19A1"",""id"":""1588""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP1A2"",""id"":""1544""},{""label"":""EFEMP2"",""id"":""30008""},{""label"":""EGF"",""id"":""1950""},{""label"":""JAK1"",""id"":""3716""},{""label"":""LTA"",""id"":""4049""},{""label"":""MRE11"",""id"":""4361""},{""label"":""MSH6"",""id"":""2956""},{""label"":""PGM1"",""id"":""5236""},{""label"":""PIK3CD"",""id"":""5293""},{""label"":""POLE"",""id"":""5426""},{""label"":""RNF43"",""id"":""54894""},{""label"":""SHBG"",""id"":""6462""},{""label"":""SULT1E1"",""id"":""6783""},{""label"":""UGT1A1"",""id"":""54658""}]"	"[""1312"",""1543"",""1544"",""155"",""1588"",""1950"",""208"",""2956"",""30008"",""324"",""328"",""367"",""3716"",""4049"",""4361"",""472"",""5236"",""5293"",""5426"",""54658"",""54894"",""572"",""6462"",""675"",""6783"",""684"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1380""}]"
DOID:1380	"[""endometrial cancer"",""endometrial Ca"",""endometrial neoplasm"",""malignant endometrial neoplasm"",""malignant neoplasm of endometrium"",""neoplasm of endometrium"",""primary malignant neoplasm of endometrium"",""tumor of Endometrium""]"	"[{""label"":""Errfi1"",""id"":""74155""},{""label"":""Trp53"",""id"":""22059""}]"	"[""22059"",""74155""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1380""}]"
DOID:13809	"[""familial combined hyperlipidemia"",""familial multiple lipoprotein-type hyperlipidemia"",""hyperbetalipoproteinemia with prebetalipoproteinemia"",""mixed hyperlipidaemia"",""type IIb hyperlipoproteinemia""]"	"[{""label"":""ADD1"",""id"":""118""},{""label"":""APOC3"",""id"":""345""},{""label"":""APOE"",""id"":""348""},{""label"":""HNF4A"",""id"":""3172""},{""label"":""LIPC"",""id"":""3990""},{""label"":""LPL"",""id"":""4023""}]"	"[""118"",""3172"",""345"",""348"",""3990"",""4023""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13809""}]"
DOID:13810	"[""familial hypercholesterolemia"",""Fredrickson type IIa hyperlipoproteinemia"",""Fredrickson type IIa lipidaemia"",""familial hyperbetalipoproteinaemia"",""familial hypercholesteremia"",""hyperbetalipoproteinemia"",""type II hyperlipidemia""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""APOA1"",""id"":""335""},{""label"":""APOB"",""id"":""338""},{""label"":""EPHX2"",""id"":""2053""},{""label"":""GHR"",""id"":""2690""},{""label"":""LDLR"",""id"":""3949""},{""label"":""PCSK9"",""id"":""255738""},{""label"":""PON2"",""id"":""5445""}]"	"[""154"",""2053"",""255738"",""2690"",""335"",""338"",""3949"",""5445""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13810""}]"
DOID:13810	"[""familial hypercholesterolemia"",""Fredrickson type IIa hyperlipoproteinemia"",""Fredrickson type IIa lipidaemia"",""familial hyperbetalipoproteinaemia"",""familial hypercholesteremia"",""hyperbetalipoproteinemia"",""type II hyperlipidemia""]"	"[{""label"":""Gk"",""id"":""79223""}]"	"[""79223""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13810""}]"
DOID:13810	"[""familial hypercholesterolemia"",""Fredrickson type IIa hyperlipoproteinemia"",""Fredrickson type IIa lipidaemia"",""familial hyperbetalipoproteinaemia"",""familial hypercholesteremia"",""hyperbetalipoproteinemia"",""type II hyperlipidemia""]"	"[{""label"":""Ldlr"",""id"":""16835""}]"	"[""16835""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13810""}]"
DOID:13812	"[""adhesions of uterus"",""Band of uterus"",""Intrauterine adhesions"",""Intrauterine synechiae""]"	"[{""label"":""Kdr"",""id"":""25589""}]"	"[""25589""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13812""}]"
DOID:13832	"[""patent ductus arteriosus"",""Patent ductus Botalli""]"	"[{""label"":""Tfap2b"",""id"":""21419""}]"	"[""21419""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13832""}]"
DOID:13832	"[""patent ductus arteriosus"",""Patent ductus Botalli""]"	"[{""label"":""MYH11"",""id"":""4629""},{""label"":""PTGIS"",""id"":""5740""},{""label"":""TFAP2B"",""id"":""7021""}]"	"[""4629"",""5740"",""7021""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13832""}]"
DOID:1387	"[""hypolipoproteinemia"",""Hypolipoproteinaemia""]"	"[{""label"":""ABCA1"",""id"":""19""},{""label"":""APOA1"",""id"":""335""}]"	"[""19"",""335""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1387""}]"
DOID:1388	"[""Tangier disease"",""familial alpha-lipoprotein deficiency"",""familial high density lipoprotein deficiency""]"	"[{""label"":""Abca1"",""id"":""11303""}]"	"[""11303""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1388""}]"
DOID:1388	"[""Tangier disease"",""familial alpha-lipoprotein deficiency"",""familial high density lipoprotein deficiency""]"	"[{""label"":""ABCA1"",""id"":""19""}]"	"[""19""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1388""}]"
DOID:13884	"[""sick sinus syndrome"",""sinus node infection""]"	"[{""label"":""Hcn1"",""id"":""15165""},{""label"":""Scn5a"",""id"":""20271""}]"	"[""15165"",""20271""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13884""}]"
DOID:13884	"[""sick sinus syndrome"",""sinus node infection""]"	"[{""label"":""AGT"",""id"":""183""},{""label"":""ANK2"",""id"":""287""},{""label"":""HCN4"",""id"":""10021""},{""label"":""SCN5A"",""id"":""6331""}]"	"[""10021"",""183"",""287"",""6331""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13884""}]"
DOID:1389	"[""polyneuropathy""]"	"[{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SOD3"",""id"":""6649""}]"	"[""2214"",""3123"",""6648"",""6649""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1389""}]"
DOID:1390	"[""hypobetalipoproteinemia"",""Hypo-beta-lipoproteinemia""]"	"[{""label"":""APOB"",""id"":""338""},{""label"":""PCSK9"",""id"":""255738""}]"	"[""255738"",""338""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1390""}]"
DOID:13909	"[""red-green color blindness"",""Deutan defect"",""Deuteranopia"",""Reduced red-green discrimination""]"	"[{""label"":""OPN1MW"",""id"":""2652""}]"	"[""2652""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13909""}]"
DOID:1391	"[""Norum disease"",""LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY"",""lecithin acyltransferase deficiency""]"	"[{""label"":""Lcat"",""id"":""16816""}]"	"[""16816""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1391""}]"
DOID:1391	"[""Norum disease"",""LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY"",""lecithin acyltransferase deficiency""]"	"[{""label"":""LCAT"",""id"":""3931""}]"	"[""3931""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1391""}]"
DOID:13910	"[""red color blindness"",""Protan defect"",""Protanopia""]"	"[{""label"":""OPN1LW"",""id"":""5956""}]"	"[""5956""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13910""}]"
DOID:13922	"[""eosinophilic esophagitis""]"	"[{""label"":""CYP2C19"",""id"":""1557""},{""label"":""TGFB1"",""id"":""7040""}]"	"[""1557"",""7040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13922""}]"
DOID:13929	"[""lacrimal duct obstruction"",""Blocked lacrimal canaliculus"",""Obstruction of lacrimal canaliculus"",""Obstruction of lacrimal ducts""]"	"[{""label"":""IGSF3"",""id"":""3321""}]"	"[""3321""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13929""}]"
DOID:13938	"[""amenorrhea"",""absence of menstruation"",""amenia""]"	"[{""label"":""FSHB"",""id"":""2488""}]"	"[""2488""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13938""}]"
DOID:1394	"[""urinary schistosomiasis"",""Schistosoma Hematobium Infection"",""Schistosoma haematobium"",""Schistosoma hematobium infectious disease"",""Schistosomiasis due to schistosoma haematobium"",""Schistosomiasis of bladder"",""Vesical schistosomiasis"",""bladder Schistosomiasis"",""cystitis with bilharziasis""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""STAT6"",""id"":""6778""}]"	"[""1493"",""6778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1394""}]"
DOID:13948	"[""bladder neck obstruction"",""Obstruction of bladder neck or vesicourethral orifice""]"	"[{""label"":""Adra1a"",""id"":""29412""},{""label"":""Ngf"",""id"":""310738""}]"	"[""29412"",""310738""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13948""}]"
DOID:13948	"[""bladder neck obstruction"",""Obstruction of bladder neck or vesicourethral orifice""]"	"[{""label"":""CYP19A1"",""id"":""1588""}]"	"[""1588""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13948""}]"
DOID:13949	"[""interstitial cystitis"",""ulcerative cystitis""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""CSF1"",""id"":""1435""},{""label"":""NGF"",""id"":""4803""}]"	"[""1435"",""154"",""4803""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13949""}]"
DOID:1395	"[""schistosomiasis""]"	"[{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1395""}]"
DOID:13963	"[""nuclear senile cataract"",""Senile nuclear cataract"",""Senile nuclear sclerosis""]"	"[{""label"":""FTO"",""id"":""79068""}]"	"[""79068""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13963""}]"
DOID:13976	"[""peptic esophagitis"",""Peptic reflux disease"",""Reflux oesophagitis"",""reflux esophagitis""]"	"[{""label"":""Tnf"",""id"":""24835""}]"	"[""24835""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13976""}]"
DOID:13994	"[""cleidocranial dysplasia"",""Marie-Sainton Disease"",""cleidocranial dysostosis""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13994""}]"
DOID:13994	"[""cleidocranial dysplasia"",""Marie-Sainton Disease"",""cleidocranial dysostosis""]"	"[{""label"":""RUNX2"",""id"":""860""}]"	"[""860""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13994""}]"
DOID:13994	"[""cleidocranial dysplasia"",""Marie-Sainton Disease"",""cleidocranial dysostosis""]"	"[{""label"":""Runx2"",""id"":""12393""}]"	"[""12393""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:13994""}]"
DOID:14004	"[""thoracic aortic aneurysm""]"	"[{""label"":""ACTA2"",""id"":""59""},{""label"":""LOX"",""id"":""4015""},{""label"":""MFAP5"",""id"":""8076""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP9"",""id"":""4318""},{""label"":""MYH11"",""id"":""4629""},{""label"":""MYLK"",""id"":""4638""},{""label"":""PRKG1"",""id"":""5592""},{""label"":""THSD4"",""id"":""79875""}]"	"[""4015"",""4312"",""4318"",""4629"",""4638"",""5592"",""59"",""79875"",""8076""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14004""}]"
DOID:14018	"[""alcoholic liver cirrhosis"",""Alcoholic Cirrhosis"",""Alcoholic cirrhosis of liver"",""Laennec's cirrhosis"",""Laennec's cirrhosis, alcoholic"",""Portal cirrhosis""]"	"[{""label"":""ALDH2"",""id"":""217""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""GABRG2"",""id"":""2566""},{""label"":""LEP"",""id"":""3952""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TG"",""id"":""7038""}]"	"[""1571"",""217"",""2566"",""3952"",""5054"",""6648"",""7038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14018""}]"
DOID:14018	"[""alcoholic liver cirrhosis"",""Alcoholic Cirrhosis"",""Alcoholic cirrhosis of liver"",""Laennec's cirrhosis"",""Laennec's cirrhosis, alcoholic"",""Portal cirrhosis""]"	"[{""label"":""Lep"",""id"":""25608""}]"	"[""25608""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14018""}]"
DOID:14021	"[""Tietze's syndrome"",""Costalchondritis"",""Costochondral junction syndrome"",""Costochondritis"",""Slipping rib syndrome"",""Tietze's disease""]"	"[{""label"":""MITF"",""id"":""4286""}]"	"[""4286""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14021""}]"
DOID:14040	"[""autoimmune polyendocrine syndrome"",""Autoimmune polyglandular failure"",""Lloyd's syndrome"",""autoimmune polyendocrinopathy""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3117"",""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14040""}]"
DOID:1405	"[""primary angle-closure glaucoma"",""primary Angle Closure Glaucoma""]"	"[{""label"":""ACVR1"",""id"":""90""},{""label"":""COL18A1"",""id"":""80781""},{""label"":""MYRF"",""id"":""745""}]"	"[""745"",""80781"",""90""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1405""}]"
DOID:14067	"[""Plasmodium falciparum malaria"",""Malaria fever, subtertian"",""falciparum malaria"",""malignant tertian fever""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""CYP2C19"",""id"":""1557""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""G6PD"",""id"":""2539""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HP"",""id"":""3240""},{""label"":""MBL2"",""id"":""4153""}]"	"[""1557"",""2212"",""2539"",""28"",""3119"",""3240"",""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14067""}]"
DOID:14069	"[""cerebral malaria"",""Malarial encephalitis""]"	"[{""label"":""ACE2"",""id"":""59272""},{""label"":""NRG1"",""id"":""3084""}]"	"[""3084"",""59272""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14069""}]"
DOID:1407	"[""anterior uveitis""]"	"[{""label"":""Cd59b"",""id"":""25407""}]"	"[""25407""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1407""}]"
DOID:1407	"[""anterior uveitis""]"	"[{""label"":""CCL2"",""id"":""6347""},{""label"":""CFB"",""id"":""629""},{""label"":""CFH"",""id"":""3075""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""}]"	"[""3075"",""3106"",""3557"",""629"",""6347"",""7097"",""7099"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1407""}]"
DOID:14080	"[""glucocorticoid-remediable aldosteronism"",""GRA"",""GRS"",""familial hyperaldosteronism type I"",""glucocorticoid-suppressible hyperaldosteronism""]"	"[{""label"":""CYP11B1"",""id"":""1584""}]"	"[""1584""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14080""}]"
DOID:14115	"[""toxic shock syndrome"",""TSS"",""toxic shock""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ADRB2"",""id"":""154""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MBL2"",""id"":""4153""},{""label"":""PROC"",""id"":""5624""},{""label"":""SERPINC1"",""id"":""462""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SERPING1"",""id"":""710""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""TFPI"",""id"":""7035""}]"	"[""154"",""1636"",""3304"",""3557"",""3586"",""4153"",""462"",""5054"",""5624"",""6439"",""7035"",""710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14115""}]"
DOID:14115	"[""toxic shock syndrome"",""TSS"",""toxic shock""]"	"[{""label"":""A2m"",""id"":""24153""},{""label"":""Tbxa2r"",""id"":""24816""}]"	"[""24153"",""24816""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14115""}]"
DOID:14118	"[""familial lipoprotein lipase deficiency"",""Fredrickson type I hyperlipoproteinemia"",""Fredrickson type I lipaemia"",""familial LPL deficiency"",""familial hyperlipoproteinemia type I"",""hypercholesterinaemic xanthomatosis"",""hyperchylomicronemia"",""mixed hyperglyceridemia""]"	"[{""label"":""LPL"",""id"":""4023""}]"	"[""4023""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14118""}]"
DOID:14118	"[""familial lipoprotein lipase deficiency"",""Fredrickson type I hyperlipoproteinemia"",""Fredrickson type I lipaemia"",""familial LPL deficiency"",""familial hyperlipoproteinemia type I"",""hypercholesterinaemic xanthomatosis"",""hyperchylomicronemia"",""mixed hyperglyceridemia""]"	"[{""label"":""Lpl"",""id"":""16956""}]"	"[""16956""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14118""}]"
DOID:1415	"[""gyrate atrophy"",""Gyrate atrophy of the choroid and/or retina"",""Ornithinemia with gyrate atrophy"",""gyrate atrophy of the retina""]"	"[{""label"":""OAT"",""id"":""4942""}]"	"[""4942""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1415""}]"
DOID:14159	"[""obstructive hydrocephalus""]"	"[{""label"":""Myo9a"",""id"":""270163""}]"	"[""270163""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14159""}]"
DOID:1417	"[""choroid disease""]"	"[{""label"":""IL10"",""id"":""3586""}]"	"[""3586""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1417""}]"
DOID:14175	"[""von Hippel-Lindau disease"",""Hippel Lindau syndrome"",""von Hippel-Lindau syndrome""]"	"[{""label"":""MMP3"",""id"":""4314""}]"	"[""4314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14175""}]"
DOID:14179	"[""X-linked agammaglobulinemia"",""BTK deficiency"",""Bruton agammaglobulinemia tyrosine kinase deficiency"",""Bruton disease"",""Bruton's Sex-Linked Agammaglobulinemia"",""Bruton's agammaglobulinaemia"",""Bruton's type agammaglobulinemia"",""Bruton-type agammaglobulinemia""]"	"[{""label"":""Btk"",""id"":""12229""},{""label"":""Pik3r1"",""id"":""18708""}]"	"[""12229"",""18708""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14179""}]"
DOID:14179	"[""X-linked agammaglobulinemia"",""BTK deficiency"",""Bruton agammaglobulinemia tyrosine kinase deficiency"",""Bruton disease"",""Bruton's Sex-Linked Agammaglobulinemia"",""Bruton's agammaglobulinaemia"",""Bruton's type agammaglobulinemia"",""Bruton-type agammaglobulinemia""]"	"[{""label"":""BTK"",""id"":""695""}]"	"[""695""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14179""}]"
DOID:14184	"[""polyneuropathy due to drug""]"	"[{""label"":""ERCC6"",""id"":""2074""}]"	"[""2074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14184""}]"
DOID:14213	"[""hypophosphatasia"",""deficiency of alkaline phosphatase""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14213""}]"
DOID:14213	"[""hypophosphatasia"",""deficiency of alkaline phosphatase""]"	"[{""label"":""ALPL"",""id"":""249""}]"	"[""249""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14213""}]"
DOID:14218	"[""dihydropyrimidine dehydrogenase deficiency"",""Dihydrouracil Dehydrogenase deficiency"",""familial pyrimidinaemia"",""thymine-uracilurea""]"	"[{""label"":""DPYD"",""id"":""1806""}]"	"[""1806""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14218""}]"
DOID:14219	"[""renal tubular acidosis""]"	"[{""label"":""Slc4a1"",""id"":""20533""},{""label"":""Slc4a4"",""id"":""54403""}]"	"[""20533"",""54403""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14219""}]"
DOID:14219	"[""renal tubular acidosis""]"	"[{""label"":""ATP6V0A4"",""id"":""50617""},{""label"":""SLC4A1"",""id"":""6521""},{""label"":""SLC4A4"",""id"":""8671""}]"	"[""50617"",""6521"",""8671""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14219""}]"
DOID:14219	"[""renal tubular acidosis""]"	"[{""label"":""MEP2"",""id"":""855580""}]"	"[""855580""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14219""}]"
DOID:14221	"[""abdominal obesity-metabolic syndrome 1"",""dysmetabolic syndrome X"",""metabolic syndrome X""]"	"[{""label"":""Lep"",""id"":""16846""}]"	"[""16846""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14221""}]"
DOID:14221	"[""abdominal obesity-metabolic syndrome 1"",""dysmetabolic syndrome X"",""metabolic syndrome X""]"	"[{""label"":""Lpl"",""id"":""24539""}]"	"[""24539""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14221""}]"
DOID:14227	"[""azoospermia""]"	"[{""label"":""Bscl2"",""id"":""361722""}]"	"[""361722""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14227""}]"
DOID:14227	"[""azoospermia""]"	"[{""label"":""Lar"",""id"":""35259""},{""label"":""sfl"",""id"":""38736""}]"	"[""35259"",""38736""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14227""}]"
DOID:14250	"[""Down syndrome"",""Complete trisomy 21 syndrome"",""Down's syndrome"",""Down's syndrome - trisomy 21"",""Downs syndrome"",""G Trisomy"",""trisomy 21 syndrome""]"	"[{""label"":""pad-2"",""id"":""259529""}]"	"[""259529""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14250""}]"
DOID:14250	"[""Down syndrome"",""Complete trisomy 21 syndrome"",""Down's syndrome"",""Down's syndrome - trisomy 21"",""Downs syndrome"",""G Trisomy"",""trisomy 21 syndrome""]"	"[{""label"":""Dscam1"",""id"":""35652""},{""label"":""mnb"",""id"":""32771""}]"	"[""32771"",""35652""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14250""}]"
DOID:14250	"[""Down syndrome"",""Complete trisomy 21 syndrome"",""Down's syndrome"",""Down's syndrome - trisomy 21"",""Downs syndrome"",""G Trisomy"",""trisomy 21 syndrome""]"	"[{""label"":""MMP9"",""id"":""4318""},{""label"":""MTHFD1"",""id"":""4522""},{""label"":""SNAP25"",""id"":""6616""},{""label"":""SOD1"",""id"":""6647""}]"	"[""4318"",""4522"",""6616"",""6647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14250""}]"
DOID:14261	"[""fragile X syndrome"",""FRAGILE X MENTAL RETARDATION SYNDROME"",""MARKER X SYNDROME"",""MARTIN-BELL SYNDROME""]"	"[{""label"":""FMR1"",""id"":""2332""}]"	"[""2332""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14261""}]"
DOID:14264	"[""benign neonatal seizures"",""benign familial neonatal seizures"",""benign neonatal convulsions""]"	"[{""label"":""Kcnq2"",""id"":""16536""},{""label"":""Kcnq3"",""id"":""110862""}]"	"[""110862"",""16536""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14264""}]"
DOID:14264	"[""benign neonatal seizures"",""benign familial neonatal seizures"",""benign neonatal convulsions""]"	"[{""label"":""ATP1A2"",""id"":""477""},{""label"":""KCNQ2"",""id"":""3785""},{""label"":""KCNQ3"",""id"":""3786""}]"	"[""3785"",""3786"",""477""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14264""}]"
DOID:14283	"[""primary hypertrophic osteoarthropathy"",""Pachydermoperiostosis of nail"",""Pachydermoperiostosis syndrome""]"	"[{""label"":""SLCO2A1"",""id"":""6578""}]"	"[""6578""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14283""}]"
DOID:14289	"[""Ebstein anomaly"",""Ebstein's anomaly"",""Ebstein's anomaly of common atrioventricular valve"",""Ebstein's anomaly of right atrioventricular valve"",""Ebstein's anomaly of tricuspid valve""]"	"[{""label"":""Bmpr1a"",""id"":""12166""}]"	"[""12166""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14289""}]"
DOID:14291	"[""Noonan syndrome with multiple lentigines"",""Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome"",""Generalized lentiginosis"",""Gorlin syndrome II"",""LEOPARD syndrome"",""Lentiginosis profusa syndrome"",""Moynahan syndrome"",""Multiple lentigines syndrome"",""Progressive cardiomyopathic lentiginosis""]"	"[{""label"":""Ptpn11"",""id"":""19247""}]"	"[""19247""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14291""}]"
DOID:1432	"[""blindness"",""vision impairment"",""vision loss"",""visual impairment""]"	"[{""label"":""AQP4"",""id"":""361""}]"	"[""361""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1432""}]"
DOID:1432	"[""blindness"",""vision impairment"",""vision loss"",""visual impairment""]"	"[{""label"":""Slc7a14"",""id"":""241919""}]"	"[""241919""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1432""}]"
DOID:14320	"[""generalized anxiety disorder""]"	"[{""label"":""Zfp462"",""id"":""242466""}]"	"[""242466""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14320""}]"
DOID:14320	"[""generalized anxiety disorder""]"	"[{""label"":""5-HT1B"",""id"":""37191""},{""label"":""SerT"",""id"":""37895""}]"	"[""37191"",""37895""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14320""}]"
DOID:14320	"[""generalized anxiety disorder""]"	"[{""label"":""HTR1B"",""id"":""3351""},{""label"":""SLC6A4"",""id"":""6532""}]"	"[""3351"",""6532""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14320""}]"
DOID:14323	"[""Marfan syndrome"",""Marfan's syndrome""]"	"[{""label"":""Fbn1"",""id"":""14118""}]"	"[""14118""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14323""}]"
DOID:14323	"[""Marfan syndrome"",""Marfan's syndrome""]"	"[{""label"":""FBN1"",""id"":""2200""},{""label"":""TGFBR2"",""id"":""7048""}]"	"[""2200"",""7048""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14323""}]"
DOID:14323	"[""Marfan syndrome"",""Marfan's syndrome""]"	"[{""label"":""daf-4"",""id"":""175781""},{""label"":""dbl-1"",""id"":""179068""},{""label"":""mua-3"",""id"":""176430""}]"	"[""175781"",""176430"",""179068""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14323""}]"
DOID:14330	"[""Parkinson's disease"",""Parkinson disease"",""paralysis agitans""]"	"[{""label"":""A2M"",""id"":""2""},{""label"":""AKT1"",""id"":""207""},{""label"":""ATM"",""id"":""472""},{""label"":""ATP13A2"",""id"":""23400""},{""label"":""CASP9"",""id"":""842""},{""label"":""CAST"",""id"":""831""},{""label"":""CHRNB3"",""id"":""1142""},{""label"":""CREB1"",""id"":""1385""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""DBH"",""id"":""1621""},{""label"":""DNAJC13"",""id"":""23317""},{""label"":""EIF2AK2"",""id"":""5610""},{""label"":""EPO"",""id"":""2056""},{""label"":""FBXO7"",""id"":""25793""},{""label"":""GBA1"",""id"":""2629""},{""label"":""GDF5"",""id"":""8200""},{""label"":""GIGYF2"",""id"":""26058""},{""label"":""GSTO1"",""id"":""9446""},{""label"":""GSTO2"",""id"":""119391""},{""label"":""HLA-DRA"",""id"":""3122""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""HSPA8"",""id"":""3312""},{""label"":""HSPA9"",""id"":""3313""},{""label"":""HTT"",""id"":""3064""},{""label"":""KLK6"",""id"":""5653""},{""label"":""LRRK2"",""id"":""120892""},{""label"":""MAPT"",""id"":""4137""},{""label"":""NAT2"",""id"":""10""},{""label"":""ND3"",""id"":""4537""},{""label"":""NOS1"",""id"":""4842""},{""label"":""PARK7"",""id"":""11315""},{""label"":""PARP1"",""id"":""142""},{""label"":""PHACTR2"",""id"":""9749""},{""label"":""PINK1"",""id"":""65018""},{""label"":""PLA2G6"",""id"":""8398""},{""label"":""PPARGC1A"",""id"":""10891""},{""label"":""PTGIS"",""id"":""5740""},{""label"":""SLC11A2"",""id"":""4891""},{""label"":""SLC18A2"",""id"":""6571""},{""label"":""SNCA"",""id"":""6622""},{""label"":""SNCB"",""id"":""6620""},{""label"":""SOD1"",""id"":""6647""},{""label"":""SYNJ1"",""id"":""8867""},{""label"":""TARDBP"",""id"":""23435""},{""label"":""TFAM"",""id"":""7019""}]"	"[""10"",""10891"",""11315"",""1142"",""119391"",""120892"",""1385"",""142"",""1543"",""1621"",""2"",""2056"",""207"",""23317"",""23400"",""23435"",""25793"",""26058"",""2629"",""3064"",""3122"",""3123"",""3156"",""3312"",""3313"",""4137"",""4537"",""472"",""4842"",""4891"",""5610"",""5653"",""5740"",""65018"",""6571"",""6620"",""6622"",""6647"",""7019"",""8200"",""831"",""8398"",""842"",""8867"",""9446"",""9749""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14330""}]"
DOID:14330	"[""Parkinson's disease"",""Parkinson disease"",""paralysis agitans""]"	"[{""label"":""daf-2"",""id"":""175410""},{""label"":""dop-2"",""id"":""179347""},{""label"":""glit-1"",""id"":""180747""},{""label"":""ida-1"",""id"":""175807""},{""label"":""ptc-1"",""id"":""174274""}]"	"[""174274"",""175410"",""175807"",""179347"",""180747""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14330""}]"
DOID:14330	"[""Parkinson's disease"",""Parkinson disease"",""paralysis agitans""]"	"[{""label"":""Gsk3b"",""id"":""84027""},{""label"":""Htr1a"",""id"":""24473""},{""label"":""Igf1r"",""id"":""25718""},{""label"":""Lep"",""id"":""25608""},{""label"":""Nox1"",""id"":""114243""},{""label"":""Slc18a2"",""id"":""25549""},{""label"":""Snca"",""id"":""29219""},{""label"":""Th"",""id"":""25085""}]"	"[""114243"",""24473"",""25085"",""25549"",""25608"",""25718"",""29219"",""84027""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14330""}]"
DOID:14330	"[""Parkinson's disease"",""Parkinson disease"",""paralysis agitans""]"	"[{""label"":""Adcy5"",""id"":""224129""},{""label"":""Adh7"",""id"":""11529""},{""label"":""Atg7"",""id"":""74244""},{""label"":""Drd2"",""id"":""13489""},{""label"":""Kcnn2"",""id"":""140492""},{""label"":""Minar2"",""id"":""225583""},{""label"":""Ppargc1a"",""id"":""19017""}]"	"[""11529"",""13489"",""140492"",""19017"",""224129"",""225583"",""74244""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14330""}]"
DOID:14330	"[""Parkinson's disease"",""Parkinson disease"",""paralysis agitans""]"	"[{""label"":""PSD1"",""id"":""855552""},{""label"":""TIF4631"",""id"":""853071""}]"	"[""853071"",""855552""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14330""}]"
DOID:14330	"[""Parkinson's disease"",""Parkinson disease"",""paralysis agitans""]"	"[{""label"":""Pgk"",""id"":""33461""}]"	"[""33461""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14330""}]"
DOID:14365	"[""systemic primary carnitine deficiency disease"",""carnitine transporter deficiency"",""carnitine uptake defect"",""deficiency of plasma-membrane carnitine transporter"",""primary carnitine deficiency"",""renal carnitine transport defect""]"	"[{""label"":""Slc22a5"",""id"":""20520""}]"	"[""20520""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14365""}]"
DOID:14365	"[""systemic primary carnitine deficiency disease"",""carnitine transporter deficiency"",""carnitine uptake defect"",""deficiency of plasma-membrane carnitine transporter"",""primary carnitine deficiency"",""renal carnitine transport defect""]"	"[{""label"":""SLC22A5"",""id"":""6584""}]"	"[""6584""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14365""}]"
DOID:1440	"[""Machado-Joseph disease"",""Azorean disease"",""MJD"",""SCA3"",""spinocerebellar ataxia 3"",""spinocerebellar ataxia type 3""]"	"[{""label"":""ATXN3"",""id"":""4287""}]"	"[""4287""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1440""}]"
DOID:14400	"[""capillary leak syndrome""]"	"[{""label"":""PON1"",""id"":""5444""}]"	"[""5444""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14400""}]"
DOID:1441	"[""autosomal dominant cerebellar ataxia"",""spinocerebellar ataxia""]"	"[{""label"":""NPTX1"",""id"":""4884""},{""label"":""SAMD9L"",""id"":""219285""}]"	"[""219285"",""4884""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1441""}]"
DOID:14415	"[""Legg-Calve-Perthes disease"",""Calve - Perthes' disease"",""Coxa plana"",""Juvenile osteochond-hip/pelvis"",""Juvenile osteochondrosis of hip and/or pelvis"",""Perthe's disease"",""Perthes disease"",""juvenile osteochondrosis of hip and pelvis"",""osteochondrosis of Legg-Calve-Perthes"",""pseudocoxalgia""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14415""}]"
DOID:14448	"[""46,XY complete gonadal dysgenesis"",""46 XY gonadal dysgenesis"",""46,XY sex reversal"",""Pure gonadal dysgenesis 46,XY"",""Swyer syndrome""]"	"[{""label"":""DHX37"",""id"":""57647""}]"	"[""57647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14448""}]"
DOID:14450	"[""46 XX gonadal dysgenesis"",""ovarian dysgenesis""]"	"[{""label"":""FSHR"",""id"":""2492""}]"	"[""2492""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14450""}]"
DOID:14451	"[""hyperkalemic periodic paralysis"",""familial hyperkalemic periodic paralysis""]"	"[{""label"":""Scn4a"",""id"":""110880""}]"	"[""110880""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14451""}]"
DOID:14451	"[""hyperkalemic periodic paralysis"",""familial hyperkalemic periodic paralysis""]"	"[{""label"":""SCN4A"",""id"":""6329""}]"	"[""6329""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14451""}]"
DOID:14452	"[""hypokalemic periodic paralysis"",""Hypokalemic familial periodic paralysis"",""Periodic paralysis I"",""Westphal disease"",""familial hypokalemic periodic paralysis"",""periodic hypokalemic paralysis""]"	"[{""label"":""Cacna1s"",""id"":""12292""},{""label"":""Scn4a"",""id"":""110880""}]"	"[""110880"",""12292""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14452""}]"
DOID:14452	"[""hypokalemic periodic paralysis"",""Hypokalemic familial periodic paralysis"",""Periodic paralysis I"",""Westphal disease"",""familial hypokalemic periodic paralysis"",""periodic hypokalemic paralysis""]"	"[{""label"":""deg-1"",""id"":""181035""}]"	"[""181035""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14452""}]"
DOID:14452	"[""hypokalemic periodic paralysis"",""Hypokalemic familial periodic paralysis"",""Periodic paralysis I"",""Westphal disease"",""familial hypokalemic periodic paralysis"",""periodic hypokalemic paralysis""]"	"[{""label"":""CACNA1S"",""id"":""779""},{""label"":""KCNE3"",""id"":""10008""}]"	"[""10008"",""779""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14452""}]"
DOID:14453	"[""farmer's lung"",""Farmers lung"",""farmer lung""]"	"[{""label"":""TNF"",""id"":""7124""}]"	"[""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14453""}]"
DOID:14497	"[""Wolman disease"",""Acid esterase deficiency"",""Acid lipase deficiency"",""Wolman xanthomatosis"",""Wolman's disease"",""Wolman's or triglyceride storage type III disease"",""Xanthomatosis, familial"",""acute infantile lysosomal acid lipase deficiency"",""complete LAL deficiency"",""complete LIPA deficiency"",""complete cholesterol ester hydrolase deficiency"",""complete lysosomal acid lipase deficiency""]"	"[{""label"":""Lipa"",""id"":""16889""}]"	"[""16889""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14497""}]"
DOID:14497	"[""Wolman disease"",""Acid esterase deficiency"",""Acid lipase deficiency"",""Wolman xanthomatosis"",""Wolman's disease"",""Wolman's or triglyceride storage type III disease"",""Xanthomatosis, familial"",""acute infantile lysosomal acid lipase deficiency"",""complete LAL deficiency"",""complete LIPA deficiency"",""complete cholesterol ester hydrolase deficiency"",""complete lysosomal acid lipase deficiency""]"	"[{""label"":""LIPA"",""id"":""3988""}]"	"[""3988""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00100""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14497""}]"
DOID:14498	"[""lipoid proteinosis"",""Lipid proteinosis"",""URBACH-WIETHE DISEASE""]"	"[{""label"":""ECM1"",""id"":""1893""}]"	"[""1893""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14498""}]"
DOID:14499	"[""Fabry disease"",""Alpha-galactosidase A deficiency"",""Angiokeratoma Corporis Diffusum"",""Fabry Disease, Cardiac Variant"",""Fabry's disease"",""alpha galactosidase deficiency"",""deficiency of melibiase""]"	"[{""label"":""gana-1"",""id"":""179660""}]"	"[""179660""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14499""}]"
DOID:14499	"[""Fabry disease"",""Alpha-galactosidase A deficiency"",""Angiokeratoma Corporis Diffusum"",""Fabry Disease, Cardiac Variant"",""Fabry's disease"",""alpha galactosidase deficiency"",""deficiency of melibiase""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGT"",""id"":""183""},{""label"":""GLA"",""id"":""2717""},{""label"":""IL1A"",""id"":""3552""}]"	"[""1636"",""183"",""2717"",""3552""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00064""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14499""}]"
DOID:14499	"[""Fabry disease"",""Alpha-galactosidase A deficiency"",""Angiokeratoma Corporis Diffusum"",""Fabry Disease, Cardiac Variant"",""Fabry's disease"",""alpha galactosidase deficiency"",""deficiency of melibiase""]"	"[{""label"":""Gla"",""id"":""11605""}]"	"[""11605""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14499""}]"
DOID:14500	"[""fucosidosis"",""A-fucosidase deficiency"",""alpha fucosidase deficiency""]"	"[{""label"":""Fuca1"",""id"":""71665""}]"	"[""71665""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14500""}]"
DOID:14500	"[""fucosidosis"",""A-fucosidase deficiency"",""alpha fucosidase deficiency""]"	"[{""label"":""FUCA1"",""id"":""2517""}]"	"[""2517""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00006""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14500""}]"
DOID:14501	"[""Sjogren-Larsson syndrome"",""FALDH deficiency"",""SLS"",""Sjogren Larsson syndrome"",""Sjogren-Larsson's syndrome"",""fatty acid alcohol oxidoreductase deficiency""]"	"[{""label"":""ALDH3A2"",""id"":""224""}]"	"[""224""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14501""}]"
DOID:14502	"[""cholesterol ester storage disease"",""CESD"",""partial LAL deficiency"",""partial LIPA deficiency"",""partial cholesterol ester hydrolase deficiency"",""partial lysosomal acid lipase deficiency""]"	"[{""label"":""LIPA"",""id"":""3988""}]"	"[""3988""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14502""}]"
DOID:14503	"[""neuronal ceroid lipofuscinosis"",""hereditary ceroid lipofuscinosis""]"	"[{""label"":""Ppt1"",""id"":""31805""},{""label"":""spin"",""id"":""45380""}]"	"[""31805"",""45380""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14503""}]"
DOID:14503	"[""neuronal ceroid lipofuscinosis"",""hereditary ceroid lipofuscinosis""]"	"[{""label"":""Ppt2"",""id"":""54397""}]"	"[""54397""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14503""}]"
DOID:14503	"[""neuronal ceroid lipofuscinosis"",""hereditary ceroid lipofuscinosis""]"	"[{""label"":""SOD2"",""id"":""6648""}]"	"[""6648""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14503""}]"
DOID:14503	"[""neuronal ceroid lipofuscinosis"",""hereditary ceroid lipofuscinosis""]"	"[{""label"":""ppt-1"",""id"":""191744""}]"	"[""191744""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14503""}]"
DOID:14504	"[""Niemann-Pick disease"",""Sphingomyelinase Deficiency Disease"",""lipoid histiocytosis"",""sphingomyelin lipidosis""]"	"[{""label"":""ncr-1"",""id"":""180719""},{""label"":""ncr-2"",""id"":""176165""}]"	"[""176165"",""180719""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14504""}]"
DOID:14504	"[""Niemann-Pick disease"",""Sphingomyelinase Deficiency Disease"",""lipoid histiocytosis"",""sphingomyelin lipidosis""]"	"[{""label"":""NCR1"",""id"":""856101""}]"	"[""856101""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14504""}]"
DOID:14504	"[""Niemann-Pick disease"",""Sphingomyelinase Deficiency Disease"",""lipoid histiocytosis"",""sphingomyelin lipidosis""]"	"[{""label"":""Npc1"",""id"":""18145""},{""label"":""Npc2"",""id"":""67963""},{""label"":""Smpd1"",""id"":""20597""}]"	"[""18145"",""20597"",""67963""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14504""}]"
DOID:14504	"[""Niemann-Pick disease"",""Sphingomyelinase Deficiency Disease"",""lipoid histiocytosis"",""sphingomyelin lipidosis""]"	"[{""label"":""NPC2"",""id"":""10577""},{""label"":""SMPD1"",""id"":""6609""}]"	"[""10577"",""6609""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14504""}]"
DOID:14557	"[""primary pulmonary hypertension"",""Idiopathic pulmonary arterial hypertension""]"	"[{""label"":""ATP13A3"",""id"":""79572""},{""label"":""BMPR2"",""id"":""659""},{""label"":""KCNK3"",""id"":""3777""},{""label"":""PTGIS"",""id"":""5740""},{""label"":""RYR1"",""id"":""6261""}]"	"[""3777"",""5740"",""6261"",""659"",""79572""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14557""}]"
DOID:14557	"[""primary pulmonary hypertension"",""Idiopathic pulmonary arterial hypertension""]"	"[{""label"":""Adora2a"",""id"":""11540""},{""label"":""Bmpr2"",""id"":""12168""},{""label"":""Pparg"",""id"":""19016""},{""label"":""Tnfsf4"",""id"":""22164""},{""label"":""Vip"",""id"":""22353""}]"	"[""11540"",""12168"",""19016"",""22164"",""22353""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14557""}]"
DOID:14566	"[""disease of cellular proliferation"",""cell process disease"",""neoplasm""]"	"[{""label"":""SPP1"",""id"":""6696""}]"	"[""6696""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14566""}]"
DOID:14566	"[""disease of cellular proliferation"",""cell process disease"",""neoplasm""]"	"[{""label"":""Tp53"",""id"":""24842""}]"	"[""24842""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14566""}]"
DOID:1459	"[""hypothyroidism"",""Thyroid deficiency"",""Thyroid insufficiency""]"	"[{""label"":""Col2a1"",""id"":""25412""},{""label"":""Cs"",""id"":""170587""}]"	"[""170587"",""25412""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1459""}]"
DOID:1459	"[""hypothyroidism"",""Thyroid deficiency"",""Thyroid insufficiency""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""TSHB"",""id"":""7252""}]"	"[""3119"",""3123"",""7252""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1459""}]"
DOID:14654	"[""prostatitis""]"	"[{""label"":""CYP19A1"",""id"":""1588""}]"	"[""1588""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14654""}]"
DOID:14669	"[""acrodysostosis""]"	"[{""label"":""PRKAR1A"",""id"":""5573""}]"	"[""5573""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14669""}]"
DOID:14671	"[""multiple intestinal atresia"",""GIDID"",""Multiple gastrointestinal atresias"",""familial intestinal polyatresia syndrome"",""gastrointestinal defects and immunodeficiency syndrome""]"	"[{""label"":""TTC7A"",""id"":""57217""}]"	"[""57217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14671""}]"
DOID:14679	"[""VACTERL association""]"	"[{""label"":""Dync2h1"",""id"":""110350""},{""label"":""Pcsk5"",""id"":""18552""},{""label"":""Qsox1"",""id"":""104009""}]"	"[""104009"",""110350"",""18552""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14679""}]"
DOID:14681	"[""Silver-Russell syndrome"",""Silver Russell Dwarfism""]"	"[{""label"":""HMGA2"",""id"":""8091""},{""label"":""IGF2"",""id"":""3481""}]"	"[""3481"",""8091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14681""}]"
DOID:14686	"[""Axenfeld-Rieger syndrome"",""Anomaly, Rieger's"",""Axenfeld syndrome"",""RGS - Rieger syndrome"",""Rieger's anomaly""]"	"[{""label"":""FOXC1"",""id"":""2296""},{""label"":""PITX2"",""id"":""5308""}]"	"[""2296"",""5308""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14686""}]"
DOID:14687	"[""diastrophic dysplasia""]"	"[{""label"":""SLC26A2"",""id"":""1836""}]"	"[""1836""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00395""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14687""}]"
DOID:14687	"[""diastrophic dysplasia""]"	"[{""label"":""Slc26a2"",""id"":""13521""}]"	"[""13521""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14687""}]"
DOID:14692	"[""Smith-Lemli-Opitz syndrome"",""Rutledge lethal multiple congenital anomaly syndrome"",""Smith-Opitz-Inborn syndrome""]"	"[{""label"":""DHCR7"",""id"":""1717""}]"	"[""1717""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14692""}]"
DOID:14693	"[""Clouston syndrome"",""Clouston's hidrotic ectodermal dysplasia"",""Clouston's syndrome"",""Hidrotic ectodermal dysplasia syndrome"",""ectodermal dysplasia 2, Clouston type"",""hidrotic ectodermal dysplasia""]"	"[{""label"":""Gjb6"",""id"":""14623""}]"	"[""14623""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14693""}]"
DOID:14694	"[""Johanson-Blizzard syndrome"",""JBS""]"	"[{""label"":""UBR1"",""id"":""197131""}]"	"[""197131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14694""}]"
DOID:14695	"[""galactokinase deficiency"",""Galactosemia II""]"	"[{""label"":""GALK1"",""id"":""2584""}]"	"[""2584""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14695""}]"
DOID:1470	"[""major depressive disorder"",""clinical depression"",""major depression"",""recurrent major depression"",""single major depressive episode"",""unipolar depression""]"	"[{""label"":""Htr2c"",""id"":""25187""}]"	"[""25187""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1470""}]"
DOID:1470	"[""major depressive disorder"",""clinical depression"",""major depression"",""recurrent major depression"",""single major depressive episode"",""unipolar depression""]"	"[{""label"":""CHRM2"",""id"":""1129""},{""label"":""CNTNAP2"",""id"":""26047""},{""label"":""CTNND2"",""id"":""1501""},{""label"":""FOXP2"",""id"":""93986""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""HSPA1L"",""id"":""3305""},{""label"":""HTR1B"",""id"":""3351""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL6"",""id"":""3569""},{""label"":""MC1R"",""id"":""4157""},{""label"":""MED12"",""id"":""9968""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""NTRK2"",""id"":""4915""},{""label"":""SLC6A4"",""id"":""6532""}]"	"[""1129"",""1501"",""26047"",""2908"",""3303"",""3305"",""3351"",""3356"",""3569"",""3586"",""4157"",""4915"",""6532"",""93986"",""9968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1470""}]"
DOID:1470	"[""major depressive disorder"",""clinical depression"",""major depression"",""recurrent major depression"",""single major depressive episode"",""unipolar depression""]"	"[{""label"":""Adcy3"",""id"":""104111""},{""label"":""Crtc1"",""id"":""382056""}]"	"[""104111"",""382056""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1470""}]"
DOID:14701	"[""propionic acidemia"",""GLYCINEMIA, KETOTIC"",""KETOTIC HYPERGLYCINEMIA"",""ketotic II glycinemia"",""ketotic glycinemia"",""propionic aciduria"",""propionyl-CoA carboxylase deficiency""]"	"[{""label"":""PCCA"",""id"":""5095""},{""label"":""PCCB"",""id"":""5096""}]"	"[""5095"",""5096""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14701""}]"
DOID:14702	"[""branchiootorenal syndrome"",""Branchio-Oto-renal syndrome"",""Branchio-otorenal dysplasia"",""Melnick-Fraser syndrome"",""branchiootorenal dysplasia""]"	"[{""label"":""SIX1"",""id"":""6495""}]"	"[""6495""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14702""}]"
DOID:14705	"[""Pfeiffer syndrome"",""acrocephalosyndactylia type V""]"	"[{""label"":""Fgfr1"",""id"":""14182""},{""label"":""Fgfr2"",""id"":""14183""}]"	"[""14182"",""14183""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14705""}]"
DOID:14705	"[""Pfeiffer syndrome"",""acrocephalosyndactylia type V""]"	"[{""label"":""FGFR1"",""id"":""2260""},{""label"":""FGFR2"",""id"":""2263""}]"	"[""2260"",""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14705""}]"
DOID:14711	"[""FG syndrome"",""Keller syndrome"",""Opitz-Kaveggia syndrome""]"	"[{""label"":""CASK"",""id"":""8573""},{""label"":""MED12"",""id"":""9968""}]"	"[""8573"",""9968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14711""}]"
DOID:14717	"[""centronuclear myopathy"",""myotubular myopathy""]"	"[{""label"":""Dnm2"",""id"":""13430""}]"	"[""13430""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14717""}]"
DOID:14720	"[""Ehlers-Danlos syndrome classic type 1"",""Ehlers-Danlos syndrome, type 1"",""type I Ehlers-Danlos syndrome""]"	"[{""label"":""Col5a1"",""id"":""12831""},{""label"":""Col5a2"",""id"":""12832""},{""label"":""Lum"",""id"":""17022""}]"	"[""12831"",""12832"",""17022""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14720""}]"
DOID:14720	"[""Ehlers-Danlos syndrome classic type 1"",""Ehlers-Danlos syndrome, type 1"",""type I Ehlers-Danlos syndrome""]"	"[{""label"":""COL5A1"",""id"":""1289""}]"	"[""1289""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14720""}]"
DOID:14723	"[""beta-ketothiolase deficiency"",""2-methyl-3-hydroxybutyricacidemia"",""3-ketothiolase deficiency"",""3-oxothiolase deficiency"",""Mitochondrial acetoacetyl-CoA Thiolase deficiency"",""alpha-methylacetoaceticaciduria"",""peroxisomal thiolase deficiency""]"	"[{""label"":""ACAT1"",""id"":""38""}]"	"[""38""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14723""}]"
DOID:14731	"[""Weaver syndrome"",""WEAVER-LIKE SYNDROME"",""Weaver-Williams syndrome""]"	"[{""label"":""Ezh2"",""id"":""14056""}]"	"[""14056""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14731""}]"
DOID:14731	"[""Weaver syndrome"",""WEAVER-LIKE SYNDROME"",""Weaver-Williams syndrome""]"	"[{""label"":""EZH2"",""id"":""2146""}]"	"[""2146""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14731""}]"
DOID:14735	"[""hereditary angioedema"",""HANE"",""Hereditary angioneurotic edema""]"	"[{""label"":""ANGPT1"",""id"":""284""},{""label"":""F12"",""id"":""2161""},{""label"":""HS3ST6"",""id"":""64711""},{""label"":""KNG1"",""id"":""3827""},{""label"":""MYOF"",""id"":""26509""},{""label"":""PLG"",""id"":""5340""},{""label"":""SERPING1"",""id"":""710""}]"	"[""2161"",""26509"",""284"",""3827"",""5340"",""64711"",""710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14735""}]"
DOID:14737	"[""craniofrontonasal syndrome"",""CFND"",""CFNS"",""craniofrontonasal dysostosis"",""craniofrontonasal dysplasia""]"	"[{""label"":""Efnb1"",""id"":""13641""}]"	"[""13641""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14737""}]"
DOID:14737	"[""craniofrontonasal syndrome"",""CFND"",""CFNS"",""craniofrontonasal dysostosis"",""craniofrontonasal dysplasia""]"	"[{""label"":""EFNB1"",""id"":""1947""}]"	"[""1947""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14737""}]"
DOID:1474	"[""aggressive periodontitis"",""juvenile periodontitis""]"	"[{""label"":""Postn"",""id"":""50706""}]"	"[""50706""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1474""}]"
DOID:1474	"[""aggressive periodontitis"",""juvenile periodontitis""]"	"[{""label"":""CCL2"",""id"":""6347""},{""label"":""CCR2"",""id"":""729230""},{""label"":""COL1A1"",""id"":""1277""},{""label"":""CTSC"",""id"":""1075""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1R2"",""id"":""7850""},{""label"":""IL6"",""id"":""3569""}]"	"[""1075"",""1277"",""3569"",""3586"",""6347"",""729230"",""7850""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1474""}]"
DOID:14743	"[""trichorhinophalangeal syndrome type I"",""trichorhinophalangeal syndrome type 1"",""type I trichorhinophalangeal syndrome""]"	"[{""label"":""TRPS1"",""id"":""7227""}]"	"[""7227""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14743""}]"
DOID:14744	"[""Partington syndrome"",""X-linked Russell-Silver syndrome""]"	"[{""label"":""ARX"",""id"":""170302""}]"	"[""170302""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14744""}]"
DOID:14748	"[""Sotos syndrome"",""cerebral gigantism""]"	"[{""label"":""NSD1"",""id"":""64324""}]"	"[""64324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14748""}]"
DOID:14755	"[""argininosuccinic aciduria"",""Argininosuccinate lyase deficiency"",""argininosuccinic acidemia"",""arginosuccinase deficiency"",""deficiency of argininosuccinate lyase""]"	"[{""label"":""Asl"",""id"":""109900""}]"	"[""109900""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14755""}]"
DOID:14756	"[""vascular type Ehlers-Danlos syndrome"",""Ehlers-Danlos syndrome type 4"",""Ehlers-Danlos syndrome type IV"",""autosomal dominant type IV Ehlers-Danlos syndrome""]"	"[{""label"":""COL3A1"",""id"":""1281""}]"	"[""1281""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14756""}]"
DOID:14756	"[""vascular type Ehlers-Danlos syndrome"",""Ehlers-Danlos syndrome type 4"",""Ehlers-Danlos syndrome type IV"",""autosomal dominant type IV Ehlers-Danlos syndrome""]"	"[{""label"":""Col3a1"",""id"":""12825""}]"	"[""12825""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14756""}]"
DOID:14757	"[""Ehlers-Danlos syndrome hypermobility type"",""Ehlers-Danlos syndrome, type 3"",""type III Ehlers-Danlos syndrome""]"	"[{""label"":""COL3A1"",""id"":""1281""}]"	"[""1281""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14757""}]"
DOID:14761	"[""Greig cephalopolysyndactyly syndrome"",""polysyndactyly with peculiars skull shape""]"	"[{""label"":""GLI3"",""id"":""2737""}]"	"[""2737""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14761""}]"
DOID:14761	"[""Greig cephalopolysyndactyly syndrome"",""polysyndactyly with peculiars skull shape""]"	"[{""label"":""Gli3"",""id"":""14634""}]"	"[""14634""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14761""}]"
DOID:14764	"[""Larsen syndrome"",""dominant larsen syndrome""]"	"[{""label"":""FLNB"",""id"":""2317""}]"	"[""2317""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14764""}]"
DOID:14766	"[""renal agenesis"",""hereditary renal aplasia"",""hereditary urogenital adysplasia"",""renal adysplasia"",""renal aplasia""]"	"[{""label"":""GFRA1"",""id"":""2674""},{""label"":""GREB1L"",""id"":""80000""},{""label"":""ITGA8"",""id"":""8516""}]"	"[""2674"",""80000"",""8516""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14766""}]"
DOID:14768	"[""Saethre-Chotzen syndrome""]"	"[{""label"":""FGFR2"",""id"":""2263""},{""label"":""TWIST1"",""id"":""7291""}]"	"[""2263"",""7291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14768""}]"
DOID:14775	"[""brittle cornea syndrome 1"",""type VIB Ehlers-Danlos syndrome""]"	"[{""label"":""PLOD1"",""id"":""5351""}]"	"[""5351""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00407""}]"
DOID:14778	"[""blepharophimosis, ptosis, and epicanthus inversus syndrome""]"	"[{""label"":""FOXL2"",""id"":""668""}]"	"[""668""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14778""}]"
DOID:14780	"[""KBG syndrome""]"	"[{""label"":""ANKRD11"",""id"":""29123""}]"	"[""29123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14780""}]"
DOID:14780	"[""KBG syndrome""]"	"[{""label"":""Ankrd11"",""id"":""77087""}]"	"[""77087""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14780""}]"
DOID:14784	"[""olivopontocerebellar atrophy"",""Dejerine-Thomas syndrome"",""Thomas' syndrome"",""WADIA-SWAMI SYNDROME""]"	"[{""label"":""APTX"",""id"":""54840""}]"	"[""54840""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14784""}]"
DOID:14789	"[""spondyloepiphyseal dysplasia congenita"",""Late Spondyloepiphyseal Dysplasia""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14789""}]"
DOID:14789	"[""spondyloepiphyseal dysplasia congenita"",""Late Spondyloepiphyseal Dysplasia""]"	"[{""label"":""Col2a1"",""id"":""12824""},{""label"":""Hapln1"",""id"":""12950""}]"	"[""12824"",""12950""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14789""}]"
DOID:14791	"[""Leber congenital amaurosis"",""LCA"",""Leber's amaurosis"",""Leber's congenital amaurosis"",""Leber's disease""]"	"[{""label"":""CRB1"",""id"":""23418""},{""label"":""MYO7A"",""id"":""4647""},{""label"":""PRPH2"",""id"":""5961""}]"	"[""23418"",""4647"",""5961""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14791""}]"
DOID:14791	"[""Leber congenital amaurosis"",""LCA"",""Leber's amaurosis"",""Leber's congenital amaurosis"",""Leber's disease""]"	"[{""label"":""Pals1"",""id"":""56217""}]"	"[""56217""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14791""}]"
DOID:14791	"[""Leber congenital amaurosis"",""LCA"",""Leber's amaurosis"",""Leber's congenital amaurosis"",""Leber's disease""]"	"[{""label"":""crb"",""id"":""42896""}]"	"[""42896""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14791""}]"
DOID:14791	"[""Leber congenital amaurosis"",""LCA"",""Leber's amaurosis"",""Leber's congenital amaurosis"",""Leber's disease""]"	"[{""label"":""ENV9"",""id"":""854420""}]"	"[""854420""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14791""}]"
DOID:14793	"[""hypohidrotic ectodermal dysplasia""]"	"[{""label"":""Eda"",""id"":""13607""},{""label"":""Edar"",""id"":""13608""}]"	"[""13607"",""13608""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:14793""}]"
DOID:1485	"[""cystic fibrosis"",""CF"",""mucoviscidosis""]"	"[{""label"":""Cftr"",""id"":""24255""}]"	"[""24255""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1485""}]"
DOID:1485	"[""cystic fibrosis"",""CF"",""mucoviscidosis""]"	"[{""label"":""Cftr"",""id"":""12638""},{""label"":""Scnn1b"",""id"":""20277""}]"	"[""12638"",""20277""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1485""}]"
DOID:1485	"[""cystic fibrosis"",""CF"",""mucoviscidosis""]"	"[{""label"":""cftr"",""id"":""559080""}]"	"[""559080""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1485""}]"
DOID:1485	"[""cystic fibrosis"",""CF"",""mucoviscidosis""]"	"[{""label"":""MNL1"",""id"":""856611""},{""label"":""STE6"",""id"":""853671""},{""label"":""YOR1"",""id"":""853198""}]"	"[""853198"",""853671"",""856611""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1485""}]"
DOID:1485	"[""cystic fibrosis"",""CF"",""mucoviscidosis""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""AGER"",""id"":""177""},{""label"":""CD14"",""id"":""929""},{""label"":""CFTR"",""id"":""1080""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""FAS"",""id"":""355""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""GCLC"",""id"":""2729""},{""label"":""HFE"",""id"":""3077""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""LTA"",""id"":""4049""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MIF"",""id"":""4282""},{""label"":""MPO"",""id"":""4353""},{""label"":""NOS1"",""id"":""4842""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""PTX3"",""id"":""5806""},{""label"":""SERPINA3"",""id"":""12""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TLR5"",""id"":""7100""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNF"",""id"":""7124""}]"	"[""1080"",""12"",""154"",""1543"",""177"",""2212"",""2729"",""3077"",""3303"",""355"",""4049"",""4153"",""4282"",""4353"",""4842"",""4846"",""54106"",""5743"",""5806"",""7040"",""7100"",""7124"",""929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1485""}]"
DOID:1495	"[""cystic echinococcosis"",""Echinococcus granulosus infection"",""Echinococcus granulosus infection of lung"",""Echinococcus granulosus infection of thyroid"",""Liver echinococcus granulosus"",""Thyroid echinococcus granulosus"",""echinococcus granulosus"",""echinococcus granulosus infectious disease"",""echinococcus granulosus infectious disease of liver"",""echinococcus granulosus infectious disease of thyroid"",""lung echinococcus granulosus"",""unilocular echinococcosis"",""unilocular hydatid disease""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""TLR2"",""id"":""7097""}]"	"[""3119"",""3123"",""7097""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1495""}]"
DOID:1496	"[""echinococcosis"",""Echinococcosis of liver"",""echinococcal disease"",""hepatic echinococcosis"",""hydatid disease"",""hydatidosis"",""liver echinococcus"",""pulmonary echinococcosis""]"	"[{""label"":""ABO"",""id"":""28""}]"	"[""28""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1496""}]"
DOID:150	"[""disease of mental health""]"	"[{""label"":""SNRNP70"",""id"":""6625""}]"	"[""6625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:150""}]"
DOID:150	"[""disease of mental health""]"	"[{""label"":""Cic"",""id"":""71722""},{""label"":""Stx1a"",""id"":""20907""}]"	"[""20907"",""71722""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:150""}]"
DOID:1508	"[""candidiasis"",""Disseminated candidiasis"",""systemic candidiasis""]"	"[{""label"":""FucTA"",""id"":""39653""}]"	"[""39653""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1508""}]"
DOID:1508	"[""candidiasis"",""Disseminated candidiasis"",""systemic candidiasis""]"	"[{""label"":""LTF"",""id"":""4057""}]"	"[""4057""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1508""}]"
DOID:1520	"[""colon carcinoma"",""Colonic carcinoma"",""carcinoma of colon""]"	"[{""label"":""CALR"",""id"":""811""},{""label"":""EFNB2"",""id"":""1948""},{""label"":""FLT3LG"",""id"":""2323""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""TNFRSF17"",""id"":""608""},{""label"":""TYMS"",""id"":""7298""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""1948"",""2323"",""3117"",""608"",""7298"",""7422"",""811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1520""}]"
DOID:1540	"[""parathyroid carcinoma"",""Parathyroid gland neoplasm"",""carcinoma of Parathyroid gland"",""malignant neoplasm of parathyroid gland"",""malignant neoplasm of the Parathyroid"",""malignant tumor of parathyroid gland"",""neoplasm of parathyroid gland"",""parathyroid gland cancer"",""parathyroid neoplasm""]"	"[{""label"":""CDC73"",""id"":""79577""}]"	"[""79577""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1540""}]"
DOID:1554	"[""vibratory urticaria""]"	"[{""label"":""ADGRE2"",""id"":""30817""}]"	"[""30817""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1554""}]"
DOID:1555	"[""urticaria""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CCR5"",""id"":""1234""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""1234"",""154"",""3123"",""729230""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1555""}]"
DOID:1556	"[""arthus reaction"",""Arthus phenomenon"",""Arthus type urticaria""]"	"[{""label"":""Cfd"",""id"":""54249""}]"	"[""54249""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1556""}]"
DOID:1556	"[""arthus reaction"",""Arthus phenomenon"",""Arthus type urticaria""]"	"[{""label"":""FCGR2A"",""id"":""2212""}]"	"[""2212""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1556""}]"
DOID:1558	"[""angioedema"",""Angioneurotic oedema"",""Quincke's edema"",""angioneurotic edema"",""giant urticaria""]"	"[{""label"":""F12"",""id"":""2161""},{""label"":""SERPING1"",""id"":""710""}]"	"[""2161"",""710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1558""}]"
DOID:1561	"[""cognitive disorder"",""cognitive disease""]"	"[{""label"":""Chrna7"",""id"":""25302""},{""label"":""Htr7"",""id"":""65032""},{""label"":""Lamp2"",""id"":""24944""}]"	"[""24944"",""25302"",""65032""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1561""}]"
DOID:1561	"[""cognitive disorder"",""cognitive disease""]"	"[{""label"":""Comt"",""id"":""12846""}]"	"[""12846""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1561""}]"
DOID:1561	"[""cognitive disorder"",""cognitive disease""]"	"[{""label"":""APOC3"",""id"":""345""},{""label"":""APP"",""id"":""351""},{""label"":""BDNF"",""id"":""627""},{""label"":""COMT"",""id"":""1312""},{""label"":""CSF3"",""id"":""1440""},{""label"":""DMD"",""id"":""1756""},{""label"":""PPARG"",""id"":""5468""}]"	"[""1312"",""1440"",""1756"",""345"",""351"",""5468"",""627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1561""}]"
DOID:1564	"[""fungal infectious disease"",""mycosis""]"	"[{""label"":""MBL2"",""id"":""4153""}]"	"[""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1564""}]"
DOID:1572	"[""normal pressure hydrocephalus"",""Low pressure hydrocephalus""]"	"[{""label"":""Cwh43"",""id"":""231293""}]"	"[""231293""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1572""}]"
DOID:1572	"[""normal pressure hydrocephalus"",""Low pressure hydrocephalus""]"	"[{""label"":""CFAP43"",""id"":""80217""}]"	"[""80217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1572""}]"
DOID:1574	"[""alcohol use disorder"",""Ethanol abuse"",""alcohol abuse""]"	"[{""label"":""Akap200"",""id"":""34170""},{""label"":""CtsL1"",""id"":""36546""},{""label"":""Dop1R1"",""id"":""41726""},{""label"":""Dop2R"",""id"":""33007""},{""label"":""Egfr"",""id"":""37455""},{""label"":""Kdm4B"",""id"":""318918""},{""label"":""N"",""id"":""31293""},{""label"":""RhoGAP18B"",""id"":""32898""},{""label"":""Tbh"",""id"":""31718""},{""label"":""homer"",""id"":""33944""},{""label"":""rut"",""id"":""32406""},{""label"":""sca"",""id"":""36411""},{""label"":""spi"",""id"":""35253""},{""label"":""tay"",""id"":""32547""}]"	"[""31293"",""31718"",""318918"",""32406"",""32547"",""32898"",""33007"",""33944"",""34170"",""35253"",""36411"",""36546"",""37455"",""41726""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1574""}]"
DOID:1574	"[""alcohol use disorder"",""Ethanol abuse"",""alcohol abuse""]"	"[{""label"":""ACADS"",""id"":""35""},{""label"":""ALDH2"",""id"":""217""},{""label"":""CHRNA6"",""id"":""8973""},{""label"":""CLOCK"",""id"":""9575""},{""label"":""COMT"",""id"":""1312""},{""label"":""DBH"",""id"":""1621""},{""label"":""DRD4"",""id"":""1815""},{""label"":""GABBR2"",""id"":""9568""},{""label"":""GABRA2"",""id"":""2555""},{""label"":""GABRB3"",""id"":""2562""},{""label"":""GRIN1"",""id"":""2902""},{""label"":""GRIN2B"",""id"":""2904""},{""label"":""HTR1B"",""id"":""3351""},{""label"":""HTR3B"",""id"":""9177""},{""label"":""HTR7"",""id"":""3363""},{""label"":""MAOA"",""id"":""4128""},{""label"":""NRG1"",""id"":""3084""},{""label"":""OPRD1"",""id"":""4985""},{""label"":""OPRK1"",""id"":""4986""},{""label"":""OPRM1"",""id"":""4988""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""TIMELESS"",""id"":""8914""},{""label"":""TPH1"",""id"":""7166""}]"	"[""1312"",""1621"",""1815"",""217"",""2555"",""2562"",""2902"",""2904"",""3084"",""3351"",""3363"",""35"",""4128"",""4985"",""4986"",""4988"",""6532"",""7166"",""8914"",""8973"",""9177"",""9568"",""9575""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1574""}]"
DOID:1574	"[""alcohol use disorder"",""Ethanol abuse"",""alcohol abuse""]"	"[{""label"":""dop-4"",""id"":""183715""},{""label"":""egl-3"",""id"":""179412""},{""label"":""unc-47"",""id"":""176431""},{""label"":""unc-63"",""id"":""172150""}]"	"[""172150"",""176431"",""179412"",""183715""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1574""}]"
DOID:1574	"[""alcohol use disorder"",""Ethanol abuse"",""alcohol abuse""]"	"[{""label"":""Creb1"",""id"":""81646""},{""label"":""Gdnf"",""id"":""25453""},{""label"":""Htr1a"",""id"":""24473""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Htr2c"",""id"":""25187""},{""label"":""Oprd1"",""id"":""24613""},{""label"":""Oprl1"",""id"":""29256""}]"	"[""24473"",""24613"",""25187"",""25453"",""29256"",""29595"",""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1574""}]"
DOID:1577	"[""limited scleroderma"",""Limited cutaneous systemic sclerosis"",""systemic sclerosis, limited""]"	"[{""label"":""IL2"",""id"":""3558""},{""label"":""STAT4"",""id"":""6775""}]"	"[""3558"",""6775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1577""}]"
DOID:1579	"[""respiratory system disease""]"	"[{""label"":""FCGR2A"",""id"":""2212""}]"	"[""2212""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1579""}]"
DOID:1580	"[""diffuse scleroderma"",""diffuse systemic sclerosis"",""systemic sclerosis, diffuse""]"	"[{""label"":""FCGR2A"",""id"":""2212""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""IL13"",""id"":""3596""},{""label"":""IRAK1"",""id"":""3654""},{""label"":""STAT4"",""id"":""6775""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TLR2"",""id"":""7097""}]"	"[""2212"",""3117"",""3596"",""3654"",""6775"",""6890"",""7097""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1580""}]"
DOID:1584	"[""acute chest syndrome"",""acute chest syndrome in sickle cell disease""]"	"[{""label"":""HBB"",""id"":""3043""},{""label"":""NOS3"",""id"":""4846""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""3043"",""4846"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1584""}]"
DOID:1586	"[""rheumatic fever"",""ACUTE RHEUMATIC FEVER"",""RhF - Rheumatic fever""]"	"[{""label"":""GC"",""id"":""2638""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""2638"",""3117"",""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1586""}]"
DOID:1587	"[""thrombocytopenia due to platelet alloimmunization"",""Auto-immune thrombocytopenia"",""Immune thrombocytopenia"",""Thrombocytopenia Due to Immune Destruction""]"	"[{""label"":""FCGR3A"",""id"":""2214""}]"	"[""2214""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1587""}]"
DOID:1588	"[""thrombocytopenia""]"	"[{""label"":""ACTB"",""id"":""60""},{""label"":""ANKRD26"",""id"":""22852""},{""label"":""CCL2"",""id"":""6347""},{""label"":""F7"",""id"":""2155""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FLI1"",""id"":""2313""},{""label"":""FYB1"",""id"":""2533""},{""label"":""GALE"",""id"":""2582""},{""label"":""GNE"",""id"":""10020""},{""label"":""IL10"",""id"":""3586""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""ITGA2B"",""id"":""3674""},{""label"":""ITGB3"",""id"":""3690""},{""label"":""MASTL"",""id"":""84930""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MPL"",""id"":""4352""},{""label"":""MYH9"",""id"":""4627""},{""label"":""PTPRJ"",""id"":""5795""},{""label"":""SRC"",""id"":""6714""},{""label"":""THPO"",""id"":""7066""},{""label"":""TNF"",""id"":""7124""}]"	"[""10020"",""2155"",""2212"",""22852"",""2313"",""2533"",""2582"",""3586"",""3673"",""3674"",""3690"",""4153"",""4352"",""4627"",""5795"",""60"",""6347"",""6714"",""7066"",""7124"",""84930""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1588""}]"
DOID:1588	"[""thrombocytopenia""]"	"[{""label"":""Tbxa2r"",""id"":""24816""}]"	"[""24816""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1588""}]"
DOID:1588	"[""thrombocytopenia""]"	"[{""label"":""GAL10"",""id"":""852307""}]"	"[""852307""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1588""}]"
DOID:1591	"[""renovascular hypertension""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Adrb1"",""id"":""24925""},{""label"":""Agtr1a"",""id"":""24180""},{""label"":""Agtr2"",""id"":""24182""},{""label"":""Cxcr3"",""id"":""84475""},{""label"":""Spp1"",""id"":""25353""}]"	"[""24180"",""24182"",""24310"",""24925"",""25353"",""84475""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1591""}]"
DOID:1596	"[""depressive disorder"",""mental depression""]"	"[{""label"":""Dop1R1"",""id"":""41726""},{""label"":""SerT"",""id"":""37895""}]"	"[""37895"",""41726""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1596""}]"
DOID:1596	"[""depressive disorder"",""mental depression""]"	"[{""label"":""CHRNB3"",""id"":""1142""},{""label"":""CRHBP"",""id"":""1393""},{""label"":""DRD2"",""id"":""1813""},{""label"":""GABRA5"",""id"":""2558""},{""label"":""GATA2"",""id"":""2624""},{""label"":""GDNF"",""id"":""2668""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HTR1A"",""id"":""3350""},{""label"":""HTR3B"",""id"":""9177""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL6"",""id"":""3569""},{""label"":""NGFR"",""id"":""4804""},{""label"":""NPPC"",""id"":""4880""},{""label"":""OPRK1"",""id"":""4986""},{""label"":""PANX1"",""id"":""24145""},{""label"":""SLC5A7"",""id"":""60482""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""TPH1"",""id"":""7166""},{""label"":""XIRP2"",""id"":""129446""}]"	"[""1142"",""129446"",""1393"",""1813"",""24145"",""2558"",""2624"",""2668"",""2876"",""3350"",""3557"",""3569"",""4804"",""4880"",""4986"",""60482"",""6532"",""7166"",""9177""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1596""}]"
DOID:1596	"[""depressive disorder"",""mental depression""]"	"[{""label"":""Adra2a"",""id"":""25083""},{""label"":""Atp5pd"",""id"":""641434""},{""label"":""Cdk5"",""id"":""140908""},{""label"":""Creb1"",""id"":""81646""},{""label"":""Esr2"",""id"":""25149""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Mc4r"",""id"":""25635""},{""label"":""Nos1"",""id"":""24598""},{""label"":""Nos1ap"",""id"":""192363""},{""label"":""Slc6a4"",""id"":""25553""}]"	"[""140908"",""192363"",""24598"",""25083"",""25149"",""25553"",""25635"",""29595"",""641434"",""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1596""}]"
DOID:161	"[""keratosis""]"	"[{""label"":""CAT"",""id"":""847""},{""label"":""MPO"",""id"":""4353""}]"	"[""4353"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:161""}]"
DOID:1612	"[""breast cancer"",""breast tumor"",""malignant neoplasm of breast"",""malignant tumor of the breast"",""mammary cancer"",""mammary tumor"",""primary breast cancer""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ACSL3"",""id"":""2181""},{""label"":""ADAM28"",""id"":""10863""},{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""ADM"",""id"":""133""},{""label"":""AGT"",""id"":""183""},{""label"":""AGTR1"",""id"":""185""},{""label"":""AKT1"",""id"":""207""},{""label"":""APEX1"",""id"":""328""},{""label"":""APOE"",""id"":""348""},{""label"":""AREG"",""id"":""374""},{""label"":""ARID1A"",""id"":""8289""},{""label"":""ATM"",""id"":""472""},{""label"":""BARD1"",""id"":""580""},{""label"":""BCAS2"",""id"":""10286""},{""label"":""BIRC2"",""id"":""329""},{""label"":""BRCA1"",""id"":""672""},{""label"":""BRCA2"",""id"":""675""},{""label"":""CASP7"",""id"":""840""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CDH13"",""id"":""1012""},{""label"":""CDH1"",""id"":""999""},{""label"":""CDKN1B"",""id"":""1027""},{""label"":""CHEK2"",""id"":""11200""},{""label"":""CLU"",""id"":""1191""},{""label"":""COMT"",""id"":""1312""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CTSD"",""id"":""1509""},{""label"":""CYB5R3"",""id"":""1727""},{""label"":""CYP17A1"",""id"":""1586""},{""label"":""CYP19A1"",""id"":""1588""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP1A2"",""id"":""1544""},{""label"":""CYP1B1"",""id"":""1545""},{""label"":""CYP2C19"",""id"":""1557""},{""label"":""EIF3H"",""id"":""8667""},{""label"":""ENG"",""id"":""2022""},{""label"":""ESR1"",""id"":""2099""},{""label"":""F10"",""id"":""2159""},{""label"":""F5"",""id"":""2153""},{""label"":""FANCD2"",""id"":""2177""},{""label"":""FAS"",""id"":""355""},{""label"":""FGFR2"",""id"":""2263""},{""label"":""FOXA1"",""id"":""3169""},{""label"":""GPX1"",""id"":""2876""},{""label"":""GRB2"",""id"":""2885""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HMMR"",""id"":""3161""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IGFBP3"",""id"":""3486""},{""label"":""IKBKB"",""id"":""3551""},{""label"":""IL13RA2"",""id"":""3598""},{""label"":""IL6"",""id"":""3569""},{""label"":""KAT6B"",""id"":""23522""},{""label"":""KDM4C"",""id"":""23081""},{""label"":""KDM5B"",""id"":""10765""},{""label"":""KRAS"",""id"":""3845""},{""label"":""LHCGR"",""id"":""3973""},{""label"":""LSP1"",""id"":""4046""},{""label"":""LTA"",""id"":""4049""},{""label"":""MAP3K1"",""id"":""4214""},{""label"":""MGMT"",""id"":""4255""},{""label"":""MIER3"",""id"":""166968""},{""label"":""MKI67"",""id"":""4288""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""MMP8"",""id"":""4317""},{""label"":""MSH2"",""id"":""4436""},{""label"":""MUC1"",""id"":""4582""},{""label"":""MYC"",""id"":""4609""},{""label"":""NBN"",""id"":""4683""},{""label"":""NCOA6"",""id"":""23054""},{""label"":""NFKB1"",""id"":""4790""},{""label"":""NOD2"",""id"":""64127""},{""label"":""NOS3"",""id"":""4846""},{""label"":""OGG1"",""id"":""4968""},{""label"":""PAK1"",""id"":""5058""},{""label"":""PHB1"",""id"":""5245""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PON1"",""id"":""5444""},{""label"":""PPM1D"",""id"":""8493""},{""label"":""PRKAA1"",""id"":""5562""},{""label"":""PTEN"",""id"":""5728""},{""label"":""PTPN13"",""id"":""5783""},{""label"":""RB1CC1"",""id"":""9821""},{""label"":""RELB"",""id"":""5971""},{""label"":""RNF20"",""id"":""56254""},{""label"":""RUNX3"",""id"":""864""},{""label"":""SHMT1"",""id"":""6470""},{""label"":""SNW1"",""id"":""22938""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SOX2"",""id"":""6657""},{""label"":""STAT3"",""id"":""6774""},{""label"":""SULT1E1"",""id"":""6783""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFAIP3"",""id"":""7128""},{""label"":""TP53"",""id"":""7157""},{""label"":""TSG101"",""id"":""7251""},{""label"":""TWIST1"",""id"":""7291""},{""label"":""UBR5"",""id"":""51366""},{""label"":""UGT1A1"",""id"":""54658""},{""label"":""WIF1"",""id"":""11197""},{""label"":""XPO5"",""id"":""57510""}]"	"[""1012"",""1027"",""10286"",""10765"",""10863"",""11197"",""11200"",""1191"",""1234"",""1312"",""133"",""1493"",""1509"",""1543"",""1544"",""1545"",""1557"",""1586"",""1588"",""1636"",""166968"",""1727"",""183"",""185"",""2022"",""207"",""2099"",""2153"",""2159"",""2177"",""2181"",""2263"",""22938"",""23054"",""23081"",""23522"",""2876"",""2885"",""3077"",""3117"",""3123"",""3161"",""3169"",""328"",""329"",""3458"",""348"",""3486"",""355"",""3551"",""3569"",""3598"",""374"",""3845"",""3973"",""4046"",""4049"",""4214"",""4255"",""4288"",""4312"",""4314"",""4317"",""4436"",""4582"",""4609"",""4683"",""472"",""4790"",""4846"",""4968"",""5058"",""51366"",""5245"",""5290"",""5444"",""54658"",""5562"",""56254"",""5728"",""57510"",""5783"",""580"",""5971"",""64127"",""6470"",""6648"",""6657"",""672"",""675"",""6774"",""6783"",""7040"",""7097"",""7099"",""7124"",""7128"",""7157"",""7251"",""7291"",""8289"",""840"",""8493"",""864"",""8667"",""9370"",""9821"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1612""}]"
DOID:1612	"[""breast cancer"",""breast tumor"",""malignant neoplasm of breast"",""malignant tumor of the breast"",""mammary cancer"",""mammary tumor"",""primary breast cancer""]"	"[{""label"":""DPM1"",""id"":""856313""}]"	"[""856313""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1612""}]"
DOID:1612	"[""breast cancer"",""breast tumor"",""malignant neoplasm of breast"",""malignant tumor of the breast"",""mammary cancer"",""mammary tumor"",""primary breast cancer""]"	"[{""label"":""Esr2"",""id"":""25149""}]"	"[""25149""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1612""}]"
DOID:1612	"[""breast cancer"",""breast tumor"",""malignant neoplasm of breast"",""malignant tumor of the breast"",""mammary cancer"",""mammary tumor"",""primary breast cancer""]"	"[{""label"":""Bard1"",""id"":""12021""},{""label"":""Erbb2"",""id"":""13866""},{""label"":""Esr1"",""id"":""13982""},{""label"":""Hgf"",""id"":""15234""},{""label"":""Met"",""id"":""17295""},{""label"":""Myc"",""id"":""17869""},{""label"":""Pik3ca"",""id"":""18706""},{""label"":""Smarca4"",""id"":""20586""},{""label"":""Trp53"",""id"":""22059""},{""label"":""Wnt1"",""id"":""22408""}]"	"[""12021"",""13866"",""13982"",""15234"",""17295"",""17869"",""18706"",""20586"",""22059"",""22408""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1612""}]"
DOID:1614	"[""male breast cancer"",""malignant neoplasm of male breast"",""neoplasm of male breast""]"	"[{""label"":""CHEK2"",""id"":""11200""}]"	"[""11200""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1614""}]"
DOID:162	"[""cancer"",""malignant neoplasm"",""malignant tumor"",""primary cancer""]"	"[{""label"":""glp-1"",""id"":""176286""},{""label"":""ina-1"",""id"":""176296""},{""label"":""pat-3"",""id"":""175504""},{""label"":""tsp-12"",""id"":""177890""}]"	"[""175504"",""176286"",""176296"",""177890""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:162""}]"
DOID:162	"[""cancer"",""malignant neoplasm"",""malignant tumor"",""primary cancer""]"	"[{""label"":""LRRK2"",""id"":""120892""}]"	"[""120892""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:162""}]"
DOID:162	"[""cancer"",""malignant neoplasm"",""malignant tumor"",""primary cancer""]"	"[{""label"":""CDS1"",""id"":""852317""},{""label"":""DOG2"",""id"":""856439""},{""label"":""GLC7"",""id"":""856870""},{""label"":""HRR25"",""id"":""855897""},{""label"":""IML1"",""id"":""853603""},{""label"":""MPE1"",""id"":""853806""},{""label"":""PCM1"",""id"":""856652""},{""label"":""PGK1"",""id"":""850370""},{""label"":""RFT1"",""id"":""852261""},{""label"":""SMP3"",""id"":""854320""},{""label"":""SNF2"",""id"":""854465""},{""label"":""TPI1"",""id"":""851620""},{""label"":""UGP1"",""id"":""853830""}]"	"[""850370"",""851620"",""852261"",""852317"",""853603"",""853806"",""853830"",""854320"",""854465"",""855897"",""856439"",""856652"",""856870""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:162""}]"
DOID:162	"[""cancer"",""malignant neoplasm"",""malignant tumor"",""primary cancer""]"	"[{""label"":""Axn"",""id"":""43565""},{""label"":""Delta"",""id"":""42313""},{""label"":""InR"",""id"":""42549""},{""label"":""N"",""id"":""31293""},{""label"":""Sin3A"",""id"":""36382""},{""label"":""ph-p"",""id"":""31181""},{""label"":""scrib"",""id"":""44448""},{""label"":""shg"",""id"":""37386""},{""label"":""shot"",""id"":""36542""}]"	"[""31181"",""31293"",""36382"",""36542"",""37386"",""42313"",""42549"",""43565"",""44448""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:162""}]"
DOID:1657	"[""ventricular septal defect"",""Interventricular septal defect"",""Ventricular septal abnormality""]"	"[{""label"":""GATA4"",""id"":""2626""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NFATC1"",""id"":""4772""},{""label"":""SALL4"",""id"":""57167""}]"	"[""2626"",""4318"",""4772"",""57167""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1657""}]"
DOID:1679	"[""cystitis""]"	"[{""label"":""Bdnf"",""id"":""24225""},{""label"":""Il2"",""id"":""116562""},{""label"":""Kdr"",""id"":""25589""},{""label"":""Ngf"",""id"":""310738""},{""label"":""Ptger4"",""id"":""84023""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Tacr1"",""id"":""24807""}]"	"[""116562"",""24225"",""24807"",""25589"",""29527"",""310738"",""84023""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1679""}]"
DOID:1679	"[""cystitis""]"	"[{""label"":""TLR5"",""id"":""7100""}]"	"[""7100""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1679""}]"
DOID:1681	"[""heart septal defect"",""Cardiac septal defects"",""Congenital septal defect of heart"",""septal defect""]"	"[{""label"":""BMPR2"",""id"":""659""},{""label"":""CRELD1"",""id"":""78987""},{""label"":""TBX2"",""id"":""6909""}]"	"[""659"",""6909"",""78987""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1681""}]"
DOID:1682	"[""congenital heart disease"",""Congenital Heart Defects"",""Congenital anomaly of heart"",""Heart Malformation"",""congenital heart defect"",""heart defect""]"	"[{""label"":""Hcf"",""id"":""43788""},{""label"":""apolpp"",""id"":""43827""},{""label"":""kis"",""id"":""33185""},{""label"":""trx"",""id"":""41737""}]"	"[""33185"",""41737"",""43788"",""43827""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1682""}]"
DOID:1682	"[""congenital heart disease"",""Congenital Heart Defects"",""Congenital anomaly of heart"",""Heart Malformation"",""congenital heart defect"",""heart defect""]"	"[{""label"":""ADAMTS19"",""id"":""171019""},{""label"":""CRIPTO"",""id"":""6997""},{""label"":""FOXP1"",""id"":""27086""},{""label"":""GATA4"",""id"":""2626""},{""label"":""GDF1"",""id"":""2657""},{""label"":""GPX3"",""id"":""2878""},{""label"":""JAG1"",""id"":""182""},{""label"":""LEFTY2"",""id"":""7044""},{""label"":""MYH7"",""id"":""4625""},{""label"":""NFATC1"",""id"":""4772""},{""label"":""NOTCH1"",""id"":""4851""},{""label"":""RBFOX2"",""id"":""23543""},{""label"":""RFC1"",""id"":""5981""},{""label"":""SP4"",""id"":""6671""},{""label"":""TAB2"",""id"":""23118""},{""label"":""TLL1"",""id"":""7092""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""171019"",""182"",""23118"",""23543"",""2626"",""2657"",""27086"",""2878"",""4625"",""4772"",""4851"",""5981"",""6671"",""6997"",""7044"",""7092"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1682""}]"
DOID:1682	"[""congenital heart disease"",""Congenital Heart Defects"",""Congenital anomaly of heart"",""Heart Malformation"",""congenital heart defect"",""heart defect""]"	"[{""label"":""Rxra"",""id"":""20181""},{""label"":""Sap130"",""id"":""269003""}]"	"[""20181"",""269003""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1682""}]"
DOID:1682	"[""congenital heart disease"",""Congenital Heart Defects"",""Congenital anomaly of heart"",""Heart Malformation"",""congenital heart defect"",""heart defect""]"	"[{""label"":""gnptab"",""id"":""553365""}]"	"[""553365""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1682""}]"
DOID:1686	"[""glaucoma""]"	"[{""label"":""Ace2"",""id"":""302668""},{""label"":""Bdnf"",""id"":""24225""},{""label"":""Mas1"",""id"":""25153""},{""label"":""Ngfr"",""id"":""24596""},{""label"":""Ntrk1"",""id"":""59109""},{""label"":""Ntrk2"",""id"":""25054""},{""label"":""Tnf"",""id"":""24835""},{""label"":""Vegfa"",""id"":""83785""}]"	"[""24225"",""24596"",""24835"",""25054"",""25153"",""302668"",""59109"",""83785""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1686""}]"
DOID:1686	"[""glaucoma""]"	"[{""label"":""Lgr4"",""id"":""107515""},{""label"":""Sh3pxd2b"",""id"":""268396""}]"	"[""107515"",""268396""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1686""}]"
DOID:1686	"[""glaucoma""]"	"[{""label"":""AGO2"",""id"":""27161""},{""label"":""BDNF"",""id"":""627""},{""label"":""EEF2"",""id"":""1938""},{""label"":""EPO"",""id"":""2056""},{""label"":""FOXC1"",""id"":""2296""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""LINGO1"",""id"":""84894""},{""label"":""OPTN"",""id"":""10133""},{""label"":""WDR36"",""id"":""134430""}]"	"[""10133"",""134430"",""1938"",""2056"",""2296"",""27161"",""3119"",""3123"",""627"",""84894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1686""}]"
DOID:169	"[""neuroendocrine tumor"",""neuroendocrine neoplasm""]"	"[{""label"":""CALR"",""id"":""811""}]"	"[""811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:169""}]"
DOID:1697	"[""ichthyosis"",""ichthyoses"",""non-syndromic ichthyosis""]"	"[{""label"":""KRT2"",""id"":""3849""}]"	"[""3849""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1697""}]"
DOID:1700	"[""X-linked ichthyosis"",""X-linked ichthyosis with steryl-sulphatase deficiency"",""X-linked placental steryl-sulphatase deficiency"",""X-linked recessive ichthyosis""]"	"[{""label"":""STS"",""id"":""412""}]"	"[""412""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1700""}]"
DOID:1702	"[""ichthyosis vulgaris"",""Dominant congenital ichthyosiform erythroderma""]"	"[{""label"":""Lbr"",""id"":""98386""}]"	"[""98386""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1702""}]"
DOID:1702	"[""ichthyosis vulgaris"",""Dominant congenital ichthyosiform erythroderma""]"	"[{""label"":""FLG"",""id"":""2312""}]"	"[""2312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1702""}]"
DOID:1712	"[""aortic valve stenosis"",""Aortic stenosis"",""Rheumatic aortic stenosis"",""rheumatic aortic valve stenosis""]"	"[{""label"":""Tnf"",""id"":""21926""}]"	"[""21926""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1712""}]"
DOID:1712	"[""aortic valve stenosis"",""Aortic stenosis"",""Rheumatic aortic stenosis"",""rheumatic aortic valve stenosis""]"	"[{""label"":""APOB"",""id"":""338""},{""label"":""ELN"",""id"":""2006""},{""label"":""MMP1"",""id"":""4312""}]"	"[""2006"",""338"",""4312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1712""}]"
DOID:1724	"[""duodenal ulcer"",""Curling Ulcer"",""Curling's ulcers"",""Stress Ulcer""]"	"[{""label"":""Cftr"",""id"":""24255""}]"	"[""24255""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1724""}]"
DOID:1727	"[""retinal vein occlusion"",""Occlusion, of retinal vein""]"	"[{""label"":""F2"",""id"":""2147""},{""label"":""F5"",""id"":""2153""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""MMP2"",""id"":""4313""},{""label"":""PON1"",""id"":""5444""},{""label"":""SERPINE1"",""id"":""5054""}]"	"[""2147"",""2153"",""3673"",""4313"",""5054"",""5444""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1727""}]"
DOID:1727	"[""retinal vein occlusion"",""Occlusion, of retinal vein""]"	"[{""label"":""Nrp1"",""id"":""18186""}]"	"[""18186""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1727""}]"
DOID:1733	"[""cryptosporidiosis"",""Cryptosporidial gastroenteritis"",""Infection by Cryptosporidium"",""intestinal cryptosporidiosis""]"	"[{""label"":""MBL2"",""id"":""4153""}]"	"[""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1733""}]"
DOID:1742	"[""drug psychosis"",""Drug-induced psychosis"",""Drug-induced psychotic disorder""]"	"[{""label"":""GAD1"",""id"":""2571""},{""label"":""GAD2"",""id"":""2572""},{""label"":""OPRM1"",""id"":""4988""}]"	"[""2571"",""2572"",""4988""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1742""}]"
DOID:1749	"[""squamous cell carcinoma"",""epidermoid carcinoma"",""malignant squamous cell tumor"",""squamous carcinoma"",""squamous cell Epithelioma"",""squamous cell cancer""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""HRAS"",""id"":""3265""},{""label"":""IL2"",""id"":""3558""},{""label"":""IRAK1"",""id"":""3654""},{""label"":""KMT2C"",""id"":""58508""},{""label"":""LZTS1"",""id"":""11178""},{""label"":""OCA2"",""id"":""4948""},{""label"":""STAT3"",""id"":""6774""},{""label"":""TP53"",""id"":""7157""}]"	"[""11178"",""1493"",""3265"",""3558"",""3654"",""4948"",""58508"",""6774"",""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1749""}]"
DOID:178	"[""vascular disease"",""vascular tissue disease""]"	"[{""label"":""CPS1"",""id"":""1373""},{""label"":""GLO1"",""id"":""2739""},{""label"":""IL1RN"",""id"":""3557""}]"	"[""1373"",""2739"",""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:178""}]"
DOID:1787	"[""pericarditis""]"	"[{""label"":""PRG4"",""id"":""10216""}]"	"[""10216""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1787""}]"
DOID:1788	"[""peritoneal mesothelioma"",""Advanced malignant Mesothelioma of Peritoneum"",""advanced malignant peritoneal mesothelioma"",""malignant mesothelioma of peritoneum""]"	"[{""label"":""TRAF7"",""id"":""84231""}]"	"[""84231""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1788""}]"
DOID:1790	"[""malignant mesothelioma"",""Diffuse malignant Mesothelioma"",""advanced malignant mesothelioma"",""asbestos-related malignant mesothelioma"",""malignant tumor of Mesothelium""]"	"[{""label"":""ACVR1B"",""id"":""91""},{""label"":""NAT2"",""id"":""10""},{""label"":""SETD2"",""id"":""29072""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10"",""29072"",""7515"",""91""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1790""}]"
DOID:1793	"[""pancreatic cancer"",""Ca body of pancreas"",""Ca head of pancreas"",""Ca tail of pancreas"",""malignant neoplasm of body of pancreas"",""malignant neoplasm of head of pancreas"",""malignant neoplasm of tail of pancreas"",""pancreas neoplasm"",""pancreatic neoplasm"",""pancreatic tumor""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""ACVR1B"",""id"":""91""},{""label"":""ADH1C"",""id"":""126""},{""label"":""ADM"",""id"":""133""},{""label"":""AKT1"",""id"":""207""},{""label"":""ALDH2"",""id"":""217""},{""label"":""ALOX5"",""id"":""240""},{""label"":""ANXA1"",""id"":""301""},{""label"":""APC"",""id"":""324""},{""label"":""ARPC1A"",""id"":""10552""},{""label"":""ATM"",""id"":""472""},{""label"":""ATR"",""id"":""545""},{""label"":""BAD"",""id"":""572""},{""label"":""BRCA1"",""id"":""672""},{""label"":""BRCA2"",""id"":""675""},{""label"":""CAPN10"",""id"":""11132""},{""label"":""CASP9"",""id"":""842""},{""label"":""CCKBR"",""id"":""887""},{""label"":""CFTR"",""id"":""1080""},{""label"":""CHEK1"",""id"":""1111""},{""label"":""CYP17A1"",""id"":""1586""},{""label"":""DPYD"",""id"":""1806""},{""label"":""EGFR"",""id"":""1956""},{""label"":""EPHA3"",""id"":""2042""},{""label"":""FANCG"",""id"":""2189""},{""label"":""FASLG"",""id"":""356""},{""label"":""HS3ST2"",""id"":""9956""},{""label"":""HSPB1"",""id"":""3315""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL13RA2"",""id"":""3598""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL4"",""id"":""3565""},{""label"":""INS"",""id"":""3630""},{""label"":""ITGA11"",""id"":""22801""},{""label"":""ITGA4"",""id"":""3676""},{""label"":""ITGA9"",""id"":""3680""},{""label"":""KDR"",""id"":""3791""},{""label"":""KRAS"",""id"":""3845""},{""label"":""L1CAM"",""id"":""3897""},{""label"":""LIG3"",""id"":""3980""},{""label"":""LUM"",""id"":""4060""},{""label"":""MAP2K4"",""id"":""6416""},{""label"":""MKI67"",""id"":""4288""},{""label"":""MPO"",""id"":""4353""},{""label"":""MSLN"",""id"":""10232""},{""label"":""MTR"",""id"":""4548""},{""label"":""MUC1"",""id"":""4582""},{""label"":""MUC4"",""id"":""4585""},{""label"":""NAP1L1"",""id"":""4673""},{""label"":""NAT2"",""id"":""10""},{""label"":""NCAM1"",""id"":""4684""},{""label"":""NUF2"",""id"":""83540""},{""label"":""OGG1"",""id"":""4968""},{""label"":""PALB2"",""id"":""79728""},{""label"":""PALLD"",""id"":""23022""},{""label"":""PDGFRA"",""id"":""5156""},{""label"":""PPARG"",""id"":""5468""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""RECQL"",""id"":""5965""},{""label"":""RUNX3"",""id"":""864""},{""label"":""SEL1L"",""id"":""6400""},{""label"":""SMAD4"",""id"":""4089""},{""label"":""SMO"",""id"":""6608""},{""label"":""SNW1"",""id"":""22938""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SPP1"",""id"":""6696""},{""label"":""TGFBR2"",""id"":""7048""},{""label"":""THBS1"",""id"":""7057""},{""label"":""TP53"",""id"":""7157""},{""label"":""TYMP"",""id"":""1890""},{""label"":""UGT1A7"",""id"":""54577""},{""label"":""WNT9A"",""id"":""7483""},{""label"":""XPC"",""id"":""7508""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10"",""10232"",""10552"",""1080"",""1111"",""11132"",""126"",""133"",""1586"",""1806"",""1890"",""1956"",""2042"",""207"",""217"",""2189"",""22801"",""22938"",""23022"",""240"",""28"",""301"",""324"",""3315"",""3480"",""3558"",""356"",""3565"",""3586"",""3596"",""3598"",""3630"",""3676"",""3680"",""3791"",""3845"",""3897"",""3980"",""4060"",""4089"",""4288"",""4353"",""4548"",""4582"",""4585"",""4673"",""4684"",""472"",""4968"",""5156"",""545"",""54577"",""5468"",""572"",""5743"",""5965"",""6400"",""6416"",""6608"",""6648"",""6696"",""672"",""675"",""7048"",""7057"",""7157"",""7483"",""7508"",""7515"",""79728"",""83540"",""842"",""864"",""887"",""91"",""9956""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1793""}]"
DOID:1793	"[""pancreatic cancer"",""Ca body of pancreas"",""Ca head of pancreas"",""Ca tail of pancreas"",""malignant neoplasm of body of pancreas"",""malignant neoplasm of head of pancreas"",""malignant neoplasm of tail of pancreas"",""pancreas neoplasm"",""pancreatic neoplasm"",""pancreatic tumor""]"	"[{""label"":""Cckbr"",""id"":""25706""},{""label"":""Tgfa"",""id"":""24827""}]"	"[""24827"",""25706""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1793""}]"
DOID:1798	"[""pancreatic endocrine carcinoma"",""Islet cell carcinoma"",""carcinoma of endocrine pancreas"",""malignant neoplasm of islets of Langerhans"",""pancreatic neuroendocrine carcinoma""]"	"[{""label"":""DAXX"",""id"":""1616""},{""label"":""MGMT"",""id"":""4255""},{""label"":""PGF"",""id"":""5228""}]"	"[""1616"",""4255"",""5228""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1798""}]"
DOID:1799	"[""islet cell tumor"",""Islet cell neoplasm"",""endocrine pancreas cancer"",""islet cell tumour"",""malignant pancreatic Endocrine tumor"",""malignant pancreatic Endocrine tumour"",""malignant tumor of endocrine pancreas"",""malignant tumour of endocrine pancreas"",""pancreatic Endocrine neoplasm""]"	"[{""label"":""DAXX"",""id"":""1616""}]"	"[""1616""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1799""}]"
DOID:18	"[""urinary system disease"",""Non-neoplastic urinary tract disease"",""urinary tract disease""]"	"[{""label"":""Bmp4"",""id"":""12159""}]"	"[""12159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:18""}]"
DOID:182	"[""calcinosis"",""Pathologically calcified structure"",""pathologic calcification""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:182""}]"
DOID:182	"[""calcinosis"",""Pathologically calcified structure"",""pathologic calcification""]"	"[{""label"":""GPX1"",""id"":""2876""}]"	"[""2876""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:182""}]"
DOID:1824	"[""status epilepticus"",""Grand mal status""]"	"[{""label"":""BDNF"",""id"":""627""}]"	"[""627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1824""}]"
DOID:1824	"[""status epilepticus"",""Grand mal status""]"	"[{""label"":""Aqp4"",""id"":""25293""},{""label"":""Bdnf"",""id"":""24225""},{""label"":""Cx3cl1"",""id"":""89808""},{""label"":""Erbb4"",""id"":""59323""},{""label"":""Grik1"",""id"":""29559""},{""label"":""Idh2"",""id"":""361596""},{""label"":""Plat"",""id"":""25692""},{""label"":""Ptgs2"",""id"":""29527""}]"	"[""24225"",""25293"",""25692"",""29527"",""29559"",""361596"",""59323"",""89808""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1824""}]"
DOID:1825	"[""childhood absence epilepsy"",""petit mal seizure"",""pyknolepsy""]"	"[{""label"":""Cacna1a"",""id"":""25398""},{""label"":""Htr7"",""id"":""65032""},{""label"":""Npy5r"",""id"":""25340""}]"	"[""25340"",""25398"",""65032""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1825""}]"
DOID:1825	"[""childhood absence epilepsy"",""petit mal seizure"",""pyknolepsy""]"	"[{""label"":""CACNA1H"",""id"":""8912""},{""label"":""GABRB3"",""id"":""2562""},{""label"":""GABRG2"",""id"":""2566""},{""label"":""GRIK1"",""id"":""2897""},{""label"":""LGI4"",""id"":""163175""},{""label"":""SLC2A1"",""id"":""6513""}]"	"[""163175"",""2562"",""2566"",""2897"",""6513"",""8912""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1825""}]"
DOID:1826	"[""epilepsy"",""epilepsy syndrome"",""epileptic syndrome""]"	"[{""label"":""Abcc2"",""id"":""25303""},{""label"":""Bdkrb1"",""id"":""81509""},{""label"":""Bdkrb2"",""id"":""25245""},{""label"":""Grm8"",""id"":""60590""},{""label"":""Lgi1"",""id"":""252892""},{""label"":""Ppia"",""id"":""25518""}]"	"[""25245"",""252892"",""25303"",""25518"",""60590"",""81509""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1826""}]"
DOID:1826	"[""epilepsy"",""epilepsy syndrome"",""epileptic syndrome""]"	"[{""label"":""ina-1"",""id"":""176296""}]"	"[""176296""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1826""}]"
DOID:1826	"[""epilepsy"",""epilepsy syndrome"",""epileptic syndrome""]"	"[{""label"":""Aldh5a1"",""id"":""214579""},{""label"":""Atp6v1b2"",""id"":""11966""},{""label"":""Bsn"",""id"":""12217""},{""label"":""C1qa"",""id"":""12259""},{""label"":""Cacna2d2"",""id"":""56808""},{""label"":""Kcna1"",""id"":""16485""},{""label"":""Scamp5"",""id"":""56807""},{""label"":""Scn8a"",""id"":""20273""},{""label"":""Slc12a5"",""id"":""57138""},{""label"":""Syn2"",""id"":""20965""}]"	"[""11966"",""12217"",""12259"",""16485"",""20273"",""20965"",""214579"",""56807"",""56808"",""57138""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1826""}]"
DOID:1826	"[""epilepsy"",""epilepsy syndrome"",""epileptic syndrome""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ACHE"",""id"":""43""},{""label"":""BCHE"",""id"":""590""},{""label"":""CP"",""id"":""1356""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""GDNF"",""id"":""2668""},{""label"":""GRIA1"",""id"":""2890""}]"	"[""1356"",""2212"",""2214"",""2668"",""2890"",""43"",""5243"",""590""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1826""}]"
DOID:1826	"[""epilepsy"",""epilepsy syndrome"",""epileptic syndrome""]"	"[{""label"":""Atpalpha"",""id"":""48971""},{""label"":""Nrg"",""id"":""31792""},{""label"":""Sh"",""id"":""32780""},{""label"":""Tmtc3"",""id"":""37401""},{""label"":""cac"",""id"":""32158""},{""label"":""eag"",""id"":""32428""},{""label"":""nrv2"",""id"":""33953""},{""label"":""para"",""id"":""32619""}]"	"[""31792"",""32158"",""32428"",""32619"",""32780"",""33953"",""37401"",""48971""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1826""}]"
DOID:1827	"[""generalized epilepsy"",""idiopathic generalized epilepsy""]"	"[{""label"":""Dnm1"",""id"":""13429""},{""label"":""Gabra1"",""id"":""14394""}]"	"[""13429"",""14394""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1827""}]"
DOID:1827	"[""generalized epilepsy"",""idiopathic generalized epilepsy""]"	"[{""label"":""HCN4"",""id"":""10021""},{""label"":""KCNMA1"",""id"":""3778""}]"	"[""10021"",""3778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1827""}]"
DOID:1838	"[""Menkes disease"",""COPPER TRANSPORT DISEASE"",""Menkes kinky-hair syndrome"",""steely hair syndrome""]"	"[{""label"":""ATP7A"",""id"":""538""},{""label"":""LOX"",""id"":""4015""}]"	"[""4015"",""538""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1838""}]"
DOID:1838	"[""Menkes disease"",""COPPER TRANSPORT DISEASE"",""Menkes kinky-hair syndrome"",""steely hair syndrome""]"	"[{""label"":""Atp7a"",""id"":""11977""},{""label"":""Lox"",""id"":""16948""}]"	"[""11977"",""16948""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1838""}]"
DOID:1849	"[""cannabis dependence""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ACHE"",""id"":""43""},{""label"":""COMT"",""id"":""1312""},{""label"":""NRG1"",""id"":""3084""}]"	"[""1312"",""3084"",""43"",""5243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1849""}]"
DOID:1852	"[""intrahepatic cholestasis"",""neonatal intrahepatic cholestasis""]"	"[{""label"":""ABCB11"",""id"":""8647""},{""label"":""ABCB4"",""id"":""5244""},{""label"":""HSD3B7"",""id"":""80270""}]"	"[""5244"",""80270"",""8647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1852""}]"
DOID:1852	"[""intrahepatic cholestasis"",""neonatal intrahepatic cholestasis""]"	"[{""label"":""Abcb4"",""id"":""18670""}]"	"[""18670""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1852""}]"
DOID:1856	"[""cherubism""]"	"[{""label"":""SH3BP2"",""id"":""6452""}]"	"[""6452""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1856""}]"
DOID:1875	"[""impotence"",""Sexual impotence"",""erectile dysfunction""]"	"[{""label"":""Agt"",""id"":""24179""},{""label"":""Akt1"",""id"":""24185""},{""label"":""Bad"",""id"":""64639""},{""label"":""Cnr1"",""id"":""25248""},{""label"":""Igfbp3"",""id"":""24484""},{""label"":""Nos1"",""id"":""24598""},{""label"":""P2ry1"",""id"":""25265""},{""label"":""P2ry2"",""id"":""29597""}]"	"[""24179"",""24185"",""24484"",""24598"",""25248"",""25265"",""29597"",""64639""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1875""}]"
DOID:1875	"[""impotence"",""Sexual impotence"",""erectile dysfunction""]"	"[{""label"":""XRCC1"",""id"":""7515""}]"	"[""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1875""}]"
DOID:1875	"[""impotence"",""Sexual impotence"",""erectile dysfunction""]"	"[{""label"":""Adamtsl2"",""id"":""77794""}]"	"[""77794""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1875""}]"
DOID:1882	"[""atrial heart septal defect"",""atrial septal defect"",""atrioseptal defect"",""auricular septal defect"",""congenital atrial septal defect"",""interatrial septal defect"",""interauricular septal defect""]"	"[{""label"":""BMP4"",""id"":""652""},{""label"":""GATA4"",""id"":""2626""},{""label"":""SOS1"",""id"":""6654""},{""label"":""TBX2"",""id"":""6909""}]"	"[""2626"",""652"",""6654"",""6909""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1882""}]"
DOID:1883	"[""hepatitis C"",""NANBH"",""Viral hepatitis C"",""chronic hepatitis C"",""hepatitis C infection"",""hepatitis nonA nonB""]"	"[{""label"":""AFP"",""id"":""174""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CCR5"",""id"":""1234""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HLA-G"",""id"":""3135""},{""label"":""IFNAR1"",""id"":""3454""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IFNL1"",""id"":""282618""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL12A"",""id"":""3592""},{""label"":""IL4"",""id"":""3565""},{""label"":""IL6"",""id"":""3569""},{""label"":""KIR3DL1"",""id"":""3811""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""LDLR"",""id"":""3949""},{""label"":""MBL2"",""id"":""4153""},{""label"":""PDCD1"",""id"":""5133""},{""label"":""SAMHD1"",""id"":""25939""},{""label"":""TLR3"",""id"":""7098""},{""label"":""TLR9"",""id"":""54106""}]"	"[""1234"",""174"",""25939"",""282618"",""3117"",""3119"",""3123"",""3135"",""3454"",""3458"",""3565"",""3569"",""3586"",""3592"",""3811"",""3813"",""3949"",""4153"",""5133"",""54106"",""6352"",""7098""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1883""}]"
DOID:1884	"[""viral hepatitis"",""Viral hepatitis with hepatic coma"",""animal viral hepatitis"",""human viral hepatitis""]"	"[{""label"":""IL2"",""id"":""3558""}]"	"[""3558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1884""}]"
DOID:1891	"[""optic nerve disease"",""disorder of the second nerve"",""optic nerve disorder"",""optic neuropathy""]"	"[{""label"":""ACO1"",""id"":""851013""}]"	"[""851013""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1891""}]"
DOID:1891	"[""optic nerve disease"",""disorder of the second nerve"",""optic nerve disorder"",""optic neuropathy""]"	"[{""label"":""EDN1"",""id"":""1906""}]"	"[""1906""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1891""}]"
DOID:1907	"[""malignant fibrous histiocytoma"",""Fibroxanthosarcoma"",""MFH""]"	"[{""label"":""PPARGC1A"",""id"":""10891""}]"	"[""10891""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1907""}]"
DOID:1909	"[""melanoma"",""Naevocarcinoma"",""malignant melanoma""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1909""}]"
DOID:1909	"[""melanoma"",""Naevocarcinoma"",""malignant melanoma""]"	"[{""label"":""Braf"",""id"":""109880""}]"	"[""109880""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1909""}]"
DOID:1909	"[""melanoma"",""Naevocarcinoma"",""malignant melanoma""]"	"[{""label"":""AGER"",""id"":""177""},{""label"":""ASS1"",""id"":""445""},{""label"":""BMP4"",""id"":""652""},{""label"":""BRCA2"",""id"":""675""},{""label"":""CAT"",""id"":""847""},{""label"":""CD40"",""id"":""958""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""ERCC5"",""id"":""2073""},{""label"":""FAS"",""id"":""355""},{""label"":""FASLG"",""id"":""356""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""JUNB"",""id"":""3726""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""MC1R"",""id"":""4157""},{""label"":""NFKB1"",""id"":""4790""},{""label"":""NRAS"",""id"":""4893""},{""label"":""RNASET2"",""id"":""8635""},{""label"":""SPP1"",""id"":""6696""},{""label"":""TERT"",""id"":""7015""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TP53"",""id"":""7157""},{""label"":""TYR"",""id"":""7299""}]"	"[""1493"",""177"",""2073"",""3117"",""355"",""3557"",""356"",""3726"",""4157"",""445"",""4790"",""4893"",""53353"",""652"",""6696"",""675"",""7015"",""7099"",""7157"",""7299"",""847"",""8635"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1909""}]"
DOID:1919	"[""Lesch-Nyhan syndrome"",""Complete hypoxanthine-guanine phosphoribosyltransferase deficiency"",""HG-PRT deficiency"",""HPRT1 deficiency"",""Hypoxanthine-guanine phosphoribosyltransferase deficiency"",""Hypoxanthine-guanine-phosphoribosyltransferase deficiency"",""Lesch - Nyhan syndrome"",""X-linked hyperuricemia"",""deficiency of IMP pyrophosphorylase"",""hypoxanthine guanine phosphoribosyltransferase deficiency""]"	"[{""label"":""Hprt1"",""id"":""15452""}]"	"[""15452""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1919""}]"
DOID:1919	"[""Lesch-Nyhan syndrome"",""Complete hypoxanthine-guanine phosphoribosyltransferase deficiency"",""HG-PRT deficiency"",""HPRT1 deficiency"",""Hypoxanthine-guanine phosphoribosyltransferase deficiency"",""Hypoxanthine-guanine-phosphoribosyltransferase deficiency"",""Lesch - Nyhan syndrome"",""X-linked hyperuricemia"",""deficiency of IMP pyrophosphorylase"",""hypoxanthine guanine phosphoribosyltransferase deficiency""]"	"[{""label"":""Aprt"",""id"":""48224""}]"	"[""48224""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1919""}]"
DOID:1919	"[""Lesch-Nyhan syndrome"",""Complete hypoxanthine-guanine phosphoribosyltransferase deficiency"",""HG-PRT deficiency"",""HPRT1 deficiency"",""Hypoxanthine-guanine phosphoribosyltransferase deficiency"",""Hypoxanthine-guanine-phosphoribosyltransferase deficiency"",""Lesch - Nyhan syndrome"",""X-linked hyperuricemia"",""deficiency of IMP pyrophosphorylase"",""hypoxanthine guanine phosphoribosyltransferase deficiency""]"	"[{""label"":""HPRT1"",""id"":""3251""}]"	"[""3251""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1919""}]"
DOID:1920	"[""hyperuricemia"",""Blood urate raized"",""uricacidemia""]"	"[{""label"":""APOE"",""id"":""348""}]"	"[""348""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1920""}]"
DOID:1920	"[""hyperuricemia"",""Blood urate raized"",""uricacidemia""]"	"[{""label"":""Abcg2"",""id"":""26357""},{""label"":""Slc2a9"",""id"":""117591""}]"	"[""117591"",""26357""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1920""}]"
DOID:1923	"[""disorder of sexual development"",""sex development disorder"",""sex differentiation disease""]"	"[{""label"":""AMH"",""id"":""268""},{""label"":""HSD17B3"",""id"":""3293""}]"	"[""268"",""3293""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1923""}]"
DOID:1924	"[""hypogonadism""]"	"[{""label"":""Lep"",""id"":""25608""}]"	"[""25608""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1924""}]"
DOID:1924	"[""hypogonadism""]"	"[{""label"":""KISS1R"",""id"":""84634""}]"	"[""84634""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1924""}]"
DOID:1925	"[""Coffin-Siris syndrome"",""Dwarfism-Onychodysplasia"",""Fifth Digit Syndrome"",""Short Stature-Onychodysplasia.""]"	"[{""label"":""ARID1B"",""id"":""57492""}]"	"[""57492""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1925""}]"
DOID:1925	"[""Coffin-Siris syndrome"",""Dwarfism-Onychodysplasia"",""Fifth Digit Syndrome"",""Short Stature-Onychodysplasia.""]"	"[{""label"":""Arid1a"",""id"":""93760""}]"	"[""93760""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1925""}]"
DOID:1926	"[""Gaucher's disease"",""Gaucher disease"",""acid beta-glucosidase deficiency"",""glocucerebrosidase deficiency"",""glucosylceramide beta-glucosidase deficiency"",""kerasin thesaurismosis""]"	"[{""label"":""Gba1"",""id"":""14466""}]"	"[""14466""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1926""}]"
DOID:1926	"[""Gaucher's disease"",""Gaucher disease"",""acid beta-glucosidase deficiency"",""glocucerebrosidase deficiency"",""glucosylceramide beta-glucosidase deficiency"",""kerasin thesaurismosis""]"	"[{""label"":""GBA1"",""id"":""2629""},{""label"":""PKLR"",""id"":""5313""},{""label"":""TNF"",""id"":""7124""}]"	"[""2629"",""5313"",""7124""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00066""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00067""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00068""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00070""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1926""}]"
DOID:1927	"[""sphingolipidosis"",""sphingolipidoses""]"	"[{""label"":""spin"",""id"":""45380""}]"	"[""45380""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1927""}]"
DOID:1927	"[""sphingolipidosis"",""sphingolipidoses""]"	"[{""label"":""ASAH1"",""id"":""427""}]"	"[""427""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1927""}]"
DOID:1928	"[""Williams-Beuren syndrome"",""Fanconi Schlesinger syndrome"",""WBS""]"	"[{""label"":""BUD23"",""id"":""114049""},{""label"":""EIF4H"",""id"":""7458""},{""label"":""ELN"",""id"":""2006""},{""label"":""FZD3"",""id"":""7976""}]"	"[""114049"",""2006"",""7458"",""7976""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1928""}]"
DOID:1928	"[""Williams-Beuren syndrome"",""Fanconi Schlesinger syndrome"",""WBS""]"	"[{""label"":""Clip2"",""id"":""269713""},{""label"":""Dlg4"",""id"":""13385""},{""label"":""Fzd9"",""id"":""14371""},{""label"":""Limk1"",""id"":""16885""},{""label"":""Lox"",""id"":""16948""},{""label"":""Src"",""id"":""20779""}]"	"[""13385"",""14371"",""16885"",""16948"",""20779"",""269713""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1928""}]"
DOID:1929	"[""supravalvular aortic stenosis"",""Supra-valvular aortic stenosis""]"	"[{""label"":""ELN"",""id"":""2006""}]"	"[""2006""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1929""}]"
DOID:1930	"[""Laurence-Moon syndrome"",""LNMS""]"	"[{""label"":""PNPLA6"",""id"":""10908""}]"	"[""10908""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1930""}]"
DOID:1932	"[""Angelman syndrome"",""happy puppet syndrome"",""puppetlike syndrome""]"	"[{""label"":""UBE3A"",""id"":""7337""}]"	"[""7337""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1932""}]"
DOID:1933	"[""Rubinstein-Taybi syndrome"",""Broad Thumb-Hallux syndrome"",""Rubinstein syndrome"",""proximal chromosome 16p13.3 deletion syndrome""]"	"[{""label"":""CREBBP"",""id"":""1387""},{""label"":""EP300"",""id"":""2033""}]"	"[""1387"",""2033""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1933""}]"
DOID:1934	"[""dysostosis""]"	"[{""label"":""EFNB1"",""id"":""1947""}]"	"[""1947""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1934""}]"
DOID:1934	"[""dysostosis""]"	"[{""label"":""Kif3a"",""id"":""16568""}]"	"[""16568""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1934""}]"
DOID:1935	"[""Bardet-Biedl syndrome""]"	"[{""label"":""BBS2"",""id"":""583""},{""label"":""BBS9"",""id"":""27241""},{""label"":""TMEM67"",""id"":""91147""},{""label"":""TTC8"",""id"":""123016""}]"	"[""123016"",""27241"",""583"",""91147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1935""}]"
DOID:1936	"[""atherosclerosis""]"	"[{""label"":""Agt"",""id"":""24179""},{""label"":""Cd40lg"",""id"":""84349""},{""label"":""Clu"",""id"":""24854""},{""label"":""Ldlr"",""id"":""300438""}]"	"[""24179"",""24854"",""300438"",""84349""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1936""}]"
DOID:1936	"[""atherosclerosis""]"	"[{""label"":""ADD1"",""id"":""118""},{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""APOA1"",""id"":""335""},{""label"":""APOE"",""id"":""348""},{""label"":""CLU"",""id"":""1191""},{""label"":""COL4A2"",""id"":""1284""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""MMP1"",""id"":""4312""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NPPB"",""id"":""4879""},{""label"":""PLA2G7"",""id"":""7941""},{""label"":""PON1"",""id"":""5444""},{""label"":""PON3"",""id"":""5446""},{""label"":""VIM"",""id"":""7431""}]"	"[""118"",""1191"",""1284"",""2212"",""3303"",""335"",""348"",""4312"",""4846"",""4879"",""5444"",""5446"",""7431"",""7941"",""9370""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1936""}]"
DOID:1949	"[""cholecystitis"",""acute and chronic cholecystitis"",""acute cholecystitis"",""acute on chronic cholecystitis"",""chronic cholecystitis""]"	"[{""label"":""Abcb4"",""id"":""18670""}]"	"[""18670""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1949""}]"
DOID:1962	"[""fallopian tube disease""]"	"[{""label"":""CCR5"",""id"":""1234""}]"	"[""1234""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1962""}]"
DOID:1967	"[""leiomyosarcoma"",""Leiomyosarcomas""]"	"[{""label"":""MED12"",""id"":""9968""}]"	"[""9968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1967""}]"
DOID:1984	"[""rectal benign neoplasm"",""Rectal tumor"",""neoplasm of rectum"",""rectum neoplasm""]"	"[{""label"":""PIK3CA"",""id"":""5290""}]"	"[""5290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1984""}]"
DOID:1993	"[""rectum cancer"",""carcinoma of rectum"",""carcinoma of the rectum"",""malignant Rectal tumor"",""malignant neoplasm of rectum"",""malignant rectum tumor"",""malignant tumor of rectum"",""rectal cancer""]"	"[{""label"":""CHD4"",""id"":""1108""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""GPX3"",""id"":""2878""},{""label"":""IL6"",""id"":""3569""},{""label"":""MAP3K1"",""id"":""4214""},{""label"":""MAPK14"",""id"":""1432""},{""label"":""MRE11"",""id"":""4361""},{""label"":""NBN"",""id"":""4683""},{""label"":""XRCC5"",""id"":""7520""}]"	"[""1108"",""1432"",""1591"",""2878"",""3569"",""4214"",""4361"",""4683"",""7520""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1993""}]"
DOID:1996	"[""rectum adenocarcinoma"",""Rectal adenocarcinoma""]"	"[{""label"":""STAT3"",""id"":""6774""},{""label"":""STAT4"",""id"":""6775""},{""label"":""STAT6"",""id"":""6778""}]"	"[""6774"",""6775"",""6778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:1996""}]"
DOID:2018	"[""hyperinsulinism"",""hyperinsulinemia""]"	"[{""label"":""ABCC8"",""id"":""6833""},{""label"":""AGT"",""id"":""183""},{""label"":""GCK"",""id"":""2645""},{""label"":""GLUD1"",""id"":""2746""},{""label"":""IL6"",""id"":""3569""},{""label"":""INS"",""id"":""3630""},{""label"":""KCNJ11"",""id"":""3767""},{""label"":""LTA"",""id"":""4049""},{""label"":""PTPRF"",""id"":""5792""}]"	"[""183"",""2645"",""2746"",""3569"",""3630"",""3767"",""4049"",""5792"",""6833""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2018""}]"
DOID:2018	"[""hyperinsulinism"",""hyperinsulinemia""]"	"[{""label"":""Lep"",""id"":""25608""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Npy5r"",""id"":""25340""}]"	"[""24536"",""25340"",""25608""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2018""}]"
DOID:2030	"[""anxiety disorder"",""anxiety"",""anxiety state""]"	"[{""label"":""Adra2a"",""id"":""25083""},{""label"":""Esr2"",""id"":""25149""},{""label"":""Hcn1"",""id"":""84390""},{""label"":""Htr1b"",""id"":""25075""},{""label"":""Htr2c"",""id"":""25187""},{""label"":""Htr7"",""id"":""65032""},{""label"":""Slc6a4"",""id"":""25553""}]"	"[""25075"",""25083"",""25149"",""25187"",""25553"",""65032"",""84390""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2030""}]"
DOID:2030	"[""anxiety disorder"",""anxiety"",""anxiety state""]"	"[{""label"":""Htr1a"",""id"":""15550""}]"	"[""15550""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2030""}]"
DOID:2030	"[""anxiety disorder"",""anxiety"",""anxiety state""]"	"[{""label"":""CTNND2"",""id"":""1501""},{""label"":""DRD2"",""id"":""1813""},{""label"":""GAD1"",""id"":""2571""},{""label"":""GDNF"",""id"":""2668""},{""label"":""HTR1A"",""id"":""3350""},{""label"":""MANEA"",""id"":""79694""},{""label"":""SLC6A4"",""id"":""6532""}]"	"[""1501"",""1813"",""2571"",""2668"",""3350"",""6532"",""79694""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2030""}]"
DOID:2033	"[""communication disorder""]"	"[{""label"":""COL6A3"",""id"":""1293""},{""label"":""DDB1"",""id"":""1642""}]"	"[""1293"",""1642""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2033""}]"
DOID:2043	"[""hepatitis B"",""chronic hepatitis B"",""hepatitis B infection""]"	"[{""label"":""CA9"",""id"":""768""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP27B1"",""id"":""1594""},{""label"":""DOCK8"",""id"":""81704""},{""label"":""EFTUD2"",""id"":""9343""},{""label"":""EIF2AK2"",""id"":""5610""},{""label"":""HLA-DPA1"",""id"":""3113""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IFNA2"",""id"":""3440""},{""label"":""IFNAR2"",""id"":""3455""},{""label"":""IFNGR1"",""id"":""3459""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL10RB"",""id"":""3588""},{""label"":""IL4"",""id"":""3565""},{""label"":""IL6"",""id"":""3569""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""MBL2"",""id"":""4153""},{""label"":""PDCD1"",""id"":""5133""},{""label"":""SAMHD1"",""id"":""25939""},{""label"":""TLR3"",""id"":""7098""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNF"",""id"":""7124""},{""label"":""UGT1A1"",""id"":""54658""},{""label"":""UGT1A6"",""id"":""54578""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1234"",""1493"",""1594"",""25939"",""3113"",""3115"",""3117"",""3119"",""3440"",""3455"",""3459"",""3565"",""3569"",""3586"",""3588"",""3813"",""4153"",""5133"",""54106"",""54578"",""54658"",""5610"",""6352"",""7098"",""7124"",""7515"",""768"",""81704"",""9343""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2043""}]"
DOID:2044	"[""drug-induced hepatitis"",""Drug-induced chronic hepatitis""]"	"[{""label"":""Hmgcr"",""id"":""25675""}]"	"[""25675""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2044""}]"
DOID:2044	"[""drug-induced hepatitis"",""Drug-induced chronic hepatitis""]"	"[{""label"":""ABCC2"",""id"":""1244""}]"	"[""1244""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2044""}]"
DOID:2048	"[""autoimmune hepatitis"",""Autoimmune chronic active hepatitis"",""autoimmune hepatitis with centrilobular necrosis""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""F2"",""id"":""2147""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HRAS"",""id"":""3265""},{""label"":""IL4"",""id"":""3565""},{""label"":""KIR2DL2"",""id"":""3803""},{""label"":""PDCD1"",""id"":""5133""},{""label"":""PDIA3"",""id"":""2923""},{""label"":""STAT4"",""id"":""6775""}]"	"[""1493"",""2147"",""2923"",""3115"",""3119"",""3123"",""3265"",""3565"",""3803"",""5133"",""6775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2048""}]"
DOID:2055	"[""post-traumatic stress disorder"",""PTSD"",""traumatic neurosis""]"	"[{""label"":""BDNF"",""id"":""627""},{""label"":""OPRM1"",""id"":""4988""}]"	"[""4988"",""627""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2055""}]"
DOID:2058	"[""chronic mucocutaneous candidiasis""]"	"[{""label"":""CLEC7A"",""id"":""64581""},{""label"":""IL17F"",""id"":""112744""},{""label"":""IL17RC"",""id"":""84818""},{""label"":""TRAF3IP2"",""id"":""10758""}]"	"[""10758"",""112744"",""64581"",""84818""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2058""}]"
DOID:206	"[""hereditary multiple exostoses"",""Multiple congenital exostosis"",""Multiple exostosis syndromes"",""Osteochondromatosis syndrome"",""hereditary multiple exostoses 1"",""hereditary multiple exostoses 2"",""hereditary multiple exostoses 3"",""multiple ostechondromas""]"	"[{""label"":""Ext1"",""id"":""14042""},{""label"":""Ext2"",""id"":""14043""}]"	"[""14042"",""14043""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:206""}]"
DOID:206	"[""hereditary multiple exostoses"",""Multiple congenital exostosis"",""Multiple exostosis syndromes"",""Osteochondromatosis syndrome"",""hereditary multiple exostoses 1"",""hereditary multiple exostoses 2"",""hereditary multiple exostoses 3"",""multiple ostechondromas""]"	"[{""label"":""rib-1"",""id"":""178080""},{""label"":""rib-2"",""id"":""176502""}]"	"[""176502"",""178080""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:206""}]"
DOID:206	"[""hereditary multiple exostoses"",""Multiple congenital exostosis"",""Multiple exostosis syndromes"",""Osteochondromatosis syndrome"",""hereditary multiple exostoses 1"",""hereditary multiple exostoses 2"",""hereditary multiple exostoses 3"",""multiple ostechondromas""]"	"[{""label"":""ext2"",""id"":""493780""}]"	"[""493780""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:206""}]"
DOID:206	"[""hereditary multiple exostoses"",""Multiple congenital exostosis"",""Multiple exostosis syndromes"",""Osteochondromatosis syndrome"",""hereditary multiple exostoses 1"",""hereditary multiple exostoses 2"",""hereditary multiple exostoses 3"",""multiple ostechondromas""]"	"[{""label"":""EXT1"",""id"":""2131""}]"	"[""2131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:206""}]"
DOID:2101	"[""vulva squamous cell carcinoma"",""Vulvar Epidermoid carcinoma"",""vulvar squamous cell carcinoma""]"	"[{""label"":""SFN"",""id"":""2810""}]"	"[""2810""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2101""}]"
DOID:2121	"[""ectodermal dysplasia"",""Congenital ectodermal defect"",""Congenital ectodermal dysplasia""]"	"[{""label"":""KRT17"",""id"":""3872""},{""label"":""NECTIN1"",""id"":""5818""},{""label"":""WNT10A"",""id"":""80326""}]"	"[""3872"",""5818"",""80326""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2121""}]"
DOID:2152	"[""ovary epithelial cancer"",""Ovarian Surface epithelial-Stromal tumor""]"	"[{""label"":""AKAP6"",""id"":""9472""},{""label"":""CCR3"",""id"":""1232""},{""label"":""DAXX"",""id"":""1616""},{""label"":""KIF1B"",""id"":""23095""},{""label"":""NME1"",""id"":""4830""},{""label"":""TAB2"",""id"":""23118""}]"	"[""1232"",""1616"",""23095"",""23118"",""4830"",""9472""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2152""}]"
DOID:2154	"[""nephroblastoma"",""adult nephroblastoma""]"	"[{""label"":""BRCA2"",""id"":""675""},{""label"":""CTNNB1"",""id"":""1499""},{""label"":""GPC3"",""id"":""2719""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""IGF2R"",""id"":""3482""},{""label"":""REST"",""id"":""5978""},{""label"":""SIX1"",""id"":""6495""}]"	"[""1499"",""2719"",""3480"",""3482"",""5978"",""6495"",""675""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2154""}]"
DOID:216	"[""dental caries"",""Dental caries extending into pulp"",""Dental caries of smooth surface"",""Dental caries pit and fissure""]"	"[{""label"":""BCOR"",""id"":""54880""},{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119"",""54880""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:216""}]"
DOID:218	"[""ascending colon cancer"",""Ca ascending colon"",""malignant neoplasm of right colon"",""malignant tumor of ascending colon""]"	"[{""label"":""POLE"",""id"":""5426""},{""label"":""RNF43"",""id"":""54894""}]"	"[""5426"",""54894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:218""}]"
DOID:2187	"[""amelogenesis imperfecta""]"	"[{""label"":""FAM20C"",""id"":""56975""}]"	"[""56975""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2187""}]"
DOID:219	"[""colon cancer""]"	"[{""label"":""Bad"",""id"":""64639""},{""label"":""Esr2"",""id"":""25149""}]"	"[""25149"",""64639""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:219""}]"
DOID:219	"[""colon cancer""]"	"[{""label"":""ACVR2A"",""id"":""92""},{""label"":""AKT1"",""id"":""207""},{""label"":""AKT3"",""id"":""10000""},{""label"":""ARID1A"",""id"":""8289""},{""label"":""ATR"",""id"":""545""},{""label"":""BRCA1"",""id"":""672""},{""label"":""BRD4"",""id"":""23476""},{""label"":""CALR"",""id"":""811""},{""label"":""CASP7"",""id"":""840""},{""label"":""CHAF1A"",""id"":""10036""},{""label"":""CRIPTO"",""id"":""6997""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""HS3ST2"",""id"":""9956""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL7R"",""id"":""3575""},{""label"":""KDM3A"",""id"":""55818""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""MAPK14"",""id"":""1432""},{""label"":""MRE11"",""id"":""4361""},{""label"":""MSH2"",""id"":""4436""},{""label"":""NCOA6"",""id"":""23054""},{""label"":""PPARG"",""id"":""5468""},{""label"":""PRKAA1"",""id"":""5562""},{""label"":""PTPN13"",""id"":""5783""},{""label"":""RICTOR"",""id"":""253260""},{""label"":""SLC7A5"",""id"":""8140""},{""label"":""SRC"",""id"":""6714""},{""label"":""TGFBR2"",""id"":""7048""}]"	"[""10000"",""10036"",""1432"",""1591"",""207"",""23054"",""23476"",""253260"",""3575"",""3586"",""4361"",""4436"",""53353"",""545"",""5468"",""5562"",""55818"",""5783"",""6714"",""672"",""6997"",""7048"",""811"",""8140"",""8289"",""840"",""92"",""9956""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:219""}]"
DOID:219	"[""colon cancer""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:219""}]"
DOID:2211	"[""factor XIII deficiency"",""Factor XIII deficiency disease"",""Hereditary factor XIII deficiency disease"",""deficiency, Laki-Lorand factor""]"	"[{""label"":""F13A1"",""id"":""2162""},{""label"":""LMAN1"",""id"":""3998""}]"	"[""2162"",""3998""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2211""}]"
DOID:2211	"[""factor XIII deficiency"",""Factor XIII deficiency disease"",""Hereditary factor XIII deficiency disease"",""deficiency, Laki-Lorand factor""]"	"[{""label"":""F13a1"",""id"":""74145""}]"	"[""74145""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2211""}]"
DOID:2215	"[""factor VII deficiency"",""deficiency, stable""]"	"[{""label"":""F7"",""id"":""2155""}]"	"[""2155""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2215""}]"
DOID:2216	"[""factor V deficiency"",""Hereditary hypoproaccelerinaemia"",""Labile factor deficiency"",""Proaccelerin deficiency"",""deficiency, labile""]"	"[{""label"":""F5"",""id"":""2153""},{""label"":""LMAN1"",""id"":""3998""}]"	"[""2153"",""3998""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2216""}]"
DOID:2217	"[""Bernard-Soulier syndrome"",""Bernard - Soulier thrombopathy"",""Bernard Soulier syndrome"",""Giant platelet syndrome"",""Hemorrhagic dystrophic thrombocytopenia"",""Thrombopathy, Bernard-Soulier""]"	"[{""label"":""GP1BA"",""id"":""2811""},{""label"":""GP1BB"",""id"":""2812""},{""label"":""GP9"",""id"":""2815""},{""label"":""VWF"",""id"":""7450""}]"	"[""2811"",""2812"",""2815"",""7450""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2217""}]"
DOID:2217	"[""Bernard-Soulier syndrome"",""Bernard - Soulier thrombopathy"",""Bernard Soulier syndrome"",""Giant platelet syndrome"",""Hemorrhagic dystrophic thrombocytopenia"",""Thrombopathy, Bernard-Soulier""]"	"[{""label"":""Gp1ba"",""id"":""14723""},{""label"":""Gp1bb"",""id"":""14724""}]"	"[""14723"",""14724""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2217""}]"
DOID:2218	"[""blood platelet disease"",""Thrombocytopathy"",""platelet disorder""]"	"[{""label"":""CD36"",""id"":""948""},{""label"":""EPHB2"",""id"":""2048""},{""label"":""FLI1"",""id"":""2313""},{""label"":""GP6"",""id"":""51206""},{""label"":""ITGB3"",""id"":""3690""},{""label"":""TBXA2R"",""id"":""6915""},{""label"":""TPM4"",""id"":""7171""}]"	"[""2048"",""2313"",""3690"",""51206"",""6915"",""7171"",""948""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2218""}]"
DOID:2219	"[""Glanzmann's thrombasthenia"",""BDPLT2"",""Glanzmann thrombasthenia"",""Glycoprotein IIb/IIIa defect"",""Thrombocytasthenia"",""deficiency of GP IIb-IIIa complex"",""deficiency of glycoprotein complex IIb-IIIa"",""deficiency of platelet fibrinogen receptor"",""platelet glycoprotein IIb-IIIa deficiency"",""platelet-type bleeding disorder 2"",""thrombasthenia of Glanzmann and Naegeli""]"	"[{""label"":""ITGA2"",""id"":""3673""},{""label"":""ITGA2B"",""id"":""3674""},{""label"":""ITGB3"",""id"":""3690""}]"	"[""3673"",""3674"",""3690""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2219""}]"
DOID:2219	"[""Glanzmann's thrombasthenia"",""BDPLT2"",""Glanzmann thrombasthenia"",""Glycoprotein IIb/IIIa defect"",""Thrombocytasthenia"",""deficiency of GP IIb-IIIa complex"",""deficiency of glycoprotein complex IIb-IIIa"",""deficiency of platelet fibrinogen receptor"",""platelet glycoprotein IIb-IIIa deficiency"",""platelet-type bleeding disorder 2"",""thrombasthenia of Glanzmann and Naegeli""]"	"[{""label"":""Itgb3"",""id"":""16416""}]"	"[""16416""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2219""}]"
DOID:2222	"[""factor X deficiency"",""disease, Stuart-Prower""]"	"[{""label"":""F10"",""id"":""2159""}]"	"[""2159""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2222""}]"
DOID:2223	"[""platelet storage pool deficiency"",""Dense body defect"",""Platelet dense granule deficiency"",""Platelet storage pool defect""]"	"[{""label"":""Ap3b1"",""id"":""11774""}]"	"[""11774""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2223""}]"
DOID:2224	"[""essential thrombocythemia"",""Essential thrombocythaemia"",""familial thrombocytosis"",""hemorrhagic thrombocythemia"",""hereditary thrombocythemia"",""primary Thrombocytosis""]"	"[{""label"":""CALR"",""id"":""811""},{""label"":""MPL"",""id"":""4352""},{""label"":""THPO"",""id"":""7066""},{""label"":""VWF"",""id"":""7450""}]"	"[""4352"",""7066"",""7450"",""811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2224""}]"
DOID:2224	"[""essential thrombocythemia"",""Essential thrombocythaemia"",""familial thrombocytosis"",""hemorrhagic thrombocythemia"",""hereditary thrombocythemia"",""primary Thrombocytosis""]"	"[{""label"":""Myb"",""id"":""17863""}]"	"[""17863""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2224""}]"
DOID:2226	"[""myeloproliferative neoplasm"",""CMPD"",""CMPD, U"",""chronic myeloproliferative disease""]"	"[{""label"":""Asxl1"",""id"":""228790""},{""label"":""Pdgfrb"",""id"":""18596""}]"	"[""18596"",""228790""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2226""}]"
DOID:2226	"[""myeloproliferative neoplasm"",""CMPD"",""CMPD, U"",""chronic myeloproliferative disease""]"	"[{""label"":""PDGFRB"",""id"":""5159""},{""label"":""TET2"",""id"":""54790""}]"	"[""5159"",""54790""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2226""}]"
DOID:2228	"[""thrombocytosis"",""Thrombocythaemia""]"	"[{""label"":""CALR"",""id"":""811""},{""label"":""MPL"",""id"":""4352""},{""label"":""THPO"",""id"":""7066""}]"	"[""4352"",""7066"",""811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2228""}]"
DOID:2229	"[""factor XI deficiency"",""Congenital factor XI deficiency"",""Hereditary factor XI deficiency disease"",""Rosenthal's disease"",""hemophilia C"",""plasma thromboplastin antecedent deficiency""]"	"[{""label"":""F11"",""id"":""109821""}]"	"[""109821""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2229""}]"
DOID:2229	"[""factor XI deficiency"",""Congenital factor XI deficiency"",""Hereditary factor XI deficiency disease"",""Rosenthal's disease"",""hemophilia C"",""plasma thromboplastin antecedent deficiency""]"	"[{""label"":""F11"",""id"":""2160""}]"	"[""2160""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2229""}]"
DOID:2231	"[""factor XII deficiency"",""Factor XII deficiency disease"",""Hageman Factor deficiency"",""deficiency, Hageman""]"	"[{""label"":""F12"",""id"":""2161""}]"	"[""2161""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2231""}]"
DOID:2231	"[""factor XII deficiency"",""Factor XII deficiency disease"",""Hageman Factor deficiency"",""deficiency, Hageman""]"	"[{""label"":""F12"",""id"":""58992""}]"	"[""58992""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2231""}]"
DOID:2234	"[""focal epilepsy"",""localisation-related epilepsy"",""partial epilepsy""]"	"[{""label"":""Cnr1"",""id"":""25248""}]"	"[""25248""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2234""}]"
DOID:2235	"[""prothrombin deficiency"",""Congenital factor II deficiency"",""Hereditary factor II deficiency disease"",""hypoprothrombinemia""]"	"[{""label"":""F2"",""id"":""2147""}]"	"[""2147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2235""}]"
DOID:2236	"[""congenital afibrinogenemia"",""Factor I deficiency"",""Fibrinogen deficiency""]"	"[{""label"":""Fgg"",""id"":""99571""}]"	"[""99571""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2236""}]"
DOID:2236	"[""congenital afibrinogenemia"",""Factor I deficiency"",""Fibrinogen deficiency""]"	"[{""label"":""FGA"",""id"":""2243""},{""label"":""FGB"",""id"":""2244""},{""label"":""FGG"",""id"":""2266""}]"	"[""2243"",""2244"",""2266""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2236""}]"
DOID:2237	"[""hepatitis"",""acute and subacute liver necrosis"",""acute hepatitis"",""acute/subac. necrosis of liver"",""animal hepatitis"",""chronic hepatitis"",""chronic persistent hepatitis""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""SPP1"",""id"":""6696""}]"	"[""28"",""6696""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2237""}]"
DOID:2237	"[""hepatitis"",""acute and subacute liver necrosis"",""acute hepatitis"",""acute/subac. necrosis of liver"",""animal hepatitis"",""chronic hepatitis"",""chronic persistent hepatitis""]"	"[{""label"":""Tf"",""id"":""24825""}]"	"[""24825""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2237""}]"
DOID:2237	"[""hepatitis"",""acute and subacute liver necrosis"",""acute hepatitis"",""acute/subac. necrosis of liver"",""animal hepatitis"",""chronic hepatitis"",""chronic persistent hepatitis""]"	"[{""label"":""Ifng"",""id"":""15978""}]"	"[""15978""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2237""}]"
DOID:224	"[""transient cerebral ischemia"",""TIA"",""TIA - Transient ischaemic attack"",""Transient cerebral ischaemia"",""Transient ischemic attacks"",""transient ischemic attack""]"	"[{""label"":""CSF3"",""id"":""1440""},{""label"":""EPO"",""id"":""2056""},{""label"":""F12"",""id"":""2161""},{""label"":""GOT1"",""id"":""2805""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""NAMPT"",""id"":""10135""},{""label"":""NRG1"",""id"":""3084""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""SOD1"",""id"":""6647""},{""label"":""TFPI"",""id"":""7035""}]"	"[""10135"",""1440"",""2056"",""2161"",""2805"",""3084"",""3557"",""5176"",""6647"",""7035""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:224""}]"
DOID:224	"[""transient cerebral ischemia"",""TIA"",""TIA - Transient ischaemic attack"",""Transient cerebral ischaemia"",""Transient ischemic attacks"",""transient ischemic attack""]"	"[{""label"":""Atf2"",""id"":""81647""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Creb1"",""id"":""81646""},{""label"":""Esr1"",""id"":""24890""},{""label"":""Esr2"",""id"":""25149""},{""label"":""Fas"",""id"":""246097""},{""label"":""G6pd"",""id"":""24377""},{""label"":""Got1"",""id"":""24401""},{""label"":""Grin2a"",""id"":""24409""},{""label"":""Grin2b"",""id"":""24410""},{""label"":""Ifnb1"",""id"":""24481""},{""label"":""Il10"",""id"":""25325""},{""label"":""Il1rn"",""id"":""60582""},{""label"":""Kcnk2"",""id"":""170899""},{""label"":""Lpar1"",""id"":""116744""},{""label"":""Mmp2"",""id"":""81686""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Nampt"",""id"":""297508""},{""label"":""Nos1"",""id"":""24598""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Nox1"",""id"":""114243""},{""label"":""Parp1"",""id"":""25591""},{""label"":""Pparg"",""id"":""25664""},{""label"":""Ptafr"",""id"":""58949""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Tnf"",""id"":""24835""},{""label"":""Ucp2"",""id"":""54315""}]"	"[""114243"",""116744"",""170899"",""24377"",""24401"",""24409"",""24410"",""24481"",""24598"",""24600"",""246097"",""24617"",""24770"",""24835"",""24890"",""25149"",""25325"",""25591"",""25664"",""297508"",""54315"",""58949"",""60582"",""81646"",""81647"",""81686"",""81687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:224""}]"
DOID:2247	"[""spondylosis"",""Lumbar spondylosis with myelopathy"",""Spondylogenic compression of lumbar spinal cord"",""Spondylogenic compression of thoracic spinal cord"",""Thoracic or lumbar spondylosis with myelopathy"",""lumbosacral spondylosis without myelopathy"",""spondylosis with myelopathy""]"	"[{""label"":""KL"",""id"":""9365""}]"	"[""9365""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2247""}]"
DOID:2256	"[""osteochondrodysplasia"",""Cartilage Development disorder"",""Congenital anomaly of cartilage"",""Osteochondrodysplasia syndrome"",""chondrodystrophy"",""skeletal dysplasia""]"	"[{""label"":""Tgfbr1"",""id"":""29591""}]"	"[""29591""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2256""}]"
DOID:2256	"[""osteochondrodysplasia"",""Cartilage Development disorder"",""Congenital anomaly of cartilage"",""Osteochondrodysplasia syndrome"",""chondrodystrophy"",""skeletal dysplasia""]"	"[{""label"":""BMPR1B"",""id"":""658""},{""label"":""CHST3"",""id"":""9469""},{""label"":""COL10A1"",""id"":""1300""},{""label"":""COL11A2"",""id"":""1302""},{""label"":""COL2A1"",""id"":""1280""},{""label"":""COL9A1"",""id"":""1297""},{""label"":""COL9A2"",""id"":""1298""},{""label"":""COL9A3"",""id"":""1299""},{""label"":""COMP"",""id"":""1311""},{""label"":""DYM"",""id"":""54808""},{""label"":""FLNA"",""id"":""2316""},{""label"":""FLNB"",""id"":""2317""},{""label"":""HSPG2"",""id"":""3339""},{""label"":""LIFR"",""id"":""3977""},{""label"":""MATN3"",""id"":""4148""},{""label"":""PTH1R"",""id"":""5745""},{""label"":""SLC26A2"",""id"":""1836""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TRPS1"",""id"":""7227""}]"	"[""1280"",""1297"",""1298"",""1299"",""1300"",""1302"",""1311"",""1836"",""2316"",""2317"",""3339"",""3977"",""4148"",""54808"",""5745"",""658"",""7040"",""7227"",""9469""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2256""}]"
DOID:2256	"[""osteochondrodysplasia"",""Cartilage Development disorder"",""Congenital anomaly of cartilage"",""Osteochondrodysplasia syndrome"",""chondrodystrophy"",""skeletal dysplasia""]"	"[{""label"":""Atf2"",""id"":""11909""},{""label"":""Cebpb"",""id"":""12608""},{""label"":""Rnf146"",""id"":""68031""}]"	"[""11909"",""12608"",""68031""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2256""}]"
DOID:2272	"[""vulvovaginal candidiasis"",""Candidal cervix"",""Candidal vulvovaginitis"",""Candidiasis of vulva and vagina"",""Monilial vulvovaginitis""]"	"[{""label"":""MBL2"",""id"":""4153""}]"	"[""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2272""}]"
DOID:2277	"[""gonadal disease""]"	"[{""label"":""LHCGR"",""id"":""3973""}]"	"[""3973""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2277""}]"
DOID:2280	"[""hidradenitis suppurativa"",""Acne inversa, familial""]"	"[{""label"":""NCSTN"",""id"":""23385""},{""label"":""TNF"",""id"":""7124""}]"	"[""23385"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2280""}]"
DOID:2300	"[""spondylolysis""]"	"[{""label"":""SLC26A2"",""id"":""1836""}]"	"[""1836""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2300""}]"
DOID:231	"[""motor neuron disease""]"	"[{""label"":""SOD1"",""id"":""6647""},{""label"":""TARDBP"",""id"":""23435""}]"	"[""23435"",""6647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:231""}]"
DOID:2316	"[""brain ischemia"",""Ischaemic encephalopathy"",""Ischemic encephalopathy"",""cerebral ischemia""]"	"[{""label"":""Angpt2"",""id"":""89805""},{""label"":""Cdk5"",""id"":""140908""},{""label"":""Kdr"",""id"":""25589""},{""label"":""Mdh2"",""id"":""81829""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Nos1"",""id"":""24598""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Prkcd"",""id"":""170538""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Slc29a1"",""id"":""63997""},{""label"":""Slc6a1"",""id"":""79212""},{""label"":""Slc8a1"",""id"":""29715""},{""label"":""Tnfrsf1a"",""id"":""25625""},{""label"":""Vip"",""id"":""117064""}]"	"[""117064"",""140908"",""170538"",""24598"",""24600"",""24617"",""25589"",""25625"",""29527"",""29715"",""63997"",""79212"",""81687"",""81829"",""89805""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2316""}]"
DOID:2316	"[""brain ischemia"",""Ischaemic encephalopathy"",""Ischemic encephalopathy"",""cerebral ischemia""]"	"[{""label"":""ANGPT1"",""id"":""284""},{""label"":""ANXA1"",""id"":""301""},{""label"":""CSF3"",""id"":""1440""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""MDK"",""id"":""4192""},{""label"":""PGF"",""id"":""5228""},{""label"":""PROZ"",""id"":""8858""},{""label"":""SELE"",""id"":""6401""}]"	"[""1440"",""284"",""301"",""3304"",""4192"",""5228"",""6401"",""8858""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2316""}]"
DOID:2320	"[""obstructive lung disease"",""respiratory airway obstruction""]"	"[{""label"":""A2M"",""id"":""2""},{""label"":""MMP1"",""id"":""4312""}]"	"[""2"",""4312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2320""}]"
DOID:2326	"[""gastroenteritis"",""cholera morbus"",""infectious colitis, enteritis and gastroenteritis""]"	"[{""label"":""TGFA"",""id"":""7039""}]"	"[""7039""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2326""}]"
DOID:2339	"[""Crouzon syndrome"",""Craniofacial Dysostosis""]"	"[{""label"":""FGFR2"",""id"":""2263""}]"	"[""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2339""}]"
DOID:2339	"[""Crouzon syndrome"",""Craniofacial Dysostosis""]"	"[{""label"":""Fgfr2"",""id"":""14183""}]"	"[""14183""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2339""}]"
DOID:234	"[""colon adenocarcinoma"",""Colonic adenocarcinoma"",""adenocarcinoma of colon""]"	"[{""label"":""Ctnnb1"",""id"":""84353""}]"	"[""84353""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:234""}]"
DOID:234	"[""colon adenocarcinoma"",""Colonic adenocarcinoma"",""adenocarcinoma of colon""]"	"[{""label"":""BAX"",""id"":""581""},{""label"":""CHD4"",""id"":""1108""},{""label"":""CSF1R"",""id"":""1436""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""LOX"",""id"":""4015""},{""label"":""MYD88"",""id"":""4615""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PIK3R3"",""id"":""8503""},{""label"":""RAC1"",""id"":""5879""},{""label"":""RNASET2"",""id"":""8635""},{""label"":""SMC2"",""id"":""10592""},{""label"":""SRC"",""id"":""6714""},{""label"":""STAT1"",""id"":""6772""},{""label"":""STAT3"",""id"":""6774""},{""label"":""STAT5A"",""id"":""6776""},{""label"":""STAT5B"",""id"":""6777""},{""label"":""STAT6"",""id"":""6778""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""UBR5"",""id"":""51366""}]"	"[""10592"",""1108"",""1436"",""4015"",""4615"",""51366"",""5290"",""581"",""5879"",""6714"",""6772"",""6774"",""6776"",""6777"",""6778"",""7040"",""7403"",""8503"",""8635""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:234""}]"
DOID:2340	"[""craniosynostosis"",""Premature closure of cranial sutures""]"	"[{""label"":""Nell1"",""id"":""81733""}]"	"[""81733""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2340""}]"
DOID:2340	"[""craniosynostosis"",""Premature closure of cranial sutures""]"	"[{""label"":""ALX4"",""id"":""60529""},{""label"":""BBS9"",""id"":""27241""},{""label"":""FGFR2"",""id"":""2263""},{""label"":""FGFR3"",""id"":""2261""},{""label"":""FLNA"",""id"":""2316""},{""label"":""NOG"",""id"":""9241""},{""label"":""TCF12"",""id"":""6938""},{""label"":""TWIST1"",""id"":""7291""}]"	"[""2261"",""2263"",""2316"",""27241"",""60529"",""6938"",""7291"",""9241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2340""}]"
DOID:2349	"[""arteriosclerosis"",""Arteriosclerotic vascular disease""]"	"[{""label"":""ABCG5"",""id"":""64240""},{""label"":""ABCG8"",""id"":""64241""},{""label"":""AKR1B1"",""id"":""231""},{""label"":""ALDH3A1"",""id"":""218""},{""label"":""ALOX5"",""id"":""240""},{""label"":""APOB"",""id"":""338""},{""label"":""ESR1"",""id"":""2099""},{""label"":""F13A1"",""id"":""2162""},{""label"":""HP"",""id"":""3240""},{""label"":""HSPD1"",""id"":""3329""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL6ST"",""id"":""3572""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""LCAT"",""id"":""3931""},{""label"":""LDLR"",""id"":""3949""},{""label"":""MMP12"",""id"":""4321""},{""label"":""MMP13"",""id"":""4322""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP2"",""id"":""4313""},{""label"":""MMP3"",""id"":""4314""},{""label"":""MMP9"",""id"":""4318""},{""label"":""MSR1"",""id"":""4481""},{""label"":""PON1"",""id"":""5444""},{""label"":""PTGER4"",""id"":""5734""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SERPINA1"",""id"":""5265""},{""label"":""TLR4"",""id"":""7099""}]"	"[""2099"",""2162"",""218"",""231"",""240"",""3240"",""3329"",""338"",""3572"",""3586"",""3673"",""3931"",""3949"",""4312"",""4313"",""4314"",""4318"",""4321"",""4322"",""4481"",""5265"",""5444"",""5734"",""5743"",""64240"",""64241"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2349""}]"
DOID:2349	"[""arteriosclerosis"",""Arteriosclerotic vascular disease""]"	"[{""label"":""Map3k7"",""id"":""313121""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Pparg"",""id"":""25664""}]"	"[""25664"",""313121"",""81687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2349""}]"
DOID:2352	"[""hemochromatosis"",""Haemochromatosis"",""diabetes bronze"",""iron storage disorder""]"	"[{""label"":""HFE"",""id"":""3077""},{""label"":""HJV"",""id"":""148738""},{""label"":""TFR2"",""id"":""7036""},{""label"":""TNF"",""id"":""7124""}]"	"[""148738"",""3077"",""7036"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2352""}]"
DOID:2355	"[""anemia"",""anaemia""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ANK1"",""id"":""286""},{""label"":""EPOR"",""id"":""2057""},{""label"":""G6PD"",""id"":""2539""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HK1"",""id"":""3098""},{""label"":""PON1"",""id"":""5444""},{""label"":""SLC11A2"",""id"":""4891""},{""label"":""TF"",""id"":""7018""}]"	"[""1636"",""2057"",""2539"",""286"",""2876"",""3098"",""4891"",""5444"",""7018""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2355""}]"
DOID:2361	"[""macrocytic anemia"",""ANEMIA MACROCYTIC"",""Macrocytic anaemia""]"	"[{""label"":""Kit"",""id"":""16590""}]"	"[""16590""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2361""}]"
DOID:2366	"[""West Nile fever""]"	"[{""label"":""CCR5"",""id"":""1234""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""RFC1"",""id"":""5981""}]"	"[""1234"",""3813"",""5981""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2366""}]"
DOID:2367	"[""neuroaxonal dystrophy""]"	"[{""label"":""NAGA"",""id"":""4668""},{""label"":""PLA2G6"",""id"":""8398""}]"	"[""4668"",""8398""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2367""}]"
DOID:2377	"[""multiple sclerosis"",""Generalized multiple sclerosis"",""insular sclerosis""]"	"[{""label"":""A2M"",""id"":""2""},{""label"":""AGER"",""id"":""177""},{""label"":""APOC2"",""id"":""344""},{""label"":""CCL1"",""id"":""6346""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CCL7"",""id"":""6354""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CD24"",""id"":""100133941""},{""label"":""CD28"",""id"":""940""},{""label"":""CD40"",""id"":""958""},{""label"":""CD46"",""id"":""4179""},{""label"":""CD86"",""id"":""942""},{""label"":""CIITA"",""id"":""4261""},{""label"":""CLEC16A"",""id"":""23274""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""FAS"",""id"":""355""},{""label"":""FASLG"",""id"":""356""},{""label"":""GABRA3"",""id"":""2556""},{""label"":""GC"",""id"":""2638""},{""label"":""H6PD"",""id"":""9563""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRA"",""id"":""3122""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HLA-DRB3"",""id"":""3125""},{""label"":""HSP90AB1"",""id"":""3326""},{""label"":""IFNB1"",""id"":""3456""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL21R"",""id"":""50615""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL2RA"",""id"":""3559""},{""label"":""IL4"",""id"":""3565""},{""label"":""IL4R"",""id"":""3566""},{""label"":""IL6"",""id"":""3569""},{""label"":""IRF5"",""id"":""3663""},{""label"":""JAG1"",""id"":""182""},{""label"":""KIF1B"",""id"":""23095""},{""label"":""MBP"",""id"":""4155""},{""label"":""MMP12"",""id"":""4321""},{""label"":""MMP9"",""id"":""4318""},{""label"":""MOG"",""id"":""4340""},{""label"":""MPHOSPH9"",""id"":""10198""},{""label"":""NDUFS2"",""id"":""4720""},{""label"":""NECTIN2"",""id"":""5819""},{""label"":""NOTCH4"",""id"":""4855""},{""label"":""PDCD1"",""id"":""5133""},{""label"":""PHACTR2"",""id"":""9749""},{""label"":""PRF1"",""id"":""5551""},{""label"":""PTPRC"",""id"":""5788""},{""label"":""RGMA"",""id"":""56963""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""SPP1"",""id"":""6696""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF1A"",""id"":""7132""}]"	"[""100133941"",""10198"",""1234"",""149233"",""1493"",""177"",""182"",""2"",""23095"",""23274"",""2556"",""2638"",""3115"",""3117"",""3119"",""3122"",""3123"",""3125"",""3326"",""344"",""3456"",""3458"",""355"",""3559"",""356"",""3565"",""3566"",""3569"",""3663"",""4155"",""4179"",""4261"",""4318"",""4321"",""4340"",""4720"",""4855"",""50615"",""5133"",""5551"",""56963"",""5788"",""5819"",""6346"",""6347"",""6354"",""6556"",""6696"",""7124"",""7132"",""940"",""942"",""9563"",""958"",""9749""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2377""}]"
DOID:2377	"[""multiple sclerosis"",""Generalized multiple sclerosis"",""insular sclerosis""]"	"[{""label"":""Prf1"",""id"":""18646""},{""label"":""Tnf"",""id"":""21926""}]"	"[""18646"",""21926""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2377""}]"
DOID:2378	"[""relapsing-remitting multiple sclerosis"",""RRMS"",""Relapsing-remitting MS""]"	"[{""label"":""ADAMTS14"",""id"":""140766""},{""label"":""CSPG4"",""id"":""1464""},{""label"":""FAS"",""id"":""355""},{""label"":""NOD2"",""id"":""64127""}]"	"[""140766"",""1464"",""355"",""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2378""}]"
DOID:2383	"[""neonatal jaundice"",""neonatal hyperbilirubinemia"",""neonatal icterus""]"	"[{""label"":""G6PD"",""id"":""2539""}]"	"[""2539""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2383""}]"
DOID:2384	"[""Wernicke encephalopathy"",""Wernicke's disease"",""Wernicke's encephalopathy""]"	"[{""label"":""Ptgs2"",""id"":""29527""}]"	"[""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2384""}]"
DOID:2394	"[""ovarian cancer"",""malignant Ovarian tumor"",""malignant tumour of ovary"",""ovarian neoplasm"",""ovary neoplasm"",""primary ovarian cancer"",""tumor of the Ovary""]"	"[{""label"":""AKT1"",""id"":""207""},{""label"":""APEX1"",""id"":""328""},{""label"":""APOB"",""id"":""338""},{""label"":""BARD1"",""id"":""580""},{""label"":""BRCA1"",""id"":""672""},{""label"":""BRCA2"",""id"":""675""},{""label"":""CD59"",""id"":""966""},{""label"":""CDH13"",""id"":""1012""},{""label"":""CDH1"",""id"":""999""},{""label"":""COMT"",""id"":""1312""},{""label"":""CTNNB1"",""id"":""1499""},{""label"":""CYP19A1"",""id"":""1588""},{""label"":""EEF1A2"",""id"":""1917""},{""label"":""ERBB2"",""id"":""2064""},{""label"":""HFE"",""id"":""3077""},{""label"":""HMGA2"",""id"":""8091""},{""label"":""ITGA8"",""id"":""8516""},{""label"":""JAK1"",""id"":""3716""},{""label"":""JUP"",""id"":""3728""},{""label"":""LEF1"",""id"":""51176""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MSLN"",""id"":""10232""},{""label"":""MUC16"",""id"":""94025""},{""label"":""MYO6"",""id"":""4646""},{""label"":""NBN"",""id"":""4683""},{""label"":""NOD2"",""id"":""64127""},{""label"":""NOS3"",""id"":""4846""},{""label"":""OGG1"",""id"":""4968""},{""label"":""OPCML"",""id"":""4978""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PRKCA"",""id"":""5578""},{""label"":""PTEN"",""id"":""5728""},{""label"":""RUNX3"",""id"":""864""},{""label"":""SMAD4"",""id"":""4089""},{""label"":""SOD2"",""id"":""6648""},{""label"":""STAT3"",""id"":""6774""},{""label"":""TFRC"",""id"":""7037""},{""label"":""UGT1A1"",""id"":""54658""}]"	"[""1012"",""10232"",""1312"",""1499"",""1588"",""1917"",""2064"",""207"",""3077"",""328"",""338"",""3716"",""3728"",""4089"",""4153"",""4312"",""4646"",""4683"",""4846"",""4968"",""4978"",""51176"",""5290"",""54658"",""5578"",""5728"",""580"",""64127"",""6648"",""672"",""675"",""6774"",""7037"",""8091"",""8516"",""864"",""94025"",""966"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2394""}]"
DOID:2394	"[""ovarian cancer"",""malignant Ovarian tumor"",""malignant tumour of ovary"",""ovarian neoplasm"",""ovary neoplasm"",""primary ovarian cancer"",""tumor of the Ovary""]"	"[{""label"":""Ctnnb1"",""id"":""12387""}]"	"[""12387""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2394""}]"
DOID:2431	"[""glomus tumor"",""Glomus neoplasm"",""Glomus tumour""]"	"[{""label"":""GLMN"",""id"":""11146""}]"	"[""11146""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2431""}]"
DOID:2436	"[""glomangioma"",""Glomuvenous Malformation""]"	"[{""label"":""GLMN"",""id"":""11146""}]"	"[""11146""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2436""}]"
DOID:2450	"[""central retinal vein occlusion""]"	"[{""label"":""PROC"",""id"":""5624""}]"	"[""5624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2450""}]"
DOID:2451	"[""protein S deficiency"",""Protein S deficiency disease""]"	"[{""label"":""PROS1"",""id"":""5627""},{""label"":""TFPI"",""id"":""7035""}]"	"[""5627"",""7035""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2451""}]"
DOID:2452	"[""thrombophilia"",""hypercoagulability state""]"	"[{""label"":""FGA"",""id"":""2243""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""PLG"",""id"":""5340""},{""label"":""PROC"",""id"":""5624""},{""label"":""SERPINA10"",""id"":""51156""}]"	"[""2243"",""3117"",""51156"",""5340"",""5624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2452""}]"
DOID:2452	"[""thrombophilia"",""hypercoagulability state""]"	"[{""label"":""Thbd"",""id"":""21824""}]"	"[""21824""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2452""}]"
DOID:2468	"[""psychotic disorder"",""mental or behavioural disorder""]"	"[{""label"":""NRG1"",""id"":""3084""}]"	"[""3084""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2468""}]"
DOID:2475	"[""chronic conjunctivitis""]"	"[{""label"":""Lamp2"",""id"":""24944""}]"	"[""24944""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2475""}]"
DOID:2476	"[""hereditary spastic paraplegia"",""French settlement disease"",""Strumpell-Lorrain disease"",""familial spastic paraplegia"",""hereditary spastic paraparesis""]"	"[{""label"":""SEY1"",""id"":""854336""},{""label"":""VPS1"",""id"":""853870""}]"	"[""853870"",""854336""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2476""}]"
DOID:2476	"[""hereditary spastic paraplegia"",""French settlement disease"",""Strumpell-Lorrain disease"",""familial spastic paraplegia"",""hereditary spastic paraparesis""]"	"[{""label"":""ALDH18A1"",""id"":""5832""},{""label"":""AP5Z1"",""id"":""9907""},{""label"":""BSCL2"",""id"":""26580""},{""label"":""HSPD1"",""id"":""3329""},{""label"":""L2HGDH"",""id"":""79944""}]"	"[""26580"",""3329"",""5832"",""79944"",""9907""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2476""}]"
DOID:2476	"[""hereditary spastic paraplegia"",""French settlement disease"",""Strumpell-Lorrain disease"",""familial spastic paraplegia"",""hereditary spastic paraparesis""]"	"[{""label"":""erl-1"",""id"":""178178""}]"	"[""178178""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2476""}]"
DOID:2477	"[""motor peripheral neuropathy"",""HSMN"",""HSMN - Hereditary sensory and motor neuropathy"",""Hereditary motor and sensory neuropathy"",""Peripheral Motor Neuropathy"",""neuropathic muscular atrophy""]"	"[{""label"":""EGR2"",""id"":""1959""}]"	"[""1959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2477""}]"
DOID:2477	"[""motor peripheral neuropathy"",""HSMN"",""HSMN - Hereditary sensory and motor neuropathy"",""Hereditary motor and sensory neuropathy"",""Peripheral Motor Neuropathy"",""neuropathic muscular atrophy""]"	"[{""label"":""Slc12a6"",""id"":""107723""}]"	"[""107723""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2477""}]"
DOID:2490	"[""congenital nervous system abnormality"",""congenital neurologic anomaly""]"	"[{""label"":""Eml1"",""id"":""68519""},{""label"":""Tuba1a"",""id"":""22142""}]"	"[""22142"",""68519""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2490""}]"
DOID:2508	"[""Takayasu's arteritis"",""Aortic arch arteritis"",""Idiopathic aortitis"",""Takayasu arteritis"",""Takayasu's disease"",""aortic arch syndrome""]"	"[{""label"":""HLA-A"",""id"":""3105""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL2"",""id"":""3558""}]"	"[""3105"",""3106"",""3123"",""3558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2508""}]"
DOID:251	"[""alcohol-induced mental disorder""]"	"[{""label"":""DRD2"",""id"":""1813""}]"	"[""1813""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:251""}]"
DOID:2512	"[""nevoid basal cell carcinoma syndrome"",""Gorlin syndrome"",""NBCCS"",""basal cell nevus syndrome""]"	"[{""label"":""PTCH1"",""id"":""5727""}]"	"[""5727""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2512""}]"
DOID:2512	"[""nevoid basal cell carcinoma syndrome"",""Gorlin syndrome"",""NBCCS"",""basal cell nevus syndrome""]"	"[{""label"":""Ptch1"",""id"":""19206""},{""label"":""Shh"",""id"":""20423""}]"	"[""19206"",""20423""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2512""}]"
DOID:2513	"[""basal cell carcinoma"",""Basal cell cancer"",""Basal cell carcinoma of skin"",""Basal cell neoplasm"",""Basal cell tumor"",""Epithelioma basal cell"",""Rodent ulcer"",""malignant Basal cell neoplasm"",""malignant basal cell tumor""]"	"[{""label"":""Ptch1"",""id"":""19206""}]"	"[""19206""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2513""}]"
DOID:2513	"[""basal cell carcinoma"",""Basal cell cancer"",""Basal cell carcinoma of skin"",""Basal cell neoplasm"",""Basal cell tumor"",""Epithelioma basal cell"",""Rodent ulcer"",""malignant Basal cell neoplasm"",""malignant basal cell tumor""]"	"[{""label"":""BAP1"",""id"":""8314""},{""label"":""CRNKL1"",""id"":""51340""},{""label"":""CTCF"",""id"":""10664""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""OCA2"",""id"":""4948""},{""label"":""PTCH1"",""id"":""5727""},{""label"":""PTCH2"",""id"":""8643""},{""label"":""RASA1"",""id"":""5921""},{""label"":""SHH"",""id"":""6469""},{""label"":""SMO"",""id"":""6608""},{""label"":""TP53"",""id"":""7157""}]"	"[""10664"",""1493"",""4948"",""51340"",""5727"",""5921"",""6469"",""6608"",""7157"",""8314"",""8643""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2513""}]"
DOID:252	"[""alcoholic psychosis"",""Alcoholic psychoses""]"	"[{""label"":""HTR2A"",""id"":""3356""}]"	"[""3356""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:252""}]"
DOID:2526	"[""prostate adenocarcinoma""]"	"[{""label"":""Igf1r"",""id"":""25718""}]"	"[""25718""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2526""}]"
DOID:2526	"[""prostate adenocarcinoma""]"	"[{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""AKT1"",""id"":""207""},{""label"":""AKT2"",""id"":""208""},{""label"":""AKT3"",""id"":""10000""},{""label"":""BIN1"",""id"":""274""},{""label"":""CD9"",""id"":""928""},{""label"":""GRB2"",""id"":""2885""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""IKBKB"",""id"":""3551""},{""label"":""INSR"",""id"":""3643""},{""label"":""MYC"",""id"":""4609""},{""label"":""NCOA2"",""id"":""10499""},{""label"":""PIK3CB"",""id"":""5291""},{""label"":""RAF1"",""id"":""5894""},{""label"":""STAT1"",""id"":""6772""}]"	"[""10000"",""10499"",""207"",""208"",""274"",""2885"",""3480"",""3551"",""3643"",""4609"",""5291"",""5894"",""6772"",""928"",""9370""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2526""}]"
DOID:2527	"[""nephrosis""]"	"[{""label"":""GATA3"",""id"":""2625""}]"	"[""2625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2527""}]"
DOID:2527	"[""nephrosis""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Angpt2"",""id"":""89805""},{""label"":""Cd59b"",""id"":""25407""}]"	"[""24310"",""25407"",""89805""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2527""}]"
DOID:2527	"[""nephrosis""]"	"[{""label"":""Lamb2"",""id"":""16779""}]"	"[""16779""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2527""}]"
DOID:2531	"[""hematologic cancer"",""Hematologic malignancy"",""Hematologic neoplasm"",""Hematological tumors"",""blood cancer"",""hematopoietic and lymphoid system tumor"",""hematopoietic cancer"",""hematopoietic neoplasm"",""hematopoietic tumors"",""malignant hematopoietic neoplasm""]"	"[{""label"":""SLC19A1"",""id"":""6573""},{""label"":""TP53"",""id"":""7157""}]"	"[""6573"",""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2531""}]"
DOID:2537	"[""inflammatory and toxic neuropathy""]"	"[{""label"":""Htr2a"",""id"":""29595""}]"	"[""29595""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2537""}]"
DOID:2548	"[""reflex epilepsy"",""epilepsy, sensory-induced""]"	"[{""label"":""Trpv1"",""id"":""83810""}]"	"[""83810""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2548""}]"
DOID:2559	"[""opiate dependence"",""Opioid type dependence""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""BMPER"",""id"":""168667""},{""label"":""C9"",""id"":""735""},{""label"":""COMT"",""id"":""1312""},{""label"":""DRD2"",""id"":""1813""},{""label"":""GAL"",""id"":""51083""},{""label"":""GALR1"",""id"":""2587""},{""label"":""NAV3"",""id"":""89795""},{""label"":""NGF"",""id"":""4803""},{""label"":""NPY1R"",""id"":""4886""},{""label"":""OPRD1"",""id"":""4985""},{""label"":""OPRK1"",""id"":""4986""},{""label"":""OPRM1"",""id"":""4988""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""1312"",""168667"",""1813"",""2587"",""4803"",""4886"",""4985"",""4986"",""4988"",""51083"",""5243"",""735"",""7422"",""89795""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2559""}]"
DOID:2560	"[""morphine dependence""]"	"[{""label"":""COMT"",""id"":""1312""}]"	"[""1312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2560""}]"
DOID:2560	"[""morphine dependence""]"	"[{""label"":""Creb1"",""id"":""81646""},{""label"":""Gria1"",""id"":""50592""}]"	"[""50592"",""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2560""}]"
DOID:2565	"[""macular corneal dystrophy"",""Fehr corneal dystrophy"",""MACULAR DYSTROPHY, CORNEAL, 1""]"	"[{""label"":""CHST6"",""id"":""4166""}]"	"[""4166""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00391""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2565""}]"
DOID:2566	"[""corneal dystrophy""]"	"[{""label"":""ELOVL4"",""id"":""6785""},{""label"":""KERA"",""id"":""11081""},{""label"":""TACSTD2"",""id"":""4070""},{""label"":""TGFBI"",""id"":""7045""}]"	"[""11081"",""4070"",""6785"",""7045""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2566""}]"
DOID:2569	"[""retinal drusen""]"	"[{""label"":""CFH"",""id"":""3075""}]"	"[""3075""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2569""}]"
DOID:2571	"[""Langerhans-cell histiocytosis"",""Histiocytosis X"",""Langerhan's cell histiocytosis"",""Langerhans cell granulomatosis"",""Letterer-Siwe disease"",""Letterer-Siwe disease involving intra-abdominal lymph nodes"",""Letterer-Siwe disease involving intrapelvic lymph nodes"",""Letterer-Siwe disease involving intrathoracic lymph nodes"",""Letterer-Siwe disease involving lymph nodes of axilla and upper limb"",""Letterer-Siwe disease involving lymph nodes of head, face and neck"",""Letterer-Siwe disease involving lymph nodes of head, face, and neck"",""Letterer-Siwe disease involving lymph nodes of inguinal region and lower limb"",""Letterer-Siwe disease involving lymph nodes of multiple sites"",""Letterer-Siwe disease involving spleen"",""Letterer-Siwe disease of intra-abdominal lymph nodes"",""Letterer-Siwe disease of intrapelvic lymph nodes"",""Letterer-Siwe disease of intrathoracic lymph nodes"",""Letterer-Siwe disease of lymph nodes of axilla and upper limb"",""Letterer-Siwe disease of lymph nodes of axilla and/or upper limb"",""Letterer-Siwe disease of lymph nodes of head, face and neck"",""Letterer-Siwe disease of lymph nodes of head, face and/or neck"",""Letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb"",""Letterer-Siwe disease of lymph nodes of inguinal region and lower limb"",""Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb"",""Letterer-Siwe disease of lymph nodes of multiple sites"",""Letterer-Siwe disease of spleen""]"	"[{""label"":""Braf"",""id"":""109880""}]"	"[""109880""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2571""}]"
DOID:2580	"[""rhizomelic chondrodysplasia punctata"",""Chondrodysplasia Punctata, Rhizomelic Form""]"	"[{""label"":""AGPS"",""id"":""8540""}]"	"[""8540""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2580""}]"
DOID:2581	"[""chondrodysplasia punctata"",""Chondrodysplasia punctata congenita""]"	"[{""label"":""ARSL"",""id"":""415""},{""label"":""EBP"",""id"":""10682""}]"	"[""10682"",""415""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2581""}]"
DOID:2582	"[""acatalasia"",""acatalasemia"",""deficiency of catalase""]"	"[{""label"":""CAT"",""id"":""847""}]"	"[""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2582""}]"
DOID:2583	"[""agammaglobulinemia"",""IGHM"",""hypogammaglobulinemia"",""mu heavy chain deficiency""]"	"[{""label"":""BTK"",""id"":""695""},{""label"":""LRRC8A"",""id"":""56262""}]"	"[""56262"",""695""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2583""}]"
DOID:2590	"[""familial nephrotic syndrome"",""Congenital nephrotic syndrome""]"	"[{""label"":""DAAM2"",""id"":""23500""},{""label"":""LAMA5"",""id"":""3911""}]"	"[""23500"",""3911""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2590""}]"
DOID:2596	"[""larynx cancer""]"	"[{""label"":""ERCC5"",""id"":""2073""},{""label"":""ERCC6"",""id"":""2074""},{""label"":""GPX1"",""id"":""2876""},{""label"":""NOD2"",""id"":""64127""}]"	"[""2073"",""2074"",""2876"",""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2596""}]"
DOID:26	"[""pancreas disease""]"	"[{""label"":""MSLN"",""id"":""10232""}]"	"[""10232""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:26""}]"
DOID:2600	"[""laryngeal carcinoma"",""cancer of larynx"",""carcinoma of larynx""]"	"[{""label"":""XRCC1"",""id"":""7515""}]"	"[""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2600""}]"
DOID:2602	"[""chondroma"",""central Chondroma""]"	"[{""label"":""PTPN11"",""id"":""5781""}]"	"[""5781""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2602""}]"
DOID:2626	"[""choroid plexus papilloma"",""childhood choroid plexus papilloma""]"	"[{""label"":""TP53"",""id"":""7157""}]"	"[""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2626""}]"
DOID:263	"[""kidney cancer"",""malignant neoplasm of kidney except pelvis"",""malignant tumour of kidney"",""renal cancer""]"	"[{""label"":""FGF9"",""id"":""2254""}]"	"[""2254""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:263""}]"
DOID:263	"[""kidney cancer"",""malignant neoplasm of kidney except pelvis"",""malignant tumour of kidney"",""renal cancer""]"	"[{""label"":""scrib"",""id"":""44448""}]"	"[""44448""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:263""}]"
DOID:2671	"[""transitional cell carcinoma"",""transitional carcinoma"",""transitional cell tumor"",""urothelial cell carcinoma""]"	"[{""label"":""APC"",""id"":""324""},{""label"":""CD44"",""id"":""960""},{""label"":""FGFR3"",""id"":""2261""},{""label"":""HRAS"",""id"":""3265""},{""label"":""IGFBP3"",""id"":""3486""},{""label"":""MSH2"",""id"":""4436""},{""label"":""NAT2"",""id"":""10""},{""label"":""OGG1"",""id"":""4968""},{""label"":""RAD50"",""id"":""10111""},{""label"":""SFN"",""id"":""2810""},{""label"":""TYMP"",""id"":""1890""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10"",""10111"",""1890"",""2261"",""2810"",""324"",""3265"",""3486"",""4436"",""4968"",""7515"",""960""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2671""}]"
DOID:2696	"[""Leydig cell tumor"",""Leydig cell neoplasm""]"	"[{""label"":""LHCGR"",""id"":""3973""}]"	"[""3973""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2696""}]"
DOID:2703	"[""synovitis""]"	"[{""label"":""HLA-B"",""id"":""3106""}]"	"[""3106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2703""}]"
DOID:2717	"[""Bloom syndrome"",""Bloom-Torre-Machacek syndrome"",""Congenital Telangiectatic Erythema syndrome""]"	"[{""label"":""BLM"",""id"":""641""}]"	"[""641""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2717""}]"
DOID:2723	"[""dermatitis"",""eczema"",""skin inflammation""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""IKBKB"",""id"":""3551""},{""label"":""IL13"",""id"":""3596""},{""label"":""TNF"",""id"":""7124""}]"	"[""154"",""3106"",""3551"",""3596"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2723""}]"
DOID:2729	"[""dyskeratosis congenita"",""DKCD""]"	"[{""label"":""DKC1"",""id"":""1736""}]"	"[""1736""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2729""}]"
DOID:2729	"[""dyskeratosis congenita"",""DKCD""]"	"[{""label"":""Dkc1"",""id"":""245474""},{""label"":""Trp53"",""id"":""22059""}]"	"[""22059"",""245474""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2729""}]"
DOID:2732	"[""Rothmund-Thomson syndrome"",""Congenital poikiloderma"",""RTS""]"	"[{""label"":""ANAPC1"",""id"":""64682""},{""label"":""RECQL4"",""id"":""9401""}]"	"[""64682"",""9401""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2732""}]"
DOID:2734	"[""keratosis follicularis"",""DARIER-WHITE DISEASE"",""Darier's disease""]"	"[{""label"":""ATP2A2"",""id"":""488""}]"	"[""488""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2734""}]"
DOID:2734	"[""keratosis follicularis"",""DARIER-WHITE DISEASE"",""Darier's disease""]"	"[{""label"":""Atp2a2"",""id"":""11938""}]"	"[""11938""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2734""}]"
DOID:2736	"[""Hajdu-Cheney syndrome"",""Cheney syndrome"",""HJCYS"",""SFPKS"",""acroosteolysis with osteoporosis and changes in skull and mandible"",""arthrodentoosteodysplasia"",""serpentine fibula-polycystic kidney syndrome""]"	"[{""label"":""Notch2"",""id"":""18129""}]"	"[""18129""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2736""}]"
DOID:2736	"[""Hajdu-Cheney syndrome"",""Cheney syndrome"",""HJCYS"",""SFPKS"",""acroosteolysis with osteoporosis and changes in skull and mandible"",""arthrodentoosteodysplasia"",""serpentine fibula-polycystic kidney syndrome""]"	"[{""label"":""NOTCH2"",""id"":""4853""}]"	"[""4853""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2736""}]"
DOID:2738	"[""pseudoxanthoma elasticum"",""Gronblad-Strandberg syndrome""]"	"[{""label"":""Abcc6"",""id"":""81642""}]"	"[""81642""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2738""}]"
DOID:2738	"[""pseudoxanthoma elasticum"",""Gronblad-Strandberg syndrome""]"	"[{""label"":""ABCC6"",""id"":""368""},{""label"":""CAT"",""id"":""847""},{""label"":""ELN"",""id"":""2006""},{""label"":""GPX1"",""id"":""2876""},{""label"":""MMP2"",""id"":""4313""},{""label"":""SOD2"",""id"":""6648""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""XYLT1"",""id"":""64131""},{""label"":""XYLT2"",""id"":""64132""}]"	"[""2006"",""2876"",""368"",""4313"",""64131"",""64132"",""6648"",""7422"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2738""}]"
DOID:2738	"[""pseudoxanthoma elasticum"",""Gronblad-Strandberg syndrome""]"	"[{""label"":""Abcc6"",""id"":""27421""}]"	"[""27421""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2738""}]"
DOID:2739	"[""Gilbert syndrome"",""Constitutional hyperbilirubinemia"",""Gilbert's disease"",""Gilbert's syndrome"",""Gilbert-Meulengracht syndrome"",""hereditary nonhemolytic jaundice""]"	"[{""label"":""UGT1A1"",""id"":""54658""}]"	"[""54658""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2739""}]"
DOID:2741	"[""bilirubin metabolic disorder"",""hereditary hyperbilirubinemia"",""hyperbilirubinemia""]"	"[{""label"":""ABCC2"",""id"":""1244""},{""label"":""HGF"",""id"":""3082""},{""label"":""SLCO1B1"",""id"":""10599""},{""label"":""SLCO1B3"",""id"":""28234""},{""label"":""SOD2"",""id"":""6648""},{""label"":""UGT1A1"",""id"":""54658""}]"	"[""10599"",""1244"",""28234"",""3082"",""54658"",""6648""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2741""}]"
DOID:2741	"[""bilirubin metabolic disorder"",""hereditary hyperbilirubinemia"",""hyperbilirubinemia""]"	"[{""label"":""Abcc2"",""id"":""25303""},{""label"":""Slco1b2"",""id"":""58978""},{""label"":""Ugt1a1"",""id"":""24861""}]"	"[""24861"",""25303"",""58978""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2741""}]"
DOID:2746	"[""glycogen storage disease V"",""Glycogen storage disease 5"",""Glycogen storage disease, type V"",""McArdle's disease"",""glycogen storage disease type V"",""myophosphorylase deficiency""]"	"[{""label"":""Pygm"",""id"":""19309""}]"	"[""19309""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2746""}]"
DOID:2746	"[""glycogen storage disease V"",""Glycogen storage disease 5"",""Glycogen storage disease, type V"",""McArdle's disease"",""glycogen storage disease type V"",""myophosphorylase deficiency""]"	"[{""label"":""PYGM"",""id"":""5837""}]"	"[""5837""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2746""}]"
DOID:2747	"[""glycogen storage disease"",""glycogenosis""]"	"[{""label"":""GYG1"",""id"":""2992""},{""label"":""GYS2"",""id"":""2998""},{""label"":""PHKA1"",""id"":""5255""},{""label"":""PHKA2"",""id"":""5256""},{""label"":""PHKG2"",""id"":""5261""},{""label"":""PRKAG2"",""id"":""51422""},{""label"":""PYGL"",""id"":""5836""},{""label"":""SLC2A2"",""id"":""6514""}]"	"[""2992"",""2998"",""51422"",""5255"",""5256"",""5261"",""5836"",""6514""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2747""}]"
DOID:2747	"[""glycogen storage disease"",""glycogenosis""]"	"[{""label"":""Phkg2"",""id"":""140671""}]"	"[""140671""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2747""}]"
DOID:2747	"[""glycogen storage disease"",""glycogenosis""]"	"[{""label"":""PFK1"",""id"":""853155""},{""label"":""PFK2"",""id"":""855245""}]"	"[""853155"",""855245""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2747""}]"
DOID:2748	"[""glycogen storage disease III"",""Glycogen storage disease 3"",""Glycogen storage disease, type III"",""amylo 1,6 glucosidase deficiency"",""deficiency of debranching enzyme"",""deficiency of dextrin""]"	"[{""label"":""AGL"",""id"":""178""}]"	"[""178""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2748""}]"
DOID:2749	"[""glycogen storage disease Ia""]"	"[{""label"":""G6pc1"",""id"":""14377""}]"	"[""14377""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2749""}]"
DOID:2749	"[""glycogen storage disease Ia""]"	"[{""label"":""G6PC1"",""id"":""2538""}]"	"[""2538""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2749""}]"
DOID:2750	"[""glycogen storage disease IV"",""Amylopectinosis"",""Branching-transferase deficiency glycogenosis"",""Glycogen storage disease 4"",""Glycogen storage disease, type IV"",""brancher deficiency glycogenosis"",""deficiency of 1,4-alpha-glucan branching enzyme""]"	"[{""label"":""GBE1"",""id"":""2632""}]"	"[""2632""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2750""}]"
DOID:2750	"[""glycogen storage disease IV"",""Amylopectinosis"",""Branching-transferase deficiency glycogenosis"",""Glycogen storage disease 4"",""Glycogen storage disease, type IV"",""brancher deficiency glycogenosis"",""deficiency of 1,4-alpha-glucan branching enzyme""]"	"[{""label"":""Gbe1"",""id"":""74185""}]"	"[""74185""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2750""}]"
DOID:2750	"[""glycogen storage disease IV"",""Amylopectinosis"",""Branching-transferase deficiency glycogenosis"",""Glycogen storage disease 4"",""Glycogen storage disease, type IV"",""brancher deficiency glycogenosis"",""deficiency of 1,4-alpha-glucan branching enzyme""]"	"[{""label"":""GLC3"",""id"":""856705""}]"	"[""856705""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2750""}]"
DOID:2752	"[""glycogen storage disease II"",""Generalized glycogenosis"",""Glycogen storage disease 2"",""Glycogen storage disease, type II"",""Glycogenosis, type 2"",""Lysosomal alpha-1,4-glucosidase deficiency"",""Pompe's disease"",""acid maltase deficiency"",""deficiency of glucoamylase"",""deficiency of maltase"",""glycogen storage disease type II""]"	"[{""label"":""GAA"",""id"":""2548""}]"	"[""2548""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00103""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00104""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00105""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2752""}]"
DOID:2752	"[""glycogen storage disease II"",""Generalized glycogenosis"",""Glycogen storage disease 2"",""Glycogen storage disease, type II"",""Glycogenosis, type 2"",""Lysosomal alpha-1,4-glucosidase deficiency"",""Pompe's disease"",""acid maltase deficiency"",""deficiency of glucoamylase"",""deficiency of maltase"",""glycogen storage disease type II""]"	"[{""label"":""Gaa"",""id"":""14387""}]"	"[""14387""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2752""}]"
DOID:2754	"[""glycogen storage disease VI"",""Glycogen storage disease 6"",""Hers' disease"",""glycogen storage disease type VI"",""hepatic glycogen phosphorylase deficiency"",""hepatophosphorylase deficiency glycogenosis""]"	"[{""label"":""Pygl"",""id"":""110095""}]"	"[""110095""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2754""}]"
DOID:2754	"[""glycogen storage disease VI"",""Glycogen storage disease 6"",""Hers' disease"",""glycogen storage disease type VI"",""hepatic glycogen phosphorylase deficiency"",""hepatophosphorylase deficiency glycogenosis""]"	"[{""label"":""PYGL"",""id"":""5836""}]"	"[""5836""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2754""}]"
DOID:2754	"[""glycogen storage disease VI"",""Glycogen storage disease 6"",""Hers' disease"",""glycogen storage disease type VI"",""hepatic glycogen phosphorylase deficiency"",""hepatophosphorylase deficiency glycogenosis""]"	"[{""label"":""Pygl"",""id"":""64035""}]"	"[""64035""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2754""}]"
DOID:2755	"[""Mycobacterium avium complex disease"",""Infection due to Mycobacterium intracellulare"",""MAC disease"",""Mycobacterium Avium Infection"",""Mycobacterium avium Complex""]"	"[{""label"":""IL17A"",""id"":""3605""}]"	"[""3605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2755""}]"
DOID:2773	"[""contact dermatitis"",""Contact dermatitis/eczema"",""Contact eczema"",""Dermatitis, venenata"",""dermatitis venenata""]"	"[{""label"":""CD46"",""id"":""4179""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""4179"",""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2773""}]"
DOID:2797	"[""idiopathic interstitial pneumonia"",""Diffuse idiopathic pulmonary fibrosis"",""Idiopathic fibrosing alveolitis""]"	"[{""label"":""MTOR"",""id"":""2475""}]"	"[""2475""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2797""}]"
DOID:2799	"[""bronchiolitis obliterans"",""Bronchiolitis exudativa"",""Bronchiolitis fibrosa obliterans"",""Obliterative bronchiolitis""]"	"[{""label"":""EDN1"",""id"":""1906""},{""label"":""MBL2"",""id"":""4153""},{""label"":""NOD2"",""id"":""64127""},{""label"":""TLR9"",""id"":""54106""}]"	"[""1906"",""4153"",""54106"",""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2799""}]"
DOID:2799	"[""bronchiolitis obliterans"",""Bronchiolitis exudativa"",""Bronchiolitis fibrosa obliterans"",""Obliterative bronchiolitis""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Ccl2"",""id"":""24770""}]"	"[""24310"",""24770""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2799""}]"
DOID:28	"[""endocrine system disease""]"	"[{""label"":""B4galt1"",""id"":""14595""},{""label"":""Pcsk1"",""id"":""18548""}]"	"[""14595"",""18548""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:28""}]"
DOID:2810	"[""middle lobe syndrome""]"	"[{""label"":""SALL1"",""id"":""6299""}]"	"[""6299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2810""}]"
DOID:2841	"[""asthma"",""bronchial hyperreactivity"",""chronic obstructive asthma"",""chronic obstructive asthma with acute exacerbation"",""chronic obstructive asthma with status asthmaticus""]"	"[{""label"":""ORMDL"",""id"":""40404""}]"	"[""40404""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2841""}]"
DOID:2841	"[""asthma"",""bronchial hyperreactivity"",""chronic obstructive asthma"",""chronic obstructive asthma with acute exacerbation"",""chronic obstructive asthma with status asthmaticus""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""ACE"",""id"":""1636""},{""label"":""ACSL3"",""id"":""2181""},{""label"":""ADAM33"",""id"":""80332""},{""label"":""ADH5"",""id"":""128""},{""label"":""ADORA1"",""id"":""134""},{""label"":""ADORA2A"",""id"":""135""},{""label"":""ADRB2"",""id"":""154""},{""label"":""ALOX5"",""id"":""240""},{""label"":""BDKRB2"",""id"":""624""},{""label"":""BDNF"",""id"":""627""},{""label"":""C3"",""id"":""718""},{""label"":""C3AR1"",""id"":""719""},{""label"":""C5"",""id"":""727""},{""label"":""CAT"",""id"":""847""},{""label"":""CCL11"",""id"":""6356""},{""label"":""CCL24"",""id"":""6369""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CCR3"",""id"":""1232""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CD14"",""id"":""929""},{""label"":""CD40"",""id"":""958""},{""label"":""CD86"",""id"":""942""},{""label"":""CDH1"",""id"":""999""},{""label"":""CFTR"",""id"":""1080""},{""label"":""CHI3L1"",""id"":""1116""},{""label"":""CHIA"",""id"":""27159""},{""label"":""CHML"",""id"":""1122""},{""label"":""CHRM1"",""id"":""1128""},{""label"":""CHRM2"",""id"":""1129""},{""label"":""CLCA1"",""id"":""1179""},{""label"":""CMA1"",""id"":""1215""},{""label"":""CRHR1"",""id"":""1394""},{""label"":""CRHR2"",""id"":""1395""},{""label"":""CSF3"",""id"":""1440""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CXCR3"",""id"":""2833""},{""label"":""CYSLTR1"",""id"":""10800""},{""label"":""CYSLTR2"",""id"":""57105""},{""label"":""DEFB1"",""id"":""1672""},{""label"":""DPP10"",""id"":""57628""},{""label"":""EDN1"",""id"":""1906""},{""label"":""EDNRB"",""id"":""1910""},{""label"":""EGR1"",""id"":""1958""},{""label"":""ELP1"",""id"":""8518""},{""label"":""F2RL1"",""id"":""2150""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""GSTO2"",""id"":""119391""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DPA1"",""id"":""3113""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQA2"",""id"":""3118""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRA"",""id"":""3122""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HLA-DRB3"",""id"":""3125""},{""label"":""HLA-G"",""id"":""3135""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""IFNGR1"",""id"":""3459""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL12B"",""id"":""3593""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL13RA1"",""id"":""3597""},{""label"":""IL15"",""id"":""3600""},{""label"":""IL16"",""id"":""3603""},{""label"":""IL17A"",""id"":""3605""},{""label"":""IL18R1"",""id"":""8809""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RL1"",""id"":""9173""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL21"",""id"":""59067""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL2RB"",""id"":""3560""},{""label"":""IL3"",""id"":""3562""},{""label"":""IL4"",""id"":""3565""},{""label"":""IL4R"",""id"":""3566""},{""label"":""IL5"",""id"":""3567""},{""label"":""IL5RA"",""id"":""3568""},{""label"":""IL9"",""id"":""3578""},{""label"":""IRAK3"",""id"":""11213""},{""label"":""ITGB3"",""id"":""3690""},{""label"":""LGALS3"",""id"":""3958""},{""label"":""LTA"",""id"":""4049""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MEFV"",""id"":""4210""},{""label"":""MIF"",""id"":""4282""},{""label"":""MMP9"",""id"":""4318""},{""label"":""MPO"",""id"":""4353""},{""label"":""MUC2"",""id"":""4583""},{""label"":""MUC7"",""id"":""4589""},{""label"":""MYLK"",""id"":""4638""},{""label"":""NAT2"",""id"":""10""},{""label"":""NGF"",""id"":""4803""},{""label"":""NOD2"",""id"":""64127""},{""label"":""NOS1"",""id"":""4842""},{""label"":""NOS2"",""id"":""4843""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NPSR1"",""id"":""387129""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""NTF3"",""id"":""4908""},{""label"":""P2RY12"",""id"":""64805""},{""label"":""PARP1"",""id"":""142""},{""label"":""PGF"",""id"":""5228""},{""label"":""PLA2G7"",""id"":""7941""},{""label"":""PROC"",""id"":""5624""},{""label"":""PTGDR2"",""id"":""11251""},{""label"":""PTGDR"",""id"":""5729""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SFTPC"",""id"":""6440""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TACR2"",""id"":""6865""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TBXA2R"",""id"":""6915""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""THBD"",""id"":""7056""},{""label"":""TLR10"",""id"":""81793""},{""label"":""TLR1"",""id"":""7096""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR3"",""id"":""7098""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TLR6"",""id"":""10333""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNC"",""id"":""3371""},{""label"":""TNF"",""id"":""7124""}]"	"[""10"",""10333"",""1080"",""10800"",""1116"",""11213"",""1122"",""11251"",""1128"",""1129"",""1179"",""119391"",""1215"",""1232"",""1234"",""128"",""134"",""135"",""1394"",""1395"",""142"",""1440"",""1493"",""154"",""1636"",""1672"",""1906"",""1910"",""1958"",""2150"",""2181"",""2214"",""240"",""27159"",""28"",""2833"",""2908"",""3106"",""3113"",""3115"",""3117"",""3118"",""3119"",""3122"",""3123"",""3125"",""3135"",""3156"",""3371"",""3459"",""3552"",""3557"",""3558"",""3560"",""3562"",""3565"",""3566"",""3567"",""3568"",""3578"",""3586"",""3593"",""3596"",""3597"",""3600"",""3603"",""3605"",""3690"",""387129"",""3958"",""4049"",""4153"",""4210"",""4282"",""4318"",""4353"",""4583"",""4589"",""4638"",""4803"",""4842"",""4843"",""4846"",""4908"",""5054"",""5228"",""54106"",""5624"",""57105"",""5729"",""5743"",""57628"",""59067"",""624"",""627"",""6347"",""6352"",""6356"",""6369"",""64127"",""6440"",""6441"",""64805"",""6532"",""6648"",""6865"",""6890"",""6915"",""7040"",""7056"",""7096"",""7097"",""7098"",""7099"",""7124"",""718"",""719"",""727"",""729230"",""7941"",""80332"",""81793"",""847"",""8518"",""8809"",""9173"",""929"",""942"",""958"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2841""}]"
DOID:2841	"[""asthma"",""bronchial hyperreactivity"",""chronic obstructive asthma"",""chronic obstructive asthma with acute exacerbation"",""chronic obstructive asthma with status asthmaticus""]"	"[{""label"":""Agtr1a"",""id"":""24180""},{""label"":""Bdkrb2"",""id"":""25245""},{""label"":""Ccl11"",""id"":""29397""},{""label"":""F7"",""id"":""260320""},{""label"":""Il10"",""id"":""25325""},{""label"":""Il13"",""id"":""116553""},{""label"":""Il2ra"",""id"":""25704""},{""label"":""Itpr1"",""id"":""25262""},{""label"":""Pdgfb"",""id"":""24628""},{""label"":""Ptger3"",""id"":""24929""},{""label"":""Trpa1"",""id"":""312896""},{""label"":""Vip"",""id"":""117064""}]"	"[""116553"",""117064"",""24180"",""24628"",""24929"",""25245"",""25262"",""25325"",""25704"",""260320"",""29397"",""312896""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2841""}]"
DOID:2841	"[""asthma"",""bronchial hyperreactivity"",""chronic obstructive asthma"",""chronic obstructive asthma with acute exacerbation"",""chronic obstructive asthma with status asthmaticus""]"	"[{""label"":""Il4ra"",""id"":""16190""},{""label"":""Itgb6"",""id"":""16420""}]"	"[""16190"",""16420""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2841""}]"
DOID:2842	"[""Jervell-Lange Nielsen syndrome"",""Jervell and Lange-Nielson syndrome""]"	"[{""label"":""Kcne1"",""id"":""16509""},{""label"":""Kcnq1"",""id"":""16535""}]"	"[""16509"",""16535""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2842""}]"
DOID:2842	"[""Jervell-Lange Nielsen syndrome"",""Jervell and Lange-Nielson syndrome""]"	"[{""label"":""KCNE1"",""id"":""3753""},{""label"":""KCNQ1"",""id"":""3784""}]"	"[""3753"",""3784""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2842""}]"
DOID:2843	"[""long QT syndrome"",""LQT"",""long Q-T syndrome""]"	"[{""label"":""Kcnq1"",""id"":""84020""}]"	"[""84020""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2843""}]"
DOID:2843	"[""long QT syndrome"",""LQT"",""long Q-T syndrome""]"	"[{""label"":""unc-103"",""id"":""175527""}]"	"[""175527""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2843""}]"
DOID:2843	"[""long QT syndrome"",""LQT"",""long Q-T syndrome""]"	"[{""label"":""ANK2"",""id"":""287""},{""label"":""KCNE1"",""id"":""3753""},{""label"":""KCNE2"",""id"":""9992""},{""label"":""KCNH2"",""id"":""3757""},{""label"":""KCNQ1"",""id"":""3784""},{""label"":""SCN5A"",""id"":""6331""}]"	"[""287"",""3753"",""3757"",""3784"",""6331"",""9992""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2843""}]"
DOID:285	"[""hairy cell leukemia""]"	"[{""label"":""GPX1"",""id"":""2876""}]"	"[""2876""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:285""}]"
DOID:2855	"[""hyperthyroxinemia""]"	"[{""label"":""ALB"",""id"":""213""}]"	"[""213""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2855""}]"
DOID:2859	"[""hemoglobin C disease"",""Hb-C disease""]"	"[{""label"":""HBB"",""id"":""3043""}]"	"[""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2859""}]"
DOID:2860	"[""hemoglobinopathy"",""hemoglobinopathies""]"	"[{""label"":""HBB"",""id"":""3043""}]"	"[""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2860""}]"
DOID:2861	"[""congenital nonspherocytic hemolytic anemia"",""HNSHA"",""congenital nonspherocytic hemolytic anaemia"",""hereditary nonspherocytic hemolytic anaemia"",""hereditary nonspherocytic hemolytic anemia""]"	"[{""label"":""Gpi1"",""id"":""14751""}]"	"[""14751""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2861""}]"
DOID:2861	"[""congenital nonspherocytic hemolytic anemia"",""HNSHA"",""congenital nonspherocytic hemolytic anaemia"",""hereditary nonspherocytic hemolytic anaemia"",""hereditary nonspherocytic hemolytic anemia""]"	"[{""label"":""ZWF1"",""id"":""855480""}]"	"[""855480""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2861""}]"
DOID:2861	"[""congenital nonspherocytic hemolytic anemia"",""HNSHA"",""congenital nonspherocytic hemolytic anaemia"",""hereditary nonspherocytic hemolytic anaemia"",""hereditary nonspherocytic hemolytic anemia""]"	"[{""label"":""G6PD"",""id"":""2539""},{""label"":""GPI"",""id"":""2821""},{""label"":""HK1"",""id"":""3098""},{""label"":""PKLR"",""id"":""5313""}]"	"[""2539"",""2821"",""3098"",""5313""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2861""}]"
DOID:2862	"[""glucosephosphate dehydrogenase deficiency"",""Glucose-6-phosphate dehydrogenase deficiency"",""deficiency of G-6PD""]"	"[{""label"":""IFNG"",""id"":""3458""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL6"",""id"":""3569""}]"	"[""3458"",""3569"",""3586""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2862""}]"
DOID:2870	"[""endometrial adenocarcinoma"",""adenocarcinoma of endometrium"",""adenocarcinoma of the Endometrium"",""adenocarcinoma of uterus"",""endometrial adenoacanthoma"",""endometrial endometrioid adenocarcinoma"",""endometrial endometrioid adenocarcinoma with squamous differentiation"",""endometrioid adenoma or carcinoma"",""endometrioid adenomas and carcinomas"",""endometrioid carcinoma of Endometrium""]"	"[{""label"":""ARID1A"",""id"":""8289""},{""label"":""TP53"",""id"":""7157""},{""label"":""TSG101"",""id"":""7251""}]"	"[""7157"",""7251"",""8289""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2870""}]"
DOID:2871	"[""endometrial carcinoma"",""carcinoma of the Endometrium"",""endometrioid carcinoma"",""endometrioid carcinoma of female Reproductive system""]"	"[{""label"":""APC"",""id"":""324""},{""label"":""CDH13"",""id"":""1012""},{""label"":""HRAS"",""id"":""3265""},{""label"":""POLE"",""id"":""5426""},{""label"":""RUNX3"",""id"":""864""},{""label"":""SMAD4"",""id"":""4089""},{""label"":""SPARC"",""id"":""6678""}]"	"[""1012"",""324"",""3265"",""4089"",""5426"",""6678"",""864""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2871""}]"
DOID:2871	"[""endometrial carcinoma"",""carcinoma of the Endometrium"",""endometrioid carcinoma"",""endometrioid carcinoma of female Reproductive system""]"	"[{""label"":""Tp53"",""id"":""24842""}]"	"[""24842""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2871""}]"
DOID:2876	"[""laryngeal squamous cell carcinoma"",""Epidermoid carcinoma of the Larynx"",""squamous cell carcinoma of larynx""]"	"[{""label"":""GPX1"",""id"":""2876""},{""label"":""NAT2"",""id"":""10""}]"	"[""10"",""2876""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2876""}]"
DOID:289	"[""endometriosis""]"	"[{""label"":""Il10"",""id"":""25325""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Tnf"",""id"":""24835""}]"	"[""24835"",""25325"",""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:289""}]"
DOID:289	"[""endometriosis""]"	"[{""label"":""ESR1"",""id"":""2099""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""PGR"",""id"":""5241""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""2099"",""3123"",""5176"",""5241"",""7133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:289""}]"
DOID:289	"[""endometriosis""]"	"[{""label"":""Kras"",""id"":""16653""}]"	"[""16653""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:289""}]"
DOID:2893	"[""cervix carcinoma"",""cancer of cervix"",""carcinoma cervix uteri"",""carcinoma of cervix"",""carcinoma of the Cervix Uteri""]"	"[{""label"":""APEX1"",""id"":""328""},{""label"":""ERAP1"",""id"":""51752""},{""label"":""FGFR3"",""id"":""2261""},{""label"":""MGMT"",""id"":""4255""},{""label"":""SPARC"",""id"":""6678""},{""label"":""TSG101"",""id"":""7251""}]"	"[""2261"",""328"",""4255"",""51752"",""6678"",""7251""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2893""}]"
DOID:2907	"[""Goldenhar syndrome"",""Facio-auriculo-vertebral spectrum"",""First AND second branchial arch syndrome"",""First arch syndrome"",""HEMIFACIAL MICROSOMIA"",""OAV (oculoauriculovertebral) dysplasia"",""Otomandibular dysostosis""]"	"[{""label"":""Zic3"",""id"":""22773""}]"	"[""22773""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2907""}]"
DOID:2907	"[""Goldenhar syndrome"",""Facio-auriculo-vertebral spectrum"",""First AND second branchial arch syndrome"",""First arch syndrome"",""HEMIFACIAL MICROSOMIA"",""OAV (oculoauriculovertebral) dysplasia"",""Otomandibular dysostosis""]"	"[{""label"":""SF3B2"",""id"":""10992""}]"	"[""10992""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2907""}]"
DOID:2908	"[""Treacher Collins syndrome"",""Franceschetti syndrome"",""mandibulofacial dysostosis""]"	"[{""label"":""Tcof1"",""id"":""21453""}]"	"[""21453""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2908""}]"
DOID:2908	"[""Treacher Collins syndrome"",""Franceschetti syndrome"",""mandibulofacial dysostosis""]"	"[{""label"":""TCOF1"",""id"":""6949""}]"	"[""6949""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2908""}]"
DOID:2913	"[""acute pancreatitis""]"	"[{""label"":""F7"",""id"":""2155""},{""label"":""IL10"",""id"":""3586""}]"	"[""2155"",""3586""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2913""}]"
DOID:2913	"[""acute pancreatitis""]"	"[{""label"":""Cx3cl1"",""id"":""89808""}]"	"[""89808""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2913""}]"
DOID:2917	"[""cryoglobulinemia"",""Cryoimmunoglobulinaemia""]"	"[{""label"":""ABCB1"",""id"":""5243""}]"	"[""5243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2917""}]"
DOID:2917	"[""cryoglobulinemia"",""Cryoimmunoglobulinaemia""]"	"[{""label"":""Tslp"",""id"":""53603""}]"	"[""53603""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2917""}]"
DOID:2920	"[""membranoproliferative glomerulonephritis"",""Lobular glomerulonephritis"",""chronic glomerulonephritis, lobular""]"	"[{""label"":""Cfh"",""id"":""12628""},{""label"":""Tslp"",""id"":""53603""}]"	"[""12628"",""53603""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2920""}]"
DOID:2920	"[""membranoproliferative glomerulonephritis"",""Lobular glomerulonephritis"",""chronic glomerulonephritis, lobular""]"	"[{""label"":""Angpt2"",""id"":""89805""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Tgfbr2"",""id"":""81810""}]"	"[""24770"",""81810"",""89805""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2920""}]"
DOID:2920	"[""membranoproliferative glomerulonephritis"",""Lobular glomerulonephritis"",""chronic glomerulonephritis, lobular""]"	"[{""label"":""CFB"",""id"":""629""},{""label"":""FN1"",""id"":""2335""}]"	"[""2335"",""629""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2920""}]"
DOID:2921	"[""glomerulonephritis""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Agtr2"",""id"":""24182""},{""label"":""C3"",""id"":""24232""},{""label"":""C6"",""id"":""24237""},{""label"":""Ccl7"",""id"":""287561""},{""label"":""Cd59b"",""id"":""25407""},{""label"":""Pdgfb"",""id"":""24628""},{""label"":""Pdgfd"",""id"":""66018""},{""label"":""Ptafr"",""id"":""58949""},{""label"":""Spp1"",""id"":""25353""}]"	"[""24182"",""24232"",""24237"",""24310"",""24628"",""25353"",""25407"",""287561"",""58949"",""66018""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2921""}]"
DOID:2921	"[""glomerulonephritis""]"	"[{""label"":""Cfi"",""id"":""12630""}]"	"[""12630""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2921""}]"
DOID:2921	"[""glomerulonephritis""]"	"[{""label"":""C1QA"",""id"":""712""},{""label"":""CNDP1"",""id"":""84735""},{""label"":""F2"",""id"":""2147""},{""label"":""FCGR2B"",""id"":""2213""},{""label"":""GDNF"",""id"":""2668""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""TPO"",""id"":""7173""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""2147"",""2213"",""2668"",""3557"",""5054"",""712"",""7173"",""7422"",""84735""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2921""}]"
DOID:2935	"[""Chediak-Higashi syndrome"",""CHS"",""Chediak - Steinbrinck anomaly""]"	"[{""label"":""LYST"",""id"":""1130""}]"	"[""1130""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2935""}]"
DOID:2938	"[""Epstein-Barr virus infectious disease"",""EBV Infection"",""Epstein-Barr virus infection""]"	"[{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""PTEN"",""id"":""5728""}]"	"[""3115"",""5728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2938""}]"
DOID:2942	"[""bronchiolitis""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""IL17A"",""id"":""3605""},{""label"":""MUC5B"",""id"":""727897""}]"	"[""154"",""3605"",""727897""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2942""}]"
DOID:2945	"[""severe acute respiratory syndrome"",""SARS"",""SARS-CoV infection""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""ACE2"",""id"":""59272""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CLEC4M"",""id"":""10332""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IFNG"",""id"":""3458""}]"	"[""10332"",""28"",""3106"",""3123"",""3458"",""59272"",""6352""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2945""}]"
DOID:2957	"[""pulmonary tuberculosis""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""AKT1"",""id"":""207""},{""label"":""ALOX5"",""id"":""240""},{""label"":""CCL1"",""id"":""6346""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CD14"",""id"":""929""},{""label"":""CD1D"",""id"":""912""},{""label"":""CD209"",""id"":""30835""},{""label"":""CD36"",""id"":""948""},{""label"":""CLEC4M"",""id"":""10332""},{""label"":""EGFR"",""id"":""1956""},{""label"":""EREG"",""id"":""2069""},{""label"":""GBE1"",""id"":""2632""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""JUN"",""id"":""3725""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""LTA"",""id"":""4049""},{""label"":""MARCO"",""id"":""8685""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MIF"",""id"":""4282""},{""label"":""NAT2"",""id"":""10""},{""label"":""NOD2"",""id"":""64127""},{""label"":""NOS2"",""id"":""4843""},{""label"":""SFTPA1"",""id"":""653509""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNF"",""id"":""7124""}]"	"[""10"",""10332"",""1956"",""2069"",""207"",""240"",""2632"",""30835"",""3115"",""3119"",""3123"",""3557"",""3725"",""3813"",""4049"",""4153"",""4282"",""4843"",""5243"",""54106"",""6346"",""6347"",""6352"",""64127"",""653509"",""6556"",""6890"",""7097"",""7099"",""7124"",""8685"",""912"",""929"",""948""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2957""}]"
DOID:2959	"[""hyperimmunoglobulin syndrome""]"	"[{""label"":""CD40"",""id"":""958""}]"	"[""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2959""}]"
DOID:2962	"[""Cockayne syndrome"",""Neill-Dingwall syndrome""]"	"[{""label"":""csa-1"",""id"":""174474""}]"	"[""174474""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2962""}]"
DOID:2962	"[""Cockayne syndrome"",""Neill-Dingwall syndrome""]"	"[{""label"":""ERCC6"",""id"":""2074""}]"	"[""2074""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2962""}]"
DOID:2975	"[""cystic kidney disease"",""renal Cyst""]"	"[{""label"":""RPGRIP1L"",""id"":""23322""}]"	"[""23322""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2975""}]"
DOID:2975	"[""cystic kidney disease"",""renal Cyst""]"	"[{""label"":""Cep290"",""id"":""216274""},{""label"":""Dnm2"",""id"":""13430""},{""label"":""Ephb4"",""id"":""13846""},{""label"":""Lama5"",""id"":""16776""},{""label"":""Robo1"",""id"":""19876""},{""label"":""Slit2"",""id"":""20563""},{""label"":""Tmem67"",""id"":""329795""},{""label"":""Ttc21b"",""id"":""73668""}]"	"[""13430"",""13846"",""16776"",""19876"",""20563"",""216274"",""329795"",""73668""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2975""}]"
DOID:2977	"[""primary hyperoxaluria""]"	"[{""label"":""GRHPR"",""id"":""9380""}]"	"[""9380""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2977""}]"
DOID:2978	"[""carbohydrate metabolic disorder"",""disorder of carbohydrate transport and metabolism"",""inborn carbohydrate metabolism disorder"",""inborn errors of carbohydrate metabolism""]"	"[{""label"":""ACAT1"",""id"":""38""},{""label"":""MPI"",""id"":""4351""},{""label"":""TALDO1"",""id"":""6888""},{""label"":""TPI1"",""id"":""7167""}]"	"[""38"",""4351"",""6888"",""7167""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2978""}]"
DOID:2978	"[""carbohydrate metabolic disorder"",""disorder of carbohydrate transport and metabolism"",""inborn carbohydrate metabolism disorder"",""inborn errors of carbohydrate metabolism""]"	"[{""label"":""gly-20"",""id"":""179562""}]"	"[""179562""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2978""}]"
DOID:2986	"[""IgA glomerulonephritis"",""Berger's IgA or IgG nephropathy"",""Focal Glomerulonephritis"",""IgA nephropathy"",""primary IgA nephropathy"",""segmental glomerulonephritis""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ACSM3"",""id"":""6296""},{""label"":""ADD1"",""id"":""118""},{""label"":""ADD2"",""id"":""119""},{""label"":""AGTR2"",""id"":""186""},{""label"":""CD14"",""id"":""929""},{""label"":""CFB"",""id"":""629""},{""label"":""CHGA"",""id"":""1113""},{""label"":""CXCR2"",""id"":""3579""},{""label"":""FCAR"",""id"":""2204""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MTR"",""id"":""4548""},{""label"":""MUC20"",""id"":""200958""},{""label"":""NGF"",""id"":""4803""},{""label"":""PDE5A"",""id"":""8654""},{""label"":""PLA2G7"",""id"":""7941""},{""label"":""SELE"",""id"":""6401""},{""label"":""SELL"",""id"":""6402""},{""label"":""SERPINB7"",""id"":""8710""},{""label"":""SPRY2"",""id"":""10253""},{""label"":""STAT4"",""id"":""6775""},{""label"":""TLR1"",""id"":""7096""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNFRSF1A"",""id"":""7132""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""10253"",""1113"",""118"",""119"",""1636"",""186"",""200958"",""2204"",""2214"",""3119"",""3480"",""3557"",""3579"",""4548"",""4803"",""54106"",""629"",""6296"",""6401"",""6402"",""6775"",""7096"",""7132"",""7133"",""7941"",""8654"",""8710"",""929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2986""}]"
DOID:2986	"[""IgA glomerulonephritis"",""Berger's IgA or IgG nephropathy"",""Focal Glomerulonephritis"",""IgA nephropathy"",""primary IgA nephropathy"",""segmental glomerulonephritis""]"	"[{""label"":""B4galt1"",""id"":""14595""},{""label"":""Tnfsf13b"",""id"":""24099""},{""label"":""Tnfsf14"",""id"":""50930""}]"	"[""14595"",""24099"",""50930""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2986""}]"
DOID:2986	"[""IgA glomerulonephritis"",""Berger's IgA or IgG nephropathy"",""Focal Glomerulonephritis"",""IgA nephropathy"",""primary IgA nephropathy"",""segmental glomerulonephritis""]"	"[{""label"":""Fas"",""id"":""246097""}]"	"[""246097""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2986""}]"
DOID:2987	"[""familial Mediterranean fever"",""FMF"",""benign paroxysmal peritonitis""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ACE"",""id"":""1636""},{""label"":""CYP3A4"",""id"":""1576""},{""label"":""MEFV"",""id"":""4210""},{""label"":""NOD2"",""id"":""64127""},{""label"":""POMC"",""id"":""5443""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""TLR4"",""id"":""7099""}]"	"[""1576"",""1636"",""4210"",""5054"",""5243"",""5443"",""64127"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2987""}]"
DOID:2988	"[""antiphospholipid syndrome"",""APS"",""antiphospholipid antibody syndrome""]"	"[{""label"":""APOH"",""id"":""350""},{""label"":""CD40LG"",""id"":""959""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""PLAT"",""id"":""5327""},{""label"":""PROC"",""id"":""5624""}]"	"[""3117"",""3119"",""3123"",""350"",""5327"",""5624"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2988""}]"
DOID:299	"[""adenocarcinoma""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:299""}]"
DOID:299	"[""adenocarcinoma""]"	"[{""label"":""APC"",""id"":""324""},{""label"":""STRAP"",""id"":""11171""}]"	"[""11171"",""324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:299""}]"
DOID:299	"[""adenocarcinoma""]"	"[{""label"":""Ptgs2"",""id"":""29527""}]"	"[""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:299""}]"
DOID:299	"[""adenocarcinoma""]"	"[{""label"":""N"",""id"":""31293""}]"	"[""31293""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:299""}]"
DOID:2994	"[""germ cell cancer"",""malignant tumor of the germ cell""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2994""}]"
DOID:2999	"[""granulosa cell tumor"",""Granulosa cell neoplasm"",""Granulosa cell tumor, adult type"",""Granulosa cell tumour, sarcomatoid"",""malignant granulosa cell neoplasm""]"	"[{""label"":""MGMT"",""id"":""4255""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""4255"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2999""}]"
DOID:2999	"[""granulosa cell tumor"",""Granulosa cell neoplasm"",""Granulosa cell tumor, adult type"",""Granulosa cell tumour, sarcomatoid"",""malignant granulosa cell neoplasm""]"	"[{""label"":""Ctnnb1"",""id"":""12387""}]"	"[""12387""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:2999""}]"
DOID:3007	"[""breast ductal carcinoma"",""duct carcinoma""]"	"[{""label"":""BCAR1"",""id"":""9564""},{""label"":""CD44"",""id"":""960""},{""label"":""RICTOR"",""id"":""253260""}]"	"[""253260"",""9564"",""960""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3007""}]"
DOID:3008	"[""invasive ductal carcinoma"",""Infiltrating ductal carcinoma of breast"",""Invasive ductal carcinoma, NST"",""ductal adenocarcinoma""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ADAM28"",""id"":""10863""},{""label"":""AKT1"",""id"":""207""},{""label"":""DLG1"",""id"":""1739""},{""label"":""NEFL"",""id"":""4747""},{""label"":""RUNX3"",""id"":""864""},{""label"":""UBR5"",""id"":""51366""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10863"",""1739"",""207"",""4747"",""51366"",""5243"",""7515"",""864""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3008""}]"
DOID:3012	"[""Li-Fraumeni syndrome"",""LFS"",""Li-Fraumeni Familiar cancer Susceptibility syndrome"",""SBLA syndrome"",""sarcoma, breast, leukaemia and adrenal gland syndrome""]"	"[{""label"":""TP53"",""id"":""7157""}]"	"[""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3012""}]"
DOID:3012	"[""Li-Fraumeni syndrome"",""LFS"",""Li-Fraumeni Familiar cancer Susceptibility syndrome"",""SBLA syndrome"",""sarcoma, breast, leukaemia and adrenal gland syndrome""]"	"[{""label"":""Trp53"",""id"":""22059""}]"	"[""22059""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3012""}]"
DOID:302	"[""substance abuse""]"	"[{""label"":""ADRA2A"",""id"":""150""},{""label"":""DRD4"",""id"":""1815""},{""label"":""HTR1A"",""id"":""3350""},{""label"":""HTR1B"",""id"":""3351""},{""label"":""NRG1"",""id"":""3084""},{""label"":""SLC6A4"",""id"":""6532""}]"	"[""150"",""1815"",""3084"",""3350"",""3351"",""6532""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:302""}]"
DOID:3021	"[""acute kidney failure""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Avpr1a"",""id"":""25107""},{""label"":""Pparg"",""id"":""25664""},{""label"":""Ptafr"",""id"":""58949""},{""label"":""Ptger4"",""id"":""84023""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Slc22a1"",""id"":""24904""},{""label"":""Slc22a2"",""id"":""29503""},{""label"":""Tlr4"",""id"":""29260""},{""label"":""Uts2r"",""id"":""57305""},{""label"":""Wnt4"",""id"":""84426""}]"	"[""24310"",""24904"",""25107"",""25664"",""29260"",""29503"",""29527"",""57305"",""58949"",""84023"",""84426""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3021""}]"
DOID:3021	"[""acute kidney failure""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""AGER"",""id"":""177""},{""label"":""AMBP"",""id"":""259""},{""label"":""EPO"",""id"":""2056""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MPO"",""id"":""4353""},{""label"":""PROC"",""id"":""5624""},{""label"":""SLC22A2"",""id"":""6582""},{""label"":""THBD"",""id"":""7056""}]"	"[""154"",""177"",""2056"",""259"",""3557"",""4353"",""5624"",""6582"",""7056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3021""}]"
DOID:3025	"[""acinar cell carcinoma"",""acinic cell carcinoma""]"	"[{""label"":""APC"",""id"":""324""}]"	"[""324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3025""}]"
DOID:303	"[""substance-related disorder""]"	"[{""label"":""Cdh13"",""id"":""192248""},{""label"":""Faslg"",""id"":""25385""},{""label"":""Gsk3b"",""id"":""84027""},{""label"":""Htr2c"",""id"":""25187""}]"	"[""192248"",""25187"",""25385"",""84027""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:303""}]"
DOID:3030	"[""mucinous adenocarcinoma"",""Mucin-Secreting adenocarcinoma"",""Mucin-Secreting carcinoma"",""Mucous carcinoma"",""Pseudomyxoma peritonei with unknown primary site"",""mucin-producing adenocarcinoma""]"	"[{""label"":""MUC1"",""id"":""4582""}]"	"[""4582""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3030""}]"
DOID:3042	"[""allergic contact dermatitis""]"	"[{""label"":""CCR1"",""id"":""1230""},{""label"":""IL18BP"",""id"":""10068""},{""label"":""NAT2"",""id"":""10""},{""label"":""TLR4"",""id"":""7099""}]"	"[""10"",""10068"",""1230"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3042""}]"
DOID:3044	"[""food allergy"",""food hypersensitivity""]"	"[{""label"":""Madcam1"",""id"":""54266""}]"	"[""54266""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3044""}]"
DOID:3049	"[""Churg-Strauss syndrome"",""Allergic Granulomatous Angiitis"",""Allergic granulomatosis angiitis"",""Churg-Strauss vasculitis""]"	"[{""label"":""VTN"",""id"":""7448""}]"	"[""7448""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3049""}]"
DOID:305	"[""carcinoma"",""epithelial cancer"",""epithelioma"",""malignant Epithelioma""]"	"[{""label"":""ERS1"",""id"":""850438""},{""label"":""PHO8"",""id"":""852092""}]"	"[""850438"",""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:305""}]"
DOID:305	"[""carcinoma"",""epithelial cancer"",""epithelioma"",""malignant Epithelioma""]"	"[{""label"":""Egfr"",""id"":""37455""},{""label"":""egr"",""id"":""36054""},{""label"":""ft"",""id"":""33627""},{""label"":""scrib"",""id"":""44448""}]"	"[""33627"",""36054"",""37455"",""44448""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:305""}]"
DOID:305	"[""carcinoma"",""epithelial cancer"",""epithelioma"",""malignant Epithelioma""]"	"[{""label"":""s1pr2"",""id"":""170457""}]"	"[""170457""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:305""}]"
DOID:3068	"[""glioblastoma"",""GBM"",""adult glioblastoma multiforme"",""glioblastoma multiforme"",""grade IV adult Astrocytic tumor"",""primary glioblastoma multiforme"",""spongioblastoma multiforme""]"	"[{""label"":""Serping1"",""id"":""295703""}]"	"[""295703""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3068""}]"
DOID:3068	"[""glioblastoma"",""GBM"",""adult glioblastoma multiforme"",""glioblastoma multiforme"",""grade IV adult Astrocytic tumor"",""primary glioblastoma multiforme"",""spongioblastoma multiforme""]"	"[{""label"":""ADGRB1"",""id"":""575""},{""label"":""AKT3"",""id"":""10000""},{""label"":""DMBT1"",""id"":""1755""},{""label"":""EGF"",""id"":""1950""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FLT3LG"",""id"":""2323""},{""label"":""IDH1"",""id"":""3417""},{""label"":""KDR"",""id"":""3791""},{""label"":""MDM2"",""id"":""4193""},{""label"":""MGMT"",""id"":""4255""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NRAS"",""id"":""4893""},{""label"":""PDGFB"",""id"":""5155""},{""label"":""PDGFRB"",""id"":""5159""},{""label"":""PGF"",""id"":""5228""},{""label"":""PIK3CB"",""id"":""5291""},{""label"":""PTPRB"",""id"":""5787""},{""label"":""RB1"",""id"":""5925""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10000"",""1755"",""1950"",""2146"",""2323"",""3417"",""3791"",""4193"",""4255"",""4318"",""4893"",""5155"",""5159"",""5228"",""5291"",""575"",""5787"",""5925"",""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3068""}]"
DOID:3068	"[""glioblastoma"",""GBM"",""adult glioblastoma multiforme"",""glioblastoma multiforme"",""grade IV adult Astrocytic tumor"",""primary glioblastoma multiforme"",""spongioblastoma multiforme""]"	"[{""label"":""Trp53"",""id"":""22059""}]"	"[""22059""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3068""}]"
DOID:3069	"[""malignant astrocytoma"",""Astrocytic tumor"",""astrocytoma of Cerebrum"",""astrocytoma of brain"",""astroglioma"",""cerebral astrocytoma""]"	"[{""label"":""CADM2"",""id"":""253559""},{""label"":""KRAS"",""id"":""3845""}]"	"[""253559"",""3845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3069""}]"
DOID:3070	"[""high grade glioma"",""Neuroglial tumor"",""glial cell tumor"",""glioma, malignant"",""malignant Neuroglial tumor"",""malignant glioma""]"	"[{""label"":""InR"",""id"":""42549""},{""label"":""htl"",""id"":""42160""}]"	"[""42160"",""42549""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3070""}]"
DOID:3070	"[""high grade glioma"",""Neuroglial tumor"",""glial cell tumor"",""glioma, malignant"",""malignant Neuroglial tumor"",""malignant glioma""]"	"[{""label"":""ATRX"",""id"":""546""},{""label"":""BRCA2"",""id"":""675""},{""label"":""CCN1"",""id"":""3491""},{""label"":""CHAF1A"",""id"":""10036""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""DCN"",""id"":""1634""},{""label"":""EGF"",""id"":""1950""},{""label"":""ENTPD2"",""id"":""954""},{""label"":""EPO"",""id"":""2056""},{""label"":""EPOR"",""id"":""2057""},{""label"":""ERBB2"",""id"":""2064""},{""label"":""ERCC5"",""id"":""2073""},{""label"":""FLT3LG"",""id"":""2323""},{""label"":""IDH1"",""id"":""3417""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL2"",""id"":""3558""},{""label"":""KDM5B"",""id"":""10765""},{""label"":""LTA"",""id"":""4049""},{""label"":""MAP2K1"",""id"":""5604""},{""label"":""NADSYN1"",""id"":""55191""},{""label"":""NF1"",""id"":""4763""},{""label"":""PDGFA"",""id"":""5154""},{""label"":""PDGFB"",""id"":""5155""},{""label"":""PRKCA"",""id"":""5578""},{""label"":""PTEN"",""id"":""5728""},{""label"":""SH3GL1"",""id"":""6455""},{""label"":""SLC44A1"",""id"":""23446""},{""label"":""SOX6"",""id"":""55553""},{""label"":""TNF"",""id"":""7124""},{""label"":""TP53"",""id"":""7157""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10036"",""10765"",""1571"",""1634"",""1950"",""2056"",""2057"",""2064"",""2073"",""2323"",""23446"",""3417"",""3480"",""3491"",""3558"",""3586"",""4049"",""4763"",""5154"",""5155"",""546"",""55191"",""55553"",""5578"",""5604"",""5728"",""6455"",""675"",""7124"",""7157"",""7515"",""954""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3070""}]"
DOID:3070	"[""high grade glioma"",""Neuroglial tumor"",""glial cell tumor"",""glioma, malignant"",""malignant Neuroglial tumor"",""malignant glioma""]"	"[{""label"":""Akt2"",""id"":""25233""},{""label"":""Areg"",""id"":""29183""},{""label"":""Bcan"",""id"":""25393""},{""label"":""Cxcr3"",""id"":""84475""},{""label"":""Hmgb1"",""id"":""25459""},{""label"":""Ifng"",""id"":""25712""},{""label"":""Spp1"",""id"":""25353""},{""label"":""St6gal1"",""id"":""25197""}]"	"[""25197"",""25233"",""25353"",""25393"",""25459"",""25712"",""29183"",""84475""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3070""}]"
DOID:3070	"[""high grade glioma"",""Neuroglial tumor"",""glial cell tumor"",""glioma, malignant"",""malignant Neuroglial tumor"",""malignant glioma""]"	"[{""label"":""IDP1"",""id"":""851493""},{""label"":""IDP2"",""id"":""850871""}]"	"[""850871"",""851493""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3070""}]"
DOID:3082	"[""interstitial lung disease"",""ILD""]"	"[{""label"":""AP3B1"",""id"":""8546""},{""label"":""HGF"",""id"":""3082""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL4R"",""id"":""3566""},{""label"":""MMP9"",""id"":""4318""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPC"",""id"":""6440""}]"	"[""3082"",""3552"",""3558"",""3566"",""4318"",""5054"",""6439"",""6440"",""8546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3082""}]"
DOID:3082	"[""interstitial lung disease"",""ILD""]"	"[{""label"":""Ccl2"",""id"":""24770""},{""label"":""Il1a"",""id"":""24493""}]"	"[""24493"",""24770""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3082""}]"
DOID:3083	"[""chronic obstructive pulmonary disease"",""COLD"",""COPD"",""chronic obstructive airway disease"",""chronic obstructive lung disease""]"	"[{""label"":""ABCC1"",""id"":""4363""},{""label"":""ACE"",""id"":""1636""},{""label"":""ADAM33"",""id"":""80332""},{""label"":""ADRB1"",""id"":""153""},{""label"":""ADRB2"",""id"":""154""},{""label"":""BDKRB2"",""id"":""624""},{""label"":""CCL1"",""id"":""6346""},{""label"":""CD86"",""id"":""942""},{""label"":""CFTR"",""id"":""1080""},{""label"":""CHRM3"",""id"":""1131""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CHRNA7"",""id"":""1139""},{""label"":""CLCA1"",""id"":""1179""},{""label"":""CRHR1"",""id"":""1394""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP1A2"",""id"":""1544""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""DEFB1"",""id"":""1672""},{""label"":""EDN1"",""id"":""1906""},{""label"":""ELN"",""id"":""2006""},{""label"":""F2RL1"",""id"":""2150""},{""label"":""GC"",""id"":""2638""},{""label"":""GRIK5"",""id"":""2901""},{""label"":""GRIN2B"",""id"":""2904""},{""label"":""HHIP"",""id"":""64399""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""IL12B"",""id"":""3593""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL13RA1"",""id"":""3597""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""LEP"",""id"":""3952""},{""label"":""LEPR"",""id"":""3953""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NAT2"",""id"":""10""},{""label"":""NOD2"",""id"":""64127""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SERPINA1"",""id"":""5265""},{""label"":""SERPINA3"",""id"":""12""},{""label"":""SFTPA1"",""id"":""653509""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPC"",""id"":""6440""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""SOD3"",""id"":""6649""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""},{""label"":""XRCC5"",""id"":""7520""}]"	"[""10"",""1080"",""1131"",""1136"",""1138"",""1139"",""1179"",""12"",""1394"",""1493"",""153"",""154"",""1543"",""1544"",""1571"",""1636"",""1672"",""1906"",""2006"",""2150"",""2638"",""2901"",""2904"",""2908"",""3115"",""3356"",""3557"",""3593"",""3596"",""3597"",""3952"",""3953"",""4153"",""4318"",""4363"",""5265"",""53353"",""5743"",""624"",""6346"",""64127"",""6439"",""64399"",""6440"",""6441"",""6532"",""653509"",""6649"",""7040"",""7099"",""7124"",""7520"",""80332"",""942""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3083""}]"
DOID:3083	"[""chronic obstructive pulmonary disease"",""COLD"",""COPD"",""chronic obstructive airway disease"",""chronic obstructive lung disease""]"	"[{""label"":""Tgfb1"",""id"":""59086""}]"	"[""59086""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3083""}]"
DOID:3114	"[""serous cystadenocarcinoma"",""serous adenocarcinoma"",""serous carcinoma""]"	"[{""label"":""XPC"",""id"":""7508""}]"	"[""7508""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3114""}]"
DOID:3119	"[""gastrointestinal system cancer"",""GI tumor"",""digestive system cancer"",""gastrointestinal tract cancer""]"	"[{""label"":""CES1"",""id"":""1066""},{""label"":""SMAD4"",""id"":""4089""}]"	"[""1066"",""4089""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3119""}]"
DOID:3121	"[""gallbladder cancer"",""gallbladder Ca"",""gallbladder neoplasm"",""localized malignant gallbladder neoplasm"",""malignant neoplasm of gallbladder"",""malignant tumor of the gallbladder"",""malignant tumour of gallbladder"",""tumor of the gallbladder""]"	"[{""label"":""APC"",""id"":""324""},{""label"":""APOB"",""id"":""338""},{""label"":""APOE"",""id"":""348""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CYP17A1"",""id"":""1586""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""EGF"",""id"":""1950""},{""label"":""GLI1"",""id"":""2735""},{""label"":""KEAP1"",""id"":""9817""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""RICTOR"",""id"":""253260""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1234"",""1543"",""1586"",""1950"",""253260"",""2735"",""324"",""338"",""348"",""53353"",""7515"",""9817""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3121""}]"
DOID:3125	"[""multiple endocrine neoplasia"",""Multiple endocrine adenomatosis"",""Multiple endocrine neoplasia syndrome""]"	"[{""label"":""Cdkn1b"",""id"":""83571""}]"	"[""83571""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3125""}]"
DOID:3132	"[""porphyria cutanea tarda""]"	"[{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP1A2"",""id"":""1544""},{""label"":""HFE"",""id"":""3077""}]"	"[""1543"",""1544"",""3077""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3132""}]"
DOID:3138	"[""acanthosis nigricans"",""keratosis nigricans""]"	"[{""label"":""FGFR3"",""id"":""2261""},{""label"":""TBC1D4"",""id"":""9882""}]"	"[""2261"",""9882""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3138""}]"
DOID:3144	"[""cutis laxa"",""loose skin""]"	"[{""label"":""ATP7A"",""id"":""538""},{""label"":""EFEMP1"",""id"":""2202""},{""label"":""ELN"",""id"":""2006""},{""label"":""FBLN5"",""id"":""10516""},{""label"":""LTBP1"",""id"":""4052""}]"	"[""10516"",""2006"",""2202"",""4052"",""538""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3144""}]"
DOID:3144	"[""cutis laxa"",""loose skin""]"	"[{""label"":""Efemp2"",""id"":""58859""},{""label"":""Fbln5"",""id"":""23876""},{""label"":""Ltbp4"",""id"":""108075""}]"	"[""108075"",""23876"",""58859""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3144""}]"
DOID:3145	"[""hyperlipoproteinemia type III"",""Remnant hyperlipidemia"",""carbohydrate induced hyperlipemia"",""familial hypercholesterolaemia with hyperlipaemia"",""familial type 3 hyperlipoproteinemia""]"	"[{""label"":""APOC3"",""id"":""345""},{""label"":""APOE"",""id"":""348""}]"	"[""345"",""348""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3145""}]"
DOID:3146	"[""lipid metabolism disorder"",""dyslipidemia"",""fatty acid metabolism disorder""]"	"[{""label"":""CPT1A"",""id"":""1374""},{""label"":""CPT2"",""id"":""1376""},{""label"":""DHCR24"",""id"":""1718""},{""label"":""MVK"",""id"":""4598""},{""label"":""NPY5R"",""id"":""4889""},{""label"":""PPARA"",""id"":""5465""}]"	"[""1374"",""1376"",""1718"",""4598"",""4889"",""5465""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3146""}]"
DOID:3151	"[""skin squamous cell carcinoma"",""Epidermoid skin carcinoma""]"	"[{""label"":""CTCF"",""id"":""10664""},{""label"":""KNSTRN"",""id"":""90417""}]"	"[""10664"",""90417""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3151""}]"
DOID:3153	"[""lipomatosis"",""multiple lipomatosis""]"	"[{""label"":""CEL"",""id"":""1056""}]"	"[""1056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3153""}]"
DOID:3159	"[""photosensitivity disease"",""Photodermatitis""]"	"[{""label"":""BRD2"",""id"":""6046""}]"	"[""6046""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3159""}]"
DOID:3165	"[""skin benign neoplasm"",""neoplasm of skin"",""neoplasm of skin by site"",""skin neoplasm"",""tumor of the skin""]"	"[{""label"":""HRAS"",""id"":""3265""}]"	"[""3265""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3165""}]"
DOID:3168	"[""squamous cell neoplasm"",""Epidermoid cell tumor"",""squamous cell tumor""]"	"[{""label"":""STRAP"",""id"":""11171""}]"	"[""11171""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3168""}]"
DOID:3181	"[""oligodendroglioma"",""oligodendroglial neoplasm"",""oligodendroglial tumor""]"	"[{""label"":""EGF"",""id"":""1950""},{""label"":""MGMT"",""id"":""4255""},{""label"":""RB1"",""id"":""5925""}]"	"[""1950"",""4255"",""5925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3181""}]"
DOID:3204	"[""schwannomatosis"",""SWN"",""neurilemmomatosis"",""neurinomatosis""]"	"[{""label"":""SMARCB1"",""id"":""6598""}]"	"[""6598""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3204""}]"
DOID:3209	"[""junctional epidermolysis bullosa"",""congenital junctional epidermolysis bullosa""]"	"[{""label"":""Col17a1"",""id"":""12821""},{""label"":""Lama3"",""id"":""16774""}]"	"[""12821"",""16774""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3209""}]"
DOID:3209	"[""junctional epidermolysis bullosa"",""congenital junctional epidermolysis bullosa""]"	"[{""label"":""COL17A1"",""id"":""1308""},{""label"":""ITGA3"",""id"":""3675""},{""label"":""ITGA6"",""id"":""3655""},{""label"":""ITGB4"",""id"":""3691""},{""label"":""LAMA3"",""id"":""3909""},{""label"":""LAMB3"",""id"":""3914""},{""label"":""LAMC2"",""id"":""3918""}]"	"[""1308"",""3655"",""3675"",""3691"",""3909"",""3914"",""3918""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3209""}]"
DOID:321	"[""HTLV-1-associated myelopathy/tropical spastic paraparesis"",""HAM/TSP"",""HTLV-associated myelopathy"",""Tropical spastic paralysis"",""Tropical spastic paraplegia"",""tropical spastic paraparesis""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HNRNPA1"",""id"":""3178""},{""label"":""KLRK1"",""id"":""22914""},{""label"":""NFKB1"",""id"":""4790""}]"	"[""22914"",""3119"",""3178"",""4790""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:321""}]"
DOID:3210	"[""Pelizaeus-Merzbacher disease"",""HLD1"",""Leukodystrophy, sudanophilic"",""PMD"",""Pelizaeus Merzbacher brain sclerosis"",""Pelizaeus-Merzbacher brain sclerosis"",""diffuse familial brain sclerosis"",""hypomyelinating leukodystrophy 1"",""sudanophilic leukodystrophy, Paelizeus-Merzbacher type""]"	"[{""label"":""PLP1"",""id"":""5354""}]"	"[""5354""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3210""}]"
DOID:3210	"[""Pelizaeus-Merzbacher disease"",""HLD1"",""Leukodystrophy, sudanophilic"",""PMD"",""Pelizaeus Merzbacher brain sclerosis"",""Pelizaeus-Merzbacher brain sclerosis"",""diffuse familial brain sclerosis"",""hypomyelinating leukodystrophy 1"",""sudanophilic leukodystrophy, Paelizeus-Merzbacher type""]"	"[{""label"":""Plp1"",""id"":""18823""}]"	"[""18823""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3210""}]"
DOID:3211	"[""lysosomal storage disease"",""disorder of lysosomal enzyme"",""inborn lysosomal enzyme disorder"",""lysosomal storage metabolism disorder""]"	"[{""label"":""Gga"",""id"":""31902""}]"	"[""31902""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3211""}]"
DOID:3211	"[""lysosomal storage disease"",""disorder of lysosomal enzyme"",""inborn lysosomal enzyme disorder"",""lysosomal storage metabolism disorder""]"	"[{""label"":""laat-1"",""id"":""3565323""}]"	"[""3565323""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3211""}]"
DOID:3211	"[""lysosomal storage disease"",""disorder of lysosomal enzyme"",""inborn lysosomal enzyme disorder"",""lysosomal storage metabolism disorder""]"	"[{""label"":""Slc17a5"",""id"":""235504""}]"	"[""235504""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3211""}]"
DOID:3211	"[""lysosomal storage disease"",""disorder of lysosomal enzyme"",""inborn lysosomal enzyme disorder"",""lysosomal storage metabolism disorder""]"	"[{""label"":""AGA"",""id"":""175""},{""label"":""CTSA"",""id"":""5476""}]"	"[""175"",""5476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3211""}]"
DOID:3213	"[""demyelinating disease"",""demyelinating disorder""]"	"[{""label"":""KLK6"",""id"":""5653""},{""label"":""MYC"",""id"":""4609""}]"	"[""4609"",""5653""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3213""}]"
DOID:3213	"[""demyelinating disease"",""demyelinating disorder""]"	"[{""label"":""Cxcr2"",""id"":""29385""}]"	"[""29385""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3213""}]"
DOID:322	"[""myelitis""]"	"[{""label"":""HLA-DPB1"",""id"":""3115""}]"	"[""3115""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:322""}]"
DOID:3227	"[""tracheal stenosis"",""Stenosis of trachea""]"	"[{""label"":""TGFB1"",""id"":""7040""}]"	"[""7040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3227""}]"
DOID:3234	"[""central nervous system lymphoma"",""Microglioma"",""primary CNS lymphoma""]"	"[{""label"":""BTK"",""id"":""695""},{""label"":""CD79B"",""id"":""974""},{""label"":""IL10"",""id"":""3586""},{""label"":""MYD88"",""id"":""4615""}]"	"[""3586"",""4615"",""695"",""974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3234""}]"
DOID:326	"[""ischemia""]"	"[{""label"":""mec-4"",""id"":""181728""}]"	"[""181728""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:326""}]"
DOID:326	"[""ischemia""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:326""}]"
DOID:326	"[""ischemia""]"	"[{""label"":""Akt2"",""id"":""25233""},{""label"":""Angpt2"",""id"":""89805""},{""label"":""Calca"",""id"":""24241""},{""label"":""Crhr2"",""id"":""64680""},{""label"":""Cx3cl1"",""id"":""89808""},{""label"":""Tnfrsf1a"",""id"":""25625""}]"	"[""24241"",""25233"",""25625"",""64680"",""89805"",""89808""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:326""}]"
DOID:326	"[""ischemia""]"	"[{""label"":""CCL2"",""id"":""6347""}]"	"[""6347""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:326""}]"
DOID:3261	"[""hyper IgE recurrent infection syndrome 1"",""Job syndrome"",""Job's syndrome"",""STAT3 Hyper IgE syndrome"",""hyperimmunoglobulin E syndrome""]"	"[{""label"":""STAT3"",""id"":""6774""}]"	"[""6774""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3261""}]"
DOID:3261	"[""hyper IgE recurrent infection syndrome 1"",""Job syndrome"",""Job's syndrome"",""STAT3 Hyper IgE syndrome"",""hyperimmunoglobulin E syndrome""]"	"[{""label"":""Stat3"",""id"":""20848""}]"	"[""20848""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3261""}]"
DOID:3263	"[""piebaldism"",""PIEBALD TRAIT"",""Partial albinism""]"	"[{""label"":""KIT"",""id"":""3815""}]"	"[""3815""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3263""}]"
DOID:3263	"[""piebaldism"",""PIEBALD TRAIT"",""Partial albinism""]"	"[{""label"":""Kit"",""id"":""16590""}]"	"[""16590""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3263""}]"
DOID:3265	"[""chronic granulomatous disease"",""Bridges-Good syndrome"",""CGD"",""Congenital dysphagocytosis"",""Quie syndrome""]"	"[{""label"":""Cybb"",""id"":""13058""}]"	"[""13058""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3265""}]"
DOID:3265	"[""chronic granulomatous disease"",""Bridges-Good syndrome"",""CGD"",""Congenital dysphagocytosis"",""Quie syndrome""]"	"[{""label"":""CYBB"",""id"":""1536""},{""label"":""IFNG"",""id"":""3458""}]"	"[""1536"",""3458""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3265""}]"
DOID:3301	"[""gonadoblastoma""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3301""}]"
DOID:3304	"[""germinoma""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3304""}]"
DOID:3307	"[""teratoma""]"	"[{""label"":""NME1"",""id"":""4830""},{""label"":""NME2"",""id"":""4831""},{""label"":""PGM1"",""id"":""5236""},{""label"":""PGM3"",""id"":""5238""}]"	"[""4830"",""4831"",""5236"",""5238""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3307""}]"
DOID:3308	"[""embryonal carcinoma"",""primary extragonadal embryonal carcinoma""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3308""}]"
DOID:3308	"[""embryonal carcinoma"",""primary extragonadal embryonal carcinoma""]"	"[{""label"":""POU5F1"",""id"":""5460""}]"	"[""5460""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3308""}]"
DOID:331	"[""central nervous system disease""]"	"[{""label"":""GluRIA"",""id"":""38742""},{""label"":""Iswi"",""id"":""36390""}]"	"[""36390"",""38742""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:331""}]"
DOID:331	"[""central nervous system disease""]"	"[{""label"":""ACO1"",""id"":""851013""}]"	"[""851013""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:331""}]"
DOID:3310	"[""atopic dermatitis"",""Atopic neurodermatitis"",""Besnier's prurigo"",""allergic dermatitis"",""atopic eczema""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""BDNF"",""id"":""627""},{""label"":""CLDN1"",""id"":""9076""},{""label"":""CMA1"",""id"":""1215""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""DOCK8"",""id"":""81704""},{""label"":""HAVCR1"",""id"":""26762""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL4"",""id"":""3565""},{""label"":""IL4R"",""id"":""3566""},{""label"":""MBL2"",""id"":""4153""},{""label"":""NAT2"",""id"":""10""},{""label"":""SELP"",""id"":""6403""},{""label"":""SHOC2"",""id"":""8036""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""}]"	"[""10"",""1215"",""1493"",""26762"",""348"",""3558"",""3565"",""3566"",""3596"",""4153"",""627"",""6403"",""7040"",""7097"",""7099"",""7124"",""8036"",""81704"",""9076""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3310""}]"
DOID:3310	"[""atopic dermatitis"",""Atopic neurodermatitis"",""Besnier's prurigo"",""allergic dermatitis"",""atopic eczema""]"	"[{""label"":""Adam17"",""id"":""11491""},{""label"":""Ctse"",""id"":""13034""},{""label"":""Il13"",""id"":""16163""},{""label"":""Il4"",""id"":""16189""},{""label"":""Tslp"",""id"":""53603""}]"	"[""11491"",""13034"",""16163"",""16189"",""53603""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3310""}]"
DOID:3312	"[""bipolar disorder"",""Manic Bipolar Affective disorder"",""Manic Depressive disorder"",""Manic bipolar I disorder"",""bipolar depression"",""bipolar disorder manic phase"",""manic depression"",""manic disorder"",""mixed bipolar disorder""]"	"[{""label"":""AKT1"",""id"":""207""},{""label"":""ANK3"",""id"":""288""},{""label"":""AVPR1B"",""id"":""553""},{""label"":""BMAL1"",""id"":""406""},{""label"":""BRD1"",""id"":""23774""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CHRM2"",""id"":""1129""},{""label"":""CHRNB3"",""id"":""1142""},{""label"":""COMT"",""id"":""1312""},{""label"":""GABRA3"",""id"":""2556""},{""label"":""GABRA5"",""id"":""2558""},{""label"":""GAD1"",""id"":""2571""},{""label"":""GRIN2A"",""id"":""2903""},{""label"":""GRIN2B"",""id"":""2904""},{""label"":""GSK3B"",""id"":""2932""},{""label"":""HTR2C"",""id"":""3358""},{""label"":""IMPA2"",""id"":""3613""},{""label"":""KAT6B"",""id"":""23522""},{""label"":""MBL2"",""id"":""4153""},{""label"":""NCAM1"",""id"":""4684""},{""label"":""NGF"",""id"":""4803""},{""label"":""NRG1"",""id"":""3084""},{""label"":""PER3"",""id"":""8863""},{""label"":""SLC18A1"",""id"":""6570""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""SSTR5"",""id"":""6755""},{""label"":""SYNE1"",""id"":""23345""}]"	"[""1129"",""1142"",""1312"",""207"",""23345"",""23522"",""23774"",""2556"",""2558"",""2571"",""288"",""2903"",""2904"",""2932"",""3084"",""3358"",""3613"",""406"",""4153"",""4684"",""4803"",""553"",""6347"",""6532"",""6570"",""6755"",""8863""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3312""}]"
DOID:3312	"[""bipolar disorder"",""Manic Bipolar Affective disorder"",""Manic Depressive disorder"",""Manic bipolar I disorder"",""bipolar depression"",""bipolar disorder manic phase"",""manic depression"",""manic disorder"",""mixed bipolar disorder""]"	"[{""label"":""ALG9"",""id"":""855502""}]"	"[""855502""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3312""}]"
DOID:3312	"[""bipolar disorder"",""Manic Bipolar Affective disorder"",""Manic Depressive disorder"",""Manic bipolar I disorder"",""bipolar depression"",""bipolar disorder manic phase"",""manic depression"",""manic disorder"",""mixed bipolar disorder""]"	"[{""label"":""Atp1a3"",""id"":""232975""},{""label"":""Camk2a"",""id"":""12322""},{""label"":""Clock"",""id"":""12753""}]"	"[""12322"",""12753"",""232975""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3312""}]"
DOID:3314	"[""angiomyolipoma""]"	"[{""label"":""OGG1"",""id"":""4968""}]"	"[""4968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3314""}]"
DOID:3315	"[""lipoma"",""Lipomatous neoplasm"",""Lipomatous tumor"",""benign lipomatous tumor"",""benign tumor of Adipose tissue"",""tumor of adipose tissue""]"	"[{""label"":""HMGA2"",""id"":""8091""}]"	"[""8091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3315""}]"
DOID:3317	"[""hepatic angiomyolipoma""]"	"[{""label"":""TSC2"",""id"":""7249""}]"	"[""7249""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3317""}]"
DOID:3319	"[""lymphangioleiomyomatosis"",""lung lymphangioleiomyomatosis"",""lymphangiomyomatosis"",""pulmonary lymphangioleiomyomatosis""]"	"[{""label"":""SRF"",""id"":""6722""},{""label"":""TSC1"",""id"":""7248""},{""label"":""TSC2"",""id"":""7249""}]"	"[""6722"",""7248"",""7249""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3319""}]"
DOID:332	"[""amyotrophic lateral sclerosis"",""ALS"",""Lou Gehrig's disease"",""motor neuron disease, bulbar""]"	"[{""label"":""tir-1"",""id"":""175502""}]"	"[""175502""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:332""}]"
DOID:332	"[""amyotrophic lateral sclerosis"",""ALS"",""Lou Gehrig's disease"",""motor neuron disease, bulbar""]"	"[{""label"":""C5ar1"",""id"":""113959""},{""label"":""Mstn"",""id"":""29152""},{""label"":""Nefm"",""id"":""24588""}]"	"[""113959"",""24588"",""29152""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:332""}]"
DOID:332	"[""amyotrophic lateral sclerosis"",""ALS"",""Lou Gehrig's disease"",""motor neuron disease, bulbar""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""CHMP2B"",""id"":""25978""},{""label"":""DPP6"",""id"":""1804""},{""label"":""FUS"",""id"":""2521""},{""label"":""GOT1"",""id"":""2805""},{""label"":""GRN"",""id"":""2896""},{""label"":""GSK3A"",""id"":""2931""},{""label"":""GSK3B"",""id"":""2932""},{""label"":""HMGB1"",""id"":""3146""},{""label"":""ITPR2"",""id"":""3709""},{""label"":""NEFH"",""id"":""4744""},{""label"":""NEFL"",""id"":""4747""},{""label"":""NRG1"",""id"":""3084""},{""label"":""OPTN"",""id"":""10133""},{""label"":""PON2"",""id"":""5445""},{""label"":""PON3"",""id"":""5446""},{""label"":""PPARGC1A"",""id"":""10891""},{""label"":""SLC11A2"",""id"":""4891""},{""label"":""SOD1"",""id"":""6647""},{""label"":""TARDBP"",""id"":""23435""},{""label"":""TFAM"",""id"":""7019""},{""label"":""UBQLN2"",""id"":""29978""},{""label"":""UNC13A"",""id"":""23025""},{""label"":""VAPB"",""id"":""9217""}]"	"[""10133"",""10891"",""1804"",""23025"",""23435"",""2521"",""25978"",""2805"",""2896"",""2931"",""2932"",""29978"",""3084"",""3146"",""348"",""3709"",""4744"",""4747"",""4891"",""5445"",""5446"",""6647"",""7019"",""9217""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:332""}]"
DOID:3320	"[""Tay-Sachs disease"",""GM2 gangliosidosis, type 1"",""hexosaminidase A deficiency""]"	"[{""label"":""HEXA"",""id"":""3073""}]"	"[""3073""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00055""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00056""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00057""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3320""}]"
DOID:3320	"[""Tay-Sachs disease"",""GM2 gangliosidosis, type 1"",""hexosaminidase A deficiency""]"	"[{""label"":""Hexa"",""id"":""15211""}]"	"[""15211""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3320""}]"
DOID:3321	"[""GM2 gangliosidosis"",""gangliosidosis GM2""]"	"[{""label"":""GM2A"",""id"":""2760""}]"	"[""2760""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3321""}]"
DOID:3322	"[""GM1 gangliosidosis"",""Beta-galactosidase deficiency"",""deficiency of beta-galactosidase"",""gangliosidosis GM1""]"	"[{""label"":""GLB1"",""id"":""2720""}]"	"[""2720""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00051""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00052""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00053""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3322""}]"
DOID:3322	"[""GM1 gangliosidosis"",""Beta-galactosidase deficiency"",""deficiency of beta-galactosidase"",""gangliosidosis GM1""]"	"[{""label"":""Glb1"",""id"":""12091""}]"	"[""12091""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3322""}]"
DOID:3323	"[""Sandhoff disease"",""Sandhoff Jatzkewitz disease""]"	"[{""label"":""Hexb"",""id"":""15212""}]"	"[""15212""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3323""}]"
DOID:3323	"[""Sandhoff disease"",""Sandhoff Jatzkewitz disease""]"	"[{""label"":""HEXB"",""id"":""3074""}]"	"[""3074""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00058""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00059""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00060""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00061""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3323""}]"
DOID:3324	"[""mood disorder"",""episodic mood disorder""]"	"[{""label"":""AVPR1B"",""id"":""553""}]"	"[""553""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3324""}]"
DOID:3324	"[""mood disorder"",""episodic mood disorder""]"	"[{""label"":""Hcn1"",""id"":""84390""}]"	"[""84390""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3324""}]"
DOID:3326	"[""purpura"",""Purpuric disorder""]"	"[{""label"":""IL13"",""id"":""3596""}]"	"[""3596""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3326""}]"
DOID:3328	"[""temporal lobe epilepsy"",""epilepsy, temporal lobe""]"	"[{""label"":""AQP4"",""id"":""361""},{""label"":""MAPT"",""id"":""4137""}]"	"[""361"",""4137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3328""}]"
DOID:3328	"[""temporal lobe epilepsy"",""epilepsy, temporal lobe""]"	"[{""label"":""Avp"",""id"":""24221""},{""label"":""Cxcr4"",""id"":""60628""},{""label"":""Gdnf"",""id"":""25453""}]"	"[""24221"",""25453"",""60628""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3328""}]"
DOID:3328	"[""temporal lobe epilepsy"",""epilepsy, temporal lobe""]"	"[{""label"":""Glul"",""id"":""14645""},{""label"":""Kcna1"",""id"":""16485""},{""label"":""Slc32a1"",""id"":""22348""}]"	"[""14645"",""16485"",""22348""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3328""}]"
DOID:3343	"[""glycoproteinosis"",""Mucolipidosis type I"",""sialidosis""]"	"[{""label"":""Neu1"",""id"":""18010""}]"	"[""18010""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3343""}]"
DOID:3343	"[""glycoproteinosis"",""Mucolipidosis type I"",""sialidosis""]"	"[{""label"":""GNPTAB"",""id"":""79158""},{""label"":""GNPTG"",""id"":""84572""},{""label"":""MCOLN1"",""id"":""57192""},{""label"":""NEU1"",""id"":""4758""}]"	"[""4758"",""57192"",""79158"",""84572""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00012""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00013""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00014""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00015""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00016""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00017""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00025""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00026""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3343""}]"
DOID:3345	"[""xanthomatosis"",""xanthelasmatosis""]"	"[{""label"":""Ldlr"",""id"":""300438""}]"	"[""300438""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3345""}]"
DOID:3347	"[""osteosarcoma"",""Osteogenic sarcoma"",""Skeletal sarcoma"",""bone tissue neoplasm"",""osteoid sarcoma""]"	"[{""label"":""CDC5L"",""id"":""988""},{""label"":""CHEK2"",""id"":""11200""},{""label"":""CXCR4"",""id"":""7852""},{""label"":""DDR1"",""id"":""780""},{""label"":""E2F1"",""id"":""1869""},{""label"":""EFEMP2"",""id"":""30008""},{""label"":""EZH2"",""id"":""2146""},{""label"":""RB1"",""id"":""5925""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""TP53"",""id"":""7157""}]"	"[""11200"",""1869"",""2146"",""30008"",""5176"",""5925"",""7157"",""780"",""7852"",""988""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3347""}]"
DOID:3347	"[""osteosarcoma"",""Osteogenic sarcoma"",""Skeletal sarcoma"",""bone tissue neoplasm"",""osteoid sarcoma""]"	"[{""label"":""Tp53"",""id"":""24842""}]"	"[""24842""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3347""}]"
DOID:3347	"[""osteosarcoma"",""Osteogenic sarcoma"",""Skeletal sarcoma"",""bone tissue neoplasm"",""osteoid sarcoma""]"	"[{""label"":""Trp53"",""id"":""22059""}]"	"[""22059""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3347""}]"
DOID:3347	"[""osteosarcoma"",""Osteogenic sarcoma"",""Skeletal sarcoma"",""bone tissue neoplasm"",""osteoid sarcoma""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3347""}]"
DOID:3355	"[""fibrosarcoma"",""Fibrocytic tumor"",""fibrosarcoma of soft tissue"",""fibrous tissue neoplasm""]"	"[{""label"":""CDC42"",""id"":""998""},{""label"":""TNFRSF1A"",""id"":""7132""}]"	"[""7132"",""998""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3355""}]"
DOID:3362	"[""coronary aneurysm"",""Aneurysm of coronary vessels"",""Aneurysmal lesion of coronary artery"",""Arteriovenous aneurysm of coronary vessels""]"	"[{""label"":""MMP12"",""id"":""4321""}]"	"[""4321""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3362""}]"
DOID:3369	"[""Ewing sarcoma"",""Ewing's family localized tumor"",""Ewing's sarcoma/peripheral primitive neuroectodermal tumor"",""Ewing's tumor"",""Ewings sarcoma"",""Ewings sarcoma-primitive neuroectodermal tumor"",""PNET of Thoracopulmonary Region"",""localized Ewing sarcoma"",""localized Ewing's sarcoma"",""localized Ewing's sarcoma/peripheral primitive neuroectodermal tumor"",""localized Ewing's tumor"",""localized peripheral primitive neuroectodermal tumor"",""peripheral primitive neuroectodermal tumor""]"	"[{""label"":""EWSR1"",""id"":""2130""}]"	"[""2130""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3369""}]"
DOID:3371	"[""chondrosarcoma"",""Cartilaginous cancer"",""chondrosarcoma of bone"",""primary chondrosarcoma of the bone""]"	"[{""label"":""COL2A1"",""id"":""1280""},{""label"":""EXT1"",""id"":""2131""}]"	"[""1280"",""2131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3371""}]"
DOID:3382	"[""liposarcoma"",""lipomatous cancer""]"	"[{""label"":""Il22"",""id"":""50929""}]"	"[""50929""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3382""}]"
DOID:3382	"[""liposarcoma"",""lipomatous cancer""]"	"[{""label"":""FUS"",""id"":""2521""}]"	"[""2521""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3382""}]"
DOID:3385	"[""bacterial vaginosis""]"	"[{""label"":""MBL2"",""id"":""4153""}]"	"[""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3385""}]"
DOID:3388	"[""periodontal disease"",""disease of supporting structures of teeth"",""periodontium disorder""]"	"[{""label"":""Dspp"",""id"":""666279""}]"	"[""666279""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3388""}]"
DOID:3388	"[""periodontal disease"",""disease of supporting structures of teeth"",""periodontium disorder""]"	"[{""label"":""IL6"",""id"":""3569""}]"	"[""3569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3388""}]"
DOID:3389	"[""Papillon-Lefevre disease"",""Papillon Lefevre syndrome"",""Papillon-Lefvre syndrome""]"	"[{""label"":""CTSC"",""id"":""1075""}]"	"[""1075""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3389""}]"
DOID:3390	"[""palmoplantar keratosis"",""Keratosis palmaris et plantaris"",""Palmoplantar Keratoderma"",""palmo-plantar keratodermas""]"	"[{""label"":""JUP"",""id"":""3728""}]"	"[""3728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3390""}]"
DOID:3393	"[""coronary artery disease"",""CHD"",""Coronary disease"",""coronary arteriosclerosis"",""coronary heart disease""]"	"[{""label"":""ABCA1"",""id"":""19""},{""label"":""ABCC6"",""id"":""368""},{""label"":""ACAT2"",""id"":""39""},{""label"":""ACE"",""id"":""1636""},{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""ADRB3"",""id"":""155""},{""label"":""AGER"",""id"":""177""},{""label"":""AGTR1"",""id"":""185""},{""label"":""AHSG"",""id"":""197""},{""label"":""APOA5"",""id"":""116519""},{""label"":""APOB"",""id"":""338""},{""label"":""APOC3"",""id"":""345""},{""label"":""APOE"",""id"":""348""},{""label"":""APOM"",""id"":""55937""},{""label"":""ARHGAP31"",""id"":""57514""},{""label"":""BCHE"",""id"":""590""},{""label"":""BRINP3"",""id"":""339479""},{""label"":""BTNL2"",""id"":""56244""},{""label"":""C1orf167"",""id"":""284498""},{""label"":""CBS"",""id"":""875""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CD40LG"",""id"":""959""},{""label"":""CLCN6"",""id"":""1185""},{""label"":""CPE"",""id"":""1363""},{""label"":""CUBN"",""id"":""8029""},{""label"":""CYP2R1"",""id"":""120227""},{""label"":""ECE1"",""id"":""1889""},{""label"":""EDN1"",""id"":""1906""},{""label"":""EPHX2"",""id"":""2053""},{""label"":""ESR1"",""id"":""2099""},{""label"":""F2"",""id"":""2147""},{""label"":""F7"",""id"":""2155""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""FGB"",""id"":""2244""},{""label"":""FTO"",""id"":""79068""},{""label"":""GCK"",""id"":""2645""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""HSPD1"",""id"":""3329""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RL1"",""id"":""9173""},{""label"":""IRS1"",""id"":""3667""},{""label"":""KALRN"",""id"":""8997""},{""label"":""KL"",""id"":""9365""},{""label"":""LEPR"",""id"":""3953""},{""label"":""LIPC"",""id"":""3990""},{""label"":""LIPG"",""id"":""9388""},{""label"":""LPL"",""id"":""4023""},{""label"":""LRP8"",""id"":""7804""},{""label"":""LTA"",""id"":""4049""},{""label"":""LUM"",""id"":""4060""},{""label"":""MLXIPL"",""id"":""51085""},{""label"":""MMP12"",""id"":""4321""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""MMP9"",""id"":""4318""},{""label"":""MYLK"",""id"":""4638""},{""label"":""NOD2"",""id"":""64127""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NPPA"",""id"":""4878""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""OGG1"",""id"":""4968""},{""label"":""OLR1"",""id"":""4973""},{""label"":""PECAM1"",""id"":""5175""},{""label"":""PLA2G7"",""id"":""7941""},{""label"":""PNPLA3"",""id"":""80339""},{""label"":""PON1"",""id"":""5444""},{""label"":""PON2"",""id"":""5445""},{""label"":""PPARA"",""id"":""5465""},{""label"":""PTPN1"",""id"":""5770""},{""label"":""PTPRD"",""id"":""5789""},{""label"":""RBP4"",""id"":""5950""},{""label"":""SELE"",""id"":""6401""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SOAT2"",""id"":""8435""},{""label"":""SOD3"",""id"":""6649""},{""label"":""SREBF1"",""id"":""6720""},{""label"":""TLL1"",""id"":""7092""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""},{""label"":""TP53"",""id"":""7157""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""116519"",""1185"",""120227"",""1363"",""155"",""1636"",""177"",""185"",""1889"",""19"",""1906"",""197"",""2053"",""2099"",""2147"",""2155"",""2212"",""2214"",""2244"",""2645"",""284498"",""2876"",""2908"",""3156"",""3329"",""338"",""339479"",""345"",""348"",""3586"",""3667"",""368"",""39"",""3953"",""3990"",""4023"",""4049"",""4060"",""4312"",""4314"",""4318"",""4321"",""4638"",""4846"",""4878"",""4968"",""4973"",""5054"",""51085"",""5175"",""5444"",""5445"",""5465"",""55937"",""56244"",""57514"",""5770"",""5789"",""590"",""5950"",""6401"",""64127"",""6649"",""6720"",""6927"",""7092"",""7099"",""7124"",""7157"",""729230"",""7515"",""7804"",""79068"",""7941"",""8029"",""80339"",""8435"",""875"",""8997"",""9173"",""9365"",""9370"",""9388"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3393""}]"
DOID:3407	"[""carotid artery disease"",""disorder of carotid artery""]"	"[{""label"":""AGT"",""id"":""183""},{""label"":""AGTR1"",""id"":""185""},{""label"":""CD14"",""id"":""929""},{""label"":""CETP"",""id"":""1071""},{""label"":""FGB"",""id"":""2244""},{""label"":""LTA"",""id"":""4049""},{""label"":""LUM"",""id"":""4060""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP2"",""id"":""4313""},{""label"":""MMP8"",""id"":""4317""},{""label"":""MMP9"",""id"":""4318""},{""label"":""PPARG"",""id"":""5468""},{""label"":""PRL"",""id"":""5617""},{""label"":""PTGDS"",""id"":""5730""},{""label"":""SELPLG"",""id"":""6404""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SREBF2"",""id"":""6721""},{""label"":""TLR4"",""id"":""7099""},{""label"":""UCP2"",""id"":""7351""}]"	"[""1071"",""183"",""185"",""2244"",""4049"",""4060"",""4312"",""4313"",""4317"",""4318"",""5468"",""5617"",""5730"",""6404"",""6648"",""6721"",""7099"",""7351"",""929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3407""}]"
DOID:3407	"[""carotid artery disease"",""disorder of carotid artery""]"	"[{""label"":""Ltb4r"",""id"":""59264""}]"	"[""59264""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3407""}]"
DOID:341	"[""peripheral vascular disease"",""arterial occlusive disease""]"	"[{""label"":""APOH"",""id"":""350""},{""label"":""IL6"",""id"":""3569""},{""label"":""LIPC"",""id"":""3990""},{""label"":""MBL2"",""id"":""4153""}]"	"[""350"",""3569"",""3990"",""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:341""}]"
DOID:341	"[""peripheral vascular disease"",""arterial occlusive disease""]"	"[{""label"":""Sell"",""id"":""29259""}]"	"[""29259""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:341""}]"
DOID:3410	"[""carotid artery thrombosis""]"	"[{""label"":""THBD"",""id"":""7056""}]"	"[""7056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3410""}]"
DOID:3413	"[""alpha-mannosidosis"",""Alpha-D-mannosidosis"",""alpha-mannosidase deficiency"",""deficiency of alpha-mannosidase""]"	"[{""label"":""Man2b1"",""id"":""17159""}]"	"[""17159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3413""}]"
DOID:3413	"[""alpha-mannosidosis"",""Alpha-D-mannosidosis"",""alpha-mannosidase deficiency"",""deficiency of alpha-mannosidase""]"	"[{""label"":""MAN2B1"",""id"":""4125""}]"	"[""4125""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00008""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00009""},{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00010""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3413""}]"
DOID:3429	"[""inclusion body myositis""]"	"[{""label"":""CLU"",""id"":""1191""},{""label"":""DAG1"",""id"":""1605""},{""label"":""SOD2"",""id"":""6648""},{""label"":""VCP"",""id"":""7415""}]"	"[""1191"",""1605"",""6648"",""7415""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3429""}]"
DOID:3443	"[""mammary Paget's disease"",""Paget cell neoplasm"",""Paget's disease"",""Paget's disease of the breast"",""mammary Paget disease""]"	"[{""label"":""ERBB2"",""id"":""2064""}]"	"[""2064""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3443""}]"
DOID:3450	"[""cutaneous Paget's disease"",""Paget's disease of skin"",""cutaneous Paget disease"",""extramammary Paget's disease""]"	"[{""label"":""PIK3CA"",""id"":""5290""}]"	"[""5290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3450""}]"
DOID:3454	"[""brain infarction""]"	"[{""label"":""ADM"",""id"":""133""},{""label"":""ALDH2"",""id"":""217""},{""label"":""CFH"",""id"":""3075""},{""label"":""CYP2R1"",""id"":""120227""},{""label"":""HLA-DQA1"",""id"":""3117""}]"	"[""120227"",""133"",""217"",""3075"",""3117""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3454""}]"
DOID:3454	"[""brain infarction""]"	"[{""label"":""Hgf"",""id"":""24446""},{""label"":""Hmgb1"",""id"":""25459""},{""label"":""Parg"",""id"":""83507""},{""label"":""Pdgfb"",""id"":""24628""}]"	"[""24446"",""24628"",""25459"",""83507""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3454""}]"
DOID:3457	"[""invasive lobular carcinoma"",""Lobular carcinoma"",""Lobular carcinoma of breast"",""Lobular carcinoma of the breast""]"	"[{""label"":""CD44"",""id"":""960""},{""label"":""CDH1"",""id"":""999""}]"	"[""960"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3457""}]"
DOID:3458	"[""breast adenocarcinoma"",""Mammary adenocarcinoma""]"	"[{""label"":""BRCA1"",""id"":""672""},{""label"":""TNF"",""id"":""7124""}]"	"[""672"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3458""}]"
DOID:3459	"[""breast carcinoma"",""Mammary carcinoma"",""carcinoma of breast""]"	"[{""label"":""BIN1"",""id"":""274""},{""label"":""CADM1"",""id"":""23705""},{""label"":""CDH13"",""id"":""1012""},{""label"":""DCN"",""id"":""1634""},{""label"":""DDR1"",""id"":""780""},{""label"":""EGFR"",""id"":""1956""},{""label"":""ESR1"",""id"":""2099""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""LZTS1"",""id"":""11178""},{""label"":""MRE11"",""id"":""4361""},{""label"":""RHOA"",""id"":""387""},{""label"":""STAT1"",""id"":""6772""},{""label"":""TFRC"",""id"":""7037""},{""label"":""THOC5"",""id"":""8563""},{""label"":""TIMP3"",""id"":""7078""},{""label"":""TSG101"",""id"":""7251""},{""label"":""TWIST1"",""id"":""7291""},{""label"":""VEGFC"",""id"":""7424""},{""label"":""WNT2"",""id"":""7472""}]"	"[""1012"",""11178"",""1634"",""1956"",""2099"",""23705"",""274"",""3123"",""387"",""4361"",""6772"",""7037"",""7078"",""7251"",""7291"",""7424"",""7472"",""780"",""8563""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3459""}]"
DOID:3482	"[""plague""]"	"[{""label"":""Ccr5"",""id"":""117029""}]"	"[""117029""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3482""}]"
DOID:3490	"[""Noonan syndrome"",""Turner's phenotype, karyotype normal""]"	"[{""label"":""Kat6b"",""id"":""54169""}]"	"[""54169""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3490""}]"
DOID:3490	"[""Noonan syndrome"",""Turner's phenotype, karyotype normal""]"	"[{""label"":""KRAS"",""id"":""3845""},{""label"":""PTPN11"",""id"":""5781""},{""label"":""RAF1"",""id"":""5894""},{""label"":""SOS1"",""id"":""6654""}]"	"[""3845"",""5781"",""5894"",""6654""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3490""}]"
DOID:3491	"[""Turner syndrome"",""Bonnevie-Ullrich syndrome"",""Gonadal dysgenesis - Turner"",""Karyotype 45, X"",""Monosomy X"",""XO syndrome"",""monosomy X syndrome""]"	"[{""label"":""IGFBP3"",""id"":""3486""}]"	"[""3486""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3491""}]"
DOID:3492	"[""mixed connective tissue disease"",""Connective tissue disease overlap syndrome"",""mixed collagen vascular disease""]"	"[{""label"":""FBN1"",""id"":""2200""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""SNRPB"",""id"":""6628""},{""label"":""SNRPC"",""id"":""6631""}]"	"[""2200"",""3123"",""6628"",""6631""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3492""}]"
DOID:3495	"[""extrahepatic bile duct adenocarcinoma"",""adenocarcinoma of extrahepatic bile duct""]"	"[{""label"":""BAP1"",""id"":""8314""},{""label"":""PBRM1"",""id"":""55193""}]"	"[""55193"",""8314""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3495""}]"
DOID:3498	"[""pancreatic ductal adenocarcinoma"",""ductal adenocarcinoma of the pancreas""]"	"[{""label"":""CALR"",""id"":""811""},{""label"":""E2F1"",""id"":""1869""},{""label"":""GOT1"",""id"":""2805""},{""label"":""TGFBR1"",""id"":""7046""}]"	"[""1869"",""2805"",""7046"",""811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3498""}]"
DOID:350	"[""mastocytosis"",""mast cell hyperplasia""]"	"[{""label"":""Kit"",""id"":""16590""}]"	"[""16590""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:350""}]"
DOID:350	"[""mastocytosis"",""mast cell hyperplasia""]"	"[{""label"":""IL13"",""id"":""3596""},{""label"":""KIT"",""id"":""3815""}]"	"[""3596"",""3815""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:350""}]"
DOID:3500	"[""gallbladder adenocarcinoma"",""adenocarcinoma of the gallbladder""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""DDR2"",""id"":""4921""}]"	"[""1636"",""4921""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3500""}]"
DOID:3507	"[""dermatofibrosarcoma protuberans""]"	"[{""label"":""COL1A1"",""id"":""1277""},{""label"":""PDGFB"",""id"":""5155""}]"	"[""1277"",""5155""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3507""}]"
DOID:3512	"[""neurofibrosarcoma"",""Neurosarcoma""]"	"[{""label"":""MXI1"",""id"":""4601""}]"	"[""4601""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3512""}]"
DOID:3525	"[""middle cerebral artery infarction""]"	"[{""label"":""Abcc8"",""id"":""25559""},{""label"":""Ace"",""id"":""24310""},{""label"":""Aqp4"",""id"":""25293""},{""label"":""Bad"",""id"":""64639""},{""label"":""Creb1"",""id"":""81646""},{""label"":""Gapdh"",""id"":""24383""},{""label"":""Gdnf"",""id"":""25453""},{""label"":""Ghsr"",""id"":""84022""},{""label"":""Gsk3b"",""id"":""84027""},{""label"":""Mag"",""id"":""29409""},{""label"":""Nampt"",""id"":""297508""},{""label"":""Ncam1"",""id"":""24586""},{""label"":""Nfe2l2"",""id"":""83619""},{""label"":""Ngf"",""id"":""310738""},{""label"":""Ngfr"",""id"":""24596""},{""label"":""Parp1"",""id"":""25591""},{""label"":""Pdgfra"",""id"":""25267""},{""label"":""Pdgfrb"",""id"":""24629""},{""label"":""Runx1"",""id"":""50662""},{""label"":""Smo"",""id"":""25273""},{""label"":""Tnf"",""id"":""24835""},{""label"":""Tnfrsf1a"",""id"":""25625""},{""label"":""Vegfa"",""id"":""83785""}]"	"[""24310"",""24383"",""24586"",""24596"",""24629"",""24835"",""25267"",""25273"",""25293"",""25453"",""25559"",""25591"",""25625"",""29409"",""297508"",""310738"",""50662"",""64639"",""81646"",""83619"",""83785"",""84022"",""84027""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3525""}]"
DOID:3525	"[""middle cerebral artery infarction""]"	"[{""label"":""ALB"",""id"":""213""},{""label"":""CSF3"",""id"":""1440""},{""label"":""EPO"",""id"":""2056""},{""label"":""F12"",""id"":""2161""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""NCAM1"",""id"":""4684""},{""label"":""NRG1"",""id"":""3084""},{""label"":""PARK7"",""id"":""11315""},{""label"":""SHH"",""id"":""6469""}]"	"[""11315"",""1440"",""2056"",""213"",""2161"",""3084"",""3557"",""4684"",""6469""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3525""}]"
DOID:3526	"[""cerebral infarction"",""CVA - Cerebral infarction"",""Cerebral infarct""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""APOA5"",""id"":""116519""},{""label"":""APOE"",""id"":""348""},{""label"":""CBS"",""id"":""875""},{""label"":""F2"",""id"":""2147""},{""label"":""F5"",""id"":""2153""},{""label"":""F7"",""id"":""2155""},{""label"":""FOLH1"",""id"":""2346""},{""label"":""GPX3"",""id"":""2878""},{""label"":""GRIN1"",""id"":""2902""},{""label"":""HLA-A"",""id"":""3105""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""IFNB1"",""id"":""3456""},{""label"":""ITGA9"",""id"":""3680""},{""label"":""KALRN"",""id"":""8997""},{""label"":""KCNN4"",""id"":""3783""},{""label"":""LIPG"",""id"":""9388""},{""label"":""LTA"",""id"":""4049""},{""label"":""MTR"",""id"":""4548""},{""label"":""MYRF"",""id"":""745""},{""label"":""NR1H3"",""id"":""10062""},{""label"":""NTRK2"",""id"":""4915""},{""label"":""PARK7"",""id"":""11315""},{""label"":""PDX1"",""id"":""3651""},{""label"":""PON1"",""id"":""5444""},{""label"":""PON2"",""id"":""5445""},{""label"":""PRKCH"",""id"":""5583""},{""label"":""PROS1"",""id"":""5627""},{""label"":""PTGIS"",""id"":""5740""},{""label"":""SERPING1"",""id"":""710""},{""label"":""TBXAS1"",""id"":""6916""},{""label"":""THBD"",""id"":""7056""},{""label"":""TNF"",""id"":""7124""},{""label"":""TOMM40"",""id"":""10452""},{""label"":""TYMS"",""id"":""7298""}]"	"[""10062"",""10452"",""11315"",""116519"",""1636"",""2147"",""2153"",""2155"",""2346"",""2878"",""2902"",""3105"",""3106"",""3123"",""3456"",""348"",""3651"",""3680"",""3783"",""4049"",""4548"",""4915"",""5444"",""5445"",""5583"",""5627"",""5740"",""6916"",""6927"",""7056"",""710"",""7124"",""7298"",""745"",""875"",""8997"",""9388""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3526""}]"
DOID:3526	"[""cerebral infarction"",""CVA - Cerebral infarction"",""Cerebral infarct""]"	"[{""label"":""Adora1"",""id"":""29290""},{""label"":""Map2"",""id"":""25595""},{""label"":""Serpine1"",""id"":""24617""}]"	"[""24617"",""25595"",""29290""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3526""}]"
DOID:3529	"[""congenital myopathy 1A"",""central core disease"",""central core myopathy""]"	"[{""label"":""RYR1"",""id"":""6261""}]"	"[""6261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3529""}]"
DOID:3529	"[""congenital myopathy 1A"",""central core disease"",""central core myopathy""]"	"[{""label"":""Ryr1"",""id"":""20190""}]"	"[""20190""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3529""}]"
DOID:3534	"[""Lafora disease"",""Lafora Progressive Myoclonic Epilepsy"",""Lafora's disease"",""MYOCLONIC EPILEPSY OF LAFORA""]"	"[{""label"":""Epm2a"",""id"":""13853""},{""label"":""Nhlrc1"",""id"":""105193""}]"	"[""105193"",""13853""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3534""}]"
DOID:3534	"[""Lafora disease"",""Lafora Progressive Myoclonic Epilepsy"",""Lafora's disease"",""MYOCLONIC EPILEPSY OF LAFORA""]"	"[{""label"":""Glys"",""id"":""41823""}]"	"[""41823""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3534""}]"
DOID:3535	"[""Unverricht-Lundborg syndrome"",""Unverricht - Lundborg disease"",""Unverricht's disease"",""Unverricht-Lundborg disease""]"	"[{""label"":""CSTB"",""id"":""1476""}]"	"[""1476""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3535""}]"
DOID:3565	"[""meningioma"",""meningeal neoplasm"",""meningothelial cell tumor"",""neoplasm of the meninges"",""primary Meningeal tumor""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3565""}]"
DOID:3565	"[""meningioma"",""meningeal neoplasm"",""meningothelial cell tumor"",""neoplasm of the meninges"",""primary Meningeal tumor""]"	"[{""label"":""MN1"",""id"":""4330""},{""label"":""SMARCB1"",""id"":""6598""},{""label"":""SMARCE1"",""id"":""6605""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""4330"",""6598"",""6605"",""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3565""}]"
DOID:3571	"[""liver cancer"",""Ca liver - primary"",""Resectable malignant neoplasm of Liver"",""hepatic cancer"",""hepatic neoplasm"",""malignant hepato-biliary neoplasm"",""malignant neoplasm of liver"",""malignant neoplasm of liver, not specified as primary or secondary"",""malignant neoplasm of liver, primary"",""malignant tumor of liver"",""neoplasm of liver"",""non-resectable primary hepatic malignant neoplasm"",""primary liver cancer"",""primary malignant neoplasm of liver"",""resectable malignant neoplasm of the liver""]"	"[{""label"":""CHUK"",""id"":""1147""},{""label"":""IKBKB"",""id"":""3551""}]"	"[""1147"",""3551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3571""}]"
DOID:3587	"[""pancreatic ductal carcinoma"",""malignant neoplasm of duct of Wirsung"",""pancreatic duct cancer""]"	"[{""label"":""CD40"",""id"":""958""},{""label"":""FASLG"",""id"":""356""},{""label"":""HEATR1"",""id"":""55127""},{""label"":""IL4"",""id"":""3565""},{""label"":""MDM2"",""id"":""4193""},{""label"":""MGMT"",""id"":""4255""},{""label"":""MSLN"",""id"":""10232""},{""label"":""MUC1"",""id"":""4582""},{""label"":""PMS1"",""id"":""5378""},{""label"":""SMO"",""id"":""6608""},{""label"":""THBS1"",""id"":""7057""}]"	"[""10232"",""356"",""3565"",""4193"",""4255"",""4582"",""5378"",""55127"",""6608"",""7057"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3587""}]"
DOID:3590	"[""gestational trophoblastic neoplasm"",""gestational trophoblastic neoplasia"",""hydatidiform mole"",""molar pregnancy""]"	"[{""label"":""MEI1"",""id"":""150365""}]"	"[""150365""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3590""}]"
DOID:3594	"[""choriocarcinoma"",""Chorioepithelioma""]"	"[{""label"":""IGF2"",""id"":""3481""},{""label"":""INSR"",""id"":""3643""}]"	"[""3481"",""3643""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3594""}]"
DOID:3594	"[""choriocarcinoma"",""Chorioepithelioma""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3594""}]"
DOID:3602	"[""toxic encephalopathy"",""neurotoxicity"",""neurotoxicity syndrome""]"	"[{""label"":""Il10"",""id"":""25325""}]"	"[""25325""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3602""}]"
DOID:3602	"[""toxic encephalopathy"",""neurotoxicity"",""neurotoxicity syndrome""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ABCG2"",""id"":""9429""},{""label"":""IGF1R"",""id"":""3480""}]"	"[""3480"",""5243"",""9429""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3602""}]"
DOID:3611	"[""acute retinal necrosis syndrome"",""acute retinal necrosis""]"	"[{""label"":""HLA-B"",""id"":""3106""}]"	"[""3106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3611""}]"
DOID:3613	"[""Canavan disease"",""ACY2 DEFICIENCY"",""AMINOACYLASE 2 DEFICIENCY"",""ASP DEFICIENCY"",""ASPA DEFICIENCY"",""ASPARTOACYLASE DEFICIENCY"",""CANAVAN-VAN BOGAERT-BERTRAND DISEASE"",""Spongy degeneration of central nervous system""]"	"[{""label"":""Sod2"",""id"":""20656""}]"	"[""20656""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3613""}]"
DOID:3620	"[""central nervous system cancer"",""CNS neoplasm"",""central nervous system tumor"",""central nervous system tumors"",""malignant neoplasm of central nervous system"",""malignant tumor of CNS"",""neoplasm of central nervous system""]"	"[{""label"":""XRCC1"",""id"":""7515""}]"	"[""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3620""}]"
DOID:3620	"[""central nervous system cancer"",""CNS neoplasm"",""central nervous system tumor"",""central nervous system tumors"",""malignant neoplasm of central nervous system"",""malignant tumor of CNS"",""neoplasm of central nervous system""]"	"[{""label"":""N"",""id"":""31293""}]"	"[""31293""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3620""}]"
DOID:3627	"[""aortic aneurysm"",""ruptured aortic aneurysm""]"	"[{""label"":""Aoc3"",""id"":""29473""},{""label"":""Serpine1"",""id"":""24617""}]"	"[""24617"",""29473""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3627""}]"
DOID:3627	"[""aortic aneurysm"",""ruptured aortic aneurysm""]"	"[{""label"":""EFEMP2"",""id"":""30008""},{""label"":""ELN"",""id"":""2006""},{""label"":""FBN1"",""id"":""2200""}]"	"[""2006"",""2200"",""30008""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3627""}]"
DOID:3627	"[""aortic aneurysm"",""ruptured aortic aneurysm""]"	"[{""label"":""Atp7a"",""id"":""11977""},{""label"":""Efemp2"",""id"":""58859""}]"	"[""11977"",""58859""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3627""}]"
DOID:3633	"[""beta-mannosidosis"",""Beta-D-mannosidosis"",""beta-mannosidase deficiency"",""lysosomal beta-mannosidase deficiency""]"	"[{""label"":""MANBA"",""id"":""4126""}]"	"[""4126""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00011""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3633""}]"
DOID:3633	"[""beta-mannosidosis"",""Beta-D-mannosidosis"",""beta-mannosidase deficiency"",""lysosomal beta-mannosidase deficiency""]"	"[{""label"":""Manba"",""id"":""110173""}]"	"[""110173""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3633""}]"
DOID:3635	"[""congenital myasthenic syndrome""]"	"[{""label"":""chrna1"",""id"":""30725""}]"	"[""30725""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3635""}]"
DOID:3635	"[""congenital myasthenic syndrome""]"	"[{""label"":""CHRNE"",""id"":""1145""},{""label"":""MYO9A"",""id"":""4649""},{""label"":""SYT2"",""id"":""127833""}]"	"[""1145"",""127833"",""4649""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3635""}]"
DOID:3635	"[""congenital myasthenic syndrome""]"	"[{""label"":""unc-63"",""id"":""172150""}]"	"[""172150""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3635""}]"
DOID:3649	"[""pyruvate decarboxylase deficiency"",""deficiency of pyruvic dehydrogenase"",""pyruvate dehydrogenase complex deficiency disease"",""pyruvate dehydrogenase deficiency""]"	"[{""label"":""Pdha1"",""id"":""29554""}]"	"[""29554""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3649""}]"
DOID:3649	"[""pyruvate decarboxylase deficiency"",""deficiency of pyruvic dehydrogenase"",""pyruvate dehydrogenase complex deficiency disease"",""pyruvate dehydrogenase deficiency""]"	"[{""label"":""DLAT"",""id"":""1737""},{""label"":""PDHA1"",""id"":""5160""},{""label"":""PDHB"",""id"":""5162""},{""label"":""PDHX"",""id"":""8050""},{""label"":""PDP1"",""id"":""54704""}]"	"[""1737"",""5160"",""5162"",""54704"",""8050""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3649""}]"
DOID:365	"[""bladder disease"",""Urinary Bladder Disease""]"	"[{""label"":""CHRM3"",""id"":""1131""}]"	"[""1131""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:365""}]"
DOID:3650	"[""lactic acidosis""]"	"[{""label"":""Pygl"",""id"":""64035""}]"	"[""64035""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3650""}]"
DOID:3650	"[""lactic acidosis""]"	"[{""label"":""PYGL"",""id"":""5836""}]"	"[""5836""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3650""}]"
DOID:3651	"[""pyruvate carboxylase deficiency disease"",""deficiency of pyruvic carboxylase""]"	"[{""label"":""PC"",""id"":""5091""}]"	"[""5091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3651""}]"
DOID:3652	"[""Leigh disease"",""Infantile necrotizing encephalomyelopathy"",""Leigh syndrome"",""juvenile subacute necrotizing encephalomyelopathy""]"	"[{""label"":""Ndufs4"",""id"":""17993""},{""label"":""Sdhc"",""id"":""66052""},{""label"":""Sod2"",""id"":""20656""}]"	"[""17993"",""20656"",""66052""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3652""}]"
DOID:3652	"[""Leigh disease"",""Infantile necrotizing encephalomyelopathy"",""Leigh syndrome"",""juvenile subacute necrotizing encephalomyelopathy""]"	"[{""label"":""LRPPRC"",""id"":""10128""},{""label"":""ND3"",""id"":""4537""},{""label"":""ND5"",""id"":""4540""},{""label"":""NDUFS2"",""id"":""4720""},{""label"":""SDHA"",""id"":""6389""},{""label"":""SURF1"",""id"":""6834""}]"	"[""10128"",""4537"",""4540"",""4720"",""6389"",""6834""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3652""}]"
DOID:3659	"[""sialuria""]"	"[{""label"":""Slc17a5"",""id"":""235504""}]"	"[""235504""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3659""}]"
DOID:3659	"[""sialuria""]"	"[{""label"":""GNE"",""id"":""10020""},{""label"":""SLC17A5"",""id"":""26503""}]"	"[""10020"",""26503""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3659""}]"
DOID:3672	"[""rhabdoid cancer"",""Rhabdoid sarcoma"",""malignant rhabdoid tumour""]"	"[{""label"":""SMARCB1"",""id"":""6598""}]"	"[""6598""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3672""}]"
DOID:3687	"[""MELAS syndrome"",""MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES""]"	"[{""label"":""ND5"",""id"":""4540""}]"	"[""4540""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3687""}]"
DOID:3689	"[""brachial plexus neuritis"",""Brachial neuritis"",""Parsonage-Aldren-Turner syndrome""]"	"[{""label"":""SEPTIN9"",""id"":""10801""}]"	"[""10801""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3689""}]"
DOID:37	"[""skin disease"",""Genodermatosis"",""skin and subcutaneous tissue disease""]"	"[{""label"":""IL10"",""id"":""3586""},{""label"":""TNF"",""id"":""7124""}]"	"[""3586"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:37""}]"
DOID:3717	"[""gastric adenocarcinoma"",""adenocarcinoma of stomach"",""stomach adenocarcinoma""]"	"[{""label"":""ABCA13"",""id"":""154664""},{""label"":""CD44"",""id"":""960""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""KMT2D"",""id"":""8085""},{""label"":""PLCE1"",""id"":""51196""},{""label"":""RNF43"",""id"":""54894""},{""label"":""TP53"",""id"":""7157""},{""label"":""UBR5"",""id"":""51366""},{""label"":""XPO1"",""id"":""7514""}]"	"[""154664"",""3117"",""51196"",""51366"",""54894"",""7157"",""7514"",""8085"",""960""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3717""}]"
DOID:3721	"[""plasmacytoma"",""Myeloma - solitary"",""Myeloma, solitary"",""Solitary myeloma"",""Solitary plasmacytoma""]"	"[{""label"":""ROBO1"",""id"":""6091""}]"	"[""6091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3721""}]"
DOID:3748	"[""esophagus squamous cell carcinoma"",""SCC of esophagus"",""SCC of oesophagus"",""oesophagus squamous cell carcinoma""]"	"[{""label"":""BRCA1"",""id"":""672""},{""label"":""BRCA2"",""id"":""675""},{""label"":""CALR"",""id"":""811""},{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CHRNA7"",""id"":""1139""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""COL14A1"",""id"":""7373""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""DCC"",""id"":""1630""},{""label"":""EFNB2"",""id"":""1948""},{""label"":""EPB41L3"",""id"":""23136""},{""label"":""ERBB4"",""id"":""2066""},{""label"":""FAT1"",""id"":""2195""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""FOXA1"",""id"":""3169""},{""label"":""GPX3"",""id"":""2878""},{""label"":""IDH2"",""id"":""3418""},{""label"":""KDM4C"",""id"":""23081""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""KMT2C"",""id"":""58508""},{""label"":""KMT2D"",""id"":""8085""},{""label"":""LZTS1"",""id"":""11178""},{""label"":""MAP3K1"",""id"":""4214""},{""label"":""MBD4"",""id"":""8930""},{""label"":""MGMT"",""id"":""4255""},{""label"":""MLH1"",""id"":""4292""},{""label"":""MSH2"",""id"":""4436""},{""label"":""PTPRT"",""id"":""11122""},{""label"":""RICTOR"",""id"":""253260""},{""label"":""RUNX1"",""id"":""861""},{""label"":""SPEN"",""id"":""23013""},{""label"":""TERT"",""id"":""7015""},{""label"":""TET2"",""id"":""54790""},{""label"":""TGFBR2"",""id"":""7048""},{""label"":""TP53"",""id"":""7157""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""11122"",""11178"",""1138"",""1139"",""1543"",""1591"",""1630"",""1948"",""2066"",""2195"",""2264"",""23013"",""23081"",""23136"",""253260"",""2878"",""3169"",""3418"",""4214"",""4255"",""4292"",""4436"",""54790"",""58508"",""672"",""675"",""7015"",""7048"",""7157"",""7373"",""7403"",""7515"",""8085"",""81037"",""811"",""861"",""8930""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3748""}]"
DOID:3753	"[""Hermansky-Pudlak syndrome""]"	"[{""label"":""AP3B1"",""id"":""8546""},{""label"":""HPS4"",""id"":""89781""},{""label"":""HPS5"",""id"":""11234""}]"	"[""11234"",""8546"",""89781""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3753""}]"
DOID:3755	"[""antithrombin III deficiency"",""AT III deficiency"",""hereditary thrombophilia due to congenital antithrombin deficiency""]"	"[{""label"":""SERPINC1"",""id"":""462""}]"	"[""462""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3755""}]"
DOID:3755	"[""antithrombin III deficiency"",""AT III deficiency"",""hereditary thrombophilia due to congenital antithrombin deficiency""]"	"[{""label"":""Serpinc1"",""id"":""11905""}]"	"[""11905""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3755""}]"
DOID:3756	"[""protein C deficiency""]"	"[{""label"":""PROC"",""id"":""5624""}]"	"[""5624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3756""}]"
DOID:3770	"[""pulmonary fibrosis"",""Fibrosis of lung""]"	"[{""label"":""AP3B1"",""id"":""8546""},{""label"":""BDKRB1"",""id"":""623""},{""label"":""CHRM3"",""id"":""1131""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MBL2"",""id"":""4153""},{""label"":""PLAU"",""id"":""5328""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SFTPA1"",""id"":""653509""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPC"",""id"":""6440""},{""label"":""TFPI"",""id"":""7035""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TNF"",""id"":""7124""}]"	"[""1131"",""3552"",""3557"",""4153"",""5054"",""5328"",""5743"",""623"",""6439"",""6440"",""653509"",""7035"",""7040"",""7124"",""8546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3770""}]"
DOID:3770	"[""pulmonary fibrosis"",""Fibrosis of lung""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Agt"",""id"":""24179""},{""label"":""Nfe2l2"",""id"":""83619""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Tgfb1"",""id"":""59086""}]"	"[""24179"",""24310"",""24617"",""59086"",""83619""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3770""}]"
DOID:3774	"[""chordoid glioma"",""Chordoid glioma of 3rd Ventricle"",""Chordoid glioma of third ventricle"",""third ventricle chordoid glioma""]"	"[{""label"":""PRKCA"",""id"":""5578""}]"	"[""5578""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3774""}]"
DOID:3783	"[""Coffin-Lowry syndrome""]"	"[{""label"":""RPS6KA3"",""id"":""6197""}]"	"[""6197""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3783""}]"
DOID:3798	"[""pleural empyema"",""Empyema of pleura"",""Empyema of pleura without fistula"",""Empyema with no fistula"",""Empyema with pleural fistula"",""Empyema without mention of fistula"",""Empyema, chest"",""Pleural empyema with fistula"",""Purulent pleurisy"",""Thorax abscess"",""abscess of pleural cavity"",""abscess of thorax"",""empyema"",""empyema with fistula"",""lung empyema"",""pleural empyema with no fistula"",""purulent pleuritis"",""pyothorax""]"	"[{""label"":""PLAU"",""id"":""5328""}]"	"[""5328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3798""}]"
DOID:3803	"[""Crigler-Najjar syndrome"",""Bilirubin UDP glucuronyl transferase deficiency"",""Crigler Najjar syndrome"",""Crigler-Najjar syndrome, type I""]"	"[{""label"":""UGT1A1"",""id"":""54658""}]"	"[""54658""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3803""}]"
DOID:3803	"[""Crigler-Najjar syndrome"",""Bilirubin UDP glucuronyl transferase deficiency"",""Crigler Najjar syndrome"",""Crigler-Najjar syndrome, type I""]"	"[{""label"":""Ugt1a1"",""id"":""24861""}]"	"[""24861""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3803""}]"
DOID:3805	"[""porokeratosis"",""disseminated superficial actinic porokeratosis""]"	"[{""label"":""FDPS"",""id"":""2224""},{""label"":""MVD"",""id"":""4597""},{""label"":""MVK"",""id"":""4598""}]"	"[""2224"",""4597"",""4598""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3805""}]"
DOID:381	"[""arthropathy"",""Ankylosis of joint of ankle and/or foot"",""Ankylosis of joint of forearm"",""Ankylosis of joint of hand"",""Ankylosis of joint of lower leg"",""Ankylosis of joint of upper arm"",""Ankylosis of multiple joints"",""Infectious arthropathy"",""Joint ankylosis of the ankle and foot"",""Joint ankylosis of the ankle and/or foot"",""Joint ankylosis of the forearm"",""Joint ankylosis of the hand"",""Joint ankylosis of the lower leg"",""Joint ankylosis of the pelvic region and thigh"",""Joint ankylosis of the shoulder region"",""Joint ankylosis of the upper arm"",""ankylosis of ankle and foot joint"",""ankylosis of forearm joint"",""ankylosis of hand joint"",""ankylosis of joint of multiple sites"",""ankylosis of joint of pelvic region and thigh"",""ankylosis of joint of shoulder region"",""ankylosis of lower leg joint"",""ankylosis of upper arm joint""]"	"[{""label"":""CCN6"",""id"":""8838""}]"	"[""8838""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:381""}]"
DOID:3827	"[""congenital diaphragmatic hernia"",""Diaphragmatic Hernia""]"	"[{""label"":""ALDH1A2"",""id"":""8854""},{""label"":""FREM1"",""id"":""158326""},{""label"":""MYRF"",""id"":""745""},{""label"":""PLS3"",""id"":""5358""}]"	"[""158326"",""5358"",""745"",""8854""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3827""}]"
DOID:3827	"[""congenital diaphragmatic hernia"",""Diaphragmatic Hernia""]"	"[{""label"":""Frem1"",""id"":""329872""},{""label"":""Gata4"",""id"":""14463""},{""label"":""Lrp1"",""id"":""16971""},{""label"":""Ndst1"",""id"":""15531""},{""label"":""Nr2f2"",""id"":""11819""},{""label"":""Pdgfra"",""id"":""18595""},{""label"":""Pls3"",""id"":""102866""},{""label"":""Slit3"",""id"":""20564""}]"	"[""102866"",""11819"",""14463"",""15531"",""16971"",""18595"",""20564"",""329872""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3827""}]"
DOID:3827	"[""congenital diaphragmatic hernia"",""Diaphragmatic Hernia""]"	"[{""label"":""Agtr2"",""id"":""24182""}]"	"[""24182""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3827""}]"
DOID:3829	"[""pituitary adenoma"",""adenoma of the Pituitary gland""]"	"[{""label"":""Cdkn1b"",""id"":""83571""}]"	"[""83571""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3829""}]"
DOID:384	"[""Wolff-Parkinson-White syndrome"",""Anomalous A-V excitation"",""Wolff-Parkinson-White pattern"",""anomalous atrioventricular excitation""]"	"[{""label"":""PRKAG2"",""id"":""51422""}]"	"[""51422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:384""}]"
DOID:384	"[""Wolff-Parkinson-White syndrome"",""Anomalous A-V excitation"",""Wolff-Parkinson-White pattern"",""anomalous atrioventricular excitation""]"	"[{""label"":""Bmpr1a"",""id"":""12166""},{""label"":""Map3k7"",""id"":""26409""}]"	"[""12166"",""26409""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:384""}]"
DOID:3875	"[""thrombophlebitis"",""Phlebitis and thrombophlebitis of superficial vessels of lower extremities"",""Superficial thrombophlebitis of leg"",""Thrombophlebitis of a superficial leg vein"",""Thrombophlebitis of superficial veins of lower extremity""]"	"[{""label"":""HLA-B"",""id"":""3106""}]"	"[""3106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3875""}]"
DOID:3883	"[""Lynch syndrome"",""HNPCC"",""Hereditary Defective Mismatch Repair syndrome"",""Hereditary non-polyposis colon cancer"",""Hereditary non-polyposis colon cancer syndrome"",""Hereditary non-polyposis colorectal cancer"",""Hereditary non-polyposis colorectal cancer syndrome"",""Hereditary nonpolyposis colon cancer"",""Hereditary nonpolyposis colon cancer syndrome"",""Hereditary nonpolyposis colorectal cancer syndrome"",""hereditary nonpolyposis colorectal cancer"",""hereditary nonpolyposis colorectal neoplasm""]"	"[{""label"":""Mlh1"",""id"":""17350""}]"	"[""17350""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3883""}]"
DOID:3883	"[""Lynch syndrome"",""HNPCC"",""Hereditary Defective Mismatch Repair syndrome"",""Hereditary non-polyposis colon cancer"",""Hereditary non-polyposis colon cancer syndrome"",""Hereditary non-polyposis colorectal cancer"",""Hereditary non-polyposis colorectal cancer syndrome"",""Hereditary nonpolyposis colon cancer"",""Hereditary nonpolyposis colon cancer syndrome"",""Hereditary nonpolyposis colorectal cancer syndrome"",""hereditary nonpolyposis colorectal cancer"",""hereditary nonpolyposis colorectal neoplasm""]"	"[{""label"":""ACVR2A"",""id"":""92""},{""label"":""E2F4"",""id"":""1874""},{""label"":""KRAS"",""id"":""3845""},{""label"":""MARCKS"",""id"":""4082""},{""label"":""MLH1"",""id"":""4292""},{""label"":""MRE11"",""id"":""4361""},{""label"":""MSH2"",""id"":""4436""},{""label"":""MSH6"",""id"":""2956""},{""label"":""PMS1"",""id"":""5378""},{""label"":""RNASEL"",""id"":""6041""},{""label"":""RNASET2"",""id"":""8635""},{""label"":""SLC22A9"",""id"":""114571""},{""label"":""SMAD4"",""id"":""4089""},{""label"":""TCF4"",""id"":""6925""},{""label"":""TGFBR1"",""id"":""7046""},{""label"":""TGFBR2"",""id"":""7048""}]"	"[""114571"",""1874"",""2956"",""3845"",""4082"",""4089"",""4292"",""4361"",""4436"",""5378"",""6041"",""6925"",""7046"",""7048"",""8635"",""92""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3883""}]"
DOID:3891	"[""placental insufficiency""]"	"[{""label"":""EPO"",""id"":""2056""}]"	"[""2056""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3891""}]"
DOID:3891	"[""placental insufficiency""]"	"[{""label"":""Emp2"",""id"":""13731""}]"	"[""13731""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3891""}]"
DOID:3892	"[""insulinoma"",""Insulin-Producing tumor of Islet cells"",""Islet cell adenoma""]"	"[{""label"":""INS"",""id"":""3630""}]"	"[""3630""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3892""}]"
DOID:3905	"[""lung carcinoma"",""cancer of lung""]"	"[{""label"":""Ctnnb1"",""id"":""84353""}]"	"[""84353""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3905""}]"
DOID:3905	"[""lung carcinoma"",""cancer of lung""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""FOXA1"",""id"":""3169""},{""label"":""SOX9"",""id"":""6662""},{""label"":""STRAP"",""id"":""11171""}]"	"[""11171"",""1136"",""1591"",""3169"",""348"",""6662""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3905""}]"
DOID:3907	"[""lung squamous cell carcinoma"",""Epidermoid cell carcinoma of the lung""]"	"[{""label"":""ATM"",""id"":""472""},{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CHRNB4"",""id"":""1143""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""CYP1B1"",""id"":""1545""},{""label"":""E2F1"",""id"":""1869""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""GPX1"",""id"":""2876""},{""label"":""IDH2"",""id"":""3418""},{""label"":""KMT2D"",""id"":""8085""},{""label"":""POLE"",""id"":""5426""},{""label"":""PTCH1"",""id"":""5727""},{""label"":""PTPN13"",""id"":""5783""},{""label"":""PTPRJ"",""id"":""5795""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SLC7A5"",""id"":""8140""},{""label"":""TERT"",""id"":""7015""}]"	"[""1138"",""1143"",""1545"",""1869"",""2264"",""2876"",""3418"",""472"",""5426"",""5727"",""5783"",""5795"",""6439"",""7015"",""8085"",""81037"",""8140""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3907""}]"
DOID:3908	"[""lung non-small cell carcinoma"",""NSCLC"",""Non-small cell lung cancer"",""non-small cell lung carcinoma""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ABCC2"",""id"":""1244""},{""label"":""ACVR1B"",""id"":""91""},{""label"":""ADAM28"",""id"":""10863""},{""label"":""ARID1A"",""id"":""8289""},{""label"":""ARID1B"",""id"":""57492""},{""label"":""ATM"",""id"":""472""},{""label"":""BAD"",""id"":""572""},{""label"":""BAG6"",""id"":""7917""},{""label"":""BRCA1"",""id"":""672""},{""label"":""CA12"",""id"":""771""},{""label"":""CA9"",""id"":""768""},{""label"":""CASP7"",""id"":""840""},{""label"":""CASP9"",""id"":""842""},{""label"":""CBL"",""id"":""867""},{""label"":""CDH13"",""id"":""1012""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CHRNA7"",""id"":""1139""},{""label"":""CHRNB4"",""id"":""1143""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""CMPK1"",""id"":""51727""},{""label"":""CSF1R"",""id"":""1436""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""DDR1"",""id"":""780""},{""label"":""DNMT1"",""id"":""1786""},{""label"":""E2F1"",""id"":""1869""},{""label"":""EGF"",""id"":""1950""},{""label"":""EGFR"",""id"":""1956""},{""label"":""EPAS1"",""id"":""2034""},{""label"":""ERBB3"",""id"":""2065""},{""label"":""ERCC5"",""id"":""2073""},{""label"":""ERCC6"",""id"":""2074""},{""label"":""ESR1"",""id"":""2099""},{""label"":""FAT1"",""id"":""2195""},{""label"":""FGFR1"",""id"":""2260""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""FH"",""id"":""2271""},{""label"":""FOXL2"",""id"":""668""},{""label"":""FRZB"",""id"":""2487""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HDAC3"",""id"":""8841""},{""label"":""HIF1A"",""id"":""3091""},{""label"":""HS3ST2"",""id"":""9956""},{""label"":""IDH2"",""id"":""3418""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL7R"",""id"":""3575""},{""label"":""JAK1"",""id"":""3716""},{""label"":""KDM2A"",""id"":""22992""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""KDR"",""id"":""3791""},{""label"":""KMT2C"",""id"":""58508""},{""label"":""KMT2D"",""id"":""8085""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""LTF"",""id"":""4057""},{""label"":""MAP2K4"",""id"":""6416""},{""label"":""MAP3K1"",""id"":""4214""},{""label"":""MSH2"",""id"":""4436""},{""label"":""MYD88"",""id"":""4615""},{""label"":""NCOA2"",""id"":""10499""},{""label"":""NFKB1"",""id"":""4790""},{""label"":""NRP1"",""id"":""8829""},{""label"":""NSD2"",""id"":""7468""},{""label"":""PBRM1"",""id"":""55193""},{""label"":""PLAU"",""id"":""5328""},{""label"":""PLCG1"",""id"":""5335""},{""label"":""POLE"",""id"":""5426""},{""label"":""PTEN"",""id"":""5728""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""PTPRB"",""id"":""5787""},{""label"":""RARB"",""id"":""5915""},{""label"":""RELA"",""id"":""5970""},{""label"":""RUNX2"",""id"":""860""},{""label"":""RUNX3"",""id"":""864""},{""label"":""SDHA"",""id"":""6389""},{""label"":""SDHC"",""id"":""6391""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""SLC3A2"",""id"":""6520""},{""label"":""SMARCA4"",""id"":""6597""},{""label"":""SPP1"",""id"":""6696""},{""label"":""TERT"",""id"":""7015""},{""label"":""TET2"",""id"":""54790""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF1A"",""id"":""7132""},{""label"":""TYMP"",""id"":""1890""},{""label"":""UGT1A1"",""id"":""54658""},{""label"":""XPO1"",""id"":""7514""},{""label"":""XPO5"",""id"":""57510""},{""label"":""XRCC1"",""id"":""7515""},{""label"":""ZFHX3"",""id"":""463""}]"	"[""1012"",""10499"",""10863"",""1136"",""1138"",""1139"",""1143"",""1244"",""1436"",""1591"",""1786"",""1869"",""1890"",""1950"",""1956"",""2034"",""2065"",""2073"",""2074"",""2099"",""2195"",""2260"",""2264"",""2271"",""22992"",""2487"",""2876"",""3091"",""3418"",""3552"",""3557"",""3575"",""3716"",""3791"",""4057"",""4214"",""4436"",""4615"",""463"",""472"",""4790"",""51727"",""5243"",""5328"",""5335"",""53353"",""5426"",""54658"",""54790"",""55193"",""572"",""5728"",""5743"",""57492"",""57510"",""5787"",""58508"",""5915"",""5970"",""6389"",""6391"",""6416"",""6439"",""6441"",""6520"",""6597"",""668"",""6696"",""672"",""7015"",""7124"",""7132"",""7403"",""7468"",""7514"",""7515"",""768"",""771"",""780"",""7917"",""8085"",""81037"",""8289"",""840"",""842"",""860"",""864"",""867"",""8829"",""8841"",""91"",""9956""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3908""}]"
DOID:3910	"[""lung adenocarcinoma"",""bronchogenic lung adenocarcinoma"",""nonsmall cell adenocarcinoma""]"	"[{""label"":""Cdh1"",""id"":""83502""}]"	"[""83502""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3910""}]"
DOID:3910	"[""lung adenocarcinoma"",""bronchogenic lung adenocarcinoma"",""nonsmall cell adenocarcinoma""]"	"[{""label"":""ADAM28"",""id"":""10863""},{""label"":""ALX4"",""id"":""60529""},{""label"":""CALR"",""id"":""811""},{""label"":""CHD4"",""id"":""1108""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CHRNB4"",""id"":""1143""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""EGF"",""id"":""1950""},{""label"":""EGFR"",""id"":""1956""},{""label"":""ERBB2"",""id"":""2064""},{""label"":""ERBB3"",""id"":""2065""},{""label"":""ERBB4"",""id"":""2066""},{""label"":""ESCO2"",""id"":""157570""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""KMT2C"",""id"":""58508""},{""label"":""KRAS"",""id"":""3845""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""MAP4K4"",""id"":""9448""},{""label"":""MIER3"",""id"":""166968""},{""label"":""MSH2"",""id"":""4436""},{""label"":""MYC"",""id"":""4609""},{""label"":""PRDM1"",""id"":""639""},{""label"":""PTCH1"",""id"":""5727""},{""label"":""PTPN13"",""id"":""5783""},{""label"":""PTPRJ"",""id"":""5795""},{""label"":""RARB"",""id"":""5915""},{""label"":""RBM10"",""id"":""8241""},{""label"":""RNF43"",""id"":""54894""},{""label"":""SETD2"",""id"":""29072""},{""label"":""SPOP"",""id"":""8405""},{""label"":""TERT"",""id"":""7015""},{""label"":""UBR5"",""id"":""51366""},{""label"":""XRCC1"",""id"":""7515""},{""label"":""ZFHX3"",""id"":""463""}]"	"[""10863"",""1108"",""1136"",""1138"",""1143"",""157570"",""1591"",""166968"",""1950"",""1956"",""2064"",""2065"",""2066"",""2264"",""29072"",""3845"",""4436"",""4609"",""463"",""51366"",""53353"",""54894"",""5727"",""5783"",""5795"",""58508"",""5915"",""60529"",""639"",""7015"",""7515"",""81037"",""811"",""8241"",""8405"",""9448""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3910""}]"
DOID:3911	"[""progeria"",""HGPS"",""Hutchinson Gilford syndrome"",""Hutchinson-Gilford Progeria syndrome"",""Hutchinson-Gilford disease""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3911""}]"
DOID:3911	"[""progeria"",""HGPS"",""Hutchinson Gilford syndrome"",""Hutchinson-Gilford Progeria syndrome"",""Hutchinson-Gilford disease""]"	"[{""label"":""Lmna"",""id"":""16905""},{""label"":""Sirt6"",""id"":""50721""},{""label"":""Vcpip1"",""id"":""70675""}]"	"[""16905"",""50721"",""70675""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3911""}]"
DOID:3963	"[""thyroid gland carcinoma"",""Thyroid carcinoma"",""head and neck cancer, Thyroid""]"	"[{""label"":""ATP6V0C"",""id"":""527""}]"	"[""527""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3963""}]"
DOID:3969	"[""papillary thyroid carcinoma"",""Papillary carcinoma of the Thyroid gland"",""Papillary carcinoma of thyroid"",""thyroid gland papillary carcinoma""]"	"[{""label"":""Braf"",""id"":""109880""}]"	"[""109880""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3969""}]"
DOID:3969	"[""papillary thyroid carcinoma"",""Papillary carcinoma of the Thyroid gland"",""Papillary carcinoma of thyroid"",""thyroid gland papillary carcinoma""]"	"[{""label"":""ATM"",""id"":""472""},{""label"":""HABP2"",""id"":""3026""},{""label"":""HRAS"",""id"":""3265""},{""label"":""KMT2D"",""id"":""8085""},{""label"":""MINPP1"",""id"":""9562""},{""label"":""NKX2-1"",""id"":""7080""},{""label"":""NRAS"",""id"":""4893""},{""label"":""SRGAP1"",""id"":""57522""},{""label"":""TP53"",""id"":""7157""},{""label"":""WDR3"",""id"":""10885""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10885"",""3026"",""3265"",""472"",""4893"",""57522"",""7080"",""7157"",""7515"",""8085"",""9562""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3969""}]"
DOID:397	"[""restrictive cardiomyopathy"",""Cardiomyopathy, constrictive"",""primary restrictive cardiomyopathy""]"	"[{""label"":""Mypn"",""id"":""68802""},{""label"":""Tnni3"",""id"":""21954""}]"	"[""21954"",""68802""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:397""}]"
DOID:397	"[""restrictive cardiomyopathy"",""Cardiomyopathy, constrictive"",""primary restrictive cardiomyopathy""]"	"[{""label"":""DES"",""id"":""1674""},{""label"":""MAP2K3"",""id"":""5606""},{""label"":""MAP2K6"",""id"":""5608""},{""label"":""TNNI3"",""id"":""7137""}]"	"[""1674"",""5606"",""5608"",""7137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:397""}]"
DOID:3981	"[""pantothenate kinase-associated neurodegeneration"",""Hallervorden-Spatz disease"",""Hallervorden-Spatz syndrome"",""NBIA1"",""Pigmentary pallidal degeneration"",""brain Iron Accumulation type I syndrome"",""neurodegeneration with brain iron accumulation 1""]"	"[{""label"":""PANK2"",""id"":""80025""}]"	"[""80025""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3981""}]"
DOID:399	"[""tuberculosis""]"	"[{""label"":""BTNL2"",""id"":""56244""},{""label"":""CCL1"",""id"":""6346""},{""label"":""CD209"",""id"":""30835""},{""label"":""CYP2B6"",""id"":""1555""},{""label"":""CYP2C19"",""id"":""1557""},{""label"":""EREG"",""id"":""2069""},{""label"":""HLA-A"",""id"":""3105""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IFNGR1"",""id"":""3459""},{""label"":""KIR3DL1"",""id"":""3811""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""NFE2L2"",""id"":""4780""},{""label"":""NRG1"",""id"":""3084""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""SPP1"",""id"":""6696""},{""label"":""TLR1"",""id"":""7096""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR6"",""id"":""10333""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""10333"",""1555"",""1557"",""2069"",""30835"",""3084"",""3105"",""3106"",""3119"",""3123"",""3458"",""3459"",""3811"",""3813"",""4780"",""56244"",""6346"",""6556"",""6696"",""7096"",""7097"",""7133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:399""}]"
DOID:3996	"[""urinary system cancer""]"	"[{""label"":""WNT2"",""id"":""7472""}]"	"[""7472""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:3996""}]"
DOID:4001	"[""ovarian carcinoma""]"	"[{""label"":""AKT2"",""id"":""208""},{""label"":""AMH"",""id"":""268""},{""label"":""CABIN1"",""id"":""23523""},{""label"":""CASP6"",""id"":""839""},{""label"":""L1CAM"",""id"":""3897""},{""label"":""MAP2K6"",""id"":""5608""},{""label"":""MMP13"",""id"":""4322""}]"	"[""208"",""23523"",""268"",""3897"",""4322"",""5608"",""839""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4001""}]"
DOID:4006	"[""bladder urothelial carcinoma"",""bladder transitional cell carcinoma"",""transitional cell carcinoma of bladder"",""urinary bladder urothelial carcinoma"",""urothelial bladder carcinoma""]"	"[{""label"":""KDM6A"",""id"":""7403""}]"	"[""7403""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4006""}]"
DOID:401	"[""multidrug-resistant tuberculosis""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:401""}]"
DOID:4029	"[""gastritis"",""Erosive Gastritis"",""Erosive gastropathy"",""acute gastric mucosal erosion""]"	"[{""label"":""ARPC1B"",""id"":""10095""},{""label"":""NOD2"",""id"":""64127""}]"	"[""10095"",""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4029""}]"
DOID:4029	"[""gastritis"",""Erosive Gastritis"",""Erosive gastropathy"",""acute gastric mucosal erosion""]"	"[{""label"":""Cblif"",""id"":""29319""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Tnf"",""id"":""24835""}]"	"[""24770"",""24835"",""29319"",""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4029""}]"
DOID:4051	"[""alveolar rhabdomyosarcoma"",""alveolar childhood rhabdomyosarcoma""]"	"[{""label"":""FOXO1"",""id"":""2308""}]"	"[""2308""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4051""}]"
DOID:4074	"[""pancreatic adenocarcinoma"",""pancreas adenocarcinoma""]"	"[{""label"":""CXCR4"",""id"":""7852""},{""label"":""E2F1"",""id"":""1869""},{""label"":""JAK1"",""id"":""3716""},{""label"":""MAP2K1"",""id"":""5604""},{""label"":""MAPK9"",""id"":""5601""},{""label"":""RAC1"",""id"":""5879""},{""label"":""RAF1"",""id"":""5894""}]"	"[""1869"",""3716"",""5601"",""5604"",""5879"",""5894"",""7852""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4074""}]"
DOID:4079	"[""heart valve disease"",""Valvular heart disease""]"	"[{""label"":""Galnt1"",""id"":""14423""},{""label"":""Tnf"",""id"":""21926""}]"	"[""14423"",""21926""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4079""}]"
DOID:4079	"[""heart valve disease"",""Valvular heart disease""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""COL1A2"",""id"":""1278""}]"	"[""1278"",""1636""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4079""}]"
DOID:4079	"[""heart valve disease"",""Valvular heart disease""]"	"[{""label"":""Htr2b"",""id"":""29581""}]"	"[""29581""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4079""}]"
DOID:409	"[""liver disease"",""disorder of liver"",""hepatic disorder""]"	"[{""label"":""ALDH2"",""id"":""217""},{""label"":""CPOX"",""id"":""1371""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""HFE"",""id"":""3077""},{""label"":""MBL2"",""id"":""4153""},{""label"":""PRKCSH"",""id"":""5589""},{""label"":""SERPINA1"",""id"":""5265""},{""label"":""THBD"",""id"":""7056""},{""label"":""TNF"",""id"":""7124""}]"	"[""1371"",""1571"",""217"",""3077"",""4153"",""5265"",""5589"",""7056"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:409""}]"
DOID:4154	"[""dentinogenesis imperfecta""]"	"[{""label"":""Dspp"",""id"":""666279""}]"	"[""666279""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4154""}]"
DOID:4154	"[""dentinogenesis imperfecta""]"	"[{""label"":""COL1A1"",""id"":""1277""},{""label"":""DSPP"",""id"":""1834""}]"	"[""1277"",""1834""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4154""}]"
DOID:4159	"[""skin cancer"",""CA - skin cancer"",""malignant neoplasm of skin"",""melanoma and Non-melanoma skin cancer""]"	"[{""label"":""Snai1"",""id"":""20613""}]"	"[""20613""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4159""}]"
DOID:4166	"[""syphilis"",""syphilitic chancre""]"	"[{""label"":""KIR3DS1"",""id"":""3813""}]"	"[""3813""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4166""}]"
DOID:417	"[""autoimmune disease"",""autoimmune hypersensitivity disease"",""hypersensitivity reaction type II disease""]"	"[{""label"":""Cd200"",""id"":""17470""},{""label"":""Gpr132"",""id"":""56696""}]"	"[""17470"",""56696""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:417""}]"
DOID:417	"[""autoimmune disease"",""autoimmune hypersensitivity disease"",""hypersensitivity reaction type II disease""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IDH1"",""id"":""3417""},{""label"":""NOD2"",""id"":""64127""},{""label"":""PARP1"",""id"":""142""},{""label"":""SIAE"",""id"":""54414""}]"	"[""142"",""3117"",""3119"",""3123"",""3417"",""54414"",""64127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:417""}]"
DOID:418	"[""systemic scleroderma"",""Scleroderma"",""Scleroderma syndrome"",""progressive systemic sclerosis"",""systemic sclerosis""]"	"[{""label"":""Col3a1"",""id"":""12825""},{""label"":""Fbn1"",""id"":""14118""},{""label"":""Fosl2"",""id"":""14284""},{""label"":""Tgfbr1"",""id"":""21812""}]"	"[""12825"",""14118"",""14284"",""21812""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:418""}]"
DOID:418	"[""systemic scleroderma"",""Scleroderma"",""Scleroderma syndrome"",""progressive systemic sclerosis"",""systemic sclerosis""]"	"[{""label"":""ANXA5"",""id"":""308""},{""label"":""CD86"",""id"":""942""},{""label"":""ELN"",""id"":""2006""},{""label"":""ESR1"",""id"":""2099""},{""label"":""FBN1"",""id"":""2200""},{""label"":""HGF"",""id"":""3082""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL1R1"",""id"":""3554""},{""label"":""IL23R"",""id"":""149233""},{""label"":""LTA"",""id"":""4049""},{""label"":""MMP3"",""id"":""4314""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NAT2"",""id"":""10""},{""label"":""NOTCH4"",""id"":""4855""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""STAT4"",""id"":""6775""}]"	"[""10"",""149233"",""2006"",""2099"",""2200"",""308"",""3082"",""3117"",""3458"",""3554"",""4049"",""4314"",""4318"",""4855"",""6556"",""6775"",""942""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:418""}]"
DOID:4183	"[""pseudopseudohypoparathyroidism"",""Normocalcemic pseudohypoparathyroidism"",""PPHP""]"	"[{""label"":""Gnas"",""id"":""14683""}]"	"[""14683""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4183""}]"
DOID:4183	"[""pseudopseudohypoparathyroidism"",""Normocalcemic pseudohypoparathyroidism"",""PPHP""]"	"[{""label"":""GNAS"",""id"":""2778""}]"	"[""2778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4183""}]"
DOID:4184	"[""pseudohypoparathyroidism"",""PHP""]"	"[{""label"":""Gnas"",""id"":""14683""}]"	"[""14683""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4184""}]"
DOID:4184	"[""pseudohypoparathyroidism"",""PHP""]"	"[{""label"":""GNAS"",""id"":""2778""}]"	"[""2778""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4184""}]"
DOID:4186	"[""articulation disorder"",""Articulation impairment"",""Phonological disorder""]"	"[{""label"":""CNTNAP2"",""id"":""26047""},{""label"":""FOXP2"",""id"":""93986""}]"	"[""26047"",""93986""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4186""}]"
DOID:4189	"[""mutism""]"	"[{""label"":""CNTNAP2"",""id"":""26047""}]"	"[""26047""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4189""}]"
DOID:419	"[""scleroderma"",""dermatosclerosis""]"	"[{""label"":""HLA-A"",""id"":""3105""}]"	"[""3105""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:419""}]"
DOID:4194	"[""glucose metabolism disease"",""disorder of glucose metabolism""]"	"[{""label"":""InR"",""id"":""42549""},{""label"":""Tl"",""id"":""43222""}]"	"[""42549"",""43222""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4194""}]"
DOID:4195	"[""hyperglycemia""]"	"[{""label"":""GLK1"",""id"":""850317""}]"	"[""850317""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4195""}]"
DOID:4195	"[""hyperglycemia""]"	"[{""label"":""CCL11"",""id"":""6356""},{""label"":""CYP2C9"",""id"":""1559""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HP"",""id"":""3240""},{""label"":""IL6"",""id"":""3569""},{""label"":""PDX1"",""id"":""3651""},{""label"":""PON1"",""id"":""5444""},{""label"":""SOD1"",""id"":""6647""},{""label"":""TF"",""id"":""7018""}]"	"[""1559"",""2876"",""3240"",""3569"",""3651"",""5444"",""6356"",""6647"",""7018""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4195""}]"
DOID:4195	"[""hyperglycemia""]"	"[{""label"":""Avp"",""id"":""24221""},{""label"":""Glp1r"",""id"":""25051""},{""label"":""Hrh3"",""id"":""85268""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Pcsk1"",""id"":""25204""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Prkcb"",""id"":""25023""},{""label"":""Prkcz"",""id"":""25522""},{""label"":""Prnp"",""id"":""24686""}]"	"[""24221"",""24536"",""24686"",""25023"",""25051"",""25204"",""25522"",""29595"",""83516"",""85268""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4195""}]"
DOID:422	"[""congenital structural myopathy""]"	"[{""label"":""MTM1"",""id"":""4534""}]"	"[""4534""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:422""}]"
DOID:423	"[""myopathy""]"	"[{""label"":""Col4a1"",""id"":""33727""},{""label"":""Hmgcr"",""id"":""42803""},{""label"":""drpr"",""id"":""38218""}]"	"[""33727"",""38218"",""42803""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:423""}]"
DOID:423	"[""myopathy""]"	"[{""label"":""Dnm2"",""id"":""13430""}]"	"[""13430""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:423""}]"
DOID:4231	"[""histiocytoma""]"	"[{""label"":""Klrk1"",""id"":""24934""}]"	"[""24934""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4231""}]"
DOID:4239	"[""alveolar soft part sarcoma""]"	"[{""label"":""ASPSCR1"",""id"":""79058""}]"	"[""79058""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4239""}]"
DOID:4247	"[""coronary restenosis""]"	"[{""label"":""BCHE"",""id"":""590""},{""label"":""ITGB2"",""id"":""3689""},{""label"":""MBL2"",""id"":""4153""},{""label"":""SPP1"",""id"":""6696""},{""label"":""TNF"",""id"":""7124""},{""label"":""TP53"",""id"":""7157""},{""label"":""UCP3"",""id"":""7352""}]"	"[""3689"",""4153"",""590"",""6696"",""7124"",""7157"",""7352""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4247""}]"
DOID:4247	"[""coronary restenosis""]"	"[{""label"":""Myc"",""id"":""24577""}]"	"[""24577""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4247""}]"
DOID:4248	"[""coronary stenosis"",""Coronary artery stenosis""]"	"[{""label"":""CYP2R1"",""id"":""120227""},{""label"":""EDN1"",""id"":""1906""},{""label"":""PECAM1"",""id"":""5175""}]"	"[""120227"",""1906"",""5175""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4248""}]"
DOID:4249	"[""Gerstmann-Straussler-Scheinker syndrome"",""Gerstmann-Straussler-Scheinker disease"",""PRION DEMENTIA""]"	"[{""label"":""Prnp"",""id"":""19122""}]"	"[""19122""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4249""}]"
DOID:4249	"[""Gerstmann-Straussler-Scheinker syndrome"",""Gerstmann-Straussler-Scheinker disease"",""PRION DEMENTIA""]"	"[{""label"":""PRNP"",""id"":""5621""}]"	"[""5621""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4249""}]"
DOID:4252	"[""Alexander disease"",""Alexander's disease""]"	"[{""label"":""Gfap"",""id"":""14580""}]"	"[""14580""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4252""}]"
DOID:4252	"[""Alexander disease"",""Alexander's disease""]"	"[{""label"":""GFAP"",""id"":""2670""}]"	"[""2670""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4252""}]"
DOID:4253	"[""melorheostosis""]"	"[{""label"":""MAP2K1"",""id"":""5604""}]"	"[""5604""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4253""}]"
DOID:4257	"[""Caffey disease"",""cortical congenital hyperostosis"",""infantile cortical hyperostosis""]"	"[{""label"":""COL1A1"",""id"":""1277""}]"	"[""1277""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4257""}]"
DOID:4258	"[""Weissenbacher-Zweymuller syndrome"",""Piere-Robin syndrome"",""Pierre Robin Malformation""]"	"[{""label"":""Acvr2a"",""id"":""11480""},{""label"":""Tfrc"",""id"":""22042""}]"	"[""11480"",""22042""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4258""}]"
DOID:4297	"[""scimitar syndrome"",""Halasz syndrome"",""congenital venolobar syndrome"",""hypogenetic lung syndrome"",""mirror-image lung syndrome"",""pulmonary venolobar syndrome"",""total anomalous pulmonary venous return"",""vena cava bronchovascular syndrome""]"	"[{""label"":""Pdgfra"",""id"":""18595""}]"	"[""18595""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4297""}]"
DOID:4306	"[""radiculopathy"",""pinched nerve""]"	"[{""label"":""Spp1"",""id"":""25353""}]"	"[""25353""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4306""}]"
DOID:431	"[""myofascial pain syndrome""]"	"[{""label"":""Ntrk1"",""id"":""59109""}]"	"[""59109""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:431""}]"
DOID:4330	"[""non-Langerhans-cell histiocytosis""]"	"[{""label"":""PRF1"",""id"":""5551""}]"	"[""5551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4330""}]"
DOID:4362	"[""cervical cancer"",""cervical neoplasm"",""cervix cancer"",""cervix uteri cancer"",""neoplasm of uterine cervix"",""tumor of the Cervix Uteri"",""uterine cervical neoplasm""]"	"[{""label"":""APEX1"",""id"":""328""},{""label"":""BRCA1"",""id"":""672""},{""label"":""CDC25A"",""id"":""993""},{""label"":""CDH13"",""id"":""1012""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""KDM3A"",""id"":""55818""},{""label"":""KMT2A"",""id"":""4297""},{""label"":""KMT2E"",""id"":""55904""},{""label"":""MAP2K3"",""id"":""5606""},{""label"":""MAP2K6"",""id"":""5608""},{""label"":""MMP1"",""id"":""4312""},{""label"":""SF3B4"",""id"":""10262""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF10A"",""id"":""8797""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1012"",""10262"",""3106"",""3115"",""3119"",""328"",""4297"",""4312"",""55818"",""55904"",""5606"",""5608"",""672"",""6890"",""7124"",""7515"",""8797"",""993""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4362""}]"
DOID:4367	"[""apparent mineralocorticoid excess syndrome"",""11-beta-hydroxysteroid dehydrogenase deficiency type 2"",""Ulick syndrome"",""cortisol 11-beta-ketoreductase deficiency"",""syndrome of apparent mineralocorticoid excess""]"	"[{""label"":""HSD11B2"",""id"":""3291""}]"	"[""3291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4367""}]"
DOID:437	"[""myasthenia gravis""]"	"[{""label"":""ACHE"",""id"":""43""},{""label"":""ADRB2"",""id"":""154""},{""label"":""CHRM1"",""id"":""1128""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL2RB"",""id"":""3560""}]"	"[""1128"",""154"",""3117"",""3119"",""3123"",""3560"",""43""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:437""}]"
DOID:4371	"[""Schnitzler syndrome""]"	"[{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""}]"	"[""3552"",""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4371""}]"
DOID:4372	"[""intracranial embolism"",""Cerebral embolism with cerebral infarction"",""cerebral embolism""]"	"[{""label"":""KL"",""id"":""9365""}]"	"[""9365""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4372""}]"
DOID:4376	"[""milk allergy"",""milk allergic reaction""]"	"[{""label"":""IL13"",""id"":""3596""}]"	"[""3596""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4376""}]"
DOID:4377	"[""egg allergy"",""Allergy to eggs""]"	"[{""label"":""IL13"",""id"":""3596""}]"	"[""3596""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4377""}]"
DOID:4378	"[""peanut allergy"",""allergy to peanuts"",""peanut allergic reaction""]"	"[{""label"":""IL13"",""id"":""3596""}]"	"[""3596""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4378""}]"
DOID:438	"[""autoimmune disease of the nervous system""]"	"[{""label"":""ALDOC"",""id"":""230""},{""label"":""ANXA5"",""id"":""308""}]"	"[""230"",""308""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:438""}]"
DOID:4398	"[""pustulosis of palm and sole"",""Acropustulosis"",""Palmoplantar Pustulosis"",""Pustular psoriasis of the palms and/or soles""]"	"[{""label"":""LTA"",""id"":""4049""},{""label"":""TNF"",""id"":""7124""}]"	"[""4049"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4398""}]"
DOID:440	"[""neuromuscular disease""]"	"[{""label"":""GPI"",""id"":""2821""}]"	"[""2821""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:440""}]"
DOID:4404	"[""occupational dermatitis"",""Occupational allergic contact dermatitis"",""Occupational eczema""]"	"[{""label"":""NAT2"",""id"":""10""}]"	"[""10""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4404""}]"
DOID:4423	"[""sea-blue histiocytosis"",""Sea-blue histiocyte syndrome""]"	"[{""label"":""APOE"",""id"":""348""}]"	"[""348""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4423""}]"
DOID:4428	"[""dyslexia""]"	"[{""label"":""DNAAF4"",""id"":""161582""},{""label"":""DRD4"",""id"":""1815""},{""label"":""FOXP2"",""id"":""93986""}]"	"[""161582"",""1815"",""93986""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4428""}]"
DOID:4440	"[""seminoma"",""Seminoma, Pure""]"	"[{""label"":""PHO8"",""id"":""852092""}]"	"[""852092""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4440""}]"
DOID:4440	"[""seminoma"",""Seminoma, Pure""]"	"[{""label"":""HRAS"",""id"":""3265""},{""label"":""KIT"",""id"":""3815""},{""label"":""KRAS"",""id"":""3845""},{""label"":""POU5F1"",""id"":""5460""},{""label"":""SMAD4"",""id"":""4089""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""3265"",""3815"",""3845"",""4089"",""5460"",""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4440""}]"
DOID:4441	"[""dysgerminoma""]"	"[{""label"":""FGFR2"",""id"":""2263""},{""label"":""KIT"",""id"":""3815""}]"	"[""2263"",""3815""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4441""}]"
DOID:4448	"[""macular degeneration"",""Macular degeneration of retina""]"	"[{""label"":""ABCA4"",""id"":""24""},{""label"":""APOE"",""id"":""348""},{""label"":""C2"",""id"":""717""},{""label"":""C3"",""id"":""718""},{""label"":""CFB"",""id"":""629""},{""label"":""CFH"",""id"":""3075""},{""label"":""CFI"",""id"":""3426""},{""label"":""ESR1"",""id"":""2099""},{""label"":""IL17A"",""id"":""3605""},{""label"":""KDR"",""id"":""3791""},{""label"":""MMP2"",""id"":""4313""},{""label"":""NFE2L2"",""id"":""4780""},{""label"":""PON1"",""id"":""5444""},{""label"":""PPARGC1A"",""id"":""10891""},{""label"":""PRPH2"",""id"":""5961""},{""label"":""SERPING1"",""id"":""710""},{""label"":""TLR4"",""id"":""7099""}]"	"[""10891"",""2099"",""24"",""3075"",""3426"",""348"",""3605"",""3791"",""4313"",""4780"",""5444"",""5961"",""629"",""7099"",""710"",""717"",""718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4448""}]"
DOID:4449	"[""macular retinal edema"",""macular edema"",""macular oedema"",""macular retinal oedema""]"	"[{""label"":""NOS3"",""id"":""4846""},{""label"":""SERPINF1"",""id"":""5176""}]"	"[""4846"",""5176""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4449""}]"
DOID:445	"[""Bartter disease"",""Aldosteronism with hyperplasia of the adrenal cortex"",""Bartter's syndrome""]"	"[{""label"":""Clcnkb"",""id"":""56365""}]"	"[""56365""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:445""}]"
DOID:445	"[""Bartter disease"",""Aldosteronism with hyperplasia of the adrenal cortex"",""Bartter's syndrome""]"	"[{""label"":""SLC12A1"",""id"":""6557""}]"	"[""6557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:445""}]"
DOID:4450	"[""renal cell carcinoma"",""RCC"",""adenocarcinoma of kidney"",""hypernephroma""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ABCG2"",""id"":""9429""},{""label"":""AKT3"",""id"":""10000""},{""label"":""APC"",""id"":""324""},{""label"":""ARNT"",""id"":""405""},{""label"":""C4A"",""id"":""720""},{""label"":""C4B"",""id"":""721""},{""label"":""CA9"",""id"":""768""},{""label"":""CDH1"",""id"":""999""},{""label"":""COMT"",""id"":""1312""},{""label"":""CSF1R"",""id"":""1436""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""ERBB2"",""id"":""2064""},{""label"":""FAS"",""id"":""355""},{""label"":""FLCN"",""id"":""201163""},{""label"":""FTO"",""id"":""79068""},{""label"":""HAVCR2"",""id"":""84868""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""HOXB13"",""id"":""10481""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL4R"",""id"":""3566""},{""label"":""JUP"",""id"":""3728""},{""label"":""KDM4C"",""id"":""23081""},{""label"":""KIT"",""id"":""3815""},{""label"":""LTF"",""id"":""4057""},{""label"":""MAP2K1"",""id"":""5604""},{""label"":""MET"",""id"":""4233""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""OGG1"",""id"":""4968""},{""label"":""PAK1"",""id"":""5058""},{""label"":""PBRM1"",""id"":""55193""},{""label"":""PDGFRB"",""id"":""5159""},{""label"":""RELA"",""id"":""5970""},{""label"":""SLC49A4"",""id"":""84925""},{""label"":""STAT3"",""id"":""6774""},{""label"":""TFE3"",""id"":""7030""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""THRA"",""id"":""7067""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF10A"",""id"":""8797""},{""label"":""WIF1"",""id"":""11197""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10000"",""10481"",""11197"",""1312"",""1436"",""1493"",""1543"",""201163"",""2064"",""23081"",""2908"",""3123"",""324"",""355"",""3557"",""3558"",""3566"",""3728"",""3815"",""405"",""4057"",""4233"",""4312"",""4314"",""4968"",""5058"",""5159"",""5243"",""55193"",""5604"",""5970"",""6774"",""6927"",""7030"",""7040"",""7067"",""7124"",""720"",""721"",""7515"",""768"",""79068"",""84868"",""84925"",""8797"",""9429"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4450""}]"
DOID:446	"[""primary hyperaldosteronism"",""Cushing syndrome"",""Cushing's syndrome"",""hyperaldosteronism""]"	"[{""label"":""Clcn2"",""id"":""12724""},{""label"":""Drd2"",""id"":""13489""},{""label"":""Nr3c1"",""id"":""14815""}]"	"[""12724"",""13489"",""14815""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:446""}]"
DOID:446	"[""primary hyperaldosteronism"",""Cushing syndrome"",""Cushing's syndrome"",""hyperaldosteronism""]"	"[{""label"":""CACNA1H"",""id"":""8912""},{""label"":""CLCN2"",""id"":""1181""},{""label"":""CYP11B1"",""id"":""1584""},{""label"":""CYP11B2"",""id"":""1585""},{""label"":""KCNJ5"",""id"":""3762""}]"	"[""1181"",""1584"",""1585"",""3762"",""8912""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:446""}]"
DOID:4465	"[""papillary renal cell carcinoma"",""Chromophil carcinoma of kidney"",""papillary kidney carcinoma"",""sporadic papillary renal cell carcinoma""]"	"[{""label"":""MET"",""id"":""4233""},{""label"":""PRCC"",""id"":""5546""}]"	"[""4233"",""5546""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4465""}]"
DOID:4467	"[""clear cell renal cell carcinoma"",""Clear cell carcinoma of kidney"",""clear cell kidney carcinoma"",""conventional (Clear cell) renal cell carcinoma"",""conventional renal cell carcinoma"",""renal clear cell carcinoma""]"	"[{""label"":""FTO"",""id"":""79068""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""PDGFB"",""id"":""5155""},{""label"":""SETD2"",""id"":""29072""}]"	"[""29072"",""3480"",""5155"",""79068""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4467""}]"
DOID:4479	"[""pseudohypoaldosteronism""]"	"[{""label"":""CUL3"",""id"":""8452""},{""label"":""NR3C2"",""id"":""4306""},{""label"":""SCNN1A"",""id"":""6337""},{""label"":""SCNN1B"",""id"":""6338""},{""label"":""SCNN1G"",""id"":""6340""},{""label"":""WNK1"",""id"":""65125""}]"	"[""4306"",""6337"",""6338"",""6340"",""65125"",""8452""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4479""}]"
DOID:4479	"[""pseudohypoaldosteronism""]"	"[{""label"":""Wnk4"",""id"":""69847""}]"	"[""69847""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4479""}]"
DOID:4480	"[""achondroplasia"",""Achondroplastic physique"",""Chondrodystrophia"",""osteosclerosis congenita""]"	"[{""label"":""Acan"",""id"":""11595""},{""label"":""Npr2"",""id"":""230103""}]"	"[""11595"",""230103""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4480""}]"
DOID:4480	"[""achondroplasia"",""Achondroplastic physique"",""Chondrodystrophia"",""osteosclerosis congenita""]"	"[{""label"":""FGFR3"",""id"":""2261""}]"	"[""2261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4480""}]"
DOID:4481	"[""allergic rhinitis"",""Non-seasonal allergic rhinitis"",""Perenial allergic rhinitis"",""atopic rhinitis"",""hay fever"",""pollenosis"",""seasonal allergic rhinitis""]"	"[{""label"":""Ccl11"",""id"":""29397""},{""label"":""Ifng"",""id"":""25712""}]"	"[""25712"",""29397""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4481""}]"
DOID:4481	"[""allergic rhinitis"",""Non-seasonal allergic rhinitis"",""Perenial allergic rhinitis"",""atopic rhinitis"",""hay fever"",""pollenosis"",""seasonal allergic rhinitis""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL17A"",""id"":""3605""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""}]"	"[""2214"",""3596"",""3605"",""5243"",""7097"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4481""}]"
DOID:4483	"[""rhinitis""]"	"[{""label"":""ADAM33"",""id"":""80332""},{""label"":""BDKRB2"",""id"":""624""},{""label"":""BDNF"",""id"":""627""},{""label"":""CCL24"",""id"":""6369""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CCR3"",""id"":""1232""},{""label"":""CD14"",""id"":""929""},{""label"":""CYSLTR1"",""id"":""10800""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL17A"",""id"":""3605""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL4R"",""id"":""3566""},{""label"":""LEP"",""id"":""3952""},{""label"":""MBL2"",""id"":""4153""},{""label"":""NOD2"",""id"":""64127""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR6"",""id"":""10333""},{""label"":""TNF"",""id"":""7124""}]"	"[""10333"",""10800"",""1232"",""149233"",""3117"",""3119"",""3557"",""3558"",""3566"",""3596"",""3605"",""3952"",""4153"",""5054"",""624"",""627"",""6369"",""64127"",""6441"",""6890"",""7097"",""7124"",""729230"",""80332"",""929""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4483""}]"
DOID:4492	"[""avian influenza"",""avian flu"",""bird flu""]"	"[{""label"":""ACE2"",""id"":""59272""},{""label"":""PTGS2"",""id"":""5743""}]"	"[""5743"",""59272""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4492""}]"
DOID:4511	"[""breast angiosarcoma"",""hemangiosarcoma of the breast""]"	"[{""label"":""KDR"",""id"":""3791""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PTPRB"",""id"":""5787""}]"	"[""3791"",""5290"",""5787""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4511""}]"
DOID:4531	"[""mucoepidermoid carcinoma"",""MEC""]"	"[{""label"":""CDH1"",""id"":""999""}]"	"[""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4531""}]"
DOID:4535	"[""hypotrichosis""]"	"[{""label"":""Dsg4"",""id"":""291754""}]"	"[""291754""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4535""}]"
DOID:4535	"[""hypotrichosis""]"	"[{""label"":""DSG4"",""id"":""147409""}]"	"[""147409""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4535""}]"
DOID:4543	"[""retrograde amnesia""]"	"[{""label"":""Ptgs2"",""id"":""29527""}]"	"[""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4543""}]"
DOID:4549	"[""extraskeletal myxoid chondrosarcoma"",""Myxoid extraosseous chondrosarcoma"",""extraosseous chondrosarcoma""]"	"[{""label"":""NR4A3"",""id"":""8013""}]"	"[""8013""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4549""}]"
DOID:4552	"[""large cell carcinoma""]"	"[{""label"":""MET"",""id"":""4233""},{""label"":""PRKCA"",""id"":""5578""},{""label"":""STRAP"",""id"":""11171""}]"	"[""11171"",""4233"",""5578""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4552""}]"
DOID:4586	"[""familial meningioma""]"	"[{""label"":""MN1"",""id"":""4330""},{""label"":""PDGFB"",""id"":""5155""},{""label"":""PTEN"",""id"":""5728""},{""label"":""SMARCE1"",""id"":""6605""}]"	"[""4330"",""5155"",""5728"",""6605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4586""}]"
DOID:4603	"[""epidermolytic hyperkeratosis"",""Bullous ichthyosiform erythroderma"",""Epidermolytic palmoplantar hyperkeratosis"",""epidermolytic ichthyosis""]"	"[{""label"":""Jup"",""id"":""16480""},{""label"":""Krt1"",""id"":""16678""}]"	"[""16480"",""16678""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4603""}]"
DOID:4603	"[""epidermolytic hyperkeratosis"",""Bullous ichthyosiform erythroderma"",""Epidermolytic palmoplantar hyperkeratosis"",""epidermolytic ichthyosis""]"	"[{""label"":""KRT10"",""id"":""3858""},{""label"":""KRT1"",""id"":""3848""}]"	"[""3848"",""3858""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4603""}]"
DOID:4606	"[""bile duct cancer"",""Ca extrahepatic bile ducts"",""bile duct tumor"",""malignant neoplasm of the extrahepatic bile duct""]"	"[{""label"":""APOB"",""id"":""338""},{""label"":""APOE"",""id"":""348""}]"	"[""338"",""348""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4606""}]"
DOID:4607	"[""biliary tract cancer"",""malignant tumour of biliary tract""]"	"[{""label"":""CYP1A1"",""id"":""1543""}]"	"[""1543""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4607""}]"
DOID:4621	"[""holoprosencephaly"",""Holoprosencephaly sequence""]"	"[{""label"":""Pgap1"",""id"":""241062""}]"	"[""241062""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4621""}]"
DOID:4621	"[""holoprosencephaly"",""Holoprosencephaly sequence""]"	"[{""label"":""PLCH1"",""id"":""23007""},{""label"":""PTCH1"",""id"":""5727""},{""label"":""SHH"",""id"":""6469""},{""label"":""TGIF1"",""id"":""7050""}]"	"[""23007"",""5727"",""6469"",""7050""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4621""}]"
DOID:4644	"[""epidermolysis bullosa simplex""]"	"[{""label"":""CD151"",""id"":""977""},{""label"":""DST"",""id"":""667""},{""label"":""KRT5"",""id"":""3852""},{""label"":""PLEC"",""id"":""5339""}]"	"[""3852"",""5339"",""667"",""977""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4644""}]"
DOID:4648	"[""familial retinoblastoma"",""Hereditary Retinoblastoma""]"	"[{""label"":""RB1"",""id"":""5925""}]"	"[""5925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4648""}]"
DOID:4661	"[""multiple chemical sensitivity"",""20th century disease"",""chemical AIDS"",""environmental illness"",""idiopathic environmental illness"",""total allergy syndrome""]"	"[{""label"":""CYP2C19"",""id"":""1557""}]"	"[""1557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4661""}]"
DOID:4667	"[""kyphosis"",""Kyphosis deformity of spine""]"	"[{""label"":""ELP1"",""id"":""8518""}]"	"[""8518""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4667""}]"
DOID:4674	"[""androgen insensitivity syndrome"",""Androgen resistance syndrome"",""Androgen-Insensitivity Syndrome"",""Feminisation - testicular"",""Goldberg - Maxwell syndrome"",""Goldberg-Maxwell syndrome"",""testicular Feminization syndrome"",""testicular feminization""]"	"[{""label"":""AR"",""id"":""367""}]"	"[""367""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4674""}]"
DOID:4676	"[""uremia"",""UREMIA OF renal ORIGIN""]"	"[{""label"":""Angpt2"",""id"":""89805""}]"	"[""89805""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4676""}]"
DOID:4676	"[""uremia"",""UREMIA OF renal ORIGIN""]"	"[{""label"":""COMT"",""id"":""1312""}]"	"[""1312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4676""}]"
DOID:4677	"[""keratitis""]"	"[{""label"":""IL6"",""id"":""3569""},{""label"":""TLR4"",""id"":""7099""}]"	"[""3569"",""7099""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4677""}]"
DOID:4680	"[""breast metaplastic carcinoma"",""Metaplastic carcinoma of the breast""]"	"[{""label"":""Ccn6"",""id"":""327743""}]"	"[""327743""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4680""}]"
DOID:4724	"[""brain edema"",""intracranial swelling"",""wet brain""]"	"[{""label"":""Abcc8"",""id"":""25559""},{""label"":""Avpr1a"",""id"":""25107""},{""label"":""Vegfa"",""id"":""83785""}]"	"[""25107"",""25559"",""83785""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4724""}]"
DOID:4724	"[""brain edema"",""intracranial swelling"",""wet brain""]"	"[{""label"":""SERPINF1"",""id"":""5176""}]"	"[""5176""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4724""}]"
DOID:4751	"[""striatonigral degeneration""]"	"[{""label"":""NUP62"",""id"":""23636""}]"	"[""23636""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4751""}]"
DOID:4752	"[""multiple system atrophy"",""Shy-Drager syndrome""]"	"[{""label"":""KLK6"",""id"":""5653""}]"	"[""5653""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4752""}]"
DOID:4769	"[""pleuropulmonary blastoma""]"	"[{""label"":""Fgf9"",""id"":""14180""}]"	"[""14180""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4769""}]"
DOID:4769	"[""pleuropulmonary blastoma""]"	"[{""label"":""DICER1"",""id"":""23405""}]"	"[""23405""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4769""}]"
DOID:4780	"[""anti-basement membrane glomerulonephritis"",""anti-GBM glomerulonephritis""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""1493"",""2214"",""3115"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4780""}]"
DOID:4780	"[""anti-basement membrane glomerulonephritis"",""anti-GBM glomerulonephritis""]"	"[{""label"":""Ccl2"",""id"":""24770""},{""label"":""Cd40lg"",""id"":""84349""},{""label"":""Il10"",""id"":""25325""},{""label"":""Il1rn"",""id"":""60582""},{""label"":""Il4"",""id"":""287287""},{""label"":""Selp"",""id"":""25651""}]"	"[""24770"",""25325"",""25651"",""287287"",""60582"",""84349""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4780""}]"
DOID:4783	"[""mesangial proliferative glomerulonephritis""]"	"[{""label"":""Pdgfd"",""id"":""66018""}]"	"[""66018""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4783""}]"
DOID:479	"[""angiokeratoma"",""Angiokeratoma of skin"",""Cutaneous Angiokeratoma"",""skin angiokeratoma""]"	"[{""label"":""NAGA"",""id"":""4668""}]"	"[""4668""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:479""}]"
DOID:4795	"[""GM2 gangliosidosis, AB variant"",""GM2 Activator Deficiency"",""Tay-Sachs disease AB variant"",""Tay-Sachs disease, variant AB""]"	"[{""label"":""GM2A"",""id"":""2760""}]"	"[""2760""]"	Homo sapiens (human)	"[{""label"":""Glyco-Disease Genes Database"",""id"":""acgg.asia/db/diseases/gdgdb?con_ui=CON00062""},{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4795""}]"
DOID:4795	"[""GM2 gangliosidosis, AB variant"",""GM2 Activator Deficiency"",""Tay-Sachs disease AB variant"",""Tay-Sachs disease, variant AB""]"	"[{""label"":""Gm2a"",""id"":""14667""}]"	"[""14667""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4795""}]"
DOID:4797	"[""SM-AHNMD"",""systemic mastocytosis with associated clonal haematological non-mast cell lineage disease"",""systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease""]"	"[{""label"":""ASXL1"",""id"":""171023""}]"	"[""171023""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4797""}]"
DOID:480	"[""movement disease""]"	"[{""label"":""Efnb3"",""id"":""13643""}]"	"[""13643""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:480""}]"
DOID:480	"[""movement disease""]"	"[{""label"":""DRD2"",""id"":""1813""}]"	"[""1813""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:480""}]"
DOID:4810	"[""cerebrotendinous xanthomatosis"",""Cholestanol storage disease""]"	"[{""label"":""CYP27A1"",""id"":""1593""}]"	"[""1593""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4810""}]"
DOID:4890	"[""juvenile myoclonic epilepsy""]"	"[{""label"":""BRD2"",""id"":""6046""}]"	"[""6046""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4890""}]"
DOID:4905	"[""pancreatic carcinoma"",""Exocrine pancreas carcinoma"",""carcinoma of pancreas""]"	"[{""label"":""Kras"",""id"":""16653""},{""label"":""Myc"",""id"":""17869""}]"	"[""16653"",""17869""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4905""}]"
DOID:4905	"[""pancreatic carcinoma"",""Exocrine pancreas carcinoma"",""carcinoma of pancreas""]"	"[{""label"":""KDR"",""id"":""3791""}]"	"[""3791""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4905""}]"
DOID:4906	"[""small intestine adenocarcinoma"",""small intestinal adenocarcinoma""]"	"[{""label"":""MAP2K1"",""id"":""5604""},{""label"":""MAP2K2"",""id"":""5605""}]"	"[""5604"",""5605""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4906""}]"
DOID:4914	"[""esophagus adenocarcinoma"",""Oesophageal adenocarcinoma""]"	"[{""label"":""Smo"",""id"":""25273""},{""label"":""Sod2"",""id"":""24787""}]"	"[""24787"",""25273""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4914""}]"
DOID:4914	"[""esophagus adenocarcinoma"",""Oesophageal adenocarcinoma""]"	"[{""label"":""ABL1"",""id"":""25""},{""label"":""CYP19A1"",""id"":""1588""},{""label"":""FOXP1"",""id"":""27086""},{""label"":""GHRL"",""id"":""51738""},{""label"":""GPX3"",""id"":""2878""},{""label"":""GRB7"",""id"":""2886""},{""label"":""KDR"",""id"":""3791""},{""label"":""MMP12"",""id"":""4321""},{""label"":""MMP14"",""id"":""4323""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""NOS3"",""id"":""4846""},{""label"":""TNFRSF10A"",""id"":""8797""}]"	"[""1588"",""25"",""27086"",""2878"",""2886"",""3791"",""4312"",""4314"",""4321"",""4323"",""4846"",""51738"",""8797""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4914""}]"
DOID:4926	"[""bronchiolo-alveolar adenocarcinoma"",""Bronchioalveolar lung carcinoma"",""Bronchioloalveolar carcinoma"",""Minimally Invasive Lung Adenocarcinoma""]"	"[{""label"":""ALX4"",""id"":""60529""},{""label"":""EGFR"",""id"":""1956""}]"	"[""1956"",""60529""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4926""}]"
DOID:4926	"[""bronchiolo-alveolar adenocarcinoma"",""Bronchioalveolar lung carcinoma"",""Bronchioloalveolar carcinoma"",""Minimally Invasive Lung Adenocarcinoma""]"	"[{""label"":""Tp53"",""id"":""24842""}]"	"[""24842""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4926""}]"
DOID:4927	"[""Klatskin's tumor"",""Klatskin tumor"",""Klatskin tumour"",""Klatskin's tumour"",""Perihilar extrahepatic bile duct carcinoma"",""hilar cholangiocarcinoma"",""hilar cholangiocellular carcinoma""]"	"[{""label"":""ARID1A"",""id"":""8289""},{""label"":""KMT2C"",""id"":""58508""},{""label"":""KRAS"",""id"":""3845""},{""label"":""PREX2"",""id"":""80243""}]"	"[""3845"",""58508"",""80243"",""8289""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4927""}]"
DOID:4928	"[""intrahepatic cholangiocarcinoma"",""Intrahepatic bile duct carcinoma"",""peripheral Cholangiocarcinoma""]"	"[{""label"":""Lcn2"",""id"":""170496""}]"	"[""170496""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4928""}]"
DOID:4928	"[""intrahepatic cholangiocarcinoma"",""Intrahepatic bile duct carcinoma"",""peripheral Cholangiocarcinoma""]"	"[{""label"":""Kras"",""id"":""16653""}]"	"[""16653""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4928""}]"
DOID:4928	"[""intrahepatic cholangiocarcinoma"",""Intrahepatic bile duct carcinoma"",""peripheral Cholangiocarcinoma""]"	"[{""label"":""IDH2"",""id"":""3418""},{""label"":""KRAS"",""id"":""3845""},{""label"":""LRP1B"",""id"":""53353""}]"	"[""3418"",""3845"",""53353""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4928""}]"
DOID:4947	"[""cholangiocarcinoma"",""adult primary Cholangiocarcinoma"",""adult primary cholangiocellular carcinoma"",""cholangiosarcoma""]"	"[{""label"":""ABCC2"",""id"":""1244""},{""label"":""ALB"",""id"":""213""},{""label"":""APC"",""id"":""324""},{""label"":""ASPH"",""id"":""444""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FASLG"",""id"":""356""},{""label"":""GNAS"",""id"":""2778""},{""label"":""MGMT"",""id"":""4255""},{""label"":""NAT2"",""id"":""10""},{""label"":""OGG1"",""id"":""4968""},{""label"":""PPIA"",""id"":""5478""},{""label"":""PREX2"",""id"":""80243""},{""label"":""RNF43"",""id"":""54894""},{""label"":""SLC7A5"",""id"":""8140""},{""label"":""THBS1"",""id"":""7057""},{""label"":""WDHD1"",""id"":""11169""}]"	"[""10"",""11169"",""1244"",""213"",""2146"",""2778"",""324"",""356"",""4255"",""444"",""4968"",""5478"",""54894"",""7057"",""80243"",""8140""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4947""}]"
DOID:4948	"[""gallbladder carcinoma"",""cancer of the gallbladder"",""carcinoma gallbladder"",""carcinoma of gallbladder""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""IL10"",""id"":""3586""},{""label"":""TERT"",""id"":""7015""},{""label"":""UBR5"",""id"":""51366""}]"	"[""28"",""3586"",""51366"",""7015"",""81037""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4948""}]"
DOID:4959	"[""epidermolysis bullosa dystrophica"",""Dystrophic epidermolysis bullosa""]"	"[{""label"":""COL7A1"",""id"":""1294""},{""label"":""MMP1"",""id"":""4312""}]"	"[""1294"",""4312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4959""}]"
DOID:4971	"[""myelofibrosis"",""Agnogenic myeloid metaplasia"",""Aleukemic myelosis"",""Megakaryocytic myelosclerosis"",""bone Marrow Fibrosis"",""myelosclerosis"",""primary myelofibrosis""]"	"[{""label"":""ASXL1"",""id"":""171023""},{""label"":""CALR"",""id"":""811""},{""label"":""EZH2"",""id"":""2146""},{""label"":""HFE"",""id"":""3077""},{""label"":""KMT2A"",""id"":""4297""},{""label"":""MPL"",""id"":""4352""}]"	"[""171023"",""2146"",""3077"",""4297"",""4352"",""811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4971""}]"
DOID:4971	"[""myelofibrosis"",""Agnogenic myeloid metaplasia"",""Aleukemic myelosis"",""Megakaryocytic myelosclerosis"",""bone Marrow Fibrosis"",""myelosclerosis"",""primary myelofibrosis""]"	"[{""label"":""Myb"",""id"":""17863""},{""label"":""Ncor2"",""id"":""20602""}]"	"[""17863"",""20602""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4971""}]"
DOID:4972	"[""myelodysplastic/myeloproliferative neoplasm"",""Myeloproliferative/Myelodysplastic syndromes"",""myelodysplastic myeloproliferative cancer""]"	"[{""label"":""Dido1"",""id"":""23856""}]"	"[""23856""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4972""}]"
DOID:4977	"[""lymphedema"",""Lymphatic edema"",""Lymphoedema""]"	"[{""label"":""GJC2"",""id"":""57165""}]"	"[""57165""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4977""}]"
DOID:4988	"[""alcoholic pancreatitis""]"	"[{""label"":""CFTR"",""id"":""1080""},{""label"":""UGT1A7"",""id"":""54577""}]"	"[""1080"",""54577""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4988""}]"
DOID:4989	"[""pancreatitis""]"	"[{""label"":""Bdkrb2"",""id"":""25245""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Il15"",""id"":""25670""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Pparg"",""id"":""25664""},{""label"":""Tacr1"",""id"":""24807""}]"	"[""24536"",""24770"",""24807"",""25245"",""25664"",""25670"",""29595""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4989""}]"
DOID:4989	"[""pancreatitis""]"	"[{""label"":""CCL2"",""id"":""6347""},{""label"":""CCL5"",""id"":""6352""},{""label"":""PRSS1"",""id"":""5644""},{""label"":""SERPING1"",""id"":""710""}]"	"[""5644"",""6347"",""6352"",""710""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4989""}]"
DOID:4990	"[""essential tremor"",""benign essential tremor"",""essential hereditary tremor"",""shaky hand syndrome""]"	"[{""label"":""Drd3"",""id"":""29238""}]"	"[""29238""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4990""}]"
DOID:4990	"[""essential tremor"",""benign essential tremor"",""essential hereditary tremor"",""shaky hand syndrome""]"	"[{""label"":""DRD3"",""id"":""1814""}]"	"[""1814""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4990""}]"
DOID:4992	"[""optic nerve glioma"",""glioma of the optic nerve""]"	"[{""label"":""NF1"",""id"":""4763""}]"	"[""4763""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4992""}]"
DOID:4997	"[""Camurati-Engelmann disease"",""Diaphyseal dysplasia"",""Engelman's disease"",""progressive diaphyseal dysplasia""]"	"[{""label"":""Mitf"",""id"":""17342""}]"	"[""17342""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4997""}]"
DOID:4997	"[""Camurati-Engelmann disease"",""Diaphyseal dysplasia"",""Engelman's disease"",""progressive diaphyseal dysplasia""]"	"[{""label"":""TGFB1"",""id"":""7040""}]"	"[""7040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:4997""}]"
DOID:50	"[""thyroid gland disease""]"	"[{""label"":""SECISBP2"",""id"":""79048""}]"	"[""79048""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:50""}]"
DOID:5015	"[""fibrolamellar carcinoma"",""Fibrolamellar hepatocellular carcinoma"",""Hepatocellular carcinoma, fibrolamellar"",""Oncocytic Hepatocellular tumor""]"	"[{""label"":""CTNNB1"",""id"":""1499""}]"	"[""1499""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5015""}]"
DOID:5016	"[""hepatocellular clear cell carcinoma"",""Clear cell carcinoma of the Liver cells"",""Hepatocellular carcinoma, clear cell type""]"	"[{""label"":""IDH1"",""id"":""3417""},{""label"":""IDH2"",""id"":""3418""}]"	"[""3417"",""3418""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5016""}]"
DOID:5041	"[""esophageal cancer"",""Ca lower third oesophagus"",""Ca middle third oesophagus"",""esophagus cancer"",""malignant neoplasm of distal third of esophagus"",""malignant neoplasm of lower third of oesophagus"",""malignant neoplasm of middle third of oesophagus"",""malignant neoplasm of proximal third of esophagus"",""malignant neoplasm of upper third esophagus"",""malignant tumor of Distal Third of esophagus"",""malignant tumor of Proximal Third of esophagus"",""malignant tumor of abdominal esophagus"",""malignant tumor of the middle Third of the esophagus""]"	"[{""label"":""CYP1A1"",""id"":""1543""},{""label"":""GPX3"",""id"":""2878""},{""label"":""IL1R2"",""id"":""7850""},{""label"":""LZTS1"",""id"":""11178""},{""label"":""PTEN"",""id"":""5728""},{""label"":""TNFAIP3"",""id"":""7128""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""11178"",""1543"",""2878"",""5728"",""7128"",""7515"",""7850""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5041""}]"
DOID:5050	"[""Ehrlich tumor carcinoma"",""Ehrlich tumour carcinoma"",""Ehrlich's tumor"",""Ehrlich's tumour""]"	"[{""label"":""Cd40lg"",""id"":""84349""}]"	"[""84349""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5050""}]"
DOID:5052	"[""melioidosis"",""Nightcliff gardener's disease"",""Pseudoglanders"",""Whitmore's disease"",""acute and fulminating melioidosis"",""subacute and chronic melioidosis""]"	"[{""label"":""TLR5"",""id"":""7100""}]"	"[""7100""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5052""}]"
DOID:5082	"[""liver cirrhosis"",""Cirrhosis"",""cirrhosis of liver""]"	"[{""label"":""Gclc"",""id"":""25283""},{""label"":""Nfe2l2"",""id"":""83619""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Smo"",""id"":""25273""},{""label"":""Tlr4"",""id"":""29260""}]"	"[""24600"",""25273"",""25283"",""29260"",""83619""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5082""}]"
DOID:5082	"[""liver cirrhosis"",""Cirrhosis"",""cirrhosis of liver""]"	"[{""label"":""ABCB11"",""id"":""8647""},{""label"":""ABCB4"",""id"":""5244""},{""label"":""ACE"",""id"":""1636""},{""label"":""ADAR"",""id"":""103""},{""label"":""C5"",""id"":""727""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CENPC"",""id"":""1060""},{""label"":""DRD4"",""id"":""1815""},{""label"":""F5"",""id"":""2153""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-DPA1"",""id"":""3113""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IFNA2"",""id"":""3440""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""IL10"",""id"":""3586""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""KRT18"",""id"":""3875""},{""label"":""KRT8"",""id"":""3856""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MPO"",""id"":""4353""},{""label"":""PHKG2"",""id"":""5261""},{""label"":""PNPLA3"",""id"":""80339""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SERPINA1"",""id"":""5265""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SPAG9"",""id"":""9043""},{""label"":""TFPI"",""id"":""7035""},{""label"":""TLR3"",""id"":""7098""},{""label"":""VASH1"",""id"":""22846""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""103"",""1060"",""1636"",""1815"",""2153"",""2264"",""22846"",""3077"",""3113"",""3117"",""3119"",""3123"",""3383"",""3440"",""3458"",""3480"",""3586"",""3813"",""3856"",""3875"",""4153"",""4353"",""5054"",""5244"",""5261"",""5265"",""5743"",""6352"",""6532"",""6648"",""7035"",""7098"",""727"",""7515"",""80339"",""8647"",""9043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5082""}]"
DOID:5151	"[""plexiform neurofibroma""]"	"[{""label"":""NF1"",""id"":""4763""}]"	"[""4763""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5151""}]"
DOID:5176	"[""renal Wilms' tumor"",""Nonanaplastic renal Wilm's tumor"",""Nonanaplastic renal Wilm's tumour"",""renal Wilms' tumour""]"	"[{""label"":""BMI1"",""id"":""648""},{""label"":""EZH2"",""id"":""2146""},{""label"":""PAX2"",""id"":""5076""},{""label"":""SALL1"",""id"":""6299""},{""label"":""SUZ12"",""id"":""23512""},{""label"":""TEK"",""id"":""7010""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""2146"",""23512"",""5076"",""6299"",""648"",""7010"",""7422""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5176""}]"
DOID:5199	"[""ureteral obstruction""]"	"[{""label"":""IL1RN"",""id"":""3557""}]"	"[""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5199""}]"
DOID:5199	"[""ureteral obstruction""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Ifng"",""id"":""25712""},{""label"":""Serpine1"",""id"":""24617""}]"	"[""24310"",""24617"",""25712""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5199""}]"
DOID:520	"[""aortic disease"",""aortic disorder"",""disorder of the aorta""]"	"[{""label"":""SMAD4"",""id"":""4089""}]"	"[""4089""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:520""}]"
DOID:5200	"[""urinary tract obstruction"",""Obstructive Uropathy"",""urinary obstruction""]"	"[{""label"":""Adamts1"",""id"":""11504""}]"	"[""11504""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5200""}]"
DOID:5204	"[""fructose-1,6-bisphosphatase deficiency"",""fructose 1 phosphate aldolase deficiency"",""fructose-1,6-diphosphatase deficiency""]"	"[{""label"":""FBP1"",""id"":""2203""}]"	"[""2203""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5204""}]"
DOID:5212	"[""congenital disorder of glycosylation"",""carbohydrate-deficient glycoprotein syndrome""]"	"[{""label"":""B4GALT1"",""id"":""2683""},{""label"":""PMM2"",""id"":""5373""}]"	"[""2683"",""5373""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5212""}]"
DOID:5212	"[""congenital disorder of glycosylation"",""carbohydrate-deficient glycoprotein syndrome""]"	"[{""label"":""ALG1"",""id"":""852407""},{""label"":""ALG3"",""id"":""852196""}]"	"[""852196"",""852407""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5212""}]"
DOID:5212	"[""congenital disorder of glycosylation"",""carbohydrate-deficient glycoprotein syndrome""]"	"[{""label"":""Ogt"",""id"":""108155""}]"	"[""108155""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5212""}]"
DOID:5212	"[""congenital disorder of glycosylation"",""carbohydrate-deficient glycoprotein syndrome""]"	"[{""label"":""ATP6AP2"",""id"":""41104""}]"	"[""41104""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5212""}]"
DOID:5223	"[""infertility""]"	"[{""label"":""Cdkn1b"",""id"":""83571""},{""label"":""Esr1"",""id"":""24890""}]"	"[""24890"",""83571""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5223""}]"
DOID:525	"[""central nervous system vasculitis""]"	"[{""label"":""HLA-A"",""id"":""3105""}]"	"[""3105""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:525""}]"
DOID:526	"[""human immunodeficiency virus infectious disease"",""HIV infection""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ABCE1"",""id"":""6059""},{""label"":""CCL11"",""id"":""6356""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CD209"",""id"":""30835""},{""label"":""CD40LG"",""id"":""959""},{""label"":""CXCR1"",""id"":""3577""},{""label"":""CYP2B6"",""id"":""1555""},{""label"":""FAS"",""id"":""355""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""GC"",""id"":""2638""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-C"",""id"":""3107""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL21R"",""id"":""50615""},{""label"":""KIR3DL1"",""id"":""3811""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MKI67"",""id"":""4288""},{""label"":""NEFM"",""id"":""4741""},{""label"":""PLA2G2A"",""id"":""5320""},{""label"":""PPIA"",""id"":""5478""},{""label"":""PRF1"",""id"":""5551""},{""label"":""SERPINA1"",""id"":""5265""},{""label"":""TLR3"",""id"":""7098""}]"	"[""1234"",""1555"",""2214"",""2638"",""30835"",""3106"",""3107"",""3117"",""3119"",""3123"",""3458"",""355"",""3577"",""3586"",""3811"",""3813"",""4153"",""4288"",""4741"",""50615"",""5243"",""5265"",""5320"",""5478"",""5551"",""6059"",""6352"",""6356"",""7098"",""729230"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:526""}]"
DOID:529	"[""blepharospasm""]"	"[{""label"":""DRD5"",""id"":""1816""}]"	"[""1816""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:529""}]"
DOID:5295	"[""intestinal disease""]"	"[{""label"":""BMPR1A"",""id"":""657""},{""label"":""NOD2"",""id"":""64127""},{""label"":""SLC10A2"",""id"":""6555""}]"	"[""64127"",""6555"",""657""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5295""}]"
DOID:5295	"[""intestinal disease""]"	"[{""label"":""Sod2"",""id"":""24787""}]"	"[""24787""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5295""}]"
DOID:5325	"[""Roberts syndrome"",""LONG BONE DEFICIENCIES ASSOCIATED WITH CLEFT LIP-PALATE"",""RBS"",""Roberts-Sc Phocomelia Syndrome"",""SC phocomelia syndrome""]"	"[{""label"":""ESCO2"",""id"":""157570""}]"	"[""157570""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5325""}]"
DOID:5327	"[""retinal detachment""]"	"[{""label"":""Epo"",""id"":""24335""},{""label"":""Fas"",""id"":""246097""},{""label"":""Tnf"",""id"":""24835""}]"	"[""24335"",""246097"",""24835""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5327""}]"
DOID:5327	"[""retinal detachment""]"	"[{""label"":""CFH"",""id"":""3075""},{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280"",""3075""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5327""}]"
DOID:5339	"[""cyclic hematopoiesis"",""Cyclic neutropenia"",""Cyclical neutropenia"",""Neutropenia, periodic"",""cyclic agranulocytosis""]"	"[{""label"":""ELANE"",""id"":""1991""}]"	"[""1991""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5339""}]"
DOID:535	"[""sleep disorder"",""Non-organic sleep disorder""]"	"[{""label"":""InR"",""id"":""42549""}]"	"[""42549""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:535""}]"
DOID:535	"[""sleep disorder"",""Non-organic sleep disorder""]"	"[{""label"":""Clock"",""id"":""12753""},{""label"":""Npsr1"",""id"":""319239""}]"	"[""12753"",""319239""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:535""}]"
DOID:5353	"[""colonic disease"",""colon disorder""]"	"[{""label"":""GHR"",""id"":""2690""}]"	"[""2690""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5353""}]"
DOID:5374	"[""pilomatrixoma"",""Pilomatricoma"",""benign pilomatricoma""]"	"[{""label"":""CTNNB1"",""id"":""1499""}]"	"[""1499""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5374""}]"
DOID:5408	"[""Paget's disease of bone"",""Paget disease of bone"",""Paget's bone disease"",""osseous Paget's disease"",""osteitis deformans""]"	"[{""label"":""OPTN"",""id"":""10133""},{""label"":""SQSTM1"",""id"":""8878""},{""label"":""TNFRSF11A"",""id"":""8792""},{""label"":""TNFRSF11B"",""id"":""4982""},{""label"":""VCP"",""id"":""7415""}]"	"[""10133"",""4982"",""7415"",""8792"",""8878""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5408""}]"
DOID:5408	"[""Paget's disease of bone"",""Paget disease of bone"",""Paget's bone disease"",""osseous Paget's disease"",""osteitis deformans""]"	"[{""label"":""Sqstm1"",""id"":""18412""},{""label"":""Tnfrsf11a"",""id"":""21934""}]"	"[""18412"",""21934""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5408""}]"
DOID:5409	"[""lung small cell carcinoma""]"	"[{""label"":""ACVR1B"",""id"":""91""},{""label"":""ATM"",""id"":""472""},{""label"":""ATRX"",""id"":""546""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CHRNA9"",""id"":""55584""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""E2F1"",""id"":""1869""},{""label"":""FAT1"",""id"":""2195""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""KMT2D"",""id"":""8085""},{""label"":""LAMA3"",""id"":""3909""},{""label"":""LAMB3"",""id"":""3914""},{""label"":""LAMC2"",""id"":""3918""},{""label"":""MTOR"",""id"":""2475""},{""label"":""PBRM1"",""id"":""55193""},{""label"":""PTK2"",""id"":""5747""},{""label"":""RARB"",""id"":""5915""},{""label"":""RICTOR"",""id"":""253260""},{""label"":""XPO5"",""id"":""57510""}]"	"[""1136"",""1591"",""1869"",""2195"",""2475"",""253260"",""3909"",""3914"",""3918"",""472"",""546"",""55193"",""55584"",""5747"",""57510"",""5915"",""7403"",""8085"",""91""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5409""}]"
DOID:5418	"[""schizoaffective disorder""]"	"[{""label"":""Gria1"",""id"":""14799""}]"	"[""14799""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5418""}]"
DOID:5419	"[""schizophrenia"",""schizophrenia-1""]"	"[{""label"":""cacna1da"",""id"":""403310""}]"	"[""403310""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5419""}]"
DOID:5419	"[""schizophrenia"",""schizophrenia-1""]"	"[{""label"":""Cnr1"",""id"":""25248""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Nos1"",""id"":""24598""}]"	"[""24598"",""25248"",""29595""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5419""}]"
DOID:5419	"[""schizophrenia"",""schizophrenia-1""]"	"[{""label"":""AGER"",""id"":""177""},{""label"":""AKT1"",""id"":""207""},{""label"":""ANK3"",""id"":""288""},{""label"":""ATN1"",""id"":""1822""},{""label"":""B3GAT2"",""id"":""135152""},{""label"":""BCL11A"",""id"":""53335""},{""label"":""BRD1"",""id"":""23774""},{""label"":""CACNA1I"",""id"":""8911""},{""label"":""CHI3L1"",""id"":""1116""},{""label"":""CHL1"",""id"":""10752""},{""label"":""CHRM2"",""id"":""1129""},{""label"":""CHRNA7"",""id"":""1139""},{""label"":""CNR1"",""id"":""1268""},{""label"":""CNTNAP2"",""id"":""26047""},{""label"":""COMT"",""id"":""1312""},{""label"":""CTNND2"",""id"":""1501""},{""label"":""CYFIP1"",""id"":""23191""},{""label"":""DRD3"",""id"":""1814""},{""label"":""DTNBP1"",""id"":""84062""},{""label"":""FOXP1"",""id"":""27086""},{""label"":""FOXP2"",""id"":""93986""},{""label"":""FZD3"",""id"":""7976""},{""label"":""GAD1"",""id"":""2571""},{""label"":""GAD2"",""id"":""2572""},{""label"":""GRIA4"",""id"":""2893""},{""label"":""GRIN2A"",""id"":""2903""},{""label"":""GRIN2B"",""id"":""2904""},{""label"":""GRM8"",""id"":""2918""},{""label"":""GSK3B"",""id"":""2932""},{""label"":""HPS4"",""id"":""89781""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""HSPA1L"",""id"":""3305""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""HTR2C"",""id"":""3358""},{""label"":""IL10"",""id"":""3586""},{""label"":""IMPA2"",""id"":""3613""},{""label"":""ITGA8"",""id"":""8516""},{""label"":""KCNN3"",""id"":""3782""},{""label"":""L1CAM"",""id"":""3897""},{""label"":""LRP8"",""id"":""7804""},{""label"":""MED15"",""id"":""51586""},{""label"":""NCSTN"",""id"":""23385""},{""label"":""NOTCH4"",""id"":""4855""},{""label"":""NTRK1"",""id"":""4914""},{""label"":""NTSR1"",""id"":""4923""},{""label"":""OPRM1"",""id"":""4988""},{""label"":""PAK1"",""id"":""5058""},{""label"":""PIK3CD"",""id"":""5293""},{""label"":""RTN4R"",""id"":""65078""},{""label"":""SLC18A1"",""id"":""6570""},{""label"":""SYN2"",""id"":""6854""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TBP"",""id"":""6908""},{""label"":""TNF"",""id"":""7124""},{""label"":""TPH1"",""id"":""7166""},{""label"":""UFD1"",""id"":""7353""}]"	"[""10752"",""1116"",""1129"",""1139"",""1268"",""1312"",""135152"",""1501"",""177"",""1814"",""1822"",""207"",""23191"",""23385"",""23774"",""2571"",""2572"",""26047"",""27086"",""288"",""2893"",""2903"",""2904"",""2918"",""2932"",""3303"",""3304"",""3305"",""3356"",""3358"",""3586"",""3613"",""3782"",""3897"",""4855"",""4914"",""4923"",""4988"",""5058"",""51586"",""5293"",""53335"",""65078"",""6570"",""6854"",""6890"",""6908"",""7124"",""7166"",""7353"",""7804"",""7976"",""84062"",""8516"",""8911"",""89781"",""93986""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5419""}]"
DOID:5419	"[""schizophrenia"",""schizophrenia-1""]"	"[{""label"":""Fur1"",""id"":""47220""}]"	"[""47220""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5419""}]"
DOID:5419	"[""schizophrenia"",""schizophrenia-1""]"	"[{""label"":""Akt1"",""id"":""11651""},{""label"":""Avpr1a"",""id"":""54140""},{""label"":""Bace1"",""id"":""23821""},{""label"":""Chrna7"",""id"":""11441""},{""label"":""Chst3"",""id"":""53374""},{""label"":""Csmd1"",""id"":""94109""},{""label"":""Ctsc"",""id"":""13032""},{""label"":""Gnas"",""id"":""14683""},{""label"":""Grin1"",""id"":""14810""},{""label"":""Grm5"",""id"":""108071""},{""label"":""Hivep2"",""id"":""15273""},{""label"":""Kif3b"",""id"":""16569""},{""label"":""Lrrtm1"",""id"":""74342""},{""label"":""Map6"",""id"":""17760""},{""label"":""Ncstn"",""id"":""59287""},{""label"":""Nlgn2"",""id"":""216856""},{""label"":""Nrxn1"",""id"":""18189""},{""label"":""Pdgfrb"",""id"":""18596""},{""label"":""Ppara"",""id"":""19013""},{""label"":""Reln"",""id"":""19699""},{""label"":""Setd1a"",""id"":""233904""},{""label"":""Shank3"",""id"":""58234""},{""label"":""Slc6a1"",""id"":""232333""},{""label"":""Slc6a3"",""id"":""13162""},{""label"":""Snap25"",""id"":""20614""},{""label"":""Srgap3"",""id"":""259302""},{""label"":""Srr"",""id"":""27364""},{""label"":""Syngap1"",""id"":""240057""},{""label"":""Taar1"",""id"":""111174""},{""label"":""Tcf4"",""id"":""21413""},{""label"":""Ywhaz"",""id"":""22631""},{""label"":""Zfp521"",""id"":""225207""}]"	"[""108071"",""111174"",""11441"",""11651"",""13032"",""13162"",""14683"",""14810"",""15273"",""16569"",""17760"",""18189"",""18596"",""19013"",""19699"",""20614"",""21413"",""216856"",""225207"",""22631"",""232333"",""233904"",""23821"",""240057"",""259302"",""27364"",""53374"",""54140"",""58234"",""59287"",""74342"",""94109""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5419""}]"
DOID:5425	"[""ovarian hyperstimulation syndrome"",""secondary Meig's syndrome""]"	"[{""label"":""FSHR"",""id"":""2492""},{""label"":""SERPINF1"",""id"":""5176""}]"	"[""2492"",""5176""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5425""}]"
DOID:5425	"[""ovarian hyperstimulation syndrome"",""secondary Meig's syndrome""]"	"[{""label"":""Drd2"",""id"":""24318""},{""label"":""Vegfa"",""id"":""83785""}]"	"[""24318"",""83785""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5425""}]"
DOID:5426	"[""primary ovarian insufficiency"",""hypergonadotropic hypogonadism"",""premature ovarian failure"",""premature ovarian insufficiency""]"	"[{""label"":""BBS9"",""id"":""27241""},{""label"":""BMP15"",""id"":""9210""},{""label"":""KASH5"",""id"":""147872""},{""label"":""MEIOB"",""id"":""254528""},{""label"":""MSH4"",""id"":""4438""},{""label"":""XPO5"",""id"":""57510""}]"	"[""147872"",""254528"",""27241"",""4438"",""57510"",""9210""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5426""}]"
DOID:543	"[""dystonia"",""dystonic disease""]"	"[{""label"":""Torsin"",""id"":""31399""}]"	"[""31399""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:543""}]"
DOID:5434	"[""scrapie""]"	"[{""label"":""Prnp"",""id"":""24686""}]"	"[""24686""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5434""}]"
DOID:5453	"[""pulmonary venoocclusive disease"",""pulmonary veno-occlusive disease""]"	"[{""label"":""Kcnk3"",""id"":""29553""}]"	"[""29553""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5453""}]"
DOID:5485	"[""synovial sarcoma""]"	"[{""label"":""SS18"",""id"":""6760""}]"	"[""6760""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5485""}]"
DOID:5517	"[""stomach carcinoma"",""cancer of the stomach"",""carcinoma of stomach"",""gastric carcinoma""]"	"[{""label"":""BCOR"",""id"":""54880""},{""label"":""FGFR2"",""id"":""2263""},{""label"":""KRAS"",""id"":""3845""},{""label"":""MRE11"",""id"":""4361""},{""label"":""MUTYH"",""id"":""4595""},{""label"":""PARP1"",""id"":""142""},{""label"":""RNF43"",""id"":""54894""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""142"",""2263"",""3845"",""4361"",""4595"",""54880"",""54894"",""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5517""}]"
DOID:552	"[""pneumonia"",""acute pneumonia""]"	"[{""label"":""C3"",""id"":""24232""},{""label"":""Ccl11"",""id"":""29397""},{""label"":""Slc11a2"",""id"":""25715""}]"	"[""24232"",""25715"",""29397""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:552""}]"
DOID:552	"[""pneumonia"",""acute pneumonia""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""ACE"",""id"":""1636""},{""label"":""C5"",""id"":""727""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MIF"",""id"":""4282""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SFTPB"",""id"":""6439""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""SOD3"",""id"":""6649""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""1543"",""1571"",""1636"",""2214"",""28"",""3557"",""4282"",""5054"",""6439"",""6441"",""6649"",""7133"",""727""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:552""}]"
DOID:5520	"[""head and neck squamous cell carcinoma"",""carcinoma of the head and neck"",""squamous cell carcinoma of the head and neck"",""squamous cell carcinomas of head and neck""]"	"[{""label"":""CYP2C19"",""id"":""1557""},{""label"":""CYP2C9"",""id"":""1559""},{""label"":""FANCB"",""id"":""2187""},{""label"":""FGFR4"",""id"":""2264""},{""label"":""IL2"",""id"":""3558""},{""label"":""JUNB"",""id"":""3726""},{""label"":""OGG1"",""id"":""4968""},{""label"":""PTPN13"",""id"":""5783""},{""label"":""STAT3"",""id"":""6774""},{""label"":""TNFRSF10A"",""id"":""8797""},{""label"":""TNFRSF10B"",""id"":""8795""}]"	"[""1557"",""1559"",""2187"",""2264"",""3558"",""3726"",""4968"",""5783"",""6774"",""8795"",""8797""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5520""}]"
DOID:5522	"[""basaloid squamous cell carcinoma"",""Basaloid carcinoma""]"	"[{""label"":""PTCH1"",""id"":""5727""}]"	"[""5727""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5522""}]"
DOID:557	"[""kidney disease"",""impaired renal function disease"",""nephropathy""]"	"[{""label"":""Cubn"",""id"":""326235""},{""label"":""kirre"",""id"":""31292""}]"	"[""31292"",""326235""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:557""}]"
DOID:557	"[""kidney disease"",""impaired renal function disease"",""nephropathy""]"	"[{""label"":""klo-1"",""id"":""177557""}]"	"[""177557""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:557""}]"
DOID:557	"[""kidney disease"",""impaired renal function disease"",""nephropathy""]"	"[{""label"":""Col4a1"",""id"":""12826""},{""label"":""Umod"",""id"":""22242""}]"	"[""12826"",""22242""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:557""}]"
DOID:557	"[""kidney disease"",""impaired renal function disease"",""nephropathy""]"	"[{""label"":""Ccl2"",""id"":""24770""}]"	"[""24770""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:557""}]"
DOID:557	"[""kidney disease"",""impaired renal function disease"",""nephropathy""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""LIPC"",""id"":""3990""},{""label"":""VPS33B"",""id"":""26276""}]"	"[""1493"",""26276"",""3990""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:557""}]"
DOID:5572	"[""Beckwith-Wiedemann syndrome""]"	"[{""label"":""Sptbn1"",""id"":""20742""}]"	"[""20742""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5572""}]"
DOID:5577	"[""gastrinoma"",""Gastrin Secreting tumor"",""Gastrin cell tumour"",""malignant gastrinoma""]"	"[{""label"":""MGMT"",""id"":""4255""}]"	"[""4255""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5577""}]"
DOID:5585	"[""Ferguson-Smith tumor"",""Multiple self-healing epithelioma of Ferguson-Smith""]"	"[{""label"":""TGFBR1"",""id"":""7046""}]"	"[""7046""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5585""}]"
DOID:559	"[""acute pyelonephritis""]"	"[{""label"":""CXCR2"",""id"":""3579""}]"	"[""3579""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:559""}]"
DOID:5602	"[""T-cell adult acute lymphocytic leukemia"",""ATLL"",""Acute Adult T-cell Leukemia-Lymphoma"",""adult Precursor T Lymphoblastic Leukemia""]"	"[{""label"":""Cntn2"",""id"":""21367""},{""label"":""Zeb2"",""id"":""24136""}]"	"[""21367"",""24136""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5602""}]"
DOID:5603	"[""T-cell acute lymphoblastic leukemia"",""Precursor T Lymphoblastic Leukemia"",""T Acute Lymphoblastic Leukemia"",""T-cell acute lymphocytic leukaemia"",""T-cell leukemia"",""T-cell lymphoblastic leukemia/lymphoma"",""acute T cell leukemia"",""precursor T-lymphoblastic lymphoma/leukemia""]"	"[{""label"":""AKR1C3"",""id"":""8644""},{""label"":""CXCR4"",""id"":""7852""},{""label"":""JAK1"",""id"":""3716""},{""label"":""JAK3"",""id"":""3718""},{""label"":""NUP98"",""id"":""4928""},{""label"":""PDGFRA"",""id"":""5156""}]"	"[""3716"",""3718"",""4928"",""5156"",""7852"",""8644""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5603""}]"
DOID:5614	"[""eye disease""]"	"[{""label"":""COL2A1"",""id"":""1280""},{""label"":""F2"",""id"":""2147""}]"	"[""1280"",""2147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5614""}]"
DOID:5627	"[""adenosquamous gallbladder carcinoma"",""Adenosquamous carcinoma of the gallbladder""]"	"[{""label"":""DDR2"",""id"":""4921""}]"	"[""4921""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5627""}]"
DOID:5637	"[""pancreatic adenosquamous carcinoma"",""Adenosquamous carcinoma of pancreas""]"	"[{""label"":""TGFB2"",""id"":""7042""}]"	"[""7042""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5637""}]"
DOID:5679	"[""retinal disease""]"	"[{""label"":""ninaE"",""id"":""42367""}]"	"[""42367""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5679""}]"
DOID:5679	"[""retinal disease""]"	"[{""label"":""APOE"",""id"":""348""}]"	"[""348""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5679""}]"
DOID:5683	"[""hereditary breast ovarian cancer syndrome"",""BRCA1- and BRCA2-associated hereditary breast and ovarian cancer"",""Breast and Ovarian Cancer syndrome"",""HBOC syndrome"",""Hereditary Breast and Ovarian Cancer syndrome"",""Hereditary breast and ovarian cancer""]"	"[{""label"":""BRCA1"",""id"":""672""},{""label"":""BRCA2"",""id"":""675""},{""label"":""PALB2"",""id"":""79728""},{""label"":""RAD51C"",""id"":""5889""}]"	"[""5889"",""672"",""675"",""79728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5683""}]"
DOID:5684	"[""spondyloepimetaphyseal dysplasia, Sponastrime type"",""Spondylar and nasal Alterations-Striated Metaphyses syndrome"",""sponastrime dysplasia""]"	"[{""label"":""TONSL"",""id"":""4796""}]"	"[""4796""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5684""}]"
DOID:5688	"[""Werner syndrome"",""WS"",""Werner's syndrome"",""adult premature ageing syndrome"",""adult progeria""]"	"[{""label"":""LMNA"",""id"":""4000""}]"	"[""4000""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5688""}]"
DOID:5688	"[""Werner syndrome"",""WS"",""Werner's syndrome"",""adult premature ageing syndrome"",""adult progeria""]"	"[{""label"":""Wrn"",""id"":""22427""}]"	"[""22427""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5688""}]"
DOID:57	"[""aortic valve insufficiency"",""Rheumatic aortic insufficiency"",""Rheumatic aortic regurgitation"",""Rheumatic aortic valve regurgitation"",""aortic incompetence"",""aortic insufficiency"",""aortic regurgitation"",""rheumatic aortic valve insufficiency""]"	"[{""label"":""MBL2"",""id"":""4153""}]"	"[""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:57""}]"
DOID:5723	"[""optic atrophy"",""atrophy of optic disc""]"	"[{""label"":""MCAT"",""id"":""27349""},{""label"":""MECR"",""id"":""51102""},{""label"":""OPA1"",""id"":""4976""},{""label"":""SSBP1"",""id"":""6742""},{""label"":""WFS1"",""id"":""7466""}]"	"[""27349"",""4976"",""51102"",""6742"",""7466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5723""}]"
DOID:574	"[""peripheral nervous system disease""]"	"[{""label"":""Artn"",""id"":""362572""}]"	"[""362572""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:574""}]"
DOID:5744	"[""ovary serous adenocarcinoma"",""malignant ovarian serous tumor"",""serous carcinoma of Ovary""]"	"[{""label"":""TP53"",""id"":""7157""}]"	"[""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5744""}]"
DOID:5750	"[""endometrial serous adenocarcinoma"",""uterine corpus serous adenocarcinoma"",""uterine papillary serous carcinoma"",""uterine serous carcinoma""]"	"[{""label"":""BRCA2"",""id"":""675""}]"	"[""675""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5750""}]"
DOID:576	"[""proteinuria""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGER"",""id"":""177""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""MYH9"",""id"":""4627""},{""label"":""PLA2G7"",""id"":""7941""},{""label"":""SNRPD1"",""id"":""6632""},{""label"":""TLR9"",""id"":""54106""}]"	"[""1636"",""177"",""3557"",""4627"",""54106"",""6632"",""7941""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:576""}]"
DOID:576	"[""proteinuria""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Agtr1a"",""id"":""24180""},{""label"":""C6"",""id"":""24237""},{""label"":""Ifnb1"",""id"":""24481""},{""label"":""Lamb2"",""id"":""25473""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Mgat5"",""id"":""65271""},{""label"":""Mmp2"",""id"":""81686""},{""label"":""Tgfb1"",""id"":""59086""}]"	"[""24180"",""24237"",""24310"",""24481"",""24536"",""25473"",""59086"",""65271"",""81686""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:576""}]"
DOID:576	"[""proteinuria""]"	"[{""label"":""vegfaa"",""id"":""30682""}]"	"[""30682""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:576""}]"
DOID:5768	"[""Nager acrofacial dysostosis"",""AFD"",""Nager syndrome"",""acrofacial dysostosis 1, Nager type"",""preaxial acrofacial dysostosis"",""preaxial manibulofacial dysostosis""]"	"[{""label"":""SF3B4"",""id"":""10262""}]"	"[""10262""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5768""}]"
DOID:5812	"[""MHC class II deficiency"",""BLSII"",""SCID due to absent class II HLA antigens"",""bare lymphocyte syndrome type II""]"	"[{""label"":""CIITA"",""id"":""4261""}]"	"[""4261""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5812""}]"
DOID:5813	"[""purine nucleoside phosphorylase deficiency"",""PNP deficiency"",""Purine-Nucleoside Phosphorylase deficiency"",""deficiency of inosine phosphorylase""]"	"[{""label"":""Pnp"",""id"":""18950""}]"	"[""18950""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5813""}]"
DOID:5813	"[""purine nucleoside phosphorylase deficiency"",""PNP deficiency"",""Purine-Nucleoside Phosphorylase deficiency"",""deficiency of inosine phosphorylase""]"	"[{""label"":""PNP"",""id"":""4860""}]"	"[""4860""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5813""}]"
DOID:583	"[""hemolytic anemia"",""ANEMIA HEMOLYTIC""]"	"[{""label"":""A2m"",""id"":""24153""}]"	"[""24153""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:583""}]"
DOID:583	"[""hemolytic anemia"",""ANEMIA HEMOLYTIC""]"	"[{""label"":""ABO"",""id"":""28""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""GCLC"",""id"":""2729""},{""label"":""HP"",""id"":""3240""},{""label"":""PGK1"",""id"":""5230""},{""label"":""RHAG"",""id"":""6005""}]"	"[""2212"",""2729"",""28"",""3240"",""5230"",""6005""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:583""}]"
DOID:5844	"[""myocardial infarction"",""Myocardial infarct"",""heart attack""]"	"[{""label"":""Ace2"",""id"":""302668""},{""label"":""Ace"",""id"":""24310""},{""label"":""Adrb1"",""id"":""24925""},{""label"":""Agt"",""id"":""24179""},{""label"":""Akt1"",""id"":""24185""},{""label"":""Avpr1a"",""id"":""25107""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Cdkn1b"",""id"":""83571""},{""label"":""Cs"",""id"":""170587""},{""label"":""Csf2"",""id"":""116630""},{""label"":""Dab2"",""id"":""79128""},{""label"":""Ednra"",""id"":""24326""},{""label"":""Ednrb"",""id"":""50672""},{""label"":""Gsk3b"",""id"":""84027""},{""label"":""Hmgb1"",""id"":""25459""},{""label"":""Itgb1"",""id"":""24511""},{""label"":""Kdr"",""id"":""25589""},{""label"":""Lcat"",""id"":""24530""},{""label"":""Mdh2"",""id"":""81829""},{""label"":""Mmp2"",""id"":""81686""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Nfe2l2"",""id"":""83619""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Oprd1"",""id"":""24613""},{""label"":""Oprk1"",""id"":""29335""},{""label"":""Pgf"",""id"":""94203""},{""label"":""Pln"",""id"":""64672""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Shh"",""id"":""29499""},{""label"":""Sod2"",""id"":""24787""},{""label"":""Tnfrsf1a"",""id"":""25625""},{""label"":""Trpv1"",""id"":""83810""},{""label"":""Vdac2"",""id"":""83531""},{""label"":""Vegfa"",""id"":""83785""}]"	"[""116630"",""170587"",""24179"",""24185"",""24310"",""24326"",""24511"",""24530"",""24600"",""24613"",""24617"",""24770"",""24787"",""24925"",""25107"",""25459"",""25589"",""25625"",""29335"",""29499"",""302668"",""50672"",""64672"",""79128"",""81686"",""81687"",""81829"",""83531"",""83571"",""83619"",""83785"",""83810"",""84027"",""94203""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5844""}]"
DOID:5844	"[""myocardial infarction"",""Myocardial infarct"",""heart attack""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ADD1"",""id"":""118""},{""label"":""ADRB2"",""id"":""154""},{""label"":""AGER"",""id"":""177""},{""label"":""AGT"",""id"":""183""},{""label"":""AGTR1"",""id"":""185""},{""label"":""ALDH2"",""id"":""217""},{""label"":""ANXA5"",""id"":""308""},{""label"":""APEX1"",""id"":""328""},{""label"":""APOA1"",""id"":""335""},{""label"":""APOA4"",""id"":""337""},{""label"":""APOE"",""id"":""348""},{""label"":""APOH"",""id"":""350""},{""label"":""BRINP3"",""id"":""339479""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CD14"",""id"":""929""},{""label"":""CIITA"",""id"":""4261""},{""label"":""CLU"",""id"":""1191""},{""label"":""COL4A1"",""id"":""1282""},{""label"":""COL6A3"",""id"":""1293""},{""label"":""CSF3"",""id"":""1440""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP2J2"",""id"":""1573""},{""label"":""CYP2R1"",""id"":""120227""},{""label"":""EPO"",""id"":""2056""},{""label"":""ESR1"",""id"":""2099""},{""label"":""F12"",""id"":""2161""},{""label"":""F13A1"",""id"":""2162""},{""label"":""F2"",""id"":""2147""},{""label"":""F5"",""id"":""2153""},{""label"":""F7"",""id"":""2155""},{""label"":""FGB"",""id"":""2244""},{""label"":""FTO"",""id"":""79068""},{""label"":""GCLC"",""id"":""2729""},{""label"":""GP1BA"",""id"":""2811""},{""label"":""GP6"",""id"":""51206""},{""label"":""HFE"",""id"":""3077""},{""label"":""HGF"",""id"":""3082""},{""label"":""HIF1A"",""id"":""3091""},{""label"":""HP"",""id"":""3240""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL18BP"",""id"":""10068""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""ITGB3"",""id"":""3690""},{""label"":""ITIH4"",""id"":""3700""},{""label"":""KCNN4"",""id"":""3783""},{""label"":""KDR"",""id"":""3791""},{""label"":""KLK1"",""id"":""3816""},{""label"":""LGALS2"",""id"":""3957""},{""label"":""LIPG"",""id"":""9388""},{""label"":""LPA"",""id"":""4018""},{""label"":""LPL"",""id"":""4023""},{""label"":""LRP1"",""id"":""4035""},{""label"":""LRP8"",""id"":""7804""},{""label"":""LRPAP1"",""id"":""4043""},{""label"":""LTA"",""id"":""4049""},{""label"":""MLXIPL"",""id"":""51085""},{""label"":""MMP14"",""id"":""4323""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NGF"",""id"":""4803""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NPPA"",""id"":""4878""},{""label"":""NPPB"",""id"":""4879""},{""label"":""NPR1"",""id"":""4881""},{""label"":""NR1H3"",""id"":""10062""},{""label"":""NRG1"",""id"":""3084""},{""label"":""OLR1"",""id"":""4973""},{""label"":""PAPPA"",""id"":""5069""},{""label"":""PCSK2"",""id"":""5126""},{""label"":""PECAM1"",""id"":""5175""},{""label"":""PGF"",""id"":""5228""},{""label"":""PLAT"",""id"":""5327""},{""label"":""PLAU"",""id"":""5328""},{""label"":""PON1"",""id"":""5444""},{""label"":""PPARA"",""id"":""5465""},{""label"":""PSMA6"",""id"":""5687""},{""label"":""PTGIS"",""id"":""5740""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SELP"",""id"":""6403""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SOD1"",""id"":""6647""},{""label"":""SOD3"",""id"":""6649""},{""label"":""SPP1"",""id"":""6696""},{""label"":""TFPI"",""id"":""7035""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNFSF4"",""id"":""7292""},{""label"":""VEGFB"",""id"":""7423""}]"	"[""10062"",""10068"",""118"",""1191"",""120227"",""1282"",""1293"",""1440"",""1493"",""154"",""1573"",""1636"",""177"",""183"",""185"",""2056"",""2099"",""2147"",""2153"",""2155"",""2161"",""2162"",""217"",""2244"",""2729"",""2811"",""3077"",""308"",""3082"",""3084"",""3091"",""3240"",""328"",""335"",""337"",""339479"",""348"",""350"",""3586"",""3673"",""3690"",""3700"",""3783"",""3791"",""3816"",""3957"",""4018"",""4023"",""4035"",""4043"",""4049"",""4261"",""4312"",""4314"",""4318"",""4323"",""4803"",""4846"",""4878"",""4879"",""4881"",""4973"",""5054"",""5069"",""51085"",""51206"",""5126"",""5175"",""5228"",""5327"",""5328"",""5444"",""5465"",""5687"",""5740"",""5743"",""6347"",""6403"",""6647"",""6649"",""6696"",""7035"",""7040"",""7099"",""7292"",""729230"",""7423"",""7804"",""79068"",""929"",""9388""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:5844""}]"
DOID:585	"[""nephrolithiasis"",""Stone - kidney/ureter"",""kidney stones""]"	"[{""label"":""CASR"",""id"":""846""},{""label"":""SLC34A1"",""id"":""6569""}]"	"[""6569"",""846""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:585""}]"
DOID:589	"[""congenital hemolytic anemia"",""congenital hemolytic anaemia"",""hereditary hemolytic anaemia"",""hereditary hemolytic anemia""]"	"[{""label"":""GPI"",""id"":""2821""},{""label"":""HBB"",""id"":""3043""},{""label"":""SLC4A1"",""id"":""6521""}]"	"[""2821"",""3043"",""6521""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:589""}]"
DOID:591	"[""phobic disorder""]"	"[{""label"":""HRAS"",""id"":""3265""},{""label"":""MED12"",""id"":""9968""}]"	"[""3265"",""9968""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:591""}]"
DOID:594	"[""panic disorder"",""panic anxiety syndrome""]"	"[{""label"":""CCKBR"",""id"":""887""},{""label"":""HTR1A"",""id"":""3350""},{""label"":""MANEA"",""id"":""79694""},{""label"":""MAOA"",""id"":""4128""},{""label"":""MBL2"",""id"":""4153""}]"	"[""3350"",""4128"",""4153"",""79694"",""887""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:594""}]"
DOID:594	"[""panic disorder"",""panic anxiety syndrome""]"	"[{""label"":""Htr1a"",""id"":""24473""}]"	"[""24473""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:594""}]"
DOID:6000	"[""congestive heart failure"",""CHF"",""Cardiac Failure Congestive"",""Congestive heart disease"",""Weak heart""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Adrb1"",""id"":""24925""},{""label"":""Agtr1a"",""id"":""24180""},{""label"":""Creb1"",""id"":""81646""},{""label"":""Cs"",""id"":""170587""},{""label"":""Hmgb1"",""id"":""25459""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Mdh2"",""id"":""81829""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Parp1"",""id"":""25591""},{""label"":""Pgf"",""id"":""94203""},{""label"":""Plcd1"",""id"":""24655""},{""label"":""Pln"",""id"":""64672""},{""label"":""Ryr2"",""id"":""689560""},{""label"":""Sox2"",""id"":""499593""},{""label"":""Tnf"",""id"":""24835""}]"	"[""170587"",""24180"",""24310"",""24536"",""24655"",""24835"",""24925"",""25459"",""25591"",""29595"",""499593"",""64672"",""689560"",""81646"",""81687"",""81829"",""94203""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6000""}]"
DOID:6000	"[""congestive heart failure"",""CHF"",""Cardiac Failure Congestive"",""Congestive heart disease"",""Weak heart""]"	"[{""label"":""Ace2"",""id"":""70008""},{""label"":""Calr"",""id"":""12317""},{""label"":""Cxcr4"",""id"":""12767""},{""label"":""Med1"",""id"":""19014""},{""label"":""Ppargc1a"",""id"":""19017""},{""label"":""Sod2"",""id"":""20656""},{""label"":""Tnf"",""id"":""21926""}]"	"[""12317"",""12767"",""19014"",""19017"",""20656"",""21926"",""70008""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6000""}]"
DOID:6000	"[""congestive heart failure"",""CHF"",""Cardiac Failure Congestive"",""Congestive heart disease"",""Weak heart""]"	"[{""label"":""ADRA2C"",""id"":""152""},{""label"":""ADRB1"",""id"":""153""},{""label"":""AGT"",""id"":""183""},{""label"":""APOE"",""id"":""348""},{""label"":""CBL"",""id"":""867""},{""label"":""CCR2"",""id"":""729230""},{""label"":""EDN1"",""id"":""1906""},{""label"":""EP300"",""id"":""2033""},{""label"":""EPO"",""id"":""2056""},{""label"":""EYA4"",""id"":""2070""},{""label"":""EZH2"",""id"":""2146""},{""label"":""GNB1"",""id"":""2782""},{""label"":""MMP1"",""id"":""4312""},{""label"":""PHF6"",""id"":""84295""},{""label"":""RYR1"",""id"":""6261""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""SLC9A1"",""id"":""6548""},{""label"":""SMC1A"",""id"":""8243""},{""label"":""SRSF2"",""id"":""6427""},{""label"":""TNFRSF1B"",""id"":""7133""},{""label"":""YY1"",""id"":""7528""}]"	"[""152"",""153"",""183"",""1906"",""2033"",""2056"",""2070"",""2146"",""2782"",""348"",""4312"",""6261"",""6427"",""6532"",""6548"",""7133"",""729230"",""7528"",""8243"",""84295"",""867""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6000""}]"
DOID:6039	"[""uveal melanoma"",""melanoma of Uvea""]"	"[{""label"":""Grm1"",""id"":""14816""}]"	"[""14816""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6039""}]"
DOID:6039	"[""uveal melanoma"",""melanoma of Uvea""]"	"[{""label"":""BAP1"",""id"":""8314""},{""label"":""BRCA2"",""id"":""675""},{""label"":""MBD4"",""id"":""8930""},{""label"":""SERPINE1"",""id"":""5054""}]"	"[""5054"",""675"",""8314"",""8930""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6039""}]"
DOID:61	"[""mitral valve disease"",""Mitral RH valve dis."",""Rheumatic mitral insufficiency"",""Rheumatic mitral valve changes"",""Rheumatic mitral valve regurgitation"",""chronic rheumatic mitral valve"",""disease of mitral valve"",""rheumatic disease of mitral valve"",""rheumatic mitral valve incompetence""]"	"[{""label"":""ACE"",""id"":""1636""}]"	"[""1636""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:61""}]"
DOID:612	"[""primary immunodeficiency disease"",""hypoimmunity"",""immune deficiency disorder"",""immunodeficiency syndrome""]"	"[{""label"":""Tl"",""id"":""43222""}]"	"[""43222""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:612""}]"
DOID:612	"[""primary immunodeficiency disease"",""hypoimmunity"",""immune deficiency disorder"",""immunodeficiency syndrome""]"	"[{""label"":""Magt1"",""id"":""67075""}]"	"[""67075""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:612""}]"
DOID:612	"[""primary immunodeficiency disease"",""hypoimmunity"",""immune deficiency disorder"",""immunodeficiency syndrome""]"	"[{""label"":""ARPC5"",""id"":""10092""},{""label"":""CARD10"",""id"":""29775""},{""label"":""CARD9"",""id"":""64170""},{""label"":""CD8A"",""id"":""925""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CTNNBL1"",""id"":""56259""},{""label"":""FADD"",""id"":""8772""},{""label"":""FCHO1"",""id"":""23149""},{""label"":""FNIP1"",""id"":""96459""},{""label"":""IFNAR1"",""id"":""3454""},{""label"":""IKZF3"",""id"":""22806""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL6ST"",""id"":""3572""},{""label"":""IL7R"",""id"":""3575""},{""label"":""IRAK4"",""id"":""51135""},{""label"":""LIG1"",""id"":""3978""},{""label"":""MCM10"",""id"":""55388""},{""label"":""MCTS1"",""id"":""28985""},{""label"":""MPEG1"",""id"":""219972""},{""label"":""MYD88"",""id"":""4615""},{""label"":""OAS1"",""id"":""4938""},{""label"":""OTULIN"",""id"":""90268""},{""label"":""PIK3CG"",""id"":""5294""},{""label"":""PTPRC"",""id"":""5788""},{""label"":""REL"",""id"":""5966""},{""label"":""SLC19A1"",""id"":""6573""},{""label"":""SPPL2A"",""id"":""84888""},{""label"":""STK4"",""id"":""6789""},{""label"":""SYK"",""id"":""6850""},{""label"":""TET2"",""id"":""54790""},{""label"":""TLR3"",""id"":""7098""},{""label"":""TLR8"",""id"":""51311""},{""label"":""TNFRSF9"",""id"":""3604""},{""label"":""TPP2"",""id"":""7174""},{""label"":""ZNFX1"",""id"":""57169""}]"	"[""10092"",""1493"",""219972"",""22806"",""23149"",""28985"",""29775"",""3454"",""3558"",""3572"",""3575"",""3604"",""3978"",""4615"",""4938"",""51135"",""51311"",""5294"",""54790"",""55388"",""56259"",""57169"",""5788"",""5966"",""64170"",""6573"",""6789"",""6850"",""7098"",""7174"",""84888"",""8772"",""90268"",""925"",""96459""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:612""}]"
DOID:6132	"[""bronchitis"",""CI - Chest infection"",""Chest infection"",""acute Bronchitis"",""chest cold"",""chronic bronchitis"",""recurrent wheezy bronchitis""]"	"[{""label"":""CYP1A1"",""id"":""1543""}]"	"[""1543""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6132""}]"
DOID:614	"[""lymphopenia"",""Lymphocytopenia""]"	"[{""label"":""Cd28"",""id"":""25660""},{""label"":""Ednrb"",""id"":""50672""}]"	"[""25660"",""50672""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:614""}]"
DOID:614	"[""lymphopenia"",""Lymphocytopenia""]"	"[{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""IL2RA"",""id"":""3559""}]"	"[""2212"",""2214"",""3559""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:614""}]"
DOID:615	"[""leukopenia"",""Leucopenia""]"	"[{""label"":""CXCR4"",""id"":""7852""}]"	"[""7852""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:615""}]"
DOID:6195	"[""conjunctivitis""]"	"[{""label"":""Mmp2"",""id"":""81686""}]"	"[""81686""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6195""}]"
DOID:6195	"[""conjunctivitis""]"	"[{""label"":""PLG"",""id"":""5340""}]"	"[""5340""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6195""}]"
DOID:6196	"[""reactive arthritis"",""Fiessinger Leroy Reiter syndrome"",""Post-bacterial arthropathy"",""Reiter disease"",""Reiter's disease"",""postdysenteric arthropathy""]"	"[{""label"":""CYP1A1"",""id"":""1543""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TAP1"",""id"":""6890""}]"	"[""1543"",""3106"",""6648"",""6890""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6196""}]"
DOID:62	"[""aortic valve disease""]"	"[{""label"":""Adamts19"",""id"":""240322""},{""label"":""Egfr"",""id"":""13649""},{""label"":""Nos3"",""id"":""18127""}]"	"[""13649"",""18127"",""240322""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:62""}]"
DOID:620	"[""blood protein disease"",""blood protein disorder""]"	"[{""label"":""ALB"",""id"":""213""}]"	"[""213""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:620""}]"
DOID:627	"[""severe combined immunodeficiency"",""SCID"",""combined T and B cell inborn immunodeficiency""]"	"[{""label"":""CD3D"",""id"":""915""},{""label"":""DCLRE1C"",""id"":""64421""},{""label"":""IL2RG"",""id"":""3561""},{""label"":""IL7R"",""id"":""3575""},{""label"":""JAK3"",""id"":""3718""},{""label"":""PTPRC"",""id"":""5788""},{""label"":""RFX5"",""id"":""5993""},{""label"":""TAPBP"",""id"":""6892""},{""label"":""ZAP70"",""id"":""7535""}]"	"[""3561"",""3575"",""3718"",""5788"",""5993"",""64421"",""6892"",""7535"",""915""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:627""}]"
DOID:6270	"[""gastric cardia carcinoma"",""carcinoma of Cardia of stomach""]"	"[{""label"":""XRCC1"",""id"":""7515""}]"	"[""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6270""}]"
DOID:6271	"[""gastric cardia adenocarcinoma"",""adenocarcinoma of Cardia of stomach""]"	"[{""label"":""XRCC1"",""id"":""7515""}]"	"[""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6271""}]"
DOID:628	"[""combined T cell and B cell immunodeficiency"",""Congenital Combined Immunodeficiency""]"	"[{""label"":""CD40LG"",""id"":""959""},{""label"":""IL2RG"",""id"":""3561""}]"	"[""3561"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:628""}]"
DOID:630	"[""genetic disease""]"	"[{""label"":""COG7"",""id"":""91949""}]"	"[""91949""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:630""}]"
DOID:631	"[""fibromyalgia""]"	"[{""label"":""COMT"",""id"":""1312""}]"	"[""1312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:631""}]"
DOID:633	"[""myositis"",""Inflammatory disorder of muscle""]"	"[{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""2214"",""3117"",""3119"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:633""}]"
DOID:633	"[""myositis"",""Inflammatory disorder of muscle""]"	"[{""label"":""H2-K1"",""id"":""14972""}]"	"[""14972""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:633""}]"
DOID:635	"[""acquired immunodeficiency syndrome"",""AIDS"",""acquired Immune deficiency""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""BST2"",""id"":""684""},{""label"":""CD209"",""id"":""30835""},{""label"":""HLA-A"",""id"":""3105""},{""label"":""KIR2DL1"",""id"":""3802""},{""label"":""KIR3DS1"",""id"":""3813""}]"	"[""30835"",""3105"",""3802"",""3813"",""5243"",""684""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:635""}]"
DOID:6364	"[""migraine"",""migraine disorder"",""migraine variant"",""migraine with or without aura""]"	"[{""label"":""Htr7"",""id"":""65032""}]"	"[""65032""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6364""}]"
DOID:6364	"[""migraine"",""migraine disorder"",""migraine variant"",""migraine with or without aura""]"	"[{""label"":""CACNA1A"",""id"":""773""},{""label"":""CALCA"",""id"":""796""},{""label"":""EDNRA"",""id"":""1909""},{""label"":""ESR1"",""id"":""2099""},{""label"":""KCNK18"",""id"":""338567""},{""label"":""NOS3"",""id"":""4846""},{""label"":""TNF"",""id"":""7124""},{""label"":""TRPV1"",""id"":""7442""}]"	"[""1909"",""2099"",""338567"",""4846"",""7124"",""7442"",""773"",""796""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6364""}]"
DOID:639	"[""acute disseminated encephalomyelitis"",""ADEM"",""acute disseminated encephalitis""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HLA-DRB5"",""id"":""3127""}]"	"[""3119"",""3123"",""3127""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:639""}]"
DOID:640	"[""encephalomyelitis"",""Encephalitis \u0026/or myelitis""]"	"[{""label"":""Ikzf4"",""id"":""22781""}]"	"[""22781""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:640""}]"
DOID:640	"[""encephalomyelitis"",""Encephalitis \u0026/or myelitis""]"	"[{""label"":""Spp1"",""id"":""25353""}]"	"[""25353""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:640""}]"
DOID:6406	"[""double outlet right ventricle"",""Dextrotransposition of aorta"",""Double outlet right ventricle with subpulmonary ventricular septal defect"",""Taussig-Bing syndrome or defect""]"	"[{""label"":""Cfc1"",""id"":""12627""},{""label"":""Ece1"",""id"":""230857""}]"	"[""12627"",""230857""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6406""}]"
DOID:6419	"[""tetralogy of Fallot"",""Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle""]"	"[{""label"":""Bmp10"",""id"":""12154""},{""label"":""Dnah5"",""id"":""110082""},{""label"":""Fgf8"",""id"":""14179""},{""label"":""Ntf3"",""id"":""18205""},{""label"":""Phc1"",""id"":""13619""}]"	"[""110082"",""12154"",""13619"",""14179"",""18205""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6419""}]"
DOID:6419	"[""tetralogy of Fallot"",""Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle""]"	"[{""label"":""popdc1"",""id"":""415107""}]"	"[""415107""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6419""}]"
DOID:6419	"[""tetralogy of Fallot"",""Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle""]"	"[{""label"":""CFC1B"",""id"":""653275""},{""label"":""GATA4"",""id"":""2626""},{""label"":""JAG1"",""id"":""182""},{""label"":""MTHFD1"",""id"":""4522""},{""label"":""NRP1"",""id"":""8829""},{""label"":""PTPN11"",""id"":""5781""}]"	"[""182"",""2626"",""4522"",""5781"",""653275"",""8829""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6419""}]"
DOID:6420	"[""pulmonary valve stenosis""]"	"[{""label"":""SOS1"",""id"":""6654""}]"	"[""6654""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6420""}]"
DOID:6432	"[""pulmonary hypertension""]"	"[{""label"":""ACE2"",""id"":""59272""},{""label"":""ACVRL1"",""id"":""94""},{""label"":""ADM"",""id"":""133""},{""label"":""AGTR1"",""id"":""185""},{""label"":""ALOX5"",""id"":""240""},{""label"":""ATP2A2"",""id"":""488""},{""label"":""BMPR2"",""id"":""659""},{""label"":""CSF3"",""id"":""1440""},{""label"":""CYP2J2"",""id"":""1573""},{""label"":""EDNRA"",""id"":""1909""},{""label"":""EPAS1"",""id"":""2034""},{""label"":""EPO"",""id"":""2056""},{""label"":""F5"",""id"":""2153""},{""label"":""HP"",""id"":""3240""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL23R"",""id"":""149233""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NOS2"",""id"":""4843""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PTGIS"",""id"":""5740""},{""label"":""PTK2"",""id"":""5747""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""VEGFB"",""id"":""7423""},{""label"":""VWF"",""id"":""7450""}]"	"[""133"",""1440"",""149233"",""1573"",""185"",""1909"",""2034"",""2056"",""2153"",""240"",""3240"",""3557"",""4318"",""4843"",""4846"",""488"",""5054"",""5740"",""5747"",""59272"",""6532"",""659"",""7040"",""7423"",""7450"",""94""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6432""}]"
DOID:6432	"[""pulmonary hypertension""]"	"[{""label"":""Cavin1"",""id"":""19285""}]"	"[""19285""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6432""}]"
DOID:6432	"[""pulmonary hypertension""]"	"[{""label"":""Agt"",""id"":""24179""},{""label"":""Atp5f1a"",""id"":""65262""},{""label"":""Atp5pf"",""id"":""94271""},{""label"":""Bdkrb2"",""id"":""25245""},{""label"":""Cxcr4"",""id"":""60628""},{""label"":""Cysltr1"",""id"":""114099""},{""label"":""Ednra"",""id"":""24326""},{""label"":""Ednrb"",""id"":""50672""},{""label"":""Esr2"",""id"":""25149""},{""label"":""Fgfr1"",""id"":""79114""},{""label"":""Hmgb1"",""id"":""25459""},{""label"":""Hmgcr"",""id"":""25675""},{""label"":""Kcnk3"",""id"":""29553""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Myc"",""id"":""24577""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Nox1"",""id"":""114243""},{""label"":""Pecam1"",""id"":""29583""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Serpina1"",""id"":""24648""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Slc6a4"",""id"":""25553""},{""label"":""Tacr1"",""id"":""24807""},{""label"":""Tacr2"",""id"":""25007""},{""label"":""Tgfbr1"",""id"":""29591""},{""label"":""Tnc"",""id"":""116640""},{""label"":""Vip"",""id"":""117064""}]"	"[""114099"",""114243"",""116640"",""117064"",""24179"",""24326"",""24577"",""24600"",""24617"",""24648"",""24807"",""25007"",""25149"",""25245"",""25459"",""25553"",""25675"",""29527"",""29553"",""29583"",""29591"",""50672"",""60628"",""65262"",""79114"",""81687"",""94271""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6432""}]"
DOID:648	"[""kuru"",""kuru encephalopathy""]"	"[{""label"":""PRNP"",""id"":""5621""}]"	"[""5621""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:648""}]"
DOID:649	"[""prion disease"",""Prion disease pathway"",""Prion protein disease"",""Spongiform Encephalopathy"",""prion induced disorder"",""transmissible spongiform encephalopathy""]"	"[{""label"":""SOD1"",""id"":""6647""}]"	"[""6647""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:649""}]"
DOID:6498	"[""seborrheic keratosis""]"	"[{""label"":""PIK3CA"",""id"":""5290""}]"	"[""5290""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6498""}]"
DOID:65	"[""connective tissue disease"",""connective tissue disorder"",""disorder of connective tissue""]"	"[{""label"":""fbn-1"",""id"":""176076""}]"	"[""176076""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:65""}]"
DOID:65	"[""connective tissue disease"",""connective tissue disorder"",""disorder of connective tissue""]"	"[{""label"":""SNRPA1"",""id"":""6627""},{""label"":""SNRPA"",""id"":""6626""},{""label"":""SNRPB2"",""id"":""6629""},{""label"":""SNRPC"",""id"":""6631""},{""label"":""SNRPD1"",""id"":""6632""}]"	"[""6626"",""6627"",""6629"",""6631"",""6632""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:65""}]"
DOID:653	"[""purine-pyrimidine metabolic disorder"",""inborn errors of purine-pyrimidine metabolism""]"	"[{""label"":""ATIC"",""id"":""471""},{""label"":""PNP"",""id"":""4860""},{""label"":""UMPS"",""id"":""7372""}]"	"[""471"",""4860"",""7372""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:653""}]"
DOID:6543	"[""acne"",""Acne varioliformis"",""acne vulgaris"",""frontalis acne""]"	"[{""label"":""IL4R"",""id"":""3566""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF1A"",""id"":""7132""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""3566"",""7097"",""7124"",""7132"",""7133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6543""}]"
DOID:655	"[""inherited metabolic disorder"",""Inborn Errors of Metabolism"",""Metabolic hereditary disorder"",""inborn metabolism disorder""]"	"[{""label"":""BCHE"",""id"":""590""},{""label"":""GPHN"",""id"":""10243""},{""label"":""HSD11B2"",""id"":""3291""},{""label"":""LIG1"",""id"":""3978""},{""label"":""MMAB"",""id"":""326625""},{""label"":""NDUFS1"",""id"":""4719""},{""label"":""NDUFS2"",""id"":""4720""},{""label"":""SLC22A5"",""id"":""6584""},{""label"":""SLC25A19"",""id"":""60386""}]"	"[""10243"",""326625"",""3291"",""3978"",""4719"",""4720"",""590"",""60386"",""6584""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:655""}]"
DOID:657	"[""adenoma"",""acinar cell adenoma"",""acinic cell adenoma"",""adenomas""]"	"[{""label"":""APC"",""id"":""324""}]"	"[""324""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:657""}]"
DOID:6612	"[""leukocyte adhesion deficiency"",""Congenital leukocyte adherence deficiency""]"	"[{""label"":""ITGB2"",""id"":""3689""}]"	"[""3689""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6612""}]"
DOID:6652	"[""diffuse idiopathic skeletal hyperostosis"",""Ankylosing vertebral hyperostosis"",""DISH"",""Disseminated idiopathic skeletal hyperostosis""]"	"[{""label"":""Slc29a1"",""id"":""63959""}]"	"[""63959""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6652""}]"
DOID:6688	"[""autoimmune lymphoproliferative syndrome"",""ALPS"",""Canale-Smith syndrome""]"	"[{""label"":""Fas"",""id"":""14102""},{""label"":""Fasl"",""id"":""14103""}]"	"[""14102"",""14103""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6688""}]"
DOID:6688	"[""autoimmune lymphoproliferative syndrome"",""ALPS"",""Canale-Smith syndrome""]"	"[{""label"":""FAS"",""id"":""355""},{""label"":""FASLG"",""id"":""356""}]"	"[""355"",""356""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6688""}]"
DOID:670	"[""amphetamine abuse""]"	"[{""label"":""AKT1"",""id"":""207""},{""label"":""COMT"",""id"":""1312""},{""label"":""GABBR1"",""id"":""2550""},{""label"":""GABRG2"",""id"":""2566""},{""label"":""GAD1"",""id"":""2571""},{""label"":""GAD2"",""id"":""2572""},{""label"":""NPY1R"",""id"":""4886""}]"	"[""1312"",""207"",""2550"",""2566"",""2571"",""2572"",""4886""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:670""}]"
DOID:670	"[""amphetamine abuse""]"	"[{""label"":""Snca"",""id"":""29219""}]"	"[""29219""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:670""}]"
DOID:670	"[""amphetamine abuse""]"	"[{""label"":""cat-1"",""id"":""180837""}]"	"[""180837""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:670""}]"
DOID:6713	"[""cerebrovascular disease"",""CVA"",""cerebrovascular disorder"",""stroke""]"	"[{""label"":""AGT"",""id"":""183""},{""label"":""AGTR1"",""id"":""185""},{""label"":""APOE"",""id"":""348""},{""label"":""G6PD"",""id"":""2539""},{""label"":""GLCE"",""id"":""26035""},{""label"":""LMNA"",""id"":""4000""},{""label"":""NR1H3"",""id"":""10062""},{""label"":""P2RY12"",""id"":""64805""},{""label"":""SELE"",""id"":""6401""}]"	"[""10062"",""183"",""185"",""2539"",""26035"",""348"",""4000"",""6401"",""64805""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6713""}]"
DOID:674	"[""cleft palate"",""Palatoschisis""]"	"[{""label"":""Specc1l"",""id"":""74392""}]"	"[""74392""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:674""}]"
DOID:674	"[""cleft palate"",""Palatoschisis""]"	"[{""label"":""COL11A2"",""id"":""1302""},{""label"":""COL2A1"",""id"":""1280""},{""label"":""FLNB"",""id"":""2317""},{""label"":""GDF6"",""id"":""392255""},{""label"":""MTHFD1"",""id"":""4522""},{""label"":""NECTIN1"",""id"":""5818""},{""label"":""ROR2"",""id"":""4920""},{""label"":""SDC2"",""id"":""6383""}]"	"[""1280"",""1302"",""2317"",""392255"",""4522"",""4920"",""5818"",""6383""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:674""}]"
DOID:676	"[""juvenile rheumatoid arthritis"",""Pauciarticular onset juvenile chronic arthritis"",""Still's disease"",""acute juvenile rheumatoid arthritis"",""juvenile chronic polyarthritis"",""juvenile idiopathic arthritis"",""monarticular juvenile rheumatoid arthritis"",""pauciarticular juvenile arthritis"",""systemic juvenile rheumatoid arthritis""]"	"[{""label"":""CCR5"",""id"":""1234""},{""label"":""CIITA"",""id"":""4261""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL1A"",""id"":""3552""},{""label"":""LACC1"",""id"":""144811""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""SLC26A2"",""id"":""1836""}]"	"[""1234"",""144811"",""1836"",""3077"",""3117"",""3119"",""3123"",""3552"",""4261"",""6556""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:676""}]"
DOID:678	"[""progressive supranuclear palsy"",""Steele-Richardson-Olszewski syndrome"",""progressive supranuclear ophthalmoplegia""]"	"[{""label"":""MAP2K6"",""id"":""5608""},{""label"":""MAPT"",""id"":""4137""},{""label"":""NAT2"",""id"":""10""}]"	"[""10"",""4137"",""5608""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:678""}]"
DOID:680	"[""tauopathy""]"	"[{""label"":""MAPT"",""id"":""4137""}]"	"[""4137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:680""}]"
DOID:684	"[""hepatocellular carcinoma"",""Hepatoma""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ACE"",""id"":""1636""},{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""ALB"",""id"":""213""},{""label"":""ALDH2"",""id"":""217""},{""label"":""ALX4"",""id"":""60529""},{""label"":""APC"",""id"":""324""},{""label"":""APOC3"",""id"":""345""},{""label"":""ARID1A"",""id"":""8289""},{""label"":""ARID2"",""id"":""196528""},{""label"":""ASS1"",""id"":""445""},{""label"":""BMI1"",""id"":""648""},{""label"":""CALR"",""id"":""811""},{""label"":""CAT"",""id"":""847""},{""label"":""CBX4"",""id"":""8535""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CDH1"",""id"":""999""},{""label"":""CDK13"",""id"":""8621""},{""label"":""CEP164"",""id"":""22897""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""CSF1R"",""id"":""1436""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CTNNB1"",""id"":""1499""},{""label"":""CYP2C19"",""id"":""1557""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""DICER1"",""id"":""23405""},{""label"":""EFTUD2"",""id"":""9343""},{""label"":""EGF"",""id"":""1950""},{""label"":""ERBB4"",""id"":""2066""},{""label"":""ERN1"",""id"":""2081""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FGFR1"",""id"":""2260""},{""label"":""FGFR2"",""id"":""2263""},{""label"":""FLT3"",""id"":""2322""},{""label"":""FOXA1"",""id"":""3169""},{""label"":""FUBP1"",""id"":""8880""},{""label"":""G6PC1"",""id"":""2538""},{""label"":""GC"",""id"":""2638""},{""label"":""GPX1"",""id"":""2876""},{""label"":""GPX3"",""id"":""2878""},{""label"":""HAVCR2"",""id"":""84868""},{""label"":""HFE"",""id"":""3077""},{""label"":""HILPDA"",""id"":""29923""},{""label"":""HLA-DPA1"",""id"":""3113""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""HNRNPAB"",""id"":""3182""},{""label"":""HRAS"",""id"":""3265""},{""label"":""IFNA2"",""id"":""3440""},{""label"":""IFNL1"",""id"":""282618""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""IGF2"",""id"":""3481""},{""label"":""IGF2R"",""id"":""3482""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL12A"",""id"":""3592""},{""label"":""IL21"",""id"":""59067""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL6"",""id"":""3569""},{""label"":""JAK1"",""id"":""3716""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""KDR"",""id"":""3791""},{""label"":""KIF1B"",""id"":""23095""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""KLF4"",""id"":""9314""},{""label"":""KMT2B"",""id"":""9757""},{""label"":""LEP"",""id"":""3952""},{""label"":""LEPR"",""id"":""3953""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""MAP4K4"",""id"":""9448""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MCM7"",""id"":""4176""},{""label"":""MDM2"",""id"":""4193""},{""label"":""MET"",""id"":""4233""},{""label"":""MPO"",""id"":""4353""},{""label"":""MTDH"",""id"":""92140""},{""label"":""MYD88"",""id"":""4615""},{""label"":""NFE2L2"",""id"":""4780""},{""label"":""NFKB1"",""id"":""4790""},{""label"":""NRAS"",""id"":""4893""},{""label"":""PDCD1"",""id"":""5133""},{""label"":""PDGFRL"",""id"":""5157""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PINX1"",""id"":""54984""},{""label"":""PLCG1"",""id"":""5335""},{""label"":""PNPLA3"",""id"":""80339""},{""label"":""PPARA"",""id"":""5465""},{""label"":""PRDM1"",""id"":""639""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""PTPN13"",""id"":""5783""},{""label"":""RECQL"",""id"":""5965""},{""label"":""RNF43"",""id"":""54894""},{""label"":""RYR3"",""id"":""6263""},{""label"":""SF3B1"",""id"":""23451""},{""label"":""SF3B4"",""id"":""10262""},{""label"":""SLC38A1"",""id"":""81539""},{""label"":""SLC7A5"",""id"":""8140""},{""label"":""SMARCA4"",""id"":""6597""},{""label"":""SMC3"",""id"":""9126""},{""label"":""SMO"",""id"":""6608""},{""label"":""SNRPE"",""id"":""6635""},{""label"":""SOAT2"",""id"":""8435""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SOX30"",""id"":""11063""},{""label"":""SPAG9"",""id"":""9043""},{""label"":""SPOCK1"",""id"":""6695""},{""label"":""SPOP"",""id"":""8405""},{""label"":""SPP1"",""id"":""6696""},{""label"":""SRSF2"",""id"":""6427""},{""label"":""STAT4"",""id"":""6775""},{""label"":""TEP1"",""id"":""7011""},{""label"":""TERT"",""id"":""7015""},{""label"":""TET2"",""id"":""54790""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNF"",""id"":""7124""},{""label"":""TP53"",""id"":""7157""},{""label"":""TRAF7"",""id"":""84231""},{""label"":""TYMS"",""id"":""7298""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""WNT2"",""id"":""7472""},{""label"":""XPO1"",""id"":""7514""},{""label"":""XPO5"",""id"":""57510""},{""label"":""XRCC1"",""id"":""7515""},{""label"":""ZFHX3"",""id"":""463""}]"	"[""10262"",""11063"",""1436"",""1493"",""1499"",""1557"",""1571"",""1636"",""1950"",""196528"",""2066"",""2081"",""213"",""2146"",""217"",""2260"",""2263"",""22897"",""23095"",""2322"",""23405"",""23451"",""2538"",""2638"",""282618"",""2876"",""2878"",""29923"",""3077"",""3113"",""3117"",""3119"",""3169"",""3182"",""324"",""3265"",""3440"",""345"",""3480"",""3481"",""3482"",""3558"",""3569"",""3586"",""3592"",""3716"",""3791"",""3813"",""3952"",""3953"",""4153"",""4176"",""4193"",""4233"",""4353"",""445"",""4615"",""463"",""4780"",""4790"",""4893"",""5133"",""5157"",""5243"",""5290"",""5335"",""53353"",""54106"",""5465"",""54790"",""54894"",""54984"",""5743"",""57510"",""5783"",""59067"",""5965"",""60529"",""6263"",""6347"",""6352"",""639"",""6427"",""648"",""6597"",""6608"",""6635"",""6648"",""6695"",""6696"",""6775"",""6927"",""7011"",""7015"",""7097"",""7099"",""7124"",""7157"",""7298"",""7403"",""7422"",""7472"",""7514"",""7515"",""80339"",""81037"",""811"",""8140"",""81539"",""8289"",""8405"",""84231"",""8435"",""847"",""84868"",""8535"",""8621"",""8880"",""9043"",""9126"",""92140"",""9314"",""9343"",""9370"",""9448"",""9757"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:684""}]"
DOID:684	"[""hepatocellular carcinoma"",""Hepatoma""]"	"[{""label"":""COX1"",""id"":""26195""},{""label"":""Cdh1"",""id"":""83502""},{""label"":""Gpc3"",""id"":""25236""},{""label"":""Il10"",""id"":""25325""},{""label"":""Lep"",""id"":""25608""},{""label"":""Lpar1"",""id"":""116744""},{""label"":""Myc"",""id"":""24577""},{""label"":""Ppara"",""id"":""25747""}]"	"[""116744"",""24577"",""25236"",""25325"",""25608"",""25747"",""26195"",""83502""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:684""}]"
DOID:684	"[""hepatocellular carcinoma"",""Hepatoma""]"	"[{""label"":""LAG1"",""id"":""856386""}]"	"[""856386""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:684""}]"
DOID:684	"[""hepatocellular carcinoma"",""Hepatoma""]"	"[{""label"":""Abcb4"",""id"":""18670""},{""label"":""Gnmt"",""id"":""14711""},{""label"":""Krt18"",""id"":""16668""},{""label"":""Myc"",""id"":""17869""},{""label"":""Nfe2l1"",""id"":""18023""},{""label"":""Uaca"",""id"":""72565""}]"	"[""14711"",""16668"",""17869"",""18023"",""18670"",""72565""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:684""}]"
DOID:6846	"[""familial melanoma""]"	"[{""label"":""MC1R"",""id"":""4157""},{""label"":""MITF"",""id"":""4286""},{""label"":""TERT"",""id"":""7015""}]"	"[""4157"",""4286"",""7015""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:6846""}]"
DOID:686	"[""liver carcinoma"",""Liver and Intrahepatic bile duct carcinoma""]"	"[{""label"":""IL10"",""id"":""3586""}]"	"[""3586""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:686""}]"
DOID:687	"[""hepatoblastoma""]"	"[{""label"":""DPEP1"",""id"":""1800""},{""label"":""MKI67"",""id"":""4288""}]"	"[""1800"",""4288""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:687""}]"
DOID:693	"[""dental enamel hypoplasia"",""enamel hypoplasia""]"	"[{""label"":""Cftr"",""id"":""24255""}]"	"[""24255""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:693""}]"
DOID:700	"[""mitochondrial metabolism disease""]"	"[{""label"":""HADHB"",""id"":""3032""}]"	"[""3032""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:700""}]"
DOID:7004	"[""ACTH-secreting pituitary adenoma"",""ACTH-Producing Pituitary Adenoma"",""Corticotroph adenoma"",""Corticotropinoma""]"	"[{""label"":""USP8"",""id"":""9101""}]"	"[""9101""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7004""}]"
DOID:705	"[""Leber hereditary optic neuropathy"",""Leber's hereditary optic neuropathy"",""Leber's optic atrophy""]"	"[{""label"":""ND3"",""id"":""4537""},{""label"":""ND5"",""id"":""4540""},{""label"":""SOD2"",""id"":""6648""},{""label"":""TP53"",""id"":""7157""}]"	"[""4537"",""4540"",""6648"",""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:705""}]"
DOID:707	"[""B-cell lymphoma"",""B-cell lymphocytic neoplasm""]"	"[{""label"":""Ezh2"",""id"":""14056""}]"	"[""14056""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:707""}]"
DOID:707	"[""B-cell lymphoma"",""B-cell lymphocytic neoplasm""]"	"[{""label"":""ABCG2"",""id"":""9429""},{""label"":""BRD2"",""id"":""6046""},{""label"":""BTK"",""id"":""695""},{""label"":""CD40"",""id"":""958""},{""label"":""EZH2"",""id"":""2146""},{""label"":""IL21R"",""id"":""50615""}]"	"[""2146"",""50615"",""6046"",""695"",""9429"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:707""}]"
DOID:7147	"[""ankylosing spondylitis"",""Bekhterev syndrome"",""Bekhterev's disease"",""Marie-Strumpell disease""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ANO6"",""id"":""196527""},{""label"":""ASPN"",""id"":""54829""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL17A"",""id"":""3605""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IRAK1"",""id"":""3654""},{""label"":""PTGER4"",""id"":""5734""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TNFRSF1B"",""id"":""7133""}]"	"[""149233"",""1543"",""1636"",""196527"",""3106"",""3117"",""3119"",""3123"",""3605"",""3654"",""54829"",""5734"",""6890"",""7133""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7147""}]"
DOID:7148	"[""rheumatoid arthritis"",""Arthritis or polyarthritis, rheumatic"",""atrophic Arthritis""]"	"[{""label"":""Dnase2a"",""id"":""13423""},{""label"":""Il6st"",""id"":""16195""},{""label"":""Tnf"",""id"":""21926""}]"	"[""13423"",""16195"",""21926""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7148""}]"
DOID:7148	"[""rheumatoid arthritis"",""Arthritis or polyarthritis, rheumatic"",""atrophic Arthritis""]"	"[{""label"":""Crp"",""id"":""25419""}]"	"[""25419""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7148""}]"
DOID:7148	"[""rheumatoid arthritis"",""Arthritis or polyarthritis, rheumatic"",""atrophic Arthritis""]"	"[{""label"":""ADRB3"",""id"":""155""},{""label"":""BTNL2"",""id"":""56244""},{""label"":""C4B"",""id"":""721""},{""label"":""CAST"",""id"":""831""},{""label"":""CCR1"",""id"":""1230""},{""label"":""CCR5"",""id"":""1234""},{""label"":""CD244"",""id"":""51744""},{""label"":""CD40"",""id"":""958""},{""label"":""CIITA"",""id"":""4261""},{""label"":""CLEC16A"",""id"":""23274""},{""label"":""EDN1"",""id"":""1906""},{""label"":""ELN"",""id"":""2006""},{""label"":""FAS"",""id"":""355""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IGF2"",""id"":""3481""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL17A"",""id"":""3605""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL3"",""id"":""3562""},{""label"":""IL4R"",""id"":""3566""},{""label"":""IRF5"",""id"":""3663""},{""label"":""MBD4"",""id"":""8930""},{""label"":""NPSR1"",""id"":""387129""},{""label"":""OPRM1"",""id"":""4988""},{""label"":""PLAUR"",""id"":""5329""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""SLC22A4"",""id"":""6583""},{""label"":""SPP1"",""id"":""6696""},{""label"":""STAT3"",""id"":""6774""},{""label"":""THBD"",""id"":""7056""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF1A"",""id"":""7132""},{""label"":""TYMS"",""id"":""7298""},{""label"":""VIM"",""id"":""7431""}]"	"[""1230"",""1234"",""149233"",""155"",""1906"",""2006"",""2212"",""2214"",""23274"",""3077"",""3117"",""3119"",""3123"",""3458"",""3481"",""355"",""3552"",""3557"",""3558"",""3562"",""3566"",""3586"",""3605"",""3663"",""387129"",""4261"",""4988"",""51744"",""5329"",""56244"",""5743"",""6556"",""6583"",""6696"",""6774"",""7056"",""7124"",""7132"",""721"",""7298"",""7431"",""831"",""8930"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7148""}]"
DOID:718	"[""autoimmune hemolytic anemia"",""Autoimmune haemolytic anaemia"",""autoimmune hemolytic anaemia""]"	"[{""label"":""CTLA4"",""id"":""1493""}]"	"[""1493""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:718""}]"
DOID:718	"[""autoimmune hemolytic anemia"",""Autoimmune haemolytic anaemia"",""autoimmune hemolytic anaemia""]"	"[{""label"":""Tslp"",""id"":""53603""}]"	"[""53603""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:718""}]"
DOID:7188	"[""autoimmune thyroiditis"",""Chronic Lymphocytic Thyroiditis"",""Hashimoto thyroiditis"",""Hashimoto's Disease"",""Hashimoto's syndrome"",""Hashimoto's thyroiditis"",""Lymphocytic Thyroiditis""]"	"[{""label"":""Il4"",""id"":""287287""}]"	"[""287287""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7188""}]"
DOID:7188	"[""autoimmune thyroiditis"",""Chronic Lymphocytic Thyroiditis"",""Hashimoto thyroiditis"",""Hashimoto's Disease"",""Hashimoto's syndrome"",""Hashimoto's thyroiditis"",""Lymphocytic Thyroiditis""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRA"",""id"":""3122""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""LRP2"",""id"":""4036""},{""label"":""MBL2"",""id"":""4153""},{""label"":""TG"",""id"":""7038""}]"	"[""1493"",""3117"",""3119"",""3122"",""3123"",""4036"",""4153"",""7038""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7188""}]"
DOID:7235	"[""pancreatic mucinous cystadenoma"",""pancreatic mucinous cystic neoplasm""]"	"[{""label"":""KRAS"",""id"":""3845""}]"	"[""3845""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7235""}]"
DOID:74	"[""hematopoietic system disease"",""Blood disease"",""Blood dyscrasia"",""DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS"",""Hematological disease"",""blood disorder"",""disease of haematopoietic system"",""disease of hematopoietic system"",""haematopoietic system disease""]"	"[{""label"":""Serpine1"",""id"":""24617""}]"	"[""24617""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:74""}]"
DOID:7400	"[""Nijmegen breakage syndrome"",""Berlin breakage syndrome"",""Microcephaly, normal intelligence and immunodeficiency"",""NBS"",""Seemanova syndrome II"",""Seemanova syndrome type 2"",""ataxia-telangiectasia variant"",""immunodeficiency-microcephaly-chromosomal instability syndrome"",""microcephaly-immunodeficiency-lymphoreticuloma syndrome""]"	"[{""label"":""NBN"",""id"":""4683""}]"	"[""4683""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7400""}]"
DOID:7442	"[""monoclonal gammopathy of uncertain significance"",""MGUS"",""Monoclonal gammopathy of undetermined significance""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""NEFH"",""id"":""4744""}]"	"[""1493"",""4744""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7442""}]"
DOID:746	"[""adenomatoid tumor"",""adenomatoid tumour"",""benign localised epithelial Mesothelioma"",""benign localized epithelial Mesothelioma""]"	"[{""label"":""TRAF7"",""id"":""84231""}]"	"[""84231""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:746""}]"
DOID:7474	"[""malignant pleural mesothelioma"",""malignant mesothelioma of pleura""]"	"[{""label"":""CHRNA7"",""id"":""1139""},{""label"":""SETD2"",""id"":""29072""},{""label"":""SMO"",""id"":""6608""}]"	"[""1139"",""29072"",""6608""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7474""}]"
DOID:75	"[""lymphatic system disease"",""Lymphangiopathy"",""Lymphatic disease"",""disease of lympoid system"",""disorder of lymph node and lymphatics"",""disorder of lymphatic system"",""disorder of lymphoid system"",""lymphatic disorder"",""lympoid system disease""]"	"[{""label"":""Lgmn"",""id"":""19141""}]"	"[""19141""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:75""}]"
DOID:750	"[""peptic ulcer disease"",""acute peptic ulcer with hemorrhage"",""acute peptic ulcer with hemorrhage and perforation"",""acute peptic ulcer without hemorrhage and without perforation""]"	"[{""label"":""Cnr1"",""id"":""25248""}]"	"[""25248""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:750""}]"
DOID:750	"[""peptic ulcer disease"",""acute peptic ulcer with hemorrhage"",""acute peptic ulcer with hemorrhage and perforation"",""acute peptic ulcer without hemorrhage and without perforation""]"	"[{""label"":""CYP2C19"",""id"":""1557""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""1557"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:750""}]"
DOID:7575	"[""pancreatic intraductal papillary-mucinous neoplasm""]"	"[{""label"":""AKT1"",""id"":""207""},{""label"":""TP53"",""id"":""7157""}]"	"[""207"",""7157""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7575""}]"
DOID:7596	"[""asbestos-related lung carcinoma""]"	"[{""label"":""RARB"",""id"":""5915""}]"	"[""5915""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7596""}]"
DOID:76	"[""stomach disease"",""Gastropathy"",""stomach disorder""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:76""}]"
DOID:76	"[""stomach disease"",""Gastropathy"",""stomach disorder""]"	"[{""label"":""Calca"",""id"":""24241""}]"	"[""24241""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:76""}]"
DOID:7614	"[""meninges sarcoma"",""Meningeal sarcoma"",""sarcoma of meninges""]"	"[{""label"":""Tp53"",""id"":""24842""}]"	"[""24842""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7614""}]"
DOID:767	"[""muscular atrophy"",""Amyotrophia"",""Muscle wasting"",""Wasting - muscle""]"	"[{""label"":""Crhr2"",""id"":""64680""}]"	"[""64680""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:767""}]"
DOID:768	"[""retinoblastoma"",""RB"",""RB - Retinoblastoma"",""neuroblastoma of Retina""]"	"[{""label"":""IFNB1"",""id"":""3456""},{""label"":""MGMT"",""id"":""4255""},{""label"":""MTR"",""id"":""4548""},{""label"":""RB1"",""id"":""5925""},{""label"":""SERPINF1"",""id"":""5176""}]"	"[""3456"",""4255"",""4548"",""5176"",""5925""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:768""}]"
DOID:769	"[""neuroblastoma""]"	"[{""label"":""ARID1A"",""id"":""8289""},{""label"":""ARID1B"",""id"":""57492""},{""label"":""CHAF1A"",""id"":""10036""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""KIF1B"",""id"":""23095""},{""label"":""NME1"",""id"":""4830""},{""label"":""NSD1"",""id"":""64324""},{""label"":""PECAM1"",""id"":""5175""}]"	"[""10036"",""23095"",""3480"",""4830"",""5175"",""57492"",""64324"",""8289""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:769""}]"
DOID:7693	"[""abdominal aortic aneurysm"",""AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1""]"	"[{""label"":""AHCY"",""id"":""191""},{""label"":""APOE"",""id"":""348""},{""label"":""ELN"",""id"":""2006""},{""label"":""FOLH1"",""id"":""2346""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""ITGAV"",""id"":""3685""},{""label"":""MMP12"",""id"":""4321""},{""label"":""MMP13"",""id"":""4322""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MTHFD1"",""id"":""4522""},{""label"":""MTR"",""id"":""4548""},{""label"":""PLA2G7"",""id"":""7941""},{""label"":""PON1"",""id"":""5444""},{""label"":""SLC19A1"",""id"":""6573""},{""label"":""SORT1"",""id"":""6272""},{""label"":""TYMS"",""id"":""7298""}]"	"[""191"",""2006"",""2346"",""3117"",""3123"",""348"",""3685"",""4312"",""4321"",""4322"",""4522"",""4548"",""5444"",""6272"",""6573"",""7298"",""7941""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7693""}]"
DOID:7693	"[""abdominal aortic aneurysm"",""AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Kng1"",""id"":""288001""},{""label"":""Mmp2"",""id"":""81686""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""P2ry12"",""id"":""64803""},{""label"":""Serpine1"",""id"":""24617""}]"	"[""24310"",""24617"",""288001"",""64803"",""81686"",""81687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7693""}]"
DOID:77	"[""gastrointestinal system disease"",""GIT disease"",""Gastroenteropathy"",""alimentary system disease"",""digestive system disorder"",""gastrointestinal disease"",""gastrointestinal disorder""]"	"[{""label"":""MECP2"",""id"":""4204""},{""label"":""TF"",""id"":""7018""},{""label"":""VCAM1"",""id"":""7412""}]"	"[""4204"",""7018"",""7412""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:77""}]"
DOID:7725	"[""epilepsy with generalized tonic-clonic seizures"",""Epileptic seizures, tonic-clonic"",""Grand Mal epilepsy"",""tonic-clonic epilepsy""]"	"[{""label"":""Kcna1"",""id"":""24520""},{""label"":""Lgi1"",""id"":""252892""}]"	"[""24520"",""252892""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7725""}]"
DOID:783	"[""end stage renal disease"",""end stage renal failure"",""end-stage kidney disease""]"	"[{""label"":""Cd2ap"",""id"":""12488""}]"	"[""12488""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:783""}]"
DOID:783	"[""end stage renal disease"",""end stage renal failure"",""end-stage kidney disease""]"	"[{""label"":""Abcc2"",""id"":""25303""},{""label"":""Ace"",""id"":""24310""},{""label"":""C6"",""id"":""24237""},{""label"":""Ccl2"",""id"":""24770""},{""label"":""Hmgcr"",""id"":""25675""},{""label"":""Irs1"",""id"":""25467""},{""label"":""Lcat"",""id"":""24530""},{""label"":""Nos1"",""id"":""24598""},{""label"":""Ptger4"",""id"":""84023""},{""label"":""Serpine1"",""id"":""24617""}]"	"[""24237"",""24310"",""24530"",""24598"",""24617"",""24770"",""25303"",""25467"",""25675"",""84023""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:783""}]"
DOID:783	"[""end stage renal disease"",""end stage renal failure"",""end-stage kidney disease""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""ADRB2"",""id"":""154""},{""label"":""AGTR2"",""id"":""186""},{""label"":""BDKRB1"",""id"":""623""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CD40"",""id"":""958""},{""label"":""CHGA"",""id"":""1113""},{""label"":""COL3A1"",""id"":""1281""},{""label"":""COL4A3"",""id"":""1285""},{""label"":""COL4A4"",""id"":""1286""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CXCR2"",""id"":""3579""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2C8"",""id"":""1558""},{""label"":""DRD2"",""id"":""1813""},{""label"":""ENPP1"",""id"":""5167""},{""label"":""F5"",""id"":""2153""},{""label"":""FGB"",""id"":""2244""},{""label"":""GLO1"",""id"":""2739""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""ITGA8"",""id"":""8516""},{""label"":""ITGB3"",""id"":""3690""},{""label"":""KLK1"",""id"":""3816""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP3"",""id"":""4314""},{""label"":""MPO"",""id"":""4353""},{""label"":""MYH9"",""id"":""4627""},{""label"":""NGF"",""id"":""4803""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PLAU"",""id"":""5328""},{""label"":""PPARG"",""id"":""5468""},{""label"":""SLC9A5"",""id"":""6553""},{""label"":""UCP2"",""id"":""7351""},{""label"":""VWF"",""id"":""7450""}]"	"[""1113"",""1281"",""1285"",""1286"",""1493"",""154"",""1543"",""1558"",""1636"",""1813"",""186"",""2153"",""2244"",""2739"",""3552"",""3557"",""3579"",""3690"",""3816"",""4153"",""4312"",""4314"",""4353"",""4627"",""4803"",""4846"",""5167"",""5328"",""5468"",""623"",""6347"",""6553"",""7351"",""7450"",""8516"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:783""}]"
DOID:784	"[""chronic kidney disease"",""CKD"",""CRF"",""chronic kidney failure"",""chronic renal disease"",""chronic renal failure syndrome"",""renal failure - chronic""]"	"[{""label"":""Agtr1a"",""id"":""24180""},{""label"":""Agtr2"",""id"":""24182""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Pcsk2"",""id"":""25121""}]"	"[""24180"",""24182"",""24536"",""25121""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:784""}]"
DOID:784	"[""chronic kidney disease"",""CKD"",""CRF"",""chronic kidney failure"",""chronic renal disease"",""chronic renal failure syndrome"",""renal failure - chronic""]"	"[{""label"":""Rtn3"",""id"":""20168""}]"	"[""20168""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:784""}]"
DOID:784	"[""chronic kidney disease"",""CKD"",""CRF"",""chronic kidney failure"",""chronic renal disease"",""chronic renal failure syndrome"",""renal failure - chronic""]"	"[{""label"":""AGER"",""id"":""177""},{""label"":""AGTR1"",""id"":""185""},{""label"":""AKAP12"",""id"":""9590""},{""label"":""APOC3"",""id"":""345""},{""label"":""COL6A3"",""id"":""1293""},{""label"":""CPB2"",""id"":""1361""},{""label"":""GPX1"",""id"":""2876""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""KLK1"",""id"":""3816""},{""label"":""SLC34A1"",""id"":""6569""},{""label"":""TLR9"",""id"":""54106""}]"	"[""1293"",""1361"",""177"",""185"",""2876"",""345"",""3557"",""3816"",""54106"",""6569"",""9590""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:784""}]"
DOID:7843	"[""female breast carcinoma"",""Mammary carcinoma of female breast""]"	"[{""label"":""FGFR2"",""id"":""2263""}]"	"[""2263""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7843""}]"
DOID:790	"[""ocular hypotension"",""Hypotony of eye""]"	"[{""label"":""Ace"",""id"":""24310""}]"	"[""24310""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:790""}]"
DOID:7941	"[""Barrett's adenocarcinoma"",""Barrett adenocarcinoma"",""adenocarcinoma Arising in Barrett's Mucosa""]"	"[{""label"":""GPX3"",""id"":""2878""},{""label"":""GPX7"",""id"":""2882""}]"	"[""2878"",""2882""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7941""}]"
DOID:799	"[""varicose veins"",""Varix"",""Venous ectasia"",""Venous varices"",""varices""]"	"[{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP9"",""id"":""4318""}]"	"[""4312"",""4318""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:799""}]"
DOID:7998	"[""hyperthyroidism"",""overactive thyroid""]"	"[{""label"":""Cs"",""id"":""170587""}]"	"[""170587""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7998""}]"
DOID:7998	"[""hyperthyroidism"",""overactive thyroid""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:7998""}]"
DOID:8029	"[""sporadic breast cancer""]"	"[{""label"":""ESR1"",""id"":""2099""},{""label"":""MLH1"",""id"":""4292""},{""label"":""PHB1"",""id"":""5245""},{""label"":""PTEN"",""id"":""5728""}]"	"[""2099"",""4292"",""5245"",""5728""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8029""}]"
DOID:809	"[""cocaine abuse""]"	"[{""label"":""Creb1"",""id"":""81646""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Htr2c"",""id"":""25187""}]"	"[""25187"",""29595"",""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:809""}]"
DOID:809	"[""cocaine abuse""]"	"[{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CHRNA6"",""id"":""8973""},{""label"":""CHRNB4"",""id"":""1143""},{""label"":""NPY1R"",""id"":""4886""}]"	"[""1138"",""1143"",""4886"",""8973""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:809""}]"
DOID:809	"[""cocaine abuse""]"	"[{""label"":""cat-1"",""id"":""180837""},{""label"":""mod-1"",""id"":""179269""}]"	"[""179269"",""180837""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:809""}]"
DOID:811	"[""lipodystrophy""]"	"[{""label"":""AGPAT2"",""id"":""10555""},{""label"":""BSCL2"",""id"":""26580""},{""label"":""LMNA"",""id"":""4000""},{""label"":""PPARG"",""id"":""5468""}]"	"[""10555"",""26580"",""4000"",""5468""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:811""}]"
DOID:811	"[""lipodystrophy""]"	"[{""label"":""Ebf1"",""id"":""13591""}]"	"[""13591""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:811""}]"
DOID:813	"[""septic arthritis"",""infectious arthritis""]"	"[{""label"":""Cd4"",""id"":""24932""}]"	"[""24932""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:813""}]"
DOID:8158	"[""complement component 5 deficiency"",""C5 deficiency""]"	"[{""label"":""C5"",""id"":""727""}]"	"[""727""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8158""}]"
DOID:820	"[""myocarditis"",""Myocardial inflammation""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:820""}]"
DOID:820	"[""myocarditis"",""Myocardial inflammation""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Cxcr3"",""id"":""84475""},{""label"":""Icos"",""id"":""64545""},{""label"":""Il10"",""id"":""25325""},{""label"":""Ptger4"",""id"":""84023""},{""label"":""Spp1"",""id"":""25353""}]"	"[""24310"",""25325"",""25353"",""64545"",""84023"",""84475""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:820""}]"
DOID:824	"[""periodontitis"",""chronic pericementitis""]"	"[{""label"":""ADRB1"",""id"":""153""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""ELANE"",""id"":""1991""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL6"",""id"":""3569""}]"	"[""153"",""1543"",""1991"",""3557"",""3569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:824""}]"
DOID:824	"[""periodontitis"",""chronic pericementitis""]"	"[{""label"":""Adrb1"",""id"":""24925""},{""label"":""Ppara"",""id"":""25747""},{""label"":""Vip"",""id"":""117064""}]"	"[""117064"",""24925"",""25747""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:824""}]"
DOID:8283	"[""peritonitis"",""Retractile mesenteritis"",""acute generalized peritonitis"",""primary bacterial peritonitis"",""sclerosing mesenteritis""]"	"[{""label"":""Esr1"",""id"":""24890""},{""label"":""Esr2"",""id"":""25149""}]"	"[""24890"",""25149""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8283""}]"
DOID:8283	"[""peritonitis"",""Retractile mesenteritis"",""acute generalized peritonitis"",""primary bacterial peritonitis"",""sclerosing mesenteritis""]"	"[{""label"":""FOXP1"",""id"":""27086""},{""label"":""NPPA"",""id"":""4878""},{""label"":""PLAT"",""id"":""5327""},{""label"":""PLAU"",""id"":""5328""}]"	"[""27086"",""4878"",""5327"",""5328""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8283""}]"
DOID:83	"[""cataract""]"	"[{""label"":""Akr1b1"",""id"":""24192""},{""label"":""Cdkn1b"",""id"":""83571""},{""label"":""Cryaa"",""id"":""24273""},{""label"":""G6pd"",""id"":""24377""}]"	"[""24192"",""24273"",""24377"",""83571""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:83""}]"
DOID:83	"[""cataract""]"	"[{""label"":""Dnase2b"",""id"":""56629""},{""label"":""Gclc"",""id"":""14629""},{""label"":""Lim2"",""id"":""233187""},{""label"":""Sord"",""id"":""20322""}]"	"[""14629"",""20322"",""233187"",""56629""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:83""}]"
DOID:83	"[""cataract""]"	"[{""label"":""crim1"",""id"":""404210""}]"	"[""404210""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:83""}]"
DOID:83	"[""cataract""]"	"[{""label"":""AKR1B1"",""id"":""231""},{""label"":""ALDH18A1"",""id"":""5832""},{""label"":""BCOR"",""id"":""54880""},{""label"":""GALK1"",""id"":""2584""},{""label"":""GCNT2"",""id"":""2651""},{""label"":""HSF4"",""id"":""3299""},{""label"":""LIM2"",""id"":""3982""},{""label"":""LSS"",""id"":""4047""},{""label"":""NFE2L2"",""id"":""4780""},{""label"":""OGG1"",""id"":""4968""},{""label"":""SOD1"",""id"":""6647""},{""label"":""TRPM3"",""id"":""80036""}]"	"[""231"",""2584"",""2651"",""3299"",""3982"",""4047"",""4780"",""4968"",""54880"",""5832"",""6647"",""80036""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:83""}]"
DOID:8337	"[""appendicitis"",""acute appendicitis"",""acute appendicitis with generalized peritonitis"",""acute appendicitis with peritoneal abscess""]"	"[{""label"":""F2"",""id"":""2147""}]"	"[""2147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8337""}]"
DOID:8354	"[""complement component 3 deficiency"",""C3 deficiency""]"	"[{""label"":""C3"",""id"":""12266""}]"	"[""12266""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8354""}]"
DOID:8354	"[""complement component 3 deficiency"",""C3 deficiency""]"	"[{""label"":""C3"",""id"":""718""}]"	"[""718""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8354""}]"
DOID:8398	"[""osteoarthritis"",""Osteoarthrosis and allied disorder"",""degenerative arthritis"",""degenerative joint disease"",""hypertrophic arthritis"",""osteoarthrosis""]"	"[{""label"":""Adamts5"",""id"":""304135""},{""label"":""Col2a1"",""id"":""25412""},{""label"":""Ngf"",""id"":""310738""}]"	"[""25412"",""304135"",""310738""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8398""}]"
DOID:8398	"[""osteoarthritis"",""Osteoarthrosis and allied disorder"",""degenerative arthritis"",""degenerative joint disease"",""hypertrophic arthritis"",""osteoarthrosis""]"	"[{""label"":""Atp7a"",""id"":""11977""},{""label"":""Bmp7"",""id"":""12162""},{""label"":""Bmpr1a"",""id"":""12166""},{""label"":""Col11a1"",""id"":""12814""},{""label"":""Enpp1"",""id"":""18605""},{""label"":""Errfi1"",""id"":""74155""},{""label"":""Gdf5"",""id"":""14563""},{""label"":""Matn3"",""id"":""17182""},{""label"":""Myl3"",""id"":""17897""},{""label"":""Tgfbr1"",""id"":""21812""}]"	"[""11977"",""12162"",""12166"",""12814"",""14563"",""17182"",""17897"",""18605"",""21812"",""74155""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8398""}]"
DOID:8398	"[""osteoarthritis"",""Osteoarthrosis and allied disorder"",""degenerative arthritis"",""degenerative joint disease"",""hypertrophic arthritis"",""osteoarthrosis""]"	"[{""label"":""ADAM12"",""id"":""8038""},{""label"":""ADAMTS14"",""id"":""140766""},{""label"":""ADAMTS5"",""id"":""11096""},{""label"":""ASPN"",""id"":""54829""},{""label"":""BAG6"",""id"":""7917""},{""label"":""BMP2"",""id"":""650""},{""label"":""CD36"",""id"":""948""},{""label"":""CILP"",""id"":""8483""},{""label"":""CLEC3B"",""id"":""7123""},{""label"":""COL2A1"",""id"":""1280""},{""label"":""DDR2"",""id"":""4921""},{""label"":""ESR1"",""id"":""2099""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FGFR1"",""id"":""2260""},{""label"":""FRZB"",""id"":""2487""},{""label"":""GDF5"",""id"":""8200""},{""label"":""GHR"",""id"":""2690""},{""label"":""HFE"",""id"":""3077""},{""label"":""MATN3"",""id"":""4148""},{""label"":""MMP13"",""id"":""4322""},{""label"":""MMP3"",""id"":""4314""},{""label"":""NCOR2"",""id"":""9612""},{""label"":""POMC"",""id"":""5443""},{""label"":""PTGS2"",""id"":""5743""},{""label"":""TNFRSF11B"",""id"":""4982""}]"	"[""11096"",""1280"",""140766"",""2099"",""2212"",""2260"",""2487"",""2690"",""3077"",""4148"",""4314"",""4322"",""4921"",""4982"",""5443"",""54829"",""5743"",""650"",""7123"",""7917"",""8038"",""8200"",""8483"",""948"",""9612""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8398""}]"
DOID:841	"[""extrinsic allergic alveolitis"",""alveolitis"",""hypersensitivity pneumonitis""]"	"[{""label"":""Il13"",""id"":""116553""}]"	"[""116553""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:841""}]"
DOID:841	"[""extrinsic allergic alveolitis"",""alveolitis"",""hypersensitivity pneumonitis""]"	"[{""label"":""TAP1"",""id"":""6890""},{""label"":""TNF"",""id"":""7124""}]"	"[""6890"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:841""}]"
DOID:8411	"[""kidney angiomyolipoma"",""Angiomyolipoma of kidney"",""renal Angiomyolipoma""]"	"[{""label"":""MTOR"",""id"":""2475""}]"	"[""2475""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8411""}]"
DOID:8432	"[""polycythemia"",""Erythrocythemia""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""EPAS1"",""id"":""2034""},{""label"":""EPOR"",""id"":""2057""},{""label"":""HBB"",""id"":""3043""}]"	"[""1636"",""2034"",""2057"",""3043""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8432""}]"
DOID:8437	"[""intestinal obstruction""]"	"[{""label"":""HFE"",""id"":""3077""}]"	"[""3077""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8437""}]"
DOID:8454	"[""riboflavin deficiency"",""ariboflavinosis"",""vitamin B2 deficiency""]"	"[{""label"":""SLC52A1"",""id"":""55065""}]"	"[""55065""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8454""}]"
DOID:8465	"[""retinoschisis""]"	"[{""label"":""TYR"",""id"":""7299""}]"	"[""7299""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8465""}]"
DOID:8466	"[""retinal degeneration"",""degeneration of retina""]"	"[{""label"":""eys"",""id"":""3771890""},{""label"":""kdn"",""id"":""31579""},{""label"":""ninaE"",""id"":""42367""}]"	"[""31579"",""3771890"",""42367""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8466""}]"
DOID:8466	"[""retinal degeneration"",""degeneration of retina""]"	"[{""label"":""ABCA4"",""id"":""24""},{""label"":""HDAC4"",""id"":""9759""},{""label"":""HGF"",""id"":""3082""},{""label"":""PKD2"",""id"":""5311""},{""label"":""PRPH2"",""id"":""5961""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""TFPI2"",""id"":""7980""}]"	"[""24"",""3082"",""5176"",""5311"",""5961"",""7980"",""9759""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8466""}]"
DOID:8466	"[""retinal degeneration"",""degeneration of retina""]"	"[{""label"":""Bdnf"",""id"":""24225""},{""label"":""Lcn2"",""id"":""170496""},{""label"":""Mertk"",""id"":""65037""},{""label"":""Nos3"",""id"":""24600""}]"	"[""170496"",""24225"",""24600"",""65037""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8466""}]"
DOID:8472	"[""localized scleroderma"",""Morphea"",""Scleroderma, circumscribed or localised"",""Scleroderma, circumscribed or localized"",""circumscribed scleroderma"",""localised morphea"",""localised morphoea"",""localised scleroderma"",""localized morphea""]"	"[{""label"":""HGF"",""id"":""3082""},{""label"":""MMP1"",""id"":""4312""}]"	"[""3082"",""4312""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8472""}]"
DOID:848	"[""arthritis"",""Inflammatory disorder of joint""]"	"[{""label"":""B2M"",""id"":""567""},{""label"":""CD40"",""id"":""958""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""GC"",""id"":""2638""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IL23R"",""id"":""149233""},{""label"":""PARP1"",""id"":""142""},{""label"":""TLR4"",""id"":""7099""}]"	"[""142"",""149233"",""2214"",""2638"",""3117"",""3119"",""567"",""7099"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:848""}]"
DOID:848	"[""arthritis"",""Inflammatory disorder of joint""]"	"[{""label"":""Cnr2"",""id"":""57302""}]"	"[""57302""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:848""}]"
DOID:8483	"[""retinal artery occlusion""]"	"[{""label"":""IL10"",""id"":""3586""},{""label"":""IL6"",""id"":""3569""}]"	"[""3569"",""3586""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8483""}]"
DOID:8499	"[""night blindness"",""nyctalopia""]"	"[{""label"":""GRK1"",""id"":""6011""},{""label"":""NYX"",""id"":""60506""},{""label"":""RDH5"",""id"":""5959""},{""label"":""RHO"",""id"":""6010""},{""label"":""RLBP1"",""id"":""6017""}]"	"[""5959"",""6010"",""6011"",""6017"",""60506""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8499""}]"
DOID:850	"[""lung disease""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Adora1"",""id"":""29290""},{""label"":""Adora2a"",""id"":""25369""},{""label"":""Bdkrb2"",""id"":""25245""},{""label"":""Il10"",""id"":""25325""},{""label"":""Mmp9"",""id"":""81687""},{""label"":""Tlr4"",""id"":""29260""}]"	"[""24310"",""25245"",""25325"",""25369"",""29260"",""29290"",""81687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:850""}]"
DOID:850	"[""lung disease""]"	"[{""label"":""CAT"",""id"":""847""},{""label"":""CFTR"",""id"":""1080""},{""label"":""CSF3"",""id"":""1440""},{""label"":""DEFB1"",""id"":""1672""},{""label"":""EDNRA"",""id"":""1909""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""MEFV"",""id"":""4210""},{""label"":""MIF"",""id"":""4282""},{""label"":""MPO"",""id"":""4353""},{""label"":""NAT2"",""id"":""10""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""SFTPA1"",""id"":""653509""},{""label"":""SFTPC"",""id"":""6440""},{""label"":""SFTPD"",""id"":""6441""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TLR2"",""id"":""7097""}]"	"[""10"",""1080"",""1440"",""1672"",""1909"",""2908"",""3115"",""4210"",""4282"",""4353"",""6440"",""6441"",""653509"",""7040"",""7097"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:850""}]"
DOID:8501	"[""fundus dystrophy"",""Retinal Dystrophy""]"	"[{""label"":""ABCA4"",""id"":""24""}]"	"[""24""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8501""}]"
DOID:8505	"[""dermatitis herpetiformis"",""Dermatosis herpetiformis"",""Duhring's disease""]"	"[{""label"":""ELN"",""id"":""2006""},{""label"":""LTA"",""id"":""4049""},{""label"":""TNF"",""id"":""7124""}]"	"[""2006"",""4049"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8505""}]"
DOID:8506	"[""bullous pemphigoid""]"	"[{""label"":""IL2"",""id"":""3558""}]"	"[""3558""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8506""}]"
DOID:8515	"[""Cor pulmonale"",""cardiopulmonary disease"",""pulmonary heart disease""]"	"[{""label"":""CX3CL1"",""id"":""6376""}]"	"[""6376""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8515""}]"
DOID:853	"[""polymyalgia rheumatica""]"	"[{""label"":""HFE"",""id"":""3077""},{""label"":""MBL2"",""id"":""4153""}]"	"[""3077"",""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:853""}]"
DOID:8534	"[""gastroesophageal reflux disease"",""Acid reflux"",""GERD"",""GERD - Gastro-esophageal reflux disease"",""Gastresophageal reflux"",""Gastro-esophageal reflux"",""Gastroesophageal reflux""]"	"[{""label"":""PLA2G2A"",""id"":""5320""}]"	"[""5320""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8534""}]"
DOID:8536	"[""herpes zoster"",""Shingles"",""herpes zona""]"	"[{""label"":""F2"",""id"":""2147""}]"	"[""2147""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8536""}]"
DOID:854	"[""collagen disease"",""collagen disorder""]"	"[{""label"":""Col4a1"",""id"":""33727""},{""label"":""Tl"",""id"":""43222""}]"	"[""33727"",""43222""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:854""}]"
DOID:8544	"[""chronic fatigue syndrome"",""CFS"",""Myalgic encephalitis"",""Myalgic encephalomyelitis"",""Postviral fatigue syndrome""]"	"[{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""KIR3DS1"",""id"":""3813""},{""label"":""SLC6A4"",""id"":""6532""},{""label"":""TRPC6"",""id"":""7225""}]"	"[""3117"",""3813"",""6532"",""7225""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8544""}]"
DOID:8545	"[""malignant hyperthermia"",""anesthesia related hyperthermia"",""malignant hyperpyrexia due to anesthesia""]"	"[{""label"":""Ryr1"",""id"":""20190""}]"	"[""20190""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8545""}]"
DOID:8545	"[""malignant hyperthermia"",""anesthesia related hyperthermia"",""malignant hyperpyrexia due to anesthesia""]"	"[{""label"":""CACNA1S"",""id"":""779""},{""label"":""CACNG1"",""id"":""786""},{""label"":""RYR1"",""id"":""6261""}]"	"[""6261"",""779"",""786""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8545""}]"
DOID:8549	"[""chronic ulcer of skin"",""Callous ulcer"",""Indolent ulcer""]"	"[{""label"":""MMP9"",""id"":""4318""}]"	"[""4318""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8549""}]"
DOID:8552	"[""chronic myeloid leukemia"",""CML"",""CML - chronic Myelogenous Leukemia"",""Myeloid Leukemia, chronic"",""chronic granulocytic leukaemia"",""chronic granulocytic leukemia"",""chronic myelogenous leukaemia"",""chronic myelogenous leukemia"",""chronic myeloid leukaemia""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ABCC2"",""id"":""1244""},{""label"":""ABCG2"",""id"":""9429""},{""label"":""ABL1"",""id"":""25""},{""label"":""AKT1"",""id"":""207""},{""label"":""BCR"",""id"":""613""},{""label"":""CRKL"",""id"":""1399""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP3A5"",""id"":""1577""},{""label"":""FAS"",""id"":""355""},{""label"":""FASLG"",""id"":""356""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IL10"",""id"":""3586""},{""label"":""MDM2"",""id"":""4193""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1244"",""1399"",""1543"",""1577"",""207"",""25"",""3117"",""3119"",""355"",""356"",""3586"",""4193"",""5243"",""613"",""7422"",""7515"",""9429""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8552""}]"
DOID:8552	"[""chronic myeloid leukemia"",""CML"",""CML - chronic Myelogenous Leukemia"",""Myeloid Leukemia, chronic"",""chronic granulocytic leukaemia"",""chronic granulocytic leukemia"",""chronic myelogenous leukaemia"",""chronic myelogenous leukemia"",""chronic myeloid leukaemia""]"	"[{""label"":""Ncstn"",""id"":""59287""}]"	"[""59287""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8552""}]"
DOID:856	"[""biotinidase deficiency"",""BTD deficiency"",""Juvenile-onset multiple carboxylase deficiency"",""Late-onset multiple carboxylase deficiency"",""deficiency of biotinidase""]"	"[{""label"":""BTD"",""id"":""686""}]"	"[""686""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:856""}]"
DOID:856	"[""biotinidase deficiency"",""BTD deficiency"",""Juvenile-onset multiple carboxylase deficiency"",""Late-onset multiple carboxylase deficiency"",""deficiency of biotinidase""]"	"[{""label"":""Btd"",""id"":""26363""}]"	"[""26363""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:856""}]"
DOID:8566	"[""herpes simplex"",""Herpesvirus hominis disease""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""IRF5"",""id"":""3663""},{""label"":""MBL2"",""id"":""4153""}]"	"[""348"",""3663"",""4153""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8566""}]"
DOID:8567	"[""Hodgkin's lymphoma"",""HL"",""Hodgkin disease"",""Hodgkin lymphoma"",""Hodgkin's sarcoma"",""Hodgkins lymphoma"",""stage I Subdiaphragmatic Hodgkin Lymphoma"",""stage II Subdiaphragmatic Hodgkin Lymphoma""]"	"[{""label"":""IL6"",""id"":""3569""},{""label"":""KLHDC8B"",""id"":""200942""}]"	"[""200942"",""3569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8567""}]"
DOID:8568	"[""infectious mononucleosis"",""Filatov's disease"",""Gammaherpesviral mononucleosis"",""Monocytic angina"",""Pfeiffer's disease"",""glandular fever"",""mononucleosis""]"	"[{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""SOD2"",""id"":""6648""}]"	"[""3123"",""6648""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8568""}]"
DOID:8577	"[""ulcerative colitis"",""Left-sided ulcerative colitis""]"	"[{""label"":""Ptgs2"",""id"":""29527""}]"	"[""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8577""}]"
DOID:8577	"[""ulcerative colitis"",""Left-sided ulcerative colitis""]"	"[{""label"":""RHO1"",""id"":""856294""}]"	"[""856294""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8577""}]"
DOID:8577	"[""ulcerative colitis"",""Left-sided ulcerative colitis""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""APOA4"",""id"":""337""},{""label"":""BTNL2"",""id"":""56244""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""GC"",""id"":""2638""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL23R"",""id"":""149233""},{""label"":""PTGER4"",""id"":""5734""},{""label"":""SELL"",""id"":""6402""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""STAT3"",""id"":""6774""}]"	"[""149233"",""1591"",""2212"",""2638"",""3119"",""337"",""3557"",""5243"",""56244"",""5734"",""6402"",""6556"",""6774""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8577""}]"
DOID:8584	"[""Burkitt lymphoma"",""Burkitt lymphoma/leukaemia"",""Burkitt's Lymphoma"",""Burkitt's tumor"",""Burkitt's tumor or lymphoma"",""malignant lymphoma, Burkitt's type"",""small Non-Cleaved cell Lymphoma, Burkitt's type""]"	"[{""label"":""BTK"",""id"":""695""},{""label"":""CALR"",""id"":""811""},{""label"":""CD40"",""id"":""958""},{""label"":""CD79B"",""id"":""974""},{""label"":""MYC"",""id"":""4609""}]"	"[""4609"",""695"",""811"",""958"",""974""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8584""}]"
DOID:8584	"[""Burkitt lymphoma"",""Burkitt lymphoma/leukaemia"",""Burkitt's Lymphoma"",""Burkitt's tumor"",""Burkitt's tumor or lymphoma"",""malignant lymphoma, Burkitt's type"",""small Non-Cleaved cell Lymphoma, Burkitt's type""]"	"[{""label"":""Myc"",""id"":""17869""}]"	"[""17869""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8584""}]"
DOID:8618	"[""oral cavity cancer"",""malignant neoplasm of floor of mouth""]"	"[{""label"":""CHRNB4"",""id"":""1143""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""SOD3"",""id"":""6649""}]"	"[""1143"",""1543"",""1571"",""6649""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8618""}]"
DOID:8619	"[""recurrent hypersomnia"",""primary recurrent hypersomnia""]"	"[{""label"":""CHKB"",""id"":""1120""}]"	"[""1120""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8619""}]"
DOID:863	"[""nervous system disease""]"	"[{""label"":""Atpalpha"",""id"":""48971""}]"	"[""48971""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:863""}]"
DOID:8632	"[""Kaposi's sarcoma"",""Kaposi sarcoma"",""Kaposi's sarcoma of Heart"",""Kaposi's sarcoma of anus"",""Kaposi's sarcoma of central nervous system"",""Kaposi's sarcoma of conjunctiva"",""Kaposi's sarcoma of cornea"",""Kaposi's sarcoma of esophagus"",""Kaposi's sarcoma of gastrointestinal sites"",""Kaposi's sarcoma of lung"",""Kaposi's sarcoma of lymph nodes"",""Kaposi's sarcoma of palate"",""Kaposi's sarcoma of penis"",""Kaposi's sarcoma of skin"",""Kaposi's sarcoma of soft tissue"",""Kaposi's sarcoma of soft tissues"",""Kaposi's sarcoma of the CNS"",""Kaposi's sarcoma of the gallbladder"",""Kaposi's sarcoma of the prostate"",""Kaposi's sarcoma, lung"",""Kaposi's sarcoma, skin"",""anal Kaposi's sarcoma"",""cardiac Kaposi's sarcoma"",""central nervous system Kaposi's sarcoma"",""conjunctival Kaposi's sarcoma"",""corneal Kaposi's sarcoma"",""cutaneous Kaposi's sarcoma"",""esophageal Kaposi's sarcoma"",""gallbladder Kaposi's sarcoma"",""gastric Kaposi's sarcoma"",""intestinal Kaposi's sarcoma"",""lymph node Kaposi's sarcoma"",""lymphadenopathic Kaposi's sarcoma"",""palate Kaposi's sarcoma"",""penis Kaposi's sarcoma"",""prostate Kaposi's sarcoma"",""pulmonary Kaposi's sarcoma"",""soft tissue Kaposi's sarcoma""]"	"[{""label"":""BPTF"",""id"":""2186""},{""label"":""IL6"",""id"":""3569""}]"	"[""2186"",""3569""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8632""}]"
DOID:8634	"[""prostate carcinoma in situ"",""PIN III"",""carcinoma in situ of prostate"",""grade III PIN""]"	"[{""label"":""Esr1"",""id"":""24890""},{""label"":""Esr2"",""id"":""25149""}]"	"[""24890"",""25149""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8634""}]"
DOID:8634	"[""prostate carcinoma in situ"",""PIN III"",""carcinoma in situ of prostate"",""grade III PIN""]"	"[{""label"":""CYP19A1"",""id"":""1588""},{""label"":""FGF8"",""id"":""2253""}]"	"[""1588"",""2253""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8634""}]"
DOID:8645	"[""subacute delirium""]"	"[{""label"":""ACHE"",""id"":""43""}]"	"[""43""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8645""}]"
DOID:865	"[""vasculitis"",""Angiitis""]"	"[{""label"":""CAST"",""id"":""831""},{""label"":""MPO"",""id"":""4353""},{""label"":""NOS3"",""id"":""4846""},{""label"":""SERPINA3"",""id"":""12""}]"	"[""12"",""4353"",""4846"",""831""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:865""}]"
DOID:8670	"[""eating disorder""]"	"[{""label"":""HDAC4"",""id"":""9759""}]"	"[""9759""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8670""}]"
DOID:8670	"[""eating disorder""]"	"[{""label"":""Hdac4"",""id"":""208727""}]"	"[""208727""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8670""}]"
DOID:8677	"[""perinatal necrotizing enterocolitis"",""ENTEROCOLITIS NECROTIZING"",""Necrotizing enterocolitis in fetus OR newborn"",""Perinatal necrotising enterocolitis"",""Pseudomembranous enterocolitis in newborn"",""necrotizing enterocolitis""]"	"[{""label"":""Cd14"",""id"":""60350""},{""label"":""Egf"",""id"":""25313""},{""label"":""Il10"",""id"":""25325""},{""label"":""Ptafr"",""id"":""58949""},{""label"":""Tnf"",""id"":""24835""}]"	"[""24835"",""25313"",""25325"",""58949"",""60350""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8677""}]"
DOID:8677	"[""perinatal necrotizing enterocolitis"",""ENTEROCOLITIS NECROTIZING"",""Necrotizing enterocolitis in fetus OR newborn"",""Perinatal necrotising enterocolitis"",""Pseudomembranous enterocolitis in newborn"",""necrotizing enterocolitis""]"	"[{""label"":""HBEGF"",""id"":""1839""}]"	"[""1839""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8677""}]"
DOID:8683	"[""myeloid sarcoma"",""Chloroma"",""Extramedullary Myeloid tumor"",""Granulocytic sarcoma""]"	"[{""label"":""KRAS"",""id"":""3845""},{""label"":""PDGFRA"",""id"":""5156""}]"	"[""3845"",""5156""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8683""}]"
DOID:8689	"[""anorexia nervosa""]"	"[{""label"":""AKAP6"",""id"":""9472""},{""label"":""NR3C1"",""id"":""2908""}]"	"[""2908"",""9472""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8689""}]"
DOID:8689	"[""anorexia nervosa""]"	"[{""label"":""Htr4"",""id"":""15562""}]"	"[""15562""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8689""}]"
DOID:8691	"[""mycosis fungoides"",""mycosis fungoides lymphoma""]"	"[{""label"":""HLA-DQB1"",""id"":""3119""}]"	"[""3119""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8691""}]"
DOID:8692	"[""myeloid leukemia"",""Non-Lymphocytic Leukemia"",""leukaemia myelogenous"",""leukemia myelogenous"",""myeloid granulocytic leukaemia"",""myeloid granulocytic leukemia"",""myeloid leukaemia""]"	"[{""label"":""FGFR1"",""id"":""2260""},{""label"":""GATA2"",""id"":""2624""},{""label"":""IFNG"",""id"":""3458""},{""label"":""MN1"",""id"":""4330""},{""label"":""NSD3"",""id"":""54904""},{""label"":""PDGFRA"",""id"":""5156""},{""label"":""UGT1A1"",""id"":""54658""}]"	"[""2260"",""2624"",""3458"",""4330"",""5156"",""54658"",""54904""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8692""}]"
DOID:870	"[""neuropathy"",""peripheral neuropathy""]"	"[{""label"":""Mpz"",""id"":""17528""}]"	"[""17528""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:870""}]"
DOID:870	"[""neuropathy"",""peripheral neuropathy""]"	"[{""label"":""CTSS"",""id"":""1520""}]"	"[""1520""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:870""}]"
DOID:8704	"[""genital herpes"",""Genital herpes simplex"",""Herpes Genitalis"",""Virus-Genital Herpes"",""venereal herpes""]"	"[{""label"":""STAT4"",""id"":""6775""}]"	"[""6775""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8704""}]"
DOID:8719	"[""in situ carcinoma""]"	"[{""label"":""IGF2R"",""id"":""3482""},{""label"":""RUNX3"",""id"":""864""}]"	"[""3482"",""864""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8719""}]"
DOID:8725	"[""vascular dementia"",""Multi Infarct Dementia"",""multifocal dementia""]"	"[{""label"":""Creb1"",""id"":""81646""},{""label"":""Gsk3b"",""id"":""84027""},{""label"":""Nox1"",""id"":""114243""}]"	"[""114243"",""81646"",""84027""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8725""}]"
DOID:8725	"[""vascular dementia"",""Multi Infarct Dementia"",""multifocal dementia""]"	"[{""label"":""HSPA1A"",""id"":""3303""},{""label"":""IGF1R"",""id"":""3480""},{""label"":""PON2"",""id"":""5445""},{""label"":""RPGRIP1L"",""id"":""23322""},{""label"":""SREBF2"",""id"":""6721""},{""label"":""TNF"",""id"":""7124""}]"	"[""23322"",""3303"",""3480"",""5445"",""6721"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8725""}]"
DOID:874	"[""bacterial pneumonia"",""Pneumonia due to other gram-negative bacteria"",""gram-negative pneumonia""]"	"[{""label"":""CSF3"",""id"":""1440""},{""label"":""MBL2"",""id"":""4153""},{""label"":""TNF"",""id"":""7124""}]"	"[""1440"",""4153"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:874""}]"
DOID:8741	"[""seborrheic dermatitis"",""SKIN SEBORRHEIC"",""Seborrhoeic dermatitis"",""Seborrhoeic eczema"",""seborrhea""]"	"[{""label"":""TLR2"",""id"":""7097""}]"	"[""7097""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8741""}]"
DOID:8761	"[""acute megakaryocytic leukemia"",""Megakaryocytic myelosis"",""Thrombocytic leukaemia""]"	"[{""label"":""EZH2"",""id"":""2146""},{""label"":""JAK3"",""id"":""3718""},{""label"":""MRTFA"",""id"":""57591""}]"	"[""2146"",""3718"",""57591""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8761""}]"
DOID:8778	"[""Crohn's disease"",""Crohn disease"",""Crohn's disease of colon"",""Crohn's disease of large bowel"",""Granulomatous Colitis"",""Pediatric Crohn's disease""]"	"[{""label"":""Madcam1"",""id"":""54266""}]"	"[""54266""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8778""}]"
DOID:8778	"[""Crohn's disease"",""Crohn disease"",""Crohn's disease of colon"",""Crohn's disease of large bowel"",""Granulomatous Colitis"",""Pediatric Crohn's disease""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""BPI"",""id"":""671""},{""label"":""CD40"",""id"":""958""},{""label"":""CLDN1"",""id"":""9076""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""GC"",""id"":""2638""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-DPA1"",""id"":""3113""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL21R"",""id"":""50615""},{""label"":""IL23R"",""id"":""149233""},{""label"":""IL6"",""id"":""3569""},{""label"":""LRRK2"",""id"":""120892""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MKI67"",""id"":""4288""},{""label"":""NOD2"",""id"":""64127""},{""label"":""OCLN"",""id"":""100506658""},{""label"":""PRF1"",""id"":""5551""},{""label"":""SELL"",""id"":""6402""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""SLC22A5"",""id"":""6584""},{""label"":""STAT3"",""id"":""6774""},{""label"":""UGT1A1"",""id"":""54658""}]"	"[""100506658"",""120892"",""149233"",""2212"",""2214"",""2638"",""3077"",""3113"",""3119"",""3383"",""3569"",""3586"",""4153"",""4288"",""50615"",""5243"",""54658"",""5551"",""6402"",""64127"",""6556"",""6584"",""671"",""6774"",""9076"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8778""}]"
DOID:8791	"[""breast carcinoma in situ"",""Non-Infiltrating carcinoma of breast"",""carcinoma in situ of breast""]"	"[{""label"":""IGF2R"",""id"":""3482""}]"	"[""3482""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8791""}]"
DOID:8805	"[""intermediate coronary syndrome"",""Angina at rest"",""Anginal chest pain at rest"",""Impending infarction"",""Preinfarction angina"",""Unstable angina"",""Worsening angina""]"	"[{""label"":""HMGCR"",""id"":""3156""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""ITIH4"",""id"":""3700""},{""label"":""MMP1"",""id"":""4312""},{""label"":""SERPINC1"",""id"":""462""}]"	"[""3156"",""3673"",""3700"",""4312"",""462""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8805""}]"
DOID:8864	"[""acute monocytic leukemia"",""acute Monoblastic Leukemia and acute Monocytic Leukemia"",""acute monocytic leukaemia"",""acute monocytic leukaemia without mention of remission"",""acute monocytic leukemia without mention of remission"",""acute monocytic leukemia, FAB M5"",""acute monocytic leukemia, morphology""]"	"[{""label"":""MLLT10"",""id"":""8028""}]"	"[""8028""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8864""}]"
DOID:8866	"[""actinic keratosis"",""SK - Solar keratosis"",""Senile hyperkeratosis"",""Solar keratosis"",""actinic (Solar) Keratosis""]"	"[{""label"":""KNSTRN"",""id"":""90417""},{""label"":""OCA2"",""id"":""4948""}]"	"[""4948"",""90417""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8866""}]"
DOID:8869	"[""neuromyelitis optica"",""Devic's disease"",""Devic's syndrome""]"	"[{""label"":""Cd59b"",""id"":""25407""}]"	"[""25407""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8869""}]"
DOID:8869	"[""neuromyelitis optica"",""Devic's disease"",""Devic's syndrome""]"	"[{""label"":""AQP4"",""id"":""361""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3119"",""3123"",""361""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8869""}]"
DOID:8886	"[""chorioretinitis"",""retinochoroiditis""]"	"[{""label"":""COL2A1"",""id"":""1280""}]"	"[""1280""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8886""}]"
DOID:8893	"[""psoriasis""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""AGER"",""id"":""177""},{""label"":""ALB"",""id"":""213""},{""label"":""APOE"",""id"":""348""},{""label"":""C2"",""id"":""717""},{""label"":""CADM2"",""id"":""253559""},{""label"":""CAST"",""id"":""831""},{""label"":""CD40"",""id"":""958""},{""label"":""CFB"",""id"":""629""},{""label"":""COMT"",""id"":""1312""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL17A"",""id"":""3605""},{""label"":""IL20"",""id"":""50604""},{""label"":""IL23R"",""id"":""149233""},{""label"":""LTA"",""id"":""4049""},{""label"":""MBL2"",""id"":""4153""},{""label"":""NAT2"",""id"":""10""},{""label"":""STAT3"",""id"":""6774""},{""label"":""STAT4"",""id"":""6775""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TNF"",""id"":""7124""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""10"",""1312"",""149233"",""1493"",""154"",""1543"",""177"",""213"",""253559"",""3117"",""3119"",""3383"",""348"",""3586"",""3596"",""3605"",""4049"",""4153"",""50604"",""629"",""6774"",""6775"",""6890"",""7124"",""717"",""7422"",""831"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8893""}]"
DOID:8893	"[""psoriasis""]"	"[{""label"":""Itgb2"",""id"":""16414""},{""label"":""Sptlc2"",""id"":""20773""},{""label"":""Stat3"",""id"":""20848""},{""label"":""Vegfa"",""id"":""22339""}]"	"[""16414"",""20773"",""20848"",""22339""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8893""}]"
DOID:890	"[""mitochondrial encephalomyopathy""]"	"[{""label"":""TYMP"",""id"":""1890""}]"	"[""1890""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:890""}]"
DOID:891	"[""progressive myoclonus epilepsy"",""PME"",""progressive myoclonic epilepsy""]"	"[{""label"":""EPM2A"",""id"":""7957""},{""label"":""SEMA6B"",""id"":""10501""}]"	"[""10501"",""7957""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:891""}]"
DOID:891	"[""progressive myoclonus epilepsy"",""PME"",""progressive myoclonic epilepsy""]"	"[{""label"":""Scarb2"",""id"":""12492""}]"	"[""12492""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:891""}]"
DOID:8923	"[""skin melanoma"",""Cutaneous Malignant Melanoma"",""cutaneous melanoma"",""malignant ear melanoma"",""malignant lip melanoma"",""malignant lower limb melanoma"",""malignant melanoma of ear and/or external auricular canal"",""malignant melanoma of skin of lower limb"",""malignant melanoma of skin of trunk except scrotum"",""malignant melanoma of skin of upper limb"",""malignant neck melanoma"",""malignant scalp melanoma"",""malignant trunk melanoma"",""malignant upper limb melanoma""]"	"[{""label"":""BRCA2"",""id"":""675""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CTCF"",""id"":""10664""},{""label"":""DDR1"",""id"":""780""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP9"",""id"":""4318""},{""label"":""OCA2"",""id"":""4948""},{""label"":""TYR"",""id"":""7299""}]"	"[""10664"",""3383"",""4312"",""4318"",""4948"",""6347"",""675"",""7299"",""780""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8923""}]"
DOID:8923	"[""skin melanoma"",""Cutaneous Malignant Melanoma"",""cutaneous melanoma"",""malignant ear melanoma"",""malignant lip melanoma"",""malignant lower limb melanoma"",""malignant melanoma of ear and/or external auricular canal"",""malignant melanoma of skin of lower limb"",""malignant melanoma of skin of trunk except scrotum"",""malignant melanoma of skin of upper limb"",""malignant neck melanoma"",""malignant scalp melanoma"",""malignant trunk melanoma"",""malignant upper limb melanoma""]"	"[{""label"":""Grm1"",""id"":""14816""}]"	"[""14816""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8923""}]"
DOID:8924	"[""autoimmune thrombocytopenic purpura"",""Immune thrombocytopenic purpura"",""idiopathic thrombocytopenic purpura"",""primary thrombocytopenic purpura""]"	"[{""label"":""CD40LG"",""id"":""959""},{""label"":""CD86"",""id"":""942""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR2B"",""id"":""2213""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL4"",""id"":""3565""},{""label"":""ITGB3"",""id"":""3690""}]"	"[""2212"",""2213"",""2214"",""3119"",""3123"",""3552"",""3557"",""3558"",""3565"",""3586"",""3690"",""942"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8924""}]"
DOID:8927	"[""learning disability"",""Academic skill disorder"",""learning disorder""]"	"[{""label"":""IL1RN"",""id"":""3557""}]"	"[""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8927""}]"
DOID:8929	"[""atrophic gastritis"",""gastric atrophy""]"	"[{""label"":""ATP4B"",""id"":""496""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""PTPN11"",""id"":""5781""}]"	"[""3119"",""3123"",""496"",""5781""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8929""}]"
DOID:893	"[""Wilson disease"",""Cerebral pseudosclerosis"",""Westphal pseudosclerosis"",""Westphal-Strumpell syndrome"",""Wilson's disease"",""hepatolenticular degeneration""]"	"[{""label"":""Hmgcr"",""id"":""25675""}]"	"[""25675""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:893""}]"
DOID:893	"[""Wilson disease"",""Cerebral pseudosclerosis"",""Westphal pseudosclerosis"",""Westphal-Strumpell syndrome"",""Wilson's disease"",""hepatolenticular degeneration""]"	"[{""label"":""ATP7B"",""id"":""540""}]"	"[""540""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:893""}]"
DOID:8946	"[""severe nonproliferative diabetic retinopathy"",""High risk non proliferative diabetic retinopathy"",""Severe NPDR""]"	"[{""label"":""Pdgfrb"",""id"":""18596""}]"	"[""18596""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8946""}]"
DOID:8947	"[""diabetic retinopathy"",""Retinal abnormality - diabetes-related""]"	"[{""label"":""Insr"",""id"":""16337""}]"	"[""16337""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8947""}]"
DOID:8947	"[""diabetic retinopathy"",""Retinal abnormality - diabetes-related""]"	"[{""label"":""ACE2"",""id"":""59272""},{""label"":""ACE"",""id"":""1636""},{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""ADRB3"",""id"":""155""},{""label"":""AGER"",""id"":""177""},{""label"":""AGT"",""id"":""183""},{""label"":""AKR1B1"",""id"":""231""},{""label"":""ANGPT1"",""id"":""284""},{""label"":""APOB"",""id"":""338""},{""label"":""APOE"",""id"":""348""},{""label"":""CDKAL1"",""id"":""54901""},{""label"":""CFB"",""id"":""629""},{""label"":""CFH"",""id"":""3075""},{""label"":""CLU"",""id"":""1191""},{""label"":""EDN1"",""id"":""1906""},{""label"":""ELN"",""id"":""2006""},{""label"":""EPO"",""id"":""2056""},{""label"":""FLT1"",""id"":""2321""},{""label"":""GLO1"",""id"":""2739""},{""label"":""HFE"",""id"":""3077""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL6"",""id"":""3569""},{""label"":""INS"",""id"":""3630""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""LTA"",""id"":""4049""},{""label"":""MMP2"",""id"":""4313""},{""label"":""MMP9"",""id"":""4318""},{""label"":""NOS3"",""id"":""4846""},{""label"":""PON1"",""id"":""5444""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""SGF29"",""id"":""112869""},{""label"":""SOD1"",""id"":""6647""},{""label"":""SOD3"",""id"":""6649""},{""label"":""TLR4"",""id"":""7099""},{""label"":""TNF"",""id"":""7124""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""VPS26A"",""id"":""9559""},{""label"":""WFS1"",""id"":""7466""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""112869"",""1191"",""155"",""1636"",""177"",""183"",""1906"",""2006"",""2056"",""231"",""2321"",""2739"",""284"",""3075"",""3077"",""3106"",""3119"",""3123"",""338"",""3383"",""348"",""3569"",""3586"",""3630"",""3673"",""4049"",""4313"",""4318"",""4846"",""5054"",""5176"",""5444"",""54901"",""59272"",""629"",""6647"",""6649"",""7099"",""7124"",""7422"",""7466"",""7515"",""9370"",""9559""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8947""}]"
DOID:8947	"[""diabetic retinopathy"",""Retinal abnormality - diabetes-related""]"	"[{""label"":""Agt"",""id"":""24179""},{""label"":""Akr1b1"",""id"":""24192""},{""label"":""Angpt2"",""id"":""89805""},{""label"":""Aqp4"",""id"":""25293""},{""label"":""Nfe2l2"",""id"":""83619""},{""label"":""Ngf"",""id"":""310738""},{""label"":""Nos3"",""id"":""24600""},{""label"":""Ppargc1a"",""id"":""83516""}]"	"[""24179"",""24192"",""24600"",""25293"",""310738"",""83516"",""83619"",""89805""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8947""}]"
DOID:8955	"[""sideroblastic anemia"",""ANEMIA SIDEROBLASTIC"",""Anemia, hypochromic with iron loading""]"	"[{""label"":""CALR"",""id"":""811""}]"	"[""811""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8955""}]"
DOID:896	"[""metal metabolism disorder"",""inborn metal metabolism disorder""]"	"[{""label"":""TRPM6"",""id"":""140803""}]"	"[""140803""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:896""}]"
DOID:8970	"[""subacute sclerosing panencephalitis"",""Immunosuppressive measles encephalitis"",""Van Bogaert's sclerosing leukoencephalitis"",""subacute sclerosing leukoencephalopathy""]"	"[{""label"":""ACE"",""id"":""1636""}]"	"[""1636""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8970""}]"
DOID:898	"[""autosomal dominant polycystic kidney disease"",""ADPKD"",""Congenital biliary ectasias"",""POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1""]"	"[{""label"":""pkd2"",""id"":""432387""}]"	"[""432387""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:898""}]"
DOID:898	"[""autosomal dominant polycystic kidney disease"",""ADPKD"",""Congenital biliary ectasias"",""POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1""]"	"[{""label"":""LRP5"",""id"":""4041""},{""label"":""MTOR"",""id"":""2475""},{""label"":""PKD1"",""id"":""5310""},{""label"":""PKD2"",""id"":""5311""}]"	"[""2475"",""4041"",""5310"",""5311""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:898""}]"
DOID:898	"[""autosomal dominant polycystic kidney disease"",""ADPKD"",""Congenital biliary ectasias"",""POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1""]"	"[{""label"":""Myc"",""id"":""17869""},{""label"":""Pkd2"",""id"":""18764""}]"	"[""17869"",""18764""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:898""}]"
DOID:898	"[""autosomal dominant polycystic kidney disease"",""ADPKD"",""Congenital biliary ectasias"",""POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1""]"	"[{""label"":""pkd-2"",""id"":""178424""}]"	"[""178424""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:898""}]"
DOID:8986	"[""narcolepsy"",""Narcolepsy, without cataplexy"",""paroxysmal sleep""]"	"[{""label"":""Hcrtr2"",""id"":""387285""}]"	"[""387285""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8986""}]"
DOID:8986	"[""narcolepsy"",""Narcolepsy, without cataplexy"",""paroxysmal sleep""]"	"[{""label"":""CHKB"",""id"":""1120""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""MOG"",""id"":""4340""}]"	"[""1120"",""3115"",""3117"",""3119"",""3123"",""4340""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8986""}]"
DOID:8991	"[""cervix uteri carcinoma in situ"",""CIN III"",""CIN III - carcinoma in situ of cervix"",""CIN III - severe dyskaryosis"",""Cervix Ca in situ"",""Severe Dysplasia of the Cervix Uteri"",""Severe dysplasia of cervix"",""carcinoma in situ of cervix"",""carcinoma in situ of uterine cervix"",""carcinoma of cervix stage 0"",""cervical intraepithelial neoplasia grade III with severe dysplasia"",""squamous intraepithelial neoplasia, grade III""]"	"[{""label"":""BRCA1"",""id"":""672""},{""label"":""CDH1"",""id"":""999""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3123"",""672"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8991""}]"
DOID:8997	"[""polycythemia vera"",""Osler-Vaquez syndrome"",""Polycythaemia rubra vera"",""Proliferative polycythaemia"",""chronic erythremia""]"	"[{""label"":""HFE"",""id"":""3077""}]"	"[""3077""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:8997""}]"
DOID:90	"[""degenerative disc disease"",""cervical disc degenerative disease"",""intervertebral disc degeneration"",""lumbar disc degeneration"",""vertebral disc disease""]"	"[{""label"":""ASPN"",""id"":""54829""},{""label"":""COL1A1"",""id"":""1277""}]"	"[""1277"",""54829""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:90""}]"
DOID:90	"[""degenerative disc disease"",""cervical disc degenerative disease"",""intervertebral disc degeneration"",""lumbar disc degeneration"",""vertebral disc disease""]"	"[{""label"":""Acan"",""id"":""58968""},{""label"":""Col2a1"",""id"":""25412""},{""label"":""Ngf"",""id"":""310738""},{""label"":""Ngfr"",""id"":""24596""},{""label"":""Timp1"",""id"":""116510""}]"	"[""116510"",""24596"",""25412"",""310738"",""58968""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:90""}]"
DOID:900	"[""hepatopulmonary syndrome""]"	"[{""label"":""Tnf"",""id"":""24835""}]"	"[""24835""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:900""}]"
DOID:9007	"[""sudden infant death syndrome"",""Cot death"",""Crib death"",""SIDS"",""Sudden death of nonspecific cause in infancy""]"	"[{""label"":""SCN5A"",""id"":""6331""}]"	"[""6331""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9007""}]"
DOID:9007	"[""sudden infant death syndrome"",""Cot death"",""Crib death"",""SIDS"",""Sudden death of nonspecific cause in infancy""]"	"[{""label"":""Slc6a4"",""id"":""15567""}]"	"[""15567""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9007""}]"
DOID:9008	"[""psoriatic arthritis"",""arthritis psoriatica"",""arthropathic psoriasis""]"	"[{""label"":""CCR2"",""id"":""729230""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""IL13"",""id"":""3596""},{""label"":""IL17A"",""id"":""3605""},{""label"":""IRAK1"",""id"":""3654""},{""label"":""LTA"",""id"":""4049""},{""label"":""PECAM1"",""id"":""5175""},{""label"":""STAT3"",""id"":""6774""},{""label"":""STAT4"",""id"":""6775""},{""label"":""TNF"",""id"":""7124""}]"	"[""1543"",""3596"",""3605"",""3654"",""4049"",""5175"",""6774"",""6775"",""7124"",""729230""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9008""}]"
DOID:905	"[""Zellweger syndrome"",""cerebrohepatorenal syndrome"",""congenital iron overload""]"	"[{""label"":""ABCD3"",""id"":""5825""}]"	"[""5825""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:905""}]"
DOID:906	"[""peroxisomal disease"",""peroxisomal disorder""]"	"[{""label"":""Acbd5"",""id"":""74159""}]"	"[""74159""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:906""}]"
DOID:9074	"[""systemic lupus erythematosus"",""Lupus Erythematosus, systemic"",""SLE - Lupus Erythematosus, systemic"",""disseminated lupus erythematosus""]"	"[{""label"":""Atg7"",""id"":""74244""},{""label"":""C1qa"",""id"":""12259""},{""label"":""C4b"",""id"":""12268""},{""label"":""Cd40lg"",""id"":""21947""},{""label"":""Cybb"",""id"":""13058""},{""label"":""Def6"",""id"":""23853""},{""label"":""Dnase1"",""id"":""13419""},{""label"":""Ep300"",""id"":""328572""},{""label"":""Fas"",""id"":""14102""},{""label"":""Fcgr2b"",""id"":""14130""},{""label"":""Lbr"",""id"":""98386""},{""label"":""Lyn"",""id"":""17096""},{""label"":""Man2a1"",""id"":""17158""},{""label"":""Pdcd1"",""id"":""18566""},{""label"":""Pld4"",""id"":""104759""},{""label"":""Pparg"",""id"":""19016""},{""label"":""Ptprc"",""id"":""19264""},{""label"":""Rxra"",""id"":""20181""},{""label"":""Timd4"",""id"":""276891""},{""label"":""Tlr7"",""id"":""170743""}]"	"[""104759"",""12259"",""12268"",""13058"",""13419"",""14102"",""14130"",""170743"",""17096"",""17158"",""18566"",""19016"",""19264"",""20181"",""21947"",""23853"",""276891"",""328572"",""74244"",""98386""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9074""}]"
DOID:9074	"[""systemic lupus erythematosus"",""Lupus Erythematosus, systemic"",""SLE - Lupus Erythematosus, systemic"",""disseminated lupus erythematosus""]"	"[{""label"":""AGER"",""id"":""177""},{""label"":""APOA1"",""id"":""335""},{""label"":""C3"",""id"":""718""},{""label"":""C4A"",""id"":""720""},{""label"":""C4B"",""id"":""721""},{""label"":""CAST"",""id"":""831""},{""label"":""CCL2"",""id"":""6347""},{""label"":""CD40"",""id"":""958""},{""label"":""CFH"",""id"":""3075""},{""label"":""CHAF1A"",""id"":""10036""},{""label"":""CIITA"",""id"":""4261""},{""label"":""CR2"",""id"":""1380""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""DNASE1"",""id"":""1773""},{""label"":""ELN"",""id"":""2006""},{""label"":""EPOR"",""id"":""2057""},{""label"":""F2"",""id"":""2147""},{""label"":""FAS"",""id"":""355""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FCGR2B"",""id"":""2213""},{""label"":""FCGR3A"",""id"":""2214""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HSPA1A"",""id"":""3303""},{""label"":""HSPA1L"",""id"":""3305""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL21"",""id"":""59067""},{""label"":""IL21R"",""id"":""50615""},{""label"":""IL2"",""id"":""3558""},{""label"":""IRF5"",""id"":""3663""},{""label"":""KLKB1"",""id"":""3818""},{""label"":""MBL2"",""id"":""4153""},{""label"":""NAT2"",""id"":""10""},{""label"":""NOD2"",""id"":""64127""},{""label"":""PDCD1"",""id"":""5133""},{""label"":""RPL14"",""id"":""9045""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""SNRNP70"",""id"":""6625""},{""label"":""SNRPC"",""id"":""6631""},{""label"":""SNRPD1"",""id"":""6632""},{""label"":""SNRPD2"",""id"":""6633""},{""label"":""SOD2"",""id"":""6648""},{""label"":""STAT4"",""id"":""6775""},{""label"":""TLR5"",""id"":""7100""},{""label"":""TLR9"",""id"":""54106""},{""label"":""TNF"",""id"":""7124""},{""label"":""VIM"",""id"":""7431""}]"	"[""10"",""10036"",""1380"",""1493"",""1543"",""177"",""1773"",""2006"",""2057"",""2147"",""2212"",""2213"",""2214"",""3075"",""3119"",""3123"",""3303"",""3305"",""335"",""355"",""3557"",""3558"",""3586"",""3663"",""3818"",""4153"",""4261"",""50615"",""5133"",""54106"",""59067"",""6347"",""64127"",""6556"",""6625"",""6631"",""6632"",""6633"",""6648"",""6775"",""7100"",""7124"",""718"",""720"",""721"",""7431"",""831"",""9045"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9074""}]"
DOID:9111	"[""cutaneous leishmaniasis"",""Asian Desert Cutaneous Leishmaniasis"",""Leproid leishmaniasis"",""diffuse cutaneous leishmaniasis""]"	"[{""label"":""CCR5"",""id"":""1234""},{""label"":""COL1A1"",""id"":""1277""},{""label"":""SLC11A1"",""id"":""6556""}]"	"[""1234"",""1277"",""6556""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9111""}]"
DOID:9119	"[""acute myeloid leukemia"",""AML - acute Myeloid Leukemia"",""Leukemia, Myelocytic, acute"",""acute myeloblastic leukaemia"",""acute myeloblastic leukemia"",""acute myelogenous leukaemia"",""acute myelogenous leukemia"",""acute myeloid leukaemia""]"	"[{""label"":""NUP145"",""id"":""852788""}]"	"[""852788""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9119""}]"
DOID:9119	"[""acute myeloid leukemia"",""AML - acute Myeloid Leukemia"",""Leukemia, Myelocytic, acute"",""acute myeloblastic leukaemia"",""acute myeloblastic leukemia"",""acute myelogenous leukaemia"",""acute myelogenous leukemia"",""acute myeloid leukaemia""]"	"[{""label"":""ABL1"",""id"":""25""},{""label"":""ACSL6"",""id"":""23305""},{""label"":""ASXL1"",""id"":""171023""},{""label"":""BMI1"",""id"":""648""},{""label"":""BRD7"",""id"":""29117""},{""label"":""CBL"",""id"":""867""},{""label"":""CDH1"",""id"":""999""},{""label"":""CDKN1B"",""id"":""1027""},{""label"":""CFHR1"",""id"":""3078""},{""label"":""CREBBP"",""id"":""1387""},{""label"":""CSF2"",""id"":""1437""},{""label"":""CSF3"",""id"":""1440""},{""label"":""CSF3R"",""id"":""1441""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CXCR4"",""id"":""7852""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2B6"",""id"":""1555""},{""label"":""EZH2"",""id"":""2146""},{""label"":""FAS"",""id"":""355""},{""label"":""FGFR1"",""id"":""2260""},{""label"":""FLT3"",""id"":""2322""},{""label"":""GATA2"",""id"":""2624""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IDH1"",""id"":""3417""},{""label"":""IDH2"",""id"":""3418""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL6"",""id"":""3569""},{""label"":""ITGAV"",""id"":""3685""},{""label"":""ITGB3"",""id"":""3690""},{""label"":""KAT6A"",""id"":""7994""},{""label"":""KIT"",""id"":""3815""},{""label"":""KMT2A"",""id"":""4297""},{""label"":""KRAS"",""id"":""3845""},{""label"":""LPP"",""id"":""4026""},{""label"":""MEFV"",""id"":""4210""},{""label"":""MLLT10"",""id"":""8028""},{""label"":""NAT2"",""id"":""10""},{""label"":""NCOA2"",""id"":""10499""},{""label"":""NF1"",""id"":""4763""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NPM1"",""id"":""4869""},{""label"":""NRAS"",""id"":""4893""},{""label"":""NSD1"",""id"":""64324""},{""label"":""NUP214"",""id"":""8021""},{""label"":""PHF6"",""id"":""84295""},{""label"":""PICALM"",""id"":""8301""},{""label"":""RUNX1"",""id"":""861""},{""label"":""SAMHD1"",""id"":""25939""},{""label"":""SH3GL1"",""id"":""6455""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SRSF2"",""id"":""6427""},{""label"":""TERT"",""id"":""7015""},{""label"":""TET2"",""id"":""54790""},{""label"":""TFPI2"",""id"":""7980""},{""label"":""TP53"",""id"":""7157""},{""label"":""TYMS"",""id"":""7298""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""ZRSR2"",""id"":""8233""}]"	"[""10"",""1027"",""10499"",""1387"",""1437"",""1440"",""1441"",""1493"",""1543"",""1555"",""171023"",""2146"",""2260"",""2322"",""23305"",""25"",""25939"",""2624"",""2876"",""29117"",""3078"",""3119"",""3417"",""3418"",""355"",""3552"",""3569"",""3685"",""3690"",""3815"",""3845"",""4026"",""4210"",""4297"",""4763"",""4846"",""4869"",""4893"",""54790"",""6427"",""64324"",""6455"",""648"",""6648"",""7015"",""7157"",""7298"",""7422"",""7852"",""7980"",""7994"",""8021"",""8028"",""8233"",""8301"",""84295"",""861"",""867"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9119""}]"
DOID:9119	"[""acute myeloid leukemia"",""AML - acute Myeloid Leukemia"",""Leukemia, Myelocytic, acute"",""acute myeloblastic leukaemia"",""acute myeloblastic leukemia"",""acute myelogenous leukaemia"",""acute myelogenous leukemia"",""acute myeloid leukaemia""]"	"[{""label"":""Asxl1"",""id"":""228790""},{""label"":""Flt3"",""id"":""14255""}]"	"[""14255"",""228790""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9119""}]"
DOID:9120	"[""amyloidosis"",""amyloid disease""]"	"[{""label"":""APCS"",""id"":""325""},{""label"":""GOT1"",""id"":""2805""},{""label"":""SERPINE1"",""id"":""5054""},{""label"":""TTR"",""id"":""7276""}]"	"[""2805"",""325"",""5054"",""7276""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9120""}]"
DOID:9123	"[""eczema herpeticum"",""Herpes simplex dermatitis of eyelid"",""Herpes simplex eyelid dermatitis"",""Herpes simplex virus dermatitis"",""herpes simplex dermatitis"",""herpes simplex virus eyelid dermatitis""]"	"[{""label"":""IFNG"",""id"":""3458""}]"	"[""3458""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9123""}]"
DOID:9146	"[""visceral leishmaniasis"",""Infection by visceral leishmaniasis"",""Kala-Azar""]"	"[{""label"":""CSF2"",""id"":""1437""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""IL2RB"",""id"":""3560""},{""label"":""LTA"",""id"":""4049""},{""label"":""MBL2"",""id"":""4153""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""TNF"",""id"":""7124""}]"	"[""1437"",""3117"",""3560"",""4049"",""4153"",""6556"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9146""}]"
DOID:9155	"[""mucocutaneous leishmaniasis"",""American cutaneous leishmaniasis"",""American mucocutaneous leishmaniasis"",""Cutaneous leishmaniasis, American"",""Mucocutaneous leishmaniasis, American"",""New World cutaneous leishmaniasis""]"	"[{""label"":""LTA"",""id"":""4049""},{""label"":""TNF"",""id"":""7124""}]"	"[""4049"",""7124""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9155""}]"
DOID:916	"[""liver benign neoplasm"",""epithelial hepatic and intrahepatic bile duct neoplasm""]"	"[{""label"":""TUT4"",""id"":""23318""}]"	"[""23318""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:916""}]"
DOID:9164	"[""achalasia"",""Lack of reflex relaxation of lower oesophageal sphincter"",""achalasia of cardia"",""achalasia of esophagus"",""cardiospasm"",""esophageal achalasia"",""hypertensive lower esophageal sphincter""]"	"[{""label"":""AAAS"",""id"":""8086""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""VIPR1"",""id"":""7433""}]"	"[""3117"",""3119"",""7433"",""8086""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9164""}]"
DOID:9164	"[""achalasia"",""Lack of reflex relaxation of lower oesophageal sphincter"",""achalasia of cardia"",""achalasia of esophagus"",""cardiospasm"",""esophageal achalasia"",""hypertensive lower esophageal sphincter""]"	"[{""label"":""Lmna"",""id"":""16905""},{""label"":""Spry2"",""id"":""24064""}]"	"[""16905"",""24064""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9164""}]"
DOID:9169	"[""Wiskott-Aldrich syndrome"",""Wiskott syndrome""]"	"[{""label"":""LAS17"",""id"":""854353""}]"	"[""854353""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9169""}]"
DOID:9169	"[""Wiskott-Aldrich syndrome"",""Wiskott syndrome""]"	"[{""label"":""Foxp3"",""id"":""20371""},{""label"":""Washc4"",""id"":""319277""}]"	"[""20371"",""319277""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9169""}]"
DOID:9182	"[""pemphigus""]"	"[{""label"":""CAST"",""id"":""831""},{""label"":""CD36"",""id"":""948""},{""label"":""CD40"",""id"":""958""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""IL2"",""id"":""3558""}]"	"[""3117"",""3119"",""3123"",""3558"",""831"",""948"",""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9182""}]"
DOID:9206	"[""Barrett's esophagus"",""Barrett esophagus"",""Barrett's esophagus with esophagitis"",""Barrett's oesophagus"",""Barrett's ulcer of esophagus"",""Barretts syndrome"",""ulcerative esophagitis""]"	"[{""label"":""B3GAT2"",""id"":""135152""},{""label"":""CTHRC1"",""id"":""115908""},{""label"":""FOXP1"",""id"":""27086""},{""label"":""GPX3"",""id"":""2878""},{""label"":""GPX7"",""id"":""2882""},{""label"":""MMP12"",""id"":""4321""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MSR1"",""id"":""4481""}]"	"[""115908"",""135152"",""27086"",""2878"",""2882"",""4312"",""4321"",""4481""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9206""}]"
DOID:9206	"[""Barrett's esophagus"",""Barrett esophagus"",""Barrett's esophagus with esophagitis"",""Barrett's oesophagus"",""Barrett's ulcer of esophagus"",""Barretts syndrome"",""ulcerative esophagitis""]"	"[{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Smo"",""id"":""25273""}]"	"[""25273"",""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9206""}]"
DOID:9212	"[""pityriasis rubra pilaris"",""Devergie's disease""]"	"[{""label"":""CARD14"",""id"":""79092""}]"	"[""79092""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9212""}]"
DOID:9220	"[""central sleep apnea"",""primary central sleep apnea""]"	"[{""label"":""Tacr1"",""id"":""24807""}]"	"[""24807""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9220""}]"
DOID:9240	"[""erythromelalgia"",""erythermalgia""]"	"[{""label"":""SCN9A"",""id"":""6335""}]"	"[""6335""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9240""}]"
DOID:9245	"[""Alagille syndrome"",""Alagille-Watson syndrome"",""Arteriohepatic dysplasia""]"	"[{""label"":""JAG1"",""id"":""182""},{""label"":""NOTCH2"",""id"":""4853""}]"	"[""182"",""4853""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9245""}]"
DOID:9245	"[""Alagille syndrome"",""Alagille-Watson syndrome"",""Arteriohepatic dysplasia""]"	"[{""label"":""Jag1"",""id"":""16449""}]"	"[""16449""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9245""}]"
DOID:9246	"[""cerebral amyloid angiopathy"",""Cerebral Hemorrhage, Hereditary, with Amyloidosis"",""Hereditary Cerebral Hemorrhage with Amyloidosis""]"	"[{""label"":""Itm2b"",""id"":""16432""}]"	"[""16432""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9246""}]"
DOID:9246	"[""cerebral amyloid angiopathy"",""Cerebral Hemorrhage, Hereditary, with Amyloidosis"",""Hereditary Cerebral Hemorrhage with Amyloidosis""]"	"[{""label"":""MME"",""id"":""4311""},{""label"":""OLR1"",""id"":""4973""}]"	"[""4311"",""4973""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9246""}]"
DOID:9248	"[""Pallister-Hall syndrome""]"	"[{""label"":""Gli3"",""id"":""14634""}]"	"[""14634""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9248""}]"
DOID:9248	"[""Pallister-Hall syndrome""]"	"[{""label"":""GLI3"",""id"":""2737""}]"	"[""2737""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9248""}]"
DOID:9252	"[""amino acid metabolic disorder"",""inborn errors of amino acid metabolism""]"	"[{""label"":""CTH"",""id"":""1491""},{""label"":""HMGCL"",""id"":""3155""},{""label"":""PCCA"",""id"":""5095""},{""label"":""PCCB"",""id"":""5096""},{""label"":""PHGDH"",""id"":""26227""}]"	"[""1491"",""26227"",""3155"",""5095"",""5096""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9252""}]"
DOID:9253	"[""gastrointestinal stromal tumor"",""GANT"",""GIST"",""Stromal tumor of gastrointestinal tract"",""Stromal tumour of gastrointestinal tract"",""gastrointestinal stromal tumour""]"	"[{""label"":""Kit"",""id"":""16590""}]"	"[""16590""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9253""}]"
DOID:9253	"[""gastrointestinal stromal tumor"",""GANT"",""GIST"",""Stromal tumor of gastrointestinal tract"",""Stromal tumour of gastrointestinal tract"",""gastrointestinal stromal tumour""]"	"[{""label"":""CSF1R"",""id"":""1436""},{""label"":""KIT"",""id"":""3815""},{""label"":""SDHB"",""id"":""6390""},{""label"":""SDHC"",""id"":""6391""},{""label"":""SETD2"",""id"":""29072""},{""label"":""SLCO1B3"",""id"":""28234""},{""label"":""STIM1"",""id"":""6786""},{""label"":""TERT"",""id"":""7015""}]"	"[""1436"",""28234"",""29072"",""3815"",""6390"",""6391"",""6786"",""7015""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9253""}]"
DOID:9255	"[""frontotemporal dementia"",""Wilhemsen-Lynch disease"",""frontotemporal lobar degeneration"",""multiple system tauopathy with presenile dementia"",""pallidopontonigral degeneration""]"	"[{""label"":""Trem2"",""id"":""83433""}]"	"[""83433""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9255""}]"
DOID:9255	"[""frontotemporal dementia"",""Wilhemsen-Lynch disease"",""frontotemporal lobar degeneration"",""multiple system tauopathy with presenile dementia"",""pallidopontonigral degeneration""]"	"[{""label"":""CHMP2B"",""id"":""25978""},{""label"":""GRN"",""id"":""2896""},{""label"":""MAPT"",""id"":""4137""}]"	"[""25978"",""2896"",""4137""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9255""}]"
DOID:9256	"[""colorectal cancer""]"	"[{""label"":""Stat3"",""id"":""20848""}]"	"[""20848""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9256""}]"
DOID:9256	"[""colorectal cancer""]"	"[{""label"":""N"",""id"":""31293""}]"	"[""31293""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9256""}]"
DOID:9256	"[""colorectal cancer""]"	"[{""label"":""ABL1"",""id"":""25""},{""label"":""AKT1"",""id"":""207""},{""label"":""ALX4"",""id"":""60529""},{""label"":""APC"",""id"":""324""},{""label"":""ARID2"",""id"":""196528""},{""label"":""ATM"",""id"":""472""},{""label"":""BAMBI"",""id"":""25805""},{""label"":""BAX"",""id"":""581""},{""label"":""BCOR"",""id"":""54880""},{""label"":""BRCA1"",""id"":""672""},{""label"":""BUB1"",""id"":""699""},{""label"":""BUB1B"",""id"":""701""},{""label"":""CASP9"",""id"":""842""},{""label"":""CES1"",""id"":""1066""},{""label"":""CHD4"",""id"":""1108""},{""label"":""CHEK2"",""id"":""11200""},{""label"":""CTNNB1"",""id"":""1499""},{""label"":""CTNNBL1"",""id"":""56259""},{""label"":""CYP24A1"",""id"":""1591""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""DCC"",""id"":""1630""},{""label"":""DDR2"",""id"":""4921""},{""label"":""DDX3X"",""id"":""1654""},{""label"":""DICER1"",""id"":""23405""},{""label"":""DLC1"",""id"":""10395""},{""label"":""EGFR"",""id"":""1956""},{""label"":""EP300"",""id"":""2033""},{""label"":""ERBB4"",""id"":""2066""},{""label"":""ERCC6"",""id"":""2074""},{""label"":""EZH2"",""id"":""2146""},{""label"":""F7"",""id"":""2155""},{""label"":""FAT1"",""id"":""2195""},{""label"":""FGFR3"",""id"":""2261""},{""label"":""FLCN"",""id"":""201163""},{""label"":""GALNT12"",""id"":""79695""},{""label"":""GPX1"",""id"":""2876""},{""label"":""GRIN2A"",""id"":""2903""},{""label"":""HFE"",""id"":""3077""},{""label"":""HILPDA"",""id"":""29923""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""IKZF1"",""id"":""10320""},{""label"":""IL6"",""id"":""3569""},{""label"":""ITPKC"",""id"":""80271""},{""label"":""JAK1"",""id"":""3716""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""KDR"",""id"":""3791""},{""label"":""KRAS"",""id"":""3845""},{""label"":""LRP1B"",""id"":""53353""},{""label"":""MAP2K4"",""id"":""6416""},{""label"":""MAPK9"",""id"":""5601""},{""label"":""MKI67"",""id"":""4288""},{""label"":""MLH1"",""id"":""4292""},{""label"":""MSH2"",""id"":""4436""},{""label"":""MYD88"",""id"":""4615""},{""label"":""NRAS"",""id"":""4893""},{""label"":""NTRK3"",""id"":""4916""},{""label"":""PDGFRL"",""id"":""5157""},{""label"":""PIK3CA"",""id"":""5290""},{""label"":""PIK3CD"",""id"":""5293""},{""label"":""PLA2G2A"",""id"":""5320""},{""label"":""POLE"",""id"":""5426""},{""label"":""PTPN12"",""id"":""5782""},{""label"":""PTPN13"",""id"":""5783""},{""label"":""PTPRJ"",""id"":""5795""},{""label"":""PTPRT"",""id"":""11122""},{""label"":""RAC1"",""id"":""5879""},{""label"":""RBM10"",""id"":""8241""},{""label"":""RNF43"",""id"":""54894""},{""label"":""SEPTIN9"",""id"":""10801""},{""label"":""SETD2"",""id"":""29072""},{""label"":""SPOP"",""id"":""8405""},{""label"":""SRC"",""id"":""6714""},{""label"":""STIM1"",""id"":""6786""},{""label"":""TCF3"",""id"":""6929""},{""label"":""TGFB2"",""id"":""7042""},{""label"":""TGFBR1"",""id"":""7046""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TNFAIP3"",""id"":""7128""},{""label"":""TP53"",""id"":""7157""},{""label"":""XPO1"",""id"":""7514""},{""label"":""XPO5"",""id"":""57510""},{""label"":""XRCC1"",""id"":""7515""},{""label"":""YTHDF1"",""id"":""54915""}]"	"[""10320"",""10395"",""1066"",""10801"",""1108"",""11122"",""11200"",""1499"",""1571"",""1591"",""1630"",""1654"",""1956"",""196528"",""201163"",""2033"",""2066"",""207"",""2074"",""2146"",""2155"",""2195"",""2261"",""23405"",""25"",""25805"",""2876"",""2903"",""29072"",""29923"",""3077"",""3119"",""324"",""3569"",""3716"",""3791"",""3845"",""4288"",""4292"",""4436"",""4615"",""472"",""4893"",""4916"",""4921"",""5157"",""5290"",""5293"",""5320"",""53353"",""5426"",""54880"",""54894"",""54915"",""5601"",""56259"",""57510"",""5782"",""5783"",""5795"",""581"",""5879"",""60529"",""6416"",""6714"",""672"",""6786"",""6927"",""6929"",""699"",""701"",""7042"",""7046"",""7097"",""7128"",""7157"",""7403"",""7514"",""7515"",""79695"",""80271"",""8241"",""8405"",""842""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9256""}]"
DOID:9256	"[""colorectal cancer""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9256""}]"
DOID:9258	"[""Waardenburg syndrome"",""Waardenburg Shah syndrome"",""Waardenburg's syndrome"",""van der Hoeve Halbertsona Waardenburg syndrome""]"	"[{""label"":""EDNRB"",""id"":""1910""},{""label"":""KITLG"",""id"":""4254""},{""label"":""MITF"",""id"":""4286""}]"	"[""1910"",""4254"",""4286""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9258""}]"
DOID:9261	"[""nasopharynx carcinoma"",""Nasopharyngeal carcinoma"",""malignant Nasopharyngeal tumor"",""malignant neoplasm of nasopharynx"",""nasopharynx cancer""]"	"[{""label"":""BRCA1"",""id"":""672""},{""label"":""CHRNA5"",""id"":""1138""},{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""CR2"",""id"":""1380""},{""label"":""CSF1R"",""id"":""1436""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""GPX1"",""id"":""2876""},{""label"":""MAP2K4"",""id"":""6416""},{""label"":""MAPK14"",""id"":""1432""},{""label"":""MST1R"",""id"":""4486""},{""label"":""TET2"",""id"":""54790""},{""label"":""TP53"",""id"":""7157""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1138"",""1380"",""1432"",""1436"",""1571"",""2876"",""4486"",""54790"",""6416"",""672"",""7157"",""7515"",""81037""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9261""}]"
DOID:9263	"[""homocystinuria"",""CBS deficiency"",""cystathionine beta synthase deficiency"",""cystathionine synthase deficiency""]"	"[{""label"":""CBS"",""id"":""875""}]"	"[""875""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9263""}]"
DOID:9266	"[""cystinuria""]"	"[{""label"":""SLC3A1"",""id"":""6519""}]"	"[""6519""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9266""}]"
DOID:9266	"[""cystinuria""]"	"[{""label"":""Slc3a1"",""id"":""20532""}]"	"[""20532""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9266""}]"
DOID:9268	"[""glycine encephalopathy"",""GCE"",""NKH"",""Non-ketotic hyperglycinemia"",""nonketotic hyperglycinemia""]"	"[{""label"":""Gldc"",""id"":""104174""}]"	"[""104174""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9268""}]"
DOID:9268	"[""glycine encephalopathy"",""GCE"",""NKH"",""Non-ketotic hyperglycinemia"",""nonketotic hyperglycinemia""]"	"[{""label"":""AMT"",""id"":""275""},{""label"":""GLDC"",""id"":""2731""}]"	"[""2731"",""275""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9268""}]"
DOID:9269	"[""maple syrup urine disease"",""Ketoacidaemia"",""branched chain ketoaciduria""]"	"[{""label"":""Bcat2"",""id"":""12036""}]"	"[""12036""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9269""}]"
DOID:9269	"[""maple syrup urine disease"",""Ketoacidaemia"",""branched chain ketoaciduria""]"	"[{""label"":""BCKDHA"",""id"":""593""},{""label"":""BCKDHB"",""id"":""594""},{""label"":""DBT"",""id"":""1629""},{""label"":""DLD"",""id"":""1738""}]"	"[""1629"",""1738"",""593"",""594""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9269""}]"
DOID:9270	"[""alkaptonuria"",""Homogentisate 1,2-dioxygenase deficiency"",""alcaptonuria""]"	"[{""label"":""HGD"",""id"":""3081""}]"	"[""3081""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9270""}]"
DOID:9273	"[""citrullinemia"",""ASS deficiency"",""deficiency of citrulline-aspartate ligase""]"	"[{""label"":""Ass1"",""id"":""11898""}]"	"[""11898""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9273""}]"
DOID:9273	"[""citrullinemia"",""ASS deficiency"",""deficiency of citrulline-aspartate ligase""]"	"[{""label"":""ASS1"",""id"":""445""}]"	"[""445""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9273""}]"
DOID:9277	"[""primary cerebellar degeneration""]"	"[{""label"":""SIL1"",""id"":""64374""}]"	"[""64374""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9277""}]"
DOID:9279	"[""hyperhomocysteinemia""]"	"[{""label"":""F10"",""id"":""29243""},{""label"":""F12"",""id"":""306761""},{""label"":""Gria1"",""id"":""50592""},{""label"":""Grin2a"",""id"":""24409""},{""label"":""Grin2b"",""id"":""24410""}]"	"[""24409"",""24410"",""29243"",""306761"",""50592""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9279""}]"
DOID:9279	"[""hyperhomocysteinemia""]"	"[{""label"":""CBS"",""id"":""875""},{""label"":""MTR"",""id"":""4548""}]"	"[""4548"",""875""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9279""}]"
DOID:9280	"[""carbamoyl phosphate synthetase I deficiency disease"",""CPS I deficiency""]"	"[{""label"":""CPS1"",""id"":""1373""}]"	"[""1373""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9280""}]"
DOID:9280	"[""carbamoyl phosphate synthetase I deficiency disease"",""CPS I deficiency""]"	"[{""label"":""Cps1"",""id"":""227231""}]"	"[""227231""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9280""}]"
DOID:9281	"[""phenylketonuria"",""Folling's disease"",""PKU"",""maternal phenylketonuria"",""phenylalaninemia""]"	"[{""label"":""bli-3"",""id"":""171608""}]"	"[""171608""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9281""}]"
DOID:9282	"[""ocular hypertension""]"	"[{""label"":""MMP1"",""id"":""4312""},{""label"":""MYOC"",""id"":""4653""}]"	"[""4312"",""4653""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9282""}]"
DOID:9286	"[""priapism"",""Mentulagra""]"	"[{""label"":""F13A1"",""id"":""2162""}]"	"[""2162""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9286""}]"
DOID:9296	"[""cleft lip"",""Labium leporinum"",""cheiloschisis"",""cleft lip, unilateral, complete"",""complete unilateral cleft lip"",""hare lip""]"	"[{""label"":""BMP4"",""id"":""652""},{""label"":""CDH1"",""id"":""999""},{""label"":""FGFR1"",""id"":""2260""},{""label"":""GDF6"",""id"":""392255""},{""label"":""MTHFD1"",""id"":""4522""},{""label"":""NECTIN1"",""id"":""5818""},{""label"":""NOG"",""id"":""9241""},{""label"":""POMT1"",""id"":""10585""},{""label"":""SDC2"",""id"":""6383""},{""label"":""SLC19A1"",""id"":""6573""}]"	"[""10585"",""2260"",""392255"",""4522"",""5818"",""6383"",""652"",""6573"",""9241"",""999""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9296""}]"
DOID:93	"[""language disorder""]"	"[{""label"":""FOXP2"",""id"":""93986""}]"	"[""93986""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:93""}]"
DOID:934	"[""viral infectious disease"",""Viral Infection"",""Viral disease"",""virus infection""]"	"[{""label"":""dome"",""id"":""32976""}]"	"[""32976""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:934""}]"
DOID:934	"[""viral infectious disease"",""Viral Infection"",""Viral disease"",""virus infection""]"	"[{""label"":""DOCK8"",""id"":""81704""}]"	"[""81704""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:934""}]"
DOID:934	"[""viral infectious disease"",""Viral Infection"",""Viral disease"",""virus infection""]"	"[{""label"":""Cebpb"",""id"":""12608""}]"	"[""12608""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:934""}]"
DOID:9351	"[""diabetes mellitus"",""diabetes""]"	"[{""label"":""daf-2"",""id"":""175410""},{""label"":""ida-1"",""id"":""175807""},{""label"":""ogt-1"",""id"":""176000""}]"	"[""175410"",""175807"",""176000""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9351""}]"
DOID:9351	"[""diabetes mellitus"",""diabetes""]"	"[{""label"":""cftr"",""id"":""559080""}]"	"[""559080""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9351""}]"
DOID:9351	"[""diabetes mellitus"",""diabetes""]"	"[{""label"":""InR"",""id"":""42549""},{""label"":""gbb"",""id"":""37778""}]"	"[""37778"",""42549""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9351""}]"
DOID:9351	"[""diabetes mellitus"",""diabetes""]"	"[{""label"":""Clock"",""id"":""12753""},{""label"":""Ppara"",""id"":""19013""}]"	"[""12753"",""19013""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9351""}]"
DOID:9351	"[""diabetes mellitus"",""diabetes""]"	"[{""label"":""APOE"",""id"":""348""},{""label"":""CDKAL1"",""id"":""54901""},{""label"":""CSF1R"",""id"":""1436""},{""label"":""CTSB"",""id"":""1508""},{""label"":""CYP11B2"",""id"":""1585""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2C9"",""id"":""1559""},{""label"":""G6PD"",""id"":""2539""},{""label"":""GCK"",""id"":""2645""},{""label"":""GIPR"",""id"":""2696""},{""label"":""HFE"",""id"":""3077""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""IL6"",""id"":""3569""},{""label"":""INS"",""id"":""3630""},{""label"":""INSR"",""id"":""3643""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""KCNJ11"",""id"":""3767""},{""label"":""NAT2"",""id"":""10""},{""label"":""PTPRD"",""id"":""5789""},{""label"":""SLC19A2"",""id"":""10560""},{""label"":""SOD3"",""id"":""6649""},{""label"":""TLR4"",""id"":""7099""},{""label"":""UCP3"",""id"":""7352""},{""label"":""WFS1"",""id"":""7466""}]"	"[""10"",""10560"",""1436"",""1508"",""1543"",""1559"",""1585"",""2539"",""2645"",""2696"",""3077"",""3156"",""348"",""3569"",""3630"",""3643"",""3673"",""3767"",""54901"",""5789"",""6649"",""7099"",""7352"",""7466""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9351""}]"
DOID:9351	"[""diabetes mellitus"",""diabetes""]"	"[{""label"":""F7"",""id"":""260320""},{""label"":""Il2ra"",""id"":""25704""},{""label"":""Lrp1"",""id"":""299858""},{""label"":""Serpine1"",""id"":""24617""}]"	"[""24617"",""25704"",""260320"",""299858""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9351""}]"
DOID:9352	"[""type 2 diabetes mellitus"",""NIDDM"",""insulin resistance"",""non-insulin-dependent diabetes mellitus"",""type 2 diabetes"",""type II diabetes mellitus""]"	"[{""label"":""Akt1"",""id"":""24185""},{""label"":""Aoc3"",""id"":""29473""},{""label"":""Cckar"",""id"":""24889""},{""label"":""Crtc2"",""id"":""310615""},{""label"":""Ednrb"",""id"":""50672""},{""label"":""F7"",""id"":""260320""},{""label"":""G6pc1"",""id"":""25634""},{""label"":""Gck"",""id"":""24385""},{""label"":""Gipr"",""id"":""25024""},{""label"":""Hmgcr"",""id"":""25675""},{""label"":""Irs1"",""id"":""25467""},{""label"":""Lep"",""id"":""25608""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Lnpep"",""id"":""171105""},{""label"":""Pck1"",""id"":""362282""},{""label"":""Pcsk1"",""id"":""25204""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Prkaa1"",""id"":""65248""},{""label"":""Serpine1"",""id"":""24617""},{""label"":""Tnf"",""id"":""24835""},{""label"":""Ucp2"",""id"":""54315""}]"	"[""171105"",""24185"",""24385"",""24536"",""24617"",""24835"",""24889"",""25024"",""25204"",""25467"",""25608"",""25634"",""25675"",""260320"",""29473"",""310615"",""362282"",""50672"",""54315"",""65248"",""83516""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9352""}]"
DOID:9352	"[""type 2 diabetes mellitus"",""NIDDM"",""insulin resistance"",""non-insulin-dependent diabetes mellitus"",""type 2 diabetes"",""type II diabetes mellitus""]"	"[{""label"":""InR"",""id"":""42549""},{""label"":""lilli"",""id"":""33496""}]"	"[""33496"",""42549""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9352""}]"
DOID:9352	"[""type 2 diabetes mellitus"",""NIDDM"",""insulin resistance"",""non-insulin-dependent diabetes mellitus"",""type 2 diabetes"",""type II diabetes mellitus""]"	"[{""label"":""ABCA1"",""id"":""19""},{""label"":""ABCB1"",""id"":""5243""},{""label"":""ABCC8"",""id"":""6833""},{""label"":""ACE"",""id"":""1636""},{""label"":""ADAM17"",""id"":""6868""},{""label"":""ADIPOQ"",""id"":""9370""},{""label"":""ADRA2A"",""id"":""150""},{""label"":""ADRB3"",""id"":""155""},{""label"":""AGER"",""id"":""177""},{""label"":""AHSG"",""id"":""197""},{""label"":""AKR1B1"",""id"":""231""},{""label"":""AKT2"",""id"":""208""},{""label"":""ALDH2"",""id"":""217""},{""label"":""ALDOB"",""id"":""229""},{""label"":""APOA5"",""id"":""116519""},{""label"":""APOB"",""id"":""338""},{""label"":""APOD"",""id"":""347""},{""label"":""APOM"",""id"":""55937""},{""label"":""AXL"",""id"":""558""},{""label"":""BCHE"",""id"":""590""},{""label"":""BTC"",""id"":""685""},{""label"":""CACNA1D"",""id"":""776""},{""label"":""CADM2"",""id"":""253559""},{""label"":""CAPN10"",""id"":""11132""},{""label"":""CASP9"",""id"":""842""},{""label"":""CASQ1"",""id"":""844""},{""label"":""CD36"",""id"":""948""},{""label"":""CD38"",""id"":""952""},{""label"":""CDKAL1"",""id"":""54901""},{""label"":""CEL"",""id"":""1056""},{""label"":""CNR1"",""id"":""1268""},{""label"":""CPE"",""id"":""1363""},{""label"":""CYB5R4"",""id"":""51167""},{""label"":""CYP11B2"",""id"":""1585""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2C9"",""id"":""1559""},{""label"":""DPP4"",""id"":""1803""},{""label"":""DRD2"",""id"":""1813""},{""label"":""ENPP1"",""id"":""5167""},{""label"":""ESR1"",""id"":""2099""},{""label"":""F7"",""id"":""2155""},{""label"":""FASLG"",""id"":""356""},{""label"":""FFAR1"",""id"":""2864""},{""label"":""FTO"",""id"":""79068""},{""label"":""GCGR"",""id"":""2642""},{""label"":""GCK"",""id"":""2645""},{""label"":""GFPT2"",""id"":""9945""},{""label"":""GHR"",""id"":""2690""},{""label"":""GHRL"",""id"":""51738""},{""label"":""GLO1"",""id"":""2739""},{""label"":""GP6"",""id"":""51206""},{""label"":""GPD2"",""id"":""2820""},{""label"":""GPX3"",""id"":""2878""},{""label"":""HFE"",""id"":""3077""},{""label"":""HIF1A"",""id"":""3091""},{""label"":""HK2"",""id"":""3099""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HMGCR"",""id"":""3156""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""HNF4A"",""id"":""3172""},{""label"":""HSD11B1"",""id"":""3290""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IGF2R"",""id"":""3482""},{""label"":""IGFBP3"",""id"":""3486""},{""label"":""IKBKB"",""id"":""3551""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL6"",""id"":""3569""},{""label"":""INPPL1"",""id"":""3636""},{""label"":""INS"",""id"":""3630""},{""label"":""INSR"",""id"":""3643""},{""label"":""IRS1"",""id"":""3667""},{""label"":""IRS2"",""id"":""8660""},{""label"":""ITGA2"",""id"":""3673""},{""label"":""KCNJ11"",""id"":""3767""},{""label"":""KCNQ1"",""id"":""3784""},{""label"":""LEP"",""id"":""3952""},{""label"":""LEPR"",""id"":""3953""},{""label"":""LIPC"",""id"":""3990""},{""label"":""LMNA"",""id"":""4000""},{""label"":""LPL"",""id"":""4023""},{""label"":""LTA"",""id"":""4049""},{""label"":""MAPK8IP1"",""id"":""9479""},{""label"":""MAPK9"",""id"":""5601""},{""label"":""MT2A"",""id"":""4502""},{""label"":""MTNR1B"",""id"":""4544""},{""label"":""MTOR"",""id"":""2475""},{""label"":""NOS2"",""id"":""4843""},{""label"":""P2RY12"",""id"":""64805""},{""label"":""PCK1"",""id"":""5105""},{""label"":""PCSK2"",""id"":""5126""},{""label"":""PDX1"",""id"":""3651""},{""label"":""PIK3C2G"",""id"":""5288""},{""label"":""PKLR"",""id"":""5313""},{""label"":""PLA2G7"",""id"":""7941""},{""label"":""PLAT"",""id"":""5327""},{""label"":""PNPLA3"",""id"":""80339""},{""label"":""PON1"",""id"":""5444""},{""label"":""PON2"",""id"":""5445""},{""label"":""PPARD"",""id"":""5467""},{""label"":""PPARG"",""id"":""5468""},{""label"":""PPARGC1A"",""id"":""10891""},{""label"":""PPP1R3A"",""id"":""5506""},{""label"":""PRKAA2"",""id"":""5563""},{""label"":""PTPN1"",""id"":""5770""},{""label"":""PTPRD"",""id"":""5789""},{""label"":""RBP4"",""id"":""5950""},{""label"":""RRAD"",""id"":""6236""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""SGCG"",""id"":""6445""},{""label"":""SHBG"",""id"":""6462""},{""label"":""SLC2A1"",""id"":""6513""},{""label"":""SLC2A2"",""id"":""6514""},{""label"":""SLC2A4"",""id"":""6517""},{""label"":""SOD1"",""id"":""6647""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SOD3"",""id"":""6649""},{""label"":""SORBS1"",""id"":""10580""},{""label"":""SPHK1"",""id"":""8877""},{""label"":""SRC"",""id"":""6714""},{""label"":""SREBF1"",""id"":""6720""},{""label"":""SREBF2"",""id"":""6721""},{""label"":""STAT3"",""id"":""6774""},{""label"":""TLR4"",""id"":""7099""},{""label"":""UCP3"",""id"":""7352""},{""label"":""VPS26A"",""id"":""9559""},{""label"":""WFS1"",""id"":""7466""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""1056"",""10580"",""10891"",""11132"",""116519"",""1268"",""1363"",""150"",""1543"",""155"",""1559"",""1585"",""1636"",""177"",""1803"",""1813"",""19"",""197"",""208"",""2099"",""2155"",""217"",""229"",""231"",""2475"",""253559"",""2642"",""2645"",""2690"",""2739"",""2820"",""2864"",""2878"",""3077"",""3091"",""3099"",""3117"",""3156"",""3172"",""3290"",""3304"",""338"",""3458"",""347"",""3482"",""3486"",""3551"",""3557"",""356"",""3569"",""3586"",""3630"",""3636"",""3643"",""3651"",""3667"",""3673"",""3767"",""3784"",""3952"",""3953"",""3990"",""4000"",""4023"",""4049"",""4502"",""4544"",""4843"",""5105"",""51167"",""51206"",""5126"",""5167"",""51738"",""5176"",""5243"",""5288"",""5313"",""5327"",""5444"",""5445"",""5467"",""5468"",""54901"",""5506"",""5563"",""558"",""55937"",""5601"",""5770"",""5789"",""590"",""5950"",""6236"",""6445"",""6462"",""64805"",""6513"",""6514"",""6517"",""6647"",""6648"",""6649"",""6714"",""6720"",""6721"",""6774"",""6833"",""685"",""6868"",""6927"",""7099"",""7352"",""7466"",""7515"",""776"",""79068"",""7941"",""80339"",""842"",""844"",""8660"",""8877"",""9370"",""9479"",""948"",""952"",""9559"",""9945""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9352""}]"
DOID:9352	"[""type 2 diabetes mellitus"",""NIDDM"",""insulin resistance"",""non-insulin-dependent diabetes mellitus"",""type 2 diabetes"",""type II diabetes mellitus""]"	"[{""label"":""Akt2"",""id"":""11652""},{""label"":""Cdkal1"",""id"":""68916""},{""label"":""Cyb5r4"",""id"":""266690""},{""label"":""Gck"",""id"":""103988""},{""label"":""Htr2c"",""id"":""15560""},{""label"":""Ins2"",""id"":""16334""},{""label"":""Irs1"",""id"":""16367""},{""label"":""Irs2"",""id"":""384783""},{""label"":""Lep"",""id"":""16846""},{""label"":""Lepr"",""id"":""16847""},{""label"":""Madd"",""id"":""228355""},{""label"":""Nfe2l1"",""id"":""18023""},{""label"":""Ppp1r3a"",""id"":""140491""},{""label"":""Ppp1r3c"",""id"":""53412""},{""label"":""Prkci"",""id"":""18759""},{""label"":""Slc2a2"",""id"":""20526""},{""label"":""Slc2a4"",""id"":""20528""},{""label"":""Snap25"",""id"":""20614""},{""label"":""a"",""id"":""50518""}]"	"[""103988"",""11652"",""140491"",""15560"",""16334"",""16367"",""16846"",""16847"",""18023"",""18759"",""20526"",""20528"",""20614"",""228355"",""266690"",""384783"",""50518"",""53412"",""68916""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9352""}]"
DOID:9352	"[""type 2 diabetes mellitus"",""NIDDM"",""insulin resistance"",""non-insulin-dependent diabetes mellitus"",""type 2 diabetes"",""type II diabetes mellitus""]"	"[{""label"":""LAG1"",""id"":""856386""}]"	"[""856386""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9352""}]"
DOID:9352	"[""type 2 diabetes mellitus"",""NIDDM"",""insulin resistance"",""non-insulin-dependent diabetes mellitus"",""type 2 diabetes"",""type II diabetes mellitus""]"	"[{""label"":""gon-1"",""id"":""177850""},{""label"":""ogt-1"",""id"":""176000""},{""label"":""parp-1"",""id"":""266823""}]"	"[""176000"",""177850"",""266823""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9352""}]"
DOID:936	"[""brain disease"",""encephalopathy""]"	"[{""label"":""CPT2"",""id"":""1376""},{""label"":""DBR1"",""id"":""51163""},{""label"":""NUP214"",""id"":""8021""},{""label"":""RANBP2"",""id"":""5903""},{""label"":""UNC93B1"",""id"":""81622""}]"	"[""1376"",""51163"",""5903"",""8021"",""81622""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:936""}]"
DOID:936	"[""brain disease"",""encephalopathy""]"	"[{""label"":""HRR25"",""id"":""855897""}]"	"[""855897""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:936""}]"
DOID:9383	"[""iridocyclitis"",""primary iridocyclitis""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IL1A"",""id"":""3552""}]"	"[""1493"",""3119"",""3383"",""3552""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9383""}]"
DOID:9408	"[""acute myocardial infarction""]"	"[{""label"":""GP6"",""id"":""51206""}]"	"[""51206""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9408""}]"
DOID:9409	"[""diabetes insipidus""]"	"[{""label"":""AVP"",""id"":""551""}]"	"[""551""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9409""}]"
DOID:9409	"[""diabetes insipidus""]"	"[{""label"":""Aqp2"",""id"":""25386""},{""label"":""Avp"",""id"":""24221""}]"	"[""24221"",""25386""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9409""}]"
DOID:9410	"[""combined pituitary hormone deficiency"",""Simmond's disease"",""Simmonds' disease"",""panhypopituitarism""]"	"[{""label"":""OTX2"",""id"":""5015""},{""label"":""RNPC3"",""id"":""55599""},{""label"":""ROBO1"",""id"":""6091""}]"	"[""5015"",""55599"",""6091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9410""}]"
DOID:9415	"[""allergic asthma"",""extrinsic asthma with acute exacerbation"",""extrinsic asthma with status asthmaticus""]"	"[{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-C"",""id"":""3107""},{""label"":""HLA-DPA1"",""id"":""3113""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DRB1"",""id"":""3123""}]"	"[""3106"",""3107"",""3113"",""3115"",""3123""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9415""}]"
DOID:9427	"[""hypertensive encephalopathy""]"	"[{""label"":""Ppara"",""id"":""25747""}]"	"[""25747""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9427""}]"
DOID:9432	"[""renal glycosuria"",""renal diabetes"",""renal glucosuria""]"	"[{""label"":""SLC5A2"",""id"":""6524""}]"	"[""6524""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9432""}]"
DOID:9452	"[""steatotic liver disease"",""Fatty change of liver"",""SLD"",""Steatosis of liver"",""alcoholic fatty liver"",""fatty liver disease"",""hepatic lipidosis"",""hepatic steatosis""]"	"[{""label"":""LAG1"",""id"":""856386""}]"	"[""856386""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9452""}]"
DOID:9452	"[""steatotic liver disease"",""Fatty change of liver"",""SLD"",""Steatosis of liver"",""alcoholic fatty liver"",""fatty liver disease"",""hepatic lipidosis"",""hepatic steatosis""]"	"[{""label"":""Ldlr"",""id"":""16835""},{""label"":""Lep"",""id"":""16846""},{""label"":""Lrp6"",""id"":""16974""},{""label"":""Mc4r"",""id"":""17202""}]"	"[""16835"",""16846"",""16974"",""17202""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9452""}]"
DOID:9452	"[""steatotic liver disease"",""Fatty change of liver"",""SLD"",""Steatosis of liver"",""alcoholic fatty liver"",""fatty liver disease"",""hepatic lipidosis"",""hepatic steatosis""]"	"[{""label"":""Dgat2"",""id"":""252900""},{""label"":""Gck"",""id"":""24385""},{""label"":""Ldlr"",""id"":""300438""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Ptgs2"",""id"":""29527""}]"	"[""24385"",""252900"",""29527"",""300438"",""83516""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9452""}]"
DOID:9452	"[""steatotic liver disease"",""Fatty change of liver"",""SLD"",""Steatosis of liver"",""alcoholic fatty liver"",""fatty liver disease"",""hepatic lipidosis"",""hepatic steatosis""]"	"[{""label"":""ADRB2"",""id"":""154""},{""label"":""CYP2E1"",""id"":""1571""},{""label"":""HADHA"",""id"":""3030""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""HTR2B"",""id"":""3357""},{""label"":""PNPLA3"",""id"":""80339""}]"	"[""154"",""1571"",""3030"",""3356"",""3357"",""80339""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9452""}]"
DOID:9455	"[""lipid storage disease"",""Lipoid storage diseas"",""inborn lipid storage disorder"",""lipoidosis""]"	"[{""label"":""ARV1"",""id"":""850943""}]"	"[""850943""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9455""}]"
DOID:9467	"[""nail-patella syndrome"",""Fong disease"",""Turner-Kiser syndrome"",""hereditary onychoostedysplasia"",""iliac horn syndrome"",""nail patella syndrome""]"	"[{""label"":""Ldb1"",""id"":""16825""}]"	"[""16825""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9467""}]"
DOID:9470	"[""bacterial meningitis""]"	"[{""label"":""MMP9"",""id"":""4318""},{""label"":""PARP1"",""id"":""142""}]"	"[""142"",""4318""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9470""}]"
DOID:9477	"[""pulmonary embolism"",""pulmonary artery embolism"",""pulmonary embolus""]"	"[{""label"":""Mmp2"",""id"":""81686""},{""label"":""Mmp9"",""id"":""81687""}]"	"[""81686"",""81687""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9477""}]"
DOID:9477	"[""pulmonary embolism"",""pulmonary artery embolism"",""pulmonary embolus""]"	"[{""label"":""F13A1"",""id"":""2162""},{""label"":""F2"",""id"":""2147""},{""label"":""F5"",""id"":""2153""},{""label"":""FTO"",""id"":""79068""}]"	"[""2147"",""2153"",""2162"",""79068""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9477""}]"
DOID:9478	"[""postpartum depression"",""Maternity blues"",""postnatal depression""]"	"[{""label"":""Gabrd"",""id"":""14403""}]"	"[""14403""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9478""}]"
DOID:9478	"[""postpartum depression"",""Maternity blues"",""postnatal depression""]"	"[{""label"":""TPH1"",""id"":""7166""}]"	"[""7166""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9478""}]"
DOID:9505	"[""cannabis abuse"",""marijuana abuse""]"	"[{""label"":""COMT"",""id"":""1312""},{""label"":""DRD4"",""id"":""1815""}]"	"[""1312"",""1815""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9505""}]"
DOID:9513	"[""plasma cell leukemia"",""plasma cell leukaemia"",""plasmacytic leukaemia"",""plasmacytic leukemia""]"	"[{""label"":""CD40"",""id"":""958""}]"	"[""958""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9513""}]"
DOID:9521	"[""Laron syndrome"",""Laron-type isolated somatotropin defect""]"	"[{""label"":""GHR"",""id"":""2690""}]"	"[""2690""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9521""}]"
DOID:9521	"[""Laron syndrome"",""Laron-type isolated somatotropin defect""]"	"[{""label"":""Ghr"",""id"":""14600""}]"	"[""14600""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9521""}]"
DOID:9538	"[""multiple myeloma"",""myeloma""]"	"[{""label"":""ABCG2"",""id"":""9429""},{""label"":""ACE"",""id"":""1636""},{""label"":""APOE"",""id"":""348""},{""label"":""CD40"",""id"":""958""},{""label"":""CD40LG"",""id"":""959""},{""label"":""CFHR1"",""id"":""3078""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP2C19"",""id"":""1557""},{""label"":""FCGR2A"",""id"":""2212""},{""label"":""FGG"",""id"":""2266""},{""label"":""GPX1"",""id"":""2876""},{""label"":""GPX3"",""id"":""2878""},{""label"":""HFE"",""id"":""3077""},{""label"":""HK1"",""id"":""3098""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IL10"",""id"":""3586""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL4R"",""id"":""3566""},{""label"":""IRF4"",""id"":""3662""},{""label"":""KRAS"",""id"":""3845""},{""label"":""MEFV"",""id"":""4210""},{""label"":""MET"",""id"":""4233""},{""label"":""MTR"",""id"":""4548""},{""label"":""NRAS"",""id"":""4893""},{""label"":""PON1"",""id"":""5444""},{""label"":""ROBO1"",""id"":""6091""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SPARC"",""id"":""6678""},{""label"":""SPP1"",""id"":""6696""},{""label"":""TFRC"",""id"":""7037""},{""label"":""TGFB1"",""id"":""7040""},{""label"":""TNF"",""id"":""7124""},{""label"":""TNFRSF10A"",""id"":""8797""},{""label"":""TNFRSF17"",""id"":""608""},{""label"":""TP53"",""id"":""7157""},{""label"":""TYMS"",""id"":""7298""},{""label"":""VEGFA"",""id"":""7422""},{""label"":""XPO5"",""id"":""57510""},{""label"":""XRCC5"",""id"":""7520""}]"	"[""1493"",""1543"",""1557"",""1636"",""2212"",""2266"",""2876"",""2878"",""3077"",""3078"",""3098"",""3383"",""348"",""3552"",""3557"",""3566"",""3586"",""3662"",""3845"",""4210"",""4233"",""4548"",""4893"",""5444"",""57510"",""608"",""6091"",""6648"",""6678"",""6696"",""7037"",""7040"",""7124"",""7157"",""7298"",""7422"",""7520"",""8797"",""9429"",""958"",""959""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9538""}]"
DOID:9540	"[""vascular skin disease""]"	"[{""label"":""AGER"",""id"":""177""}]"	"[""177""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9540""}]"
DOID:9562	"[""primary ciliary dyskinesia"",""ciliary motility disorder"",""immotile ciliary syndrome""]"	"[{""label"":""Dnah5"",""id"":""110082""},{""label"":""Pcsk5"",""id"":""18552""},{""label"":""Slit2"",""id"":""20563""}]"	"[""110082"",""18552"",""20563""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9562""}]"
DOID:9562	"[""primary ciliary dyskinesia"",""ciliary motility disorder"",""immotile ciliary syndrome""]"	"[{""label"":""BRWD1"",""id"":""54014""},{""label"":""CFAP74"",""id"":""85452""},{""label"":""DNAH7"",""id"":""56171""}]"	"[""54014"",""56171"",""85452""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9562""}]"
DOID:9563	"[""bronchiectasis"",""Polynesian bronchiectasis""]"	"[{""label"":""CFTR"",""id"":""1080""},{""label"":""TAP1"",""id"":""6890""}]"	"[""1080"",""6890""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9563""}]"
DOID:9620	"[""vesicoureteral reflux"",""vesico-ureteral reflux""]"	"[{""label"":""AGTR2"",""id"":""186""},{""label"":""IFNG"",""id"":""3458""},{""label"":""ROBO2"",""id"":""6092""},{""label"":""TNXB"",""id"":""7148""}]"	"[""186"",""3458"",""6092"",""7148""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9620""}]"
DOID:9620	"[""vesicoureteral reflux"",""vesico-ureteral reflux""]"	"[{""label"":""Upk3a"",""id"":""22270""}]"	"[""22270""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9620""}]"
DOID:9631	"[""Pelger-Huet anomaly""]"	"[{""label"":""Lbr"",""id"":""98386""}]"	"[""98386""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9631""}]"
DOID:9631	"[""Pelger-Huet anomaly""]"	"[{""label"":""LBR"",""id"":""3930""}]"	"[""3930""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9631""}]"
DOID:9649	"[""congenital nystagmus""]"	"[{""label"":""MYO7A"",""id"":""4647""},{""label"":""ROBO1"",""id"":""6091""}]"	"[""4647"",""6091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9649""}]"
DOID:9651	"[""systolic heart failure""]"	"[{""label"":""NPPB"",""id"":""4879""}]"	"[""4879""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9651""}]"
DOID:9655	"[""oral mucosa leukoplakia""]"	"[{""label"":""Tp53"",""id"":""24842""}]"	"[""24842""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9655""}]"
DOID:9655	"[""oral mucosa leukoplakia""]"	"[{""label"":""NAT2"",""id"":""10""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10"",""7515""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9655""}]"
DOID:9663	"[""aphthous stomatitis"",""Aphtha"",""Aphthous ulceration"",""Canker sore"",""Oral aphthae"",""oral ulcer""]"	"[{""label"":""HFE"",""id"":""3077""},{""label"":""IL10"",""id"":""3586""},{""label"":""TGFB1"",""id"":""7040""}]"	"[""3077"",""3586"",""7040""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9663""}]"
DOID:9667	"[""placental abruption"",""abruptio placenta"",""abruptio placentae""]"	"[{""label"":""PROC"",""id"":""5624""}]"	"[""5624""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9667""}]"
DOID:9669	"[""senile cataract""]"	"[{""label"":""ATM"",""id"":""472""},{""label"":""CAT"",""id"":""847""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""NAT2"",""id"":""10""},{""label"":""OGG1"",""id"":""4968""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10"",""3304"",""472"",""4968"",""7515"",""847""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9669""}]"
DOID:9675	"[""pulmonary emphysema""]"	"[{""label"":""CLPTM1L"",""id"":""81037""},{""label"":""CSF3"",""id"":""1440""},{""label"":""MMP1"",""id"":""4312""},{""label"":""MMP9"",""id"":""4318""},{""label"":""SERPINA1"",""id"":""5265""},{""label"":""SFTPC"",""id"":""6440""},{""label"":""TGFB1"",""id"":""7040""}]"	"[""1440"",""4312"",""4318"",""5265"",""6440"",""7040"",""81037""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9675""}]"
DOID:9675	"[""pulmonary emphysema""]"	"[{""label"":""Ednra"",""id"":""24326""},{""label"":""Gclc"",""id"":""25283""},{""label"":""Ptgs2"",""id"":""29527""}]"	"[""24326"",""25283"",""29527""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9675""}]"
DOID:9675	"[""pulmonary emphysema""]"	"[{""label"":""Fstl1"",""id"":""14314""},{""label"":""Fut8"",""id"":""53618""},{""label"":""Itgb6"",""id"":""16420""},{""label"":""Jun"",""id"":""16476""},{""label"":""Kl"",""id"":""16591""},{""label"":""Ptma"",""id"":""19231""},{""label"":""Smo"",""id"":""319757""},{""label"":""Tlr4"",""id"":""21898""}]"	"[""14314"",""16420"",""16476"",""16591"",""19231"",""21898"",""319757"",""53618""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9675""}]"
DOID:9719	"[""neovascular inflammatory vitreoretinopathy"",""ADNIV"",""Retinitis proliferans"",""autosomal dominant neovascular inflammatory vitreoretinopathy"",""proliferative vitreoretinopathy""]"	"[{""label"":""LRP5"",""id"":""4041""},{""label"":""LTA"",""id"":""4049""}]"	"[""4041"",""4049""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9719""}]"
DOID:9733	"[""renal tuberculosis"",""Tuberculosis of kidney""]"	"[{""label"":""IL4R"",""id"":""3566""}]"	"[""3566""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9733""}]"
DOID:9743	"[""diabetic neuropathy""]"	"[{""label"":""Akr1b1"",""id"":""24192""},{""label"":""Bad"",""id"":""64639""},{""label"":""Bdkrb1"",""id"":""81509""},{""label"":""Bdnf"",""id"":""24225""},{""label"":""Cnr1"",""id"":""25248""},{""label"":""Ptgs2"",""id"":""29527""},{""label"":""Sord"",""id"":""24788""},{""label"":""Tlr4"",""id"":""29260""},{""label"":""Trpa1"",""id"":""312896""}]"	"[""24192"",""24225"",""24788"",""25248"",""29260"",""29527"",""312896"",""64639"",""81509""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9743""}]"
DOID:9743	"[""diabetic neuropathy""]"	"[{""label"":""AKR1B1"",""id"":""231""},{""label"":""ALDH2"",""id"":""217""},{""label"":""EPO"",""id"":""2056""},{""label"":""FTO"",""id"":""79068""},{""label"":""GHRL"",""id"":""51738""},{""label"":""HGF"",""id"":""3082""},{""label"":""IFNG"",""id"":""3458""},{""label"":""PGF"",""id"":""5228""},{""label"":""TLR4"",""id"":""7099""},{""label"":""UCP2"",""id"":""7351""},{""label"":""UCP3"",""id"":""7352""},{""label"":""VEGFA"",""id"":""7422""}]"	"[""2056"",""217"",""231"",""3082"",""3458"",""51738"",""5228"",""7099"",""7351"",""7352"",""7422"",""79068""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9743""}]"
DOID:9743	"[""diabetic neuropathy""]"	"[{""label"":""InR"",""id"":""42549""}]"	"[""42549""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9743""}]"
DOID:9744	"[""type 1 diabetes mellitus"",""IDDM"",""insulin-dependent diabetes mellitus"",""type I diabetes mellitus""]"	"[{""label"":""Cd38"",""id"":""12494""},{""label"":""Fasl"",""id"":""14103""},{""label"":""G6pc2"",""id"":""14378""},{""label"":""Ifng"",""id"":""15978""},{""label"":""Ifngr2"",""id"":""15980""},{""label"":""Il1r1"",""id"":""16177""},{""label"":""Il4"",""id"":""16189""},{""label"":""Ins2"",""id"":""16334""},{""label"":""Pdx1"",""id"":""18609""},{""label"":""Prf1"",""id"":""18646""},{""label"":""Ptprn2"",""id"":""19276""},{""label"":""Sell"",""id"":""20343""},{""label"":""Senp1"",""id"":""223870""},{""label"":""Tnfsf4"",""id"":""22164""}]"	"[""12494"",""14103"",""14378"",""15978"",""15980"",""16177"",""16189"",""16334"",""18609"",""18646"",""19276"",""20343"",""22164"",""223870""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9744""}]"
DOID:9744	"[""type 1 diabetes mellitus"",""IDDM"",""insulin-dependent diabetes mellitus"",""type I diabetes mellitus""]"	"[{""label"":""Avp"",""id"":""24221""},{""label"":""Cd40lg"",""id"":""84349""},{""label"":""Faslg"",""id"":""25385""},{""label"":""Hp"",""id"":""24464""},{""label"":""Ifng"",""id"":""25712""},{""label"":""Ptprn"",""id"":""116660""},{""label"":""Slc18a2"",""id"":""25549""}]"	"[""116660"",""24221"",""24464"",""25385"",""25549"",""25712"",""84349""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9744""}]"
DOID:9744	"[""type 1 diabetes mellitus"",""IDDM"",""insulin-dependent diabetes mellitus"",""type I diabetes mellitus""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGER"",""id"":""177""},{""label"":""ALDH2"",""id"":""217""},{""label"":""APOC3"",""id"":""345""},{""label"":""APOM"",""id"":""55937""},{""label"":""BCHE"",""id"":""590""},{""label"":""BTC"",""id"":""685""},{""label"":""CCL5"",""id"":""6352""},{""label"":""CCR2"",""id"":""729230""},{""label"":""CD28"",""id"":""940""},{""label"":""CD38"",""id"":""952""},{""label"":""CD80"",""id"":""941""},{""label"":""CD86"",""id"":""942""},{""label"":""CEL"",""id"":""1056""},{""label"":""CFB"",""id"":""629""},{""label"":""CLEC16A"",""id"":""23274""},{""label"":""CTLA4"",""id"":""1493""},{""label"":""CYP27B1"",""id"":""1594""},{""label"":""CYP2R1"",""id"":""120227""},{""label"":""EIF2AK3"",""id"":""9451""},{""label"":""F7"",""id"":""2155""},{""label"":""GAD2"",""id"":""2572""},{""label"":""GC"",""id"":""2638""},{""label"":""HLA-DPA1"",""id"":""3113""},{""label"":""HLA-DPB1"",""id"":""3115""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HNF1A"",""id"":""6927""},{""label"":""HSD11B2"",""id"":""3291""},{""label"":""ICAM1"",""id"":""3383""},{""label"":""IGF2R"",""id"":""3482""},{""label"":""IGFBP3"",""id"":""3486""},{""label"":""IL15"",""id"":""3600""},{""label"":""IL1A"",""id"":""3552""},{""label"":""IL1R1"",""id"":""3554""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL2"",""id"":""3558""},{""label"":""IL2RA"",""id"":""3559""},{""label"":""IL6"",""id"":""3569""},{""label"":""INS"",""id"":""3630""},{""label"":""ITPR3"",""id"":""3710""},{""label"":""LTA"",""id"":""4049""},{""label"":""NOTCH4"",""id"":""4855""},{""label"":""PRRC2A"",""id"":""7916""},{""label"":""PTPRN2"",""id"":""5799""},{""label"":""PTPRN"",""id"":""5798""},{""label"":""REG1A"",""id"":""5967""},{""label"":""SLC11A1"",""id"":""6556""},{""label"":""SOD1"",""id"":""6647""},{""label"":""SOD2"",""id"":""6648""},{""label"":""SREBF2"",""id"":""6721""},{""label"":""TAP1"",""id"":""6890""},{""label"":""TBP"",""id"":""6908""},{""label"":""TF"",""id"":""7018""},{""label"":""TLR2"",""id"":""7097""},{""label"":""TLR3"",""id"":""7098""},{""label"":""TNF"",""id"":""7124""},{""label"":""WFS1"",""id"":""7466""},{""label"":""XYLT1"",""id"":""64131""}]"	"[""1056"",""120227"",""1493"",""1594"",""1636"",""177"",""2155"",""217"",""23274"",""2572"",""2638"",""3113"",""3115"",""3117"",""3119"",""3123"",""3291"",""3383"",""345"",""3482"",""3486"",""3552"",""3554"",""3557"",""3558"",""3559"",""3569"",""3600"",""3630"",""3710"",""4049"",""4855"",""55937"",""5798"",""5799"",""590"",""5967"",""629"",""6352"",""64131"",""6556"",""6647"",""6648"",""6721"",""685"",""6890"",""6908"",""6927"",""7018"",""7097"",""7098"",""7124"",""729230"",""7466"",""7916"",""940"",""941"",""942"",""9451"",""952""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9744""}]"
DOID:9775	"[""diastolic heart failure""]"	"[{""label"":""Ace"",""id"":""24310""},{""label"":""Lepr"",""id"":""24536""}]"	"[""24310"",""24536""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9775""}]"
DOID:9775	"[""diastolic heart failure""]"	"[{""label"":""ACE"",""id"":""1636""}]"	"[""1636""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9775""}]"
DOID:9778	"[""irritable bowel syndrome"",""IBD"",""Irritable colon""]"	"[{""label"":""HTR3A"",""id"":""3359""},{""label"":""RNF43"",""id"":""54894""}]"	"[""3359"",""54894""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9778""}]"
DOID:9778	"[""irritable bowel syndrome"",""IBD"",""Irritable colon""]"	"[{""label"":""Mlxipl"",""id"":""58805""}]"	"[""58805""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9778""}]"
DOID:9778	"[""irritable bowel syndrome"",""IBD"",""Irritable colon""]"	"[{""label"":""Nos3"",""id"":""24600""}]"	"[""24600""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9778""}]"
DOID:980	"[""choroidal sclerosis"",""Choroidal degenerations""]"	"[{""label"":""GUCY2D"",""id"":""3000""},{""label"":""PRPH2"",""id"":""5961""}]"	"[""3000"",""5961""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:980""}]"
DOID:9810	"[""polyarteritis nodosa""]"	"[{""label"":""ELN"",""id"":""2006""}]"	"[""2006""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9810""}]"
DOID:9821	"[""choroideremia"",""progressive Choroidal Atrophy""]"	"[{""label"":""CHM"",""id"":""1121""}]"	"[""1121""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9821""}]"
DOID:9822	"[""partial central choroid dystrophy"",""Choroidal dystrophy, central areolar""]"	"[{""label"":""Prph2"",""id"":""19133""}]"	"[""19133""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9822""}]"
DOID:9827	"[""radioulnar synostosis""]"	"[{""label"":""HOXA11"",""id"":""3207""},{""label"":""SMAD6"",""id"":""4091""}]"	"[""3207"",""4091""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9827""}]"
DOID:9828	"[""neonatal abstinence syndrome"",""Drug withdrawal syndrome in newborn""]"	"[{""label"":""COMT"",""id"":""1312""},{""label"":""CYP2B6"",""id"":""1555""},{""label"":""OPRK1"",""id"":""4986""},{""label"":""OPRM1"",""id"":""4988""}]"	"[""1312"",""1555"",""4986"",""4988""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9828""}]"
DOID:9834	"[""hyperopia"",""Far-sightedness"",""farsightedness"",""hypermetropia""]"	"[{""label"":""MYRF"",""id"":""745""},{""label"":""NOG"",""id"":""9241""}]"	"[""745"",""9241""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9834""}]"
DOID:9849	"[""Meniere's disease"",""Meniere disease"",""Mnire's vertigo"",""Otogenic vertigo""]"	"[{""label"":""AQP4"",""id"":""361""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""HLA-DRB1"",""id"":""3123""},{""label"":""HSPA1A"",""id"":""3303""}]"	"[""3106"",""3123"",""3303"",""361""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9849""}]"
DOID:986	"[""alopecia areata"",""Circumscribed alopecia""]"	"[{""label"":""CTLA4"",""id"":""1493""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IL1RN"",""id"":""3557""},{""label"":""IL2"",""id"":""3558""},{""label"":""NOTCH4"",""id"":""4855""}]"	"[""1493"",""3117"",""3119"",""3557"",""3558"",""4855""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:986""}]"
DOID:9869	"[""hereditary fructose intolerance syndrome"",""Fructosaemia"",""Fructose-1,6-bisphosphate aldolase B deficiency"",""Fructosemia""]"	"[{""label"":""ALDOB"",""id"":""229""}]"	"[""229""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9869""}]"
DOID:987	"[""alopecia""]"	"[{""label"":""CDSN"",""id"":""1041""},{""label"":""HLA-B"",""id"":""3106""}]"	"[""1041"",""3106""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:987""}]"
DOID:987	"[""alopecia""]"	"[{""label"":""Dsg4"",""id"":""291754""},{""label"":""Prss8"",""id"":""192107""}]"	"[""192107"",""291754""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:987""}]"
DOID:9870	"[""galactosemia"",""Galactosaemia"",""Galactose intolerance""]"	"[{""label"":""gale-1"",""id"":""173171""}]"	"[""173171""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9870""}]"
DOID:9870	"[""galactosemia"",""Galactosaemia"",""Galactose intolerance""]"	"[{""label"":""Gale"",""id"":""38076""},{""label"":""Galt"",""id"":""33935""}]"	"[""33935"",""38076""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9870""}]"
DOID:9870	"[""galactosemia"",""Galactosaemia"",""Galactose intolerance""]"	"[{""label"":""Galt"",""id"":""14430""}]"	"[""14430""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9870""}]"
DOID:9870	"[""galactosemia"",""Galactosaemia"",""Galactose intolerance""]"	"[{""label"":""GAL10"",""id"":""852307""},{""label"":""GAL7"",""id"":""852306""}]"	"[""852306"",""852307""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9870""}]"
DOID:988	"[""mitral valve prolapse"",""Barlow's syndrome"",""floppy mitral valve""]"	"[{""label"":""ACE"",""id"":""1636""},{""label"":""AGT"",""id"":""183""},{""label"":""DCHS1"",""id"":""8642""},{""label"":""DZIP1"",""id"":""22873""},{""label"":""FBN1"",""id"":""2200""},{""label"":""FLNA"",""id"":""2316""},{""label"":""HLA-B"",""id"":""3106""},{""label"":""PLAU"",""id"":""5328""},{""label"":""TSHR"",""id"":""7253""}]"	"[""1636"",""183"",""2200"",""22873"",""2316"",""3106"",""5328"",""7253"",""8642""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:988""}]"
DOID:988	"[""mitral valve prolapse"",""Barlow's syndrome"",""floppy mitral valve""]"	"[{""label"":""Dchs1"",""id"":""233651""}]"	"[""233651""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:988""}]"
DOID:9883	"[""Becker muscular dystrophy"",""Benign pseudohypertrophic muscular dystrophy"",""benign congenital myopathy""]"	"[{""label"":""Dmd"",""id"":""13405""}]"	"[""13405""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9883""}]"
DOID:9883	"[""Becker muscular dystrophy"",""Benign pseudohypertrophic muscular dystrophy"",""benign congenital myopathy""]"	"[{""label"":""DMD"",""id"":""1756""}]"	"[""1756""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9883""}]"
DOID:9884	"[""muscular dystrophy""]"	"[{""label"":""Fkrp"",""id"":""243853""}]"	"[""243853""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9884""}]"
DOID:9884	"[""muscular dystrophy""]"	"[{""label"":""Dg"",""id"":""36773""},{""label"":""tn"",""id"":""37190""}]"	"[""36773"",""37190""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9884""}]"
DOID:9884	"[""muscular dystrophy""]"	"[{""label"":""CAPN3"",""id"":""825""},{""label"":""CHKB"",""id"":""1120""},{""label"":""COL6A3"",""id"":""1293""},{""label"":""DYSF"",""id"":""8291""},{""label"":""FKRP"",""id"":""79147""},{""label"":""FKTN"",""id"":""2218""},{""label"":""LAMA2"",""id"":""3908""},{""label"":""POMGNT1"",""id"":""55624""},{""label"":""POMT1"",""id"":""10585""},{""label"":""POMT2"",""id"":""29954""},{""label"":""SGCA"",""id"":""6442""},{""label"":""SGCB"",""id"":""6443""},{""label"":""SGCD"",""id"":""6444""},{""label"":""SYNE1"",""id"":""23345""}]"	"[""10585"",""1120"",""1293"",""2218"",""23345"",""29954"",""3908"",""55624"",""6442"",""6443"",""6444"",""79147"",""825"",""8291""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9884""}]"
DOID:9884	"[""muscular dystrophy""]"	"[{""label"":""lam-3"",""id"":""172952""}]"	"[""172952""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9884""}]"
DOID:9884	"[""muscular dystrophy""]"	"[{""label"":""fkrp"",""id"":""571426""}]"	"[""571426""]"	Danio rerio (zebrafish)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9884""}]"
DOID:9938	"[""dacryocystitis""]"	"[{""label"":""IL1RN"",""id"":""3557""}]"	"[""3557""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9938""}]"
DOID:9952	"[""acute lymphoblastic leukemia"",""ALL"",""acute lymphoblastic leukaemia"",""acute lymphocytic leukaemia"",""precursor lymphoblastic lymphoma/leukemia""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ABCC2"",""id"":""1244""},{""label"":""ABO"",""id"":""28""},{""label"":""BAX"",""id"":""581""},{""label"":""BCR"",""id"":""613""},{""label"":""CFB"",""id"":""629""},{""label"":""CREBBP"",""id"":""1387""},{""label"":""CSF3"",""id"":""1440""},{""label"":""CYP1A1"",""id"":""1543""},{""label"":""CYP3A5"",""id"":""1577""},{""label"":""DPYD"",""id"":""1806""},{""label"":""FLT3"",""id"":""2322""},{""label"":""GNB1"",""id"":""2782""},{""label"":""GPX1"",""id"":""2876""},{""label"":""HFE"",""id"":""3077""},{""label"":""HK1"",""id"":""3098""},{""label"":""HLA-DQA1"",""id"":""3117""},{""label"":""HLA-DQB1"",""id"":""3119""},{""label"":""IFNG"",""id"":""3458""},{""label"":""IKZF1"",""id"":""10320""},{""label"":""IRF4"",""id"":""3662""},{""label"":""KDM6A"",""id"":""7403""},{""label"":""KRAS"",""id"":""3845""},{""label"":""MEFV"",""id"":""4210""},{""label"":""MTR"",""id"":""4548""},{""label"":""NAT2"",""id"":""10""},{""label"":""NBN"",""id"":""4683""},{""label"":""NOS3"",""id"":""4846""},{""label"":""NRAS"",""id"":""4893""},{""label"":""NUP214"",""id"":""8021""},{""label"":""PON1"",""id"":""5444""},{""label"":""TERT"",""id"":""7015""},{""label"":""TYMS"",""id"":""7298""},{""label"":""XRCC1"",""id"":""7515""}]"	"[""10"",""10320"",""1244"",""1387"",""1440"",""1543"",""1577"",""1806"",""2322"",""2782"",""28"",""2876"",""3077"",""3098"",""3117"",""3119"",""3458"",""3662"",""3845"",""4210"",""4548"",""4683"",""4846"",""4893"",""5243"",""5444"",""581"",""613"",""629"",""7015"",""7298"",""7403"",""7515"",""8021""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9952""}]"
DOID:9952	"[""acute lymphoblastic leukemia"",""ALL"",""acute lymphoblastic leukaemia"",""acute lymphocytic leukaemia"",""precursor lymphoblastic lymphoma/leukemia""]"	"[{""label"":""Ezh2"",""id"":""14056""},{""label"":""Notch3"",""id"":""18131""}]"	"[""14056"",""18131""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9952""}]"
DOID:9953	"[""acute biphenotypic leukemia"",""mixed phenotype acute leukemia""]"	"[{""label"":""DOT1L"",""id"":""84444""}]"	"[""84444""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9953""}]"
DOID:9955	"[""hypoplastic left heart syndrome""]"	"[{""label"":""MYH7"",""id"":""4625""}]"	"[""4625""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9955""}]"
DOID:9955	"[""hypoplastic left heart syndrome""]"	"[{""label"":""Sap130"",""id"":""269003""}]"	"[""269003""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9955""}]"
DOID:9970	"[""obesity""]"	"[{""label"":""ABCA1"",""id"":""19""},{""label"":""ABCG8"",""id"":""64241""},{""label"":""ADRB2"",""id"":""154""},{""label"":""ADRB3"",""id"":""155""},{""label"":""AGT"",""id"":""183""},{""label"":""APOD"",""id"":""347""},{""label"":""AR"",""id"":""367""},{""label"":""BBS2"",""id"":""583""},{""label"":""CADM2"",""id"":""253559""},{""label"":""CAPN10"",""id"":""11132""},{""label"":""CCKAR"",""id"":""886""},{""label"":""CNR1"",""id"":""1268""},{""label"":""COMT"",""id"":""1312""},{""label"":""CPE"",""id"":""1363""},{""label"":""CRHR1"",""id"":""1394""},{""label"":""CYP27B1"",""id"":""1594""},{""label"":""CYP2R1"",""id"":""120227""},{""label"":""DRD2"",""id"":""1813""},{""label"":""EDN1"",""id"":""1906""},{""label"":""ENPP1"",""id"":""5167""},{""label"":""F7"",""id"":""2155""},{""label"":""FTO"",""id"":""79068""},{""label"":""GFPT1"",""id"":""2673""},{""label"":""GHRL"",""id"":""51738""},{""label"":""GHSR"",""id"":""2693""},{""label"":""GIPR"",""id"":""2696""},{""label"":""GLP1R"",""id"":""2740""},{""label"":""GNAS"",""id"":""2778""},{""label"":""HFE"",""id"":""3077""},{""label"":""HK1"",""id"":""3098""},{""label"":""HK2"",""id"":""3099""},{""label"":""HSD11B2"",""id"":""3291""},{""label"":""HSPA1B"",""id"":""3304""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""HTR2C"",""id"":""3358""},{""label"":""IGFBP2"",""id"":""3485""},{""label"":""IGFBP6"",""id"":""3489""},{""label"":""IL6"",""id"":""3569""},{""label"":""IL6R"",""id"":""3570""},{""label"":""INPPL1"",""id"":""3636""},{""label"":""LEPR"",""id"":""3953""},{""label"":""MBL2"",""id"":""4153""},{""label"":""MC3R"",""id"":""4159""},{""label"":""MC4R"",""id"":""4160""},{""label"":""MIF"",""id"":""4282""},{""label"":""NCOA3"",""id"":""8202""},{""label"":""NMB"",""id"":""4828""},{""label"":""NMU"",""id"":""10874""},{""label"":""NPPB"",""id"":""4879""},{""label"":""NPY2R"",""id"":""4887""},{""label"":""NPY5R"",""id"":""4889""},{""label"":""NR1H3"",""id"":""10062""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""OPRM1"",""id"":""4988""},{""label"":""PCSK1"",""id"":""5122""},{""label"":""PDP1"",""id"":""54704""},{""label"":""PGR"",""id"":""5241""},{""label"":""PLIN1"",""id"":""5346""},{""label"":""POMC"",""id"":""5443""},{""label"":""PPARG"",""id"":""5468""},{""label"":""PPARGC1B"",""id"":""133522""},{""label"":""SDC3"",""id"":""9672""},{""label"":""SERPINF1"",""id"":""5176""},{""label"":""SLC2A1"",""id"":""6513""},{""label"":""SLC6A14"",""id"":""11254""},{""label"":""SLC6A3"",""id"":""6531""},{""label"":""SOCS3"",""id"":""9021""},{""label"":""SORBS1"",""id"":""10580""},{""label"":""STAT3"",""id"":""6774""},{""label"":""UCP2"",""id"":""7351""},{""label"":""UCP3"",""id"":""7352""},{""label"":""WNT10B"",""id"":""7480""}]"	"[""10062"",""10580"",""10874"",""11132"",""11254"",""120227"",""1268"",""1312"",""133522"",""1363"",""1394"",""154"",""155"",""1594"",""1813"",""183"",""19"",""1906"",""2155"",""253559"",""2673"",""2693"",""2696"",""2740"",""2778"",""2908"",""3077"",""3098"",""3099"",""3291"",""3304"",""3356"",""3358"",""347"",""3485"",""3489"",""3569"",""3570"",""3636"",""367"",""3953"",""4153"",""4159"",""4160"",""4282"",""4828"",""4879"",""4887"",""4889"",""4988"",""5122"",""5167"",""51738"",""5176"",""5241"",""5346"",""5443"",""5468"",""54704"",""583"",""64241"",""6513"",""6531"",""6774"",""7351"",""7352"",""7480"",""79068"",""8202"",""886"",""9021"",""9672""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9970""}]"
DOID:9970	"[""obesity""]"	"[{""label"":""PK1-R"",""id"":""41713""},{""label"":""PlexB"",""id"":""43766""},{""label"":""Stim"",""id"":""32556""},{""label"":""ds"",""id"":""33245""},{""label"":""fj"",""id"":""37089""},{""label"":""ft"",""id"":""33627""},{""label"":""gbb"",""id"":""37778""},{""label"":""sdk"",""id"":""31017""},{""label"":""wg"",""id"":""34009""}]"	"[""31017"",""32556"",""33245"",""33627"",""34009"",""37089"",""37778"",""41713"",""43766""]"	Drosophila melanogaster (fruit fly)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9970""}]"
DOID:9970	"[""obesity""]"	"[{""label"":""Alms1"",""id"":""236266""},{""label"":""Angptl6"",""id"":""70726""},{""label"":""Cpe"",""id"":""12876""},{""label"":""Gpr12"",""id"":""14738""},{""label"":""Gucy2c"",""id"":""14917""},{""label"":""Kdm3a"",""id"":""104263""},{""label"":""Lep"",""id"":""16846""},{""label"":""Lepr"",""id"":""16847""},{""label"":""Mc3r"",""id"":""17201""},{""label"":""Mc4r"",""id"":""17202""},{""label"":""Ncoa1"",""id"":""17977""},{""label"":""Neil1"",""id"":""72774""},{""label"":""Npy1r"",""id"":""18166""},{""label"":""Pcsk1"",""id"":""18548""},{""label"":""Pomc"",""id"":""18976""},{""label"":""Prkci"",""id"":""18759""},{""label"":""Snap25"",""id"":""20614""},{""label"":""a"",""id"":""50518""}]"	"[""104263"",""12876"",""14738"",""14917"",""16846"",""16847"",""17201"",""17202"",""17977"",""18166"",""18548"",""18759"",""18976"",""20614"",""236266"",""50518"",""70726"",""72774""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9970""}]"
DOID:9970	"[""obesity""]"	"[{""label"":""eif-6"",""id"":""173169""},{""label"":""glp-1"",""id"":""176286""},{""label"":""gon-1"",""id"":""177850""}]"	"[""173169"",""176286"",""177850""]"	Caenorhabditis elegans	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9970""}]"
DOID:9970	"[""obesity""]"	"[{""label"":""Aoc3"",""id"":""29473""},{""label"":""Atp4b"",""id"":""24217""},{""label"":""Atp5f1b"",""id"":""171374""},{""label"":""Atp5f1d"",""id"":""245965""},{""label"":""C3"",""id"":""24232""},{""label"":""C5ar1"",""id"":""113959""},{""label"":""Cckar"",""id"":""24889""},{""label"":""Cnr1"",""id"":""25248""},{""label"":""Esr1"",""id"":""24890""},{""label"":""Esr2"",""id"":""25149""},{""label"":""Gabra6"",""id"":""29708""},{""label"":""Gck"",""id"":""24385""},{""label"":""Hk1"",""id"":""25058""},{""label"":""Hp"",""id"":""24464""},{""label"":""Hrh3"",""id"":""85268""},{""label"":""Hsd11b1"",""id"":""25116""},{""label"":""Irs1"",""id"":""25467""},{""label"":""Lep"",""id"":""25608""},{""label"":""Lepr"",""id"":""24536""},{""label"":""Lpl"",""id"":""24539""},{""label"":""Mc4r"",""id"":""25635""},{""label"":""Oprm1"",""id"":""25601""},{""label"":""Ppargc1a"",""id"":""83516""},{""label"":""Prlhr"",""id"":""246075""},{""label"":""Tlr4"",""id"":""29260""}]"	"[""113959"",""171374"",""24217"",""24232"",""24385"",""24464"",""24536"",""24539"",""245965"",""246075"",""24889"",""24890"",""25058"",""25116"",""25149"",""25248"",""25467"",""25601"",""25608"",""25635"",""29260"",""29473"",""29708"",""83516"",""85268""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9970""}]"
DOID:9973	"[""substance dependence""]"	"[{""label"":""Creb1"",""id"":""81646""}]"	"[""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9973""}]"
DOID:9974	"[""drug dependence""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ACHE"",""id"":""43""},{""label"":""COMT"",""id"":""1312""},{""label"":""CYP2B6"",""id"":""1555""},{""label"":""NCAM1"",""id"":""4684""},{""label"":""OPRM1"",""id"":""4988""}]"	"[""1312"",""1555"",""43"",""4684"",""4988"",""5243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9974""}]"
DOID:9975	"[""cocaine dependence""]"	"[{""label"":""Creb1"",""id"":""81646""},{""label"":""Drd2"",""id"":""24318""},{""label"":""Gria1"",""id"":""50592""},{""label"":""Gria2"",""id"":""29627""},{""label"":""Htr2a"",""id"":""29595""},{""label"":""Htr2c"",""id"":""25187""}]"	"[""24318"",""25187"",""29595"",""29627"",""50592"",""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9975""}]"
DOID:9975	"[""cocaine dependence""]"	"[{""label"":""BDNF"",""id"":""627""},{""label"":""CAMK4"",""id"":""814""},{""label"":""CCSER1"",""id"":""401145""},{""label"":""CHRNA3"",""id"":""1136""},{""label"":""CHRNB3"",""id"":""1142""},{""label"":""COL21A1"",""id"":""81578""},{""label"":""COMT"",""id"":""1312""},{""label"":""DRD2"",""id"":""1813""},{""label"":""GABBR1"",""id"":""2550""},{""label"":""HTR2A"",""id"":""3356""},{""label"":""HTR3A"",""id"":""3359""},{""label"":""MANEA"",""id"":""79694""},{""label"":""OPRD1"",""id"":""4985""},{""label"":""OPRK1"",""id"":""4986""},{""label"":""PER2"",""id"":""8864""},{""label"":""TENM3"",""id"":""55714""}]"	"[""1136"",""1142"",""1312"",""1813"",""2550"",""3356"",""3359"",""401145"",""4985"",""4986"",""55714"",""627"",""79694"",""814"",""81578"",""8864""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9975""}]"
DOID:9976	"[""heroin dependence""]"	"[{""label"":""ABCB1"",""id"":""5243""},{""label"":""ACHE"",""id"":""43""},{""label"":""ADRA1A"",""id"":""148""},{""label"":""ALDH2"",""id"":""217""},{""label"":""CHRM2"",""id"":""1129""},{""label"":""COMT"",""id"":""1312""},{""label"":""CREB1"",""id"":""1385""},{""label"":""CYP2B6"",""id"":""1555""},{""label"":""CYP2C19"",""id"":""1557""},{""label"":""DRD2"",""id"":""1813""},{""label"":""DRD4"",""id"":""1815""},{""label"":""GABBR1"",""id"":""2550""},{""label"":""GABRB3"",""id"":""2562""},{""label"":""GABRG2"",""id"":""2566""},{""label"":""GAD1"",""id"":""2571""},{""label"":""GAD2"",""id"":""2572""},{""label"":""GDNF"",""id"":""2668""},{""label"":""GRIN2A"",""id"":""2903""},{""label"":""HTR3A"",""id"":""3359""},{""label"":""NGF"",""id"":""4803""},{""label"":""NPY1R"",""id"":""4886""},{""label"":""NR3C1"",""id"":""2908""},{""label"":""NTRK2"",""id"":""4915""},{""label"":""OPRD1"",""id"":""4985""},{""label"":""OPRK1"",""id"":""4986""},{""label"":""OPRM1"",""id"":""4988""}]"	"[""1129"",""1312"",""1385"",""148"",""1555"",""1557"",""1813"",""1815"",""217"",""2550"",""2562"",""2566"",""2571"",""2572"",""2668"",""2903"",""2908"",""3359"",""43"",""4803"",""4886"",""4915"",""4985"",""4986"",""4988"",""5243""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9976""}]"
DOID:9976	"[""heroin dependence""]"	"[{""label"":""Akt1"",""id"":""24185""},{""label"":""Creb1"",""id"":""81646""},{""label"":""Grm2"",""id"":""24415""},{""label"":""Oprk1"",""id"":""29335""},{""label"":""Penk"",""id"":""29237""}]"	"[""24185"",""24415"",""29237"",""29335"",""81646""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9976""}]"
DOID:999	"[""hypereosinophilic syndrome"",""Eosinophilic leukocytosis"",""eosinophilia""]"	"[{""label"":""F5"",""id"":""2153""},{""label"":""PDGFRA"",""id"":""5156""}]"	"[""2153"",""5156""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:999""}]"
DOID:9993	"[""hypoglycemia"",""Hypoglycaemia""]"	"[{""label"":""Abcc8"",""id"":""25559""}]"	"[""25559""]"	Rattus norvegicus (Norway rat)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9993""}]"
DOID:9993	"[""hypoglycemia"",""Hypoglycaemia""]"	"[{""label"":""AGTR2"",""id"":""186""},{""label"":""AKT2"",""id"":""208""},{""label"":""CYP2C9"",""id"":""1559""},{""label"":""GCK"",""id"":""2645""},{""label"":""GLUD1"",""id"":""2746""},{""label"":""HNF4A"",""id"":""3172""},{""label"":""PPP1R3A"",""id"":""5506""},{""label"":""UCP3"",""id"":""7352""}]"	"[""1559"",""186"",""208"",""2645"",""2746"",""3172"",""5506"",""7352""]"	Homo sapiens (human)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9993""}]"
DOID:9993	"[""hypoglycemia"",""Hypoglycaemia""]"	"[{""label"":""ERS1"",""id"":""850438""}]"	"[""850438""]"	Saccharomyces cerevisiae S288C	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9993""}]"
DOID:9997	"[""peripartum cardiomyopathy"",""antepartum peripartum cardiomyopathy"",""postpartum peripartum cardiomyopathy""]"	"[{""label"":""Stat3"",""id"":""20848""}]"	"[""20848""]"	Mus musculus (house mouse)	"[{""label"":""Alliance of Genome Resources"",""id"":""www.alliancegenome.org/disease/DOID:9997""}]"