GlyCosmos Portal

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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **1101 - 1125** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
9061	3'-phosphoadenosine 5'-phosphosulfate synthase 1	PAPSS1 Aliases: ATPSK1 PAPSS adenylyl-sulfate kinase sulfate adenylyltransferase	Homo sapiens (human)	cancer embryoma hepatitis B hepatocellular carcinoma liver cancer lung cancer lung non-small cell carcinoma
2262	glypican 5	GPC5 Aliases: glypican proteoglycan 5	Homo sapiens (human)	Balo concentric sclerosis Gilles de la Tourette syndrome MHC class II deficiency Marfan syndrome Simpson-Golabi-Behmel syndrome type 1 adenosine deaminase deficiency adrenoleukodystrophy bronchus cancer bronchus carcinoma cancer cardiac arrest cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types central nervous system cancer central nervous system disease central nervous system lymphoma demyelinating disease diabetes mellitus epithelioid sarcoma familial nephrotic syndrome gliosarcoma glomerulonephritis hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma lipoid nephrosis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma microphthalmia mixed glioma multiple sclerosis myelomeningocele narcolepsy nephritis nephrotic syndrome neuromyelitis optica obsolete Matthew-Wood syndrome obsolete ymphosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma prostate cancer prostate carcinoma proteinuria rhabdomyosarcoma rheumatoid arthritis sarcoma scoliosis severe combined immunodeficiency situs inversus spina bifida spindle cell sarcoma tethered spinal cord syndrome tetralogy of Fallot transthyretin amyloidosis tuberous sclerosis type 2 diabetes mellitus
342372	polycystin 1 like 3, transient receptor potential channel interacting	PKD1L3	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease cerebral infarction cerebrovascular disease episodic kinesigenic dyskinesia 1 prostate cancer prostate carcinoma
222537	heparan sulfate-glucosamine 3-sulfotransferase 5	HS3ST5 Aliases: 3-OST-5	Homo sapiens (human)	melanoma schizophrenia skin melanoma
3632	inositol polyphosphate-5-phosphatase A	INPP5A Aliases: 43 kDa inositol polyphosphate 5-phophatase 5PTASE CTCL tumor antigen HD-CL-02 InsP3 5-phosphatase inositol polyphosphate 5-phophatase, 40kDa type I inositol-1,4,5-trisphosphate 5-phosphatase	Homo sapiens (human)	actinic keratosis ascending cholangitis cancer cholangitis inverted follicular keratosis keratoacanthoma melanoacanthoma oculocerebrorenal syndrome primary sclerosing cholangitis schizophrenia sclerosing cholangitis seborrheic keratosis skin benign neoplasm skin cancer skin disease skin squamous cell carcinoma squamous cell carcinoma suppurative cholangitis tongue squamous cell carcinoma
8604	solute carrier family 25 member 12	SLC25A12	Homo sapiens (human)	Asperger syndrome autism spectrum disorder autistic disorder citrullinemia common bile duct disease developmental and epileptic encephalopathy 39 intrahepatic cholestasis
55830	glycosyltransferase 8 domain containing 1	GLT8D1 Aliases: AD-017 FLJ14611	Homo sapiens (human)	amyotrophic lateral sclerosis anxiety disorder arthritis arthropathy bipolar disorder depressive disorder dysplastic nevus syndrome dysthymic disorder generalized anxiety disorder laryngostenosis major depressive disorder melancholic depression melanoma neurotic disorder obsolete melancholia osteoarthritis progressive muscular atrophy schizophrenia skin melanoma
8879	sphingosine-1-phosphate lyase 1	SGPL1 Aliases: SPL	Homo sapiens (human)	Addison's disease Alzheimer's disease Charcot-Marie-Tooth disease Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IMAGe syndrome Marfan syndrome Niemann-Pick disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome adrenal cortical hypofunction alveolar rhabdomyosarcoma anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome autosomal recessive congenital ichthyosis 1 breast cancer breast carcinoma cancer childhood cerebral astrocytoma chondrodysplasia-pseudohermaphroditism syndrome chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital hypothyroidism congenital ptosis congestive heart failure coronary artery disease cryptorchidism embryoma endometrial cancer endometrial carcinoma epilepsy familial nephrotic syndrome fibrillary astrocytoma focal segmental glomerulosclerosis gastroenteritis gemistocytic astrocytoma glucose intolerance high grade glioma hyperglycemia hypertropia hypoglycemia hypogonadism hypothyroidism ichthyosis idiopathic interstitial pneumonia ileitis ileocolitis inherited metabolic disorder juvenile pilocytic astrocytoma keratosis follicularis kidney disease large intestine cancer laryngeal disease lipoid nephrosis lymphopenia malignant astrocytoma mechanical strabismus microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly mongolian spot multiple sclerosis myxedema nephrosis nephrotic syndrome type 14 nephrotic syndrome type 1 nephrotic syndrome neurodegenerative disease neuropathy obesity obsolete congenital ichthyosiform erythroderma ophthalmoplegia peripheral nervous system disease pilocytic astrocytoma pneumonia polyneuropathy postinflammatory pulmonary fibrosis prediabetes syndrome proteinuria protoplasmic astrocytoma pseudoxanthoma elasticum ptosis pulmonary fibrosis sensorineural hearing loss situs inversus sphingolipidosis strabismus subependymal giant cell astrocytoma tracheal disease triple-A syndrome tuberous sclerosis uterine corpus cancer visual epilepsy
10724	O-GlcNAcase	OGA Aliases: MEA5 NCOAT nuclear cytoplasmic O-GlcNAcase and acetyltransferase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Fabry disease GM1 gangliosidosis GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Gilles de la Tourette syndrome Lewy body dementia Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute myocardial infarction alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis angiomatous meningioma anterior horn cell disease aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive distal hereditary motor neuronopathy 1 benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease cerebral convexity meningioma cerebral degeneration chronic kidney disease chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis cystitis dermatitis diabetes mellitus diabetic ketoacidosis dystonia embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma essential hypertension fibrous meningioma gangliosidosis gastroenteritis gastrointestinal system disease gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis glucose intolerance glycoproteinosis heart disease hepatocellular carcinoma hydronephrosis hypertension ileitis ileocolitis intestinal disease intraorbital meningioma intraventricular meningioma kidney disease kidney failure kwashiorkor large intestine cancer lateral sclerosis lingual-facial-buccal dyskinesia lipid storage disease lipoid nephrosis liver cancer liver cirrhosis long QT syndrome 8 lung cancer lung carcinoma lymphoplasmacyte-rich meningioma lysosomal storage disease marasmus membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia motor neuron disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IVB mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple myeloma myelitis myocardial infarction nephritis nephrosis nervous system disease neurodegenerative disease nutrition disease obesity obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ovarian cancer ovarian carcinoma panic disorder parasagittal meningioma pituitary adenoma prediabetes syndrome progressive familial intrahepatic cholestasis 1 progressive muscular atrophy progressive supranuclear palsy protein-energy malnutrition psammomatous meningioma pyoureter renal osteodystrophy retrograde amnesia sarcoma secondary Parkinson disease secretory meningioma silent myocardial infarction situs inversus sphingolipidosis spinal meningioma spindle cell sarcoma tauopathy thalassemia transitional meningioma tricuspid valve stenosis trigonitis tuberous sclerosis 1 tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus visual epilepsy
119391	glutathione S-transferase omega 2	GSTO2	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder asthma
80896	N-acetylneuraminate pyruvate lyase	NPL Aliases: DHDPS1 NPL1 dihydrodipicolinate synthetase homolog 1 (E. coli)	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Crohn's colitis Crohn's disease Ewing sarcoma Pick's disease Reye syndrome alcohol dependence alcohol use disorder atopic dermatitis bipolar disorder cerebral degeneration cholestasis congestive heart failure dermatitis epilepsy essential hypertension generalized epilepsy with febrile seizures plus hypertension idiopathic generalized epilepsy inflammatory bowel disease 1 inflammatory bowel disease influenza juvenile myoclonic epilepsy myopathy obsolete major affective disorder 1 obsolete major affective disorder 2 panic disorder prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss ulcerative colitis visual epilepsy
27306	hematopoietic prostaglandin D synthase	HPGDS Aliases: GSTS GSTS1 GSTS1-1 H-PGDS PGD2 PGDS glutathione S-transferase sigma	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Barrett's esophagus Bell's palsy Burkitt lymphoma Crohn's colitis Crohn's disease Down syndrome Duchenne muscular dystrophy Fanconi anemia complementation group A Fanconi anemia Friedreich ataxia 1 Friedreich ataxia Gilles de la Tourette syndrome HELLP syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kuhnt-Junius degeneration Langerhans-cell histiocytosis Loeffler syndrome Lyme disease Meniere's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium vivax malaria Reye syndrome Richter's syndrome Sertoli cell-only syndrome T-cell acute lymphoblastic leukemia X-linked ichthyosis X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 Y-linked spermatogenic failure 1 Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acquired immunodeficiency syndrome acrodermatitis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma adult medulloblastoma adult respiratory distress syndrome age related macular degeneration alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis allergic asthma alopecia alternating hemiplegia of childhood amyotrophic lateral sclerosis anaplastic astrocytoma androgenic alopecia angioedema angiomatous meningioma anthracosilicosis aortic valve insufficiency aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asthma atherosclerosis atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autism spectrum disorder autistic disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant cerebellar ataxia autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy azoospermia basal cell carcinoma benign meningioma benign mesothelioma beta thalassemia bipolar disorder bladder carcinoma bladder urothelial carcinoma bone cancer bone osteosarcoma brain cancer brain disease brain stem infarction breast cancer breast carcinoma breast ductal carcinoma bronchiolo-alveolar adenocarcinoma bronchitis bronchus cancer bronchus carcinoma byssinosis cancer carcinoma cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease cataract celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebellar ataxia, mental retardation and dysequlibrium syndrome cerebral artery occlusion cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood acute myeloid leukemia childhood cerebral astrocytoma childhood disintegrative disease childhood leukemia childhood lymphoma childhood medulloblastoma childhood osteosarcoma childhood testicular germ cell tumor chromophobe renal cell carcinoma chronic ethmoiditis chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital heart disease congenital muscular dystrophy congestive heart failure coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma cryptorchidism cystic fibrosis cystinuria degeneration of macula and posterior pole dementia dental fluorosis depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diastrophic dysplasia diffuse large B-cell lymphoma distal myopathy drug psychosis dry eye syndrome dysthymic disorder embryoma embryonal cancer encephalitis encephalomyelitis endolymphatic hydrops endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis enterobiasis eosinophilic pneumonia epilepsy esophageal cancer esophageal carcinoma esophageal disease esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia essential tremor exanthem exanthema subitum exfoliation syndrome exocrine pancreatic insufficiency extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial periodic paralysis familial retinoblastoma fascioliasis female reproductive organ cancer fibrillary astrocytoma fibromyalgia fibrous meningioma fissured tongue follicular adenoma follicular lymphoma galactosemia gallbladder cancer gallbladder carcinoma gallbladder disease gastric adenocarcinoma gastric lymphoma gastritis gastroenteritis gastroesophageal junction adenocarcinoma gastroesophageal reflux disease gastrointestinal system cancer gemistocytic astrocytoma generalized atherosclerosis geographic tongue germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glaucoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hematologic cancer hemochromatosis type 1 hemochromatosis hemolytic anemia hepatitis A hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma hereditary sensory and autonomic neuropathy type 5 heroin dependence high grade glioma human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypothalamic disease idiopathic interstitial pneumonia ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer intestinal schistosomiasis intestinal volvulus intraorbital meningioma intraventricular meningioma intrinsic asthma invasive ductal carcinoma islet cell tumor juvenile pilocytic astrocytoma keratosis follicularis keratosis kidney cancer kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease laryngeal squamous cell carcinoma larynx cancer leiomyoma leukemia leukopenia lichen disease limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoma lymphoplasmacyte-rich meningioma macular degeneration major depressive disorder malaria male infertility malignant astrocytoma malignant mesothelioma mantle cell lymphoma marasmus medulloblastoma medulloepithelioma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma membranous glomerulonephritis meningioma meningothelial meningioma microcystic adenoma microcystic meningioma migraine without aura mixed glioma mongolian spot mood disorder mucoepidermoid carcinoma multiple myeloma multiple sclerosis muscular dystrophy myelitis myelodysplastic syndrome myeloid leukemia myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myofibroma myopathy myositis nasopharynx carcinoma neonatal jaundice neovascular inflammatory vitreoretinopathy nephroblastoma nephrolithiasis nervous system disease neuroblastoma neurodegenerative disease neuroectodermal tumor neuropathy neurotic disorder newborn respiratory distress syndrome nicotine dependence nodular prostate non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy olfactory groove meningioma oligospermia onchocerciasis oral mucosa leukoplakia osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma parathyroid gland disease peptic esophagitis periodontitis peripheral nervous system disease pilocytic astrocytoma pituitary adenoma plasmacytoma pleomorphic adenoma pneumonia polycystic ovary syndrome polycythemia vera polycythemia polyneuropathy porphyria cutanea tarda postinflammatory pulmonary fibrosis pre-eclampsia primary biliary cholangitis primary cutaneous amyloidosis primary open angle glaucoma primary pulmonary hypertension progressive multifocal leukoencephalopathy progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma prostatic adenoma protein-energy malnutrition protoplasmic astrocytoma psammomatous meningioma pseudoxanthoma elasticum psoriasis psychotic disorder pulmonary fibrosis pure red-cell aplasia pustulosis of palm and sole rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease reticulosarcoma retinoblastoma rheumatoid arthritis rhinitis rippling muscle disease 2 rubella sarcomatoid carcinoma sarcomatoid renal cell carcinoma schistosomiasis schizoaffective disorder schizophrenia schizophreniform disorder scleroderma scurvy secondary Parkinson disease secretory meningioma seminoma senile cataract sensorineural hearing loss sialuria sickle cell anemia silent myocardial infarction skin benign neoplasm skin cancer skin carcinoma skin melanoma skin squamous cell carcinoma small intestine adenocarcinoma spinal meningioma spinocerebellar ataxia type 2 sporadic breast cancer squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma stomach disease subependymal giant cell astrocytoma sudden infant death syndrome supratentorial primitive neuroectodermal tumor systemic lupus erythematosus systemic scleroderma tarsal-carpal coalition syndrome testicular cancer testicular germ cell cancer testicular malignant germ cell cancer testis seminoma thalassemia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue disease tongue squamous cell carcinoma tracheal disease transitional cell carcinoma transitional meningioma trichinosis trilateral retinoblastoma tuberculosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ureteral obstruction uric acid nephrolithiasis urinary bladder cancer urticaria uterine corpus cancer uterine fibroid varicocele visual epilepsy vitiligo white sponge nevus xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum xerophthalmia
2639	glutaryl-CoA dehydrogenase	GCDH Aliases: ACAD5 GCD	Homo sapiens (human)	D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria Fleck corneal dystrophy alternating hemiplegia of childhood autonomic neuropathy basal ganglia disease blepharospasm brain disease brain ischemia central nervous system disease central nervous system origin vertigo cerebral palsy colorectal cancer colorectal carcinoma corneal dystrophy disease of metabolism dystonia epilepsy focal hand dystonia generalized dystonia glutaric acidemia I granular corneal dystrophy 2 hemiplegia hyperlysinemia hypoglycemia inherited metabolic disorder lactic acidosis large intestine cancer lattice corneal dystrophy lingual-facial-buccal dyskinesia liver cirrhosis malignant hyperthermia migraine movement disease nervous system disease oligohydramnios spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy speech disorder transient cerebral ischemia visual epilepsy
2629	glucosylceramidase beta 1	GBA1 Aliases: glucocerebrosidase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Burkitt lymphoma Canavan disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Cogan syndrome DiGeorge syndrome Fabry disease Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Lafora disease Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Netherton syndrome Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease type C2 Niemann-Pick disease PCWH syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease REM sleep behavior disorder Reye syndrome Sjogren-Larsson syndrome Tay-Sachs disease Unverricht-Lundborg syndrome West Nile fever Wolman disease abdominal obesity-metabolic syndrome 1 achondroplasia acquired hyperkeratosis actinic keratosis adult lymphoma agenesis of the corpus callosum with peripheral neuropathy agnosia alternating hemiplegia of childhood amyotrophic lateral sclerosis anemia arthritis arthropathy atypical Gaucher's disease due to saposin c deficiency autonomic neuropathy autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis autosomal recessive osteopetrosis 7 blepharospasm brain disease cancer cardiac arrest central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma chylomicron retention disease communicating hydrocephalus congestive heart failure dementia dentatorubral-pallidoluysian atrophy depressive disorder developmental coordination disorder diffuse interstitial keratitis diffuse large B-cell lymphoma dissociated nystagmus dysthymic disorder dystonia early myoclonic encephalopathy ectropion embryoma endometriosis of uterus endometriosis esotropia essential hypertension essential tremor female stress incontinence fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome focal hand dystonia follicular lymphoma glucose intolerance hemopericardium hepatitis B hepatopulmonary syndrome hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hydrocephalus hypertension hypomyelinating leukodystrophy 2 hypomyelinating leukodystrophy 3 hypomyelinating leukodystrophy 4 hypomyelinating leukodystrophy 6 hypomyelinating leukodystrophy 9 ichthyosis interstitial lung disease intracranial aneurysm keratosis follicularis late onset Parkinson's disease leukoencephalopathy with vanishing white matter leukopenia lingual-facial-buccal dyskinesia lipid storage disease liver cirrhosis lymphoma lysosomal storage disease macrocytic anemia major depressive disorder melancholic depression metachromatic leukodystrophy microcephaly mitral valve stenosis mongolian spot monocular esotropia motor peripheral neuropathy movement disease multiple myeloma nervous system disease neuroblastoma neurodegenerative disease neurotic disorder non-Hodgkin lymphoma obsolete congenital ichthyosiform erythroderma obsolete constipation obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus ophthalmoplegia osteoarthritis osteonecrosis osteopetrosis osteosclerosis pancytopenia pathologic nystagmus pericardial effusion placental insufficiency polyhydramnios prediabetes syndrome primary pulmonary hypertension progressive muscular atrophy progressive myoclonus epilepsy 4 progressive myoclonus epilepsy progressive supranuclear palsy proteinuria pseudoxanthoma elasticum psoriasis reticulosarcoma schizophrenia seborrheic keratosis secondary Parkinson disease senile degeneration of brain sensorineural hearing loss skin disease speech disorder sphingolipidosis spontaneous ocular nystagmus thrombocytopenia velocardiofacial syndrome
5335	phospholipase C gamma 1	PLCG1 Aliases: NCKAP3 PLC-II PLC148 PLCgamma1	Homo sapiens (human)	Alzheimer's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kaposi's sarcoma Meckel syndrome Miller-Dieker lissencephaly syndrome Richter's syndrome SADDAN Sezary's disease T-cell acute lymphoblastic leukemia X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 abdominal obesity-metabolic syndrome 1 achondroplasia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult T-cell leukemia/lymphoma allergic asthma angioedema angioimmunoblastic T-cell lymphoma angiosarcoma arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrial fibrillation autosomal dominant polycystic kidney disease bacterial sepsis bipolar disorder bone osteosarcoma borderline personality disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer cerebral infarction cerebrovascular disease childhood angiosarcoma childhood osteosarcoma chromosome 17p13.1 deletion syndrome chronic lymphocytic leukemia colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease cribriform carcinoma depressive disorder diabetes mellitus diabetic ketoacidosis embryoma epilepsy essential hypertension essential thrombocythemia familial adenomatous polyposis focal segmental glomerulosclerosis fragile X syndrome gastric adenocarcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma glycoproteinosis granular cell carcinoma hepatocellular carcinoma high grade glioma hypertension ileitis ileocolitis immune system disease impulse control disorder intermittent explosive disorder intrinsic asthma irritant dermatitis kleptomania large intestine cancer laryngeal squamous cell carcinoma leukemia lissencephaly liver angiosarcoma liver cancer luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder maturity-onset diabetes of the young melancholic depression mixed glioma mucolipidosis II alpha/beta myelodysplastic syndrome obsolete melancholia oral candidiasis oral squamous cell carcinoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma placental insufficiency primary cutaneous T-cell non-Hodgkin lymphoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia squamous cell carcinoma steatotic liver disease tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urticaria visual epilepsy
4041	LDL receptor related protein 5	LRP5	Homo sapiens (human)	Worth syndrome autosomal dominant osteopetrosis 1 autosomal dominant polycystic kidney disease exudative vitreoretinopathy 4 exudative vitreoretinopathy heart valve disease idiopathic juvenile osteoporosis microphthalmia neovascular inflammatory vitreoretinopathy nonsyndromic deafness osteonecrosis osteoporosis-pseudoglioma syndrome osteoporosis polycystic liver disease tendinitis
2526	fucosyltransferase 4	FUT4 Aliases: FUC-TIV alpha (1,3) fucosyltransferase, myeloid-specific galactoside 3-L-fucosyltransferase	Homo sapiens (human)	B-cell adult acute lymphocytic leukemia Barrett's esophagus Burkitt lymphoma Castleman disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kimura disease Leber congenital amaurosis 1 T-cell acute lymphoblastic leukemia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adenosarcoma adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult medulloblastoma arthropathy autosomal recessive distal hereditary motor neuronopathy 1 bacterial sepsis benign mesothelioma benign peritoneal mesothelioma beta thalassemia bladder carcinoma bladder urothelial carcinoma bone marrow cancer brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma cardiomyopathy celiac disease central nervous system cancer chancroid childhood B-cell acute lymphoblastic leukemia childhood acute lymphocytic leukemia childhood leukemia childhood medulloblastoma chromophobe renal cell carcinoma chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc coronary thrombosis cribriform carcinoma cystic fibrosis embryoma embryonal carcinoma endometrial adenocarcinoma endomyocardial fibrosis esophagus squamous cell carcinoma essential thrombocythemia familial adenomatous polyposis 1 familial adenomatous polyposis familial medullary thyroid carcinoma follicular adenoma gastric ulcer gastritis gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease 1 inflammatory bowel disease islet cell tumor juvenile myelomonocytic leukemia large intestine cancer laryngeal carcinoma larynx cancer leptospirosis leukemia leukocyte adhesion deficiency 2 leukocyte adhesion deficiency liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphogranuloma venereum malignant mesothelioma medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma microcystic adenoma microphthalmia mixed glioma monoclonal gammopathy of uncertain significance multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A mycosis fungoides myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction myocarditis necrotizing ulcerative gingivitis nephroblastoma neuromyelitis optica nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete leukocyte-adhesion deficiency syndrome osteoarthritis pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma paroxysmal nocturnal hemoglobinuria peptic ulcer disease peritoneal mesothelioma primary mediastinal B-cell lymphoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma septic arthritis silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma teratocarcinoma thrombosis thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma ulcerative colitis urinary bladder cancer yaws
3631	inositol polyphosphate-4-phosphatase type I A	INPP4A Aliases: Type I inositol 3,4-bisphosphate 4-phosphatase	Homo sapiens (human)	Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma autosomal dominant dyskeratosis congenita 1 bladder carcinoma cancer early myoclonic encephalopathy embryoma intrinsic asthma lung cancer lung non-small cell carcinoma pancreatic cancer pancreatic carcinoma situs inversus tuberous sclerosis urinary bladder cancer
1056	carboxyl ester lipase	CEL	Homo sapiens (human)	B-cell lymphoma Bloch-Sulzberger syndrome Goodpasture syndrome Loeffler syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Takayasu's arteritis Wolman disease X-linked chronic granulomatous disease acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute pancreatitis adamantinous craniopharyngioma adenocarcinoma adenoma adiposis dolorosa adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome aggressive systemic mastocytosis agranulocytosis alcoholic liver cirrhosis alcoholic pancreatitis allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma ataxic cerebral palsy atherosclerosis autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bone marrow cancer brain disease breast cancer breast carcinoma bronchiectasis cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood lymphoma chronic eosinophilic leukemia chronic granulomatous disease chronic neutrophilic leukemia chronic obstructive pulmonary disease complement deficiency coronary artery disease craniopharyngioma cribriform carcinoma cutaneous porphyria cystic fibrosis cystic kidney disease diabetes mellitus diabetic ketoacidosis embryoma eosinophilic pneumonia epithelioid sarcoma erythropoietic protoporphyria exocrine pancreatic insufficiency extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue extrinsic allergic alveolitis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperlipidemia farmer's lung gastric lymphoma giardiasis glomerulonephritis granular cell carcinoma granulomatosis with polyangiitis hematologic cancer hepatitis C hepatitis hepatocellular carcinoma histoplasmosis hypereosinophilic syndrome hyperglycemia hyperinsulinemic hypoglycemia hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis indolent systemic mastocytosis influenza interstitial lung disease intrinsic asthma kidney disease kwashiorkor leukopenia lipid storage disease lipomatosis liver cancer lung disease lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 lysosomal acid lipase deficiency malaria marasmus mastocytosis maturity-onset diabetes of the young type 8 maturity-onset diabetes of the young microphthalmia multiple symmetric lipomatosis myeloproliferative neoplasm nasopharynx carcinoma nephritis nephrosis neurofibromatosis 1 neurofibromatosis neutropenia newborn respiratory distress syndrome non-congenital cyst of kidney nutmeg liver nutrition disease obesity obsolete Matthew-Wood syndrome obsolete multiple symmetrical lipomatosis obsolete ymphosarcoma pancreas disease pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis papillary craniopharyngioma placental insufficiency plasmacytoma pneumocystosis pneumonia polyarteritis nodosa polycythemia vera polycythemia postinflammatory pulmonary fibrosis primary ciliary dyskinesia 1 primary ciliary dyskinesia protein-energy malnutrition pulmonary alveolar proteinosis pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pyoureter red-green color blindness retinal disease retinitis sarcoidosis sarcoma scleroderma severe congenital neutropenia spindle cell sarcoma steatotic liver disease substance abuse substance-related disorder systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic mastocytosis systemic scleroderma tuberculosis tuberculous pneumothorax tubular adenocarcinoma type 1 diabetes mellitus type 2 diabetes mellitus uveoparotid fever
10039	poly(ADP-ribose) polymerase family member 3	PARP3 Aliases: ADPRT3 ARTD3 IRT1 NAD+ ADP-ribosyltransferase 3 hPARP-3 pADPRT-3 poly(ADP-ribose) polymerase 3 poly(ADP-ribose) synthetase-3	Homo sapiens (human)	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer coronary artery disease cystic fibrosis embryoma giant cell glioblastoma glioblastoma high grade glioma neuroblastoma
10559	solute carrier family 35 member A1	SLC35A1 Aliases: CMP-Sia-Tr CMP-sialic acid transporter CMPST hCST	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Behcet's disease Marfan syndrome Papillon-Lefevre disease Pick's disease Reye syndrome acute myocardial infarction agranulocytosis amyotrophic lateral sclerosis anhidrosis anterior horn cell disease aortic valve insufficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain disease brain stem infarction cancer cardiovascular system disease cellulitis central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cone-rod dystrophy 2 cone-rod dystrophy congenital disorder of glycosylation Iq congenital disorder of glycosylation type II congenital disorder of glycosylation type IIf congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis diabetic macular edema dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma glucose intolerance heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability lateral sclerosis learning disability lingual-facial-buccal dyskinesia liver cancer microcephaly mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 neutropenia obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pathologic nystagmus placental insufficiency pneumonia prediabetes syndrome progressive bulbar palsy progressive muscular atrophy proteinuria severe congenital neutropenia silent myocardial infarction situs inversus spontaneous ocular nystagmus substance abuse substance-related disorder thrombocytopenia tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis viral infectious disease visual epilepsy
57016	aldo-keto reductase family 1 member B10	AKR1B10 Aliases: AKR1B12 ALDRLn ARL-1 ARL1 HIS HSI aldo-keto reductase family 1, member B11 (aldose reductase-like) aldose reductase-like 1 aldose reductase-like peptide aldose reductase-related protein small intestine reductase	Homo sapiens (human)	Barrett's esophagus Burkitt lymphoma Schimke immuno-osseous dysplasia actinic keratosis acute pancreatitis adenocarcinoma adenoma adrenal cortex cancer adult respiratory distress syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bile duct adenocarcinoma bile duct carcinoma bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ cholangiocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma contact dermatitis coronary artery disease cribriform carcinoma cystic fibrosis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma follicular adenoma gallbladder disease gastrointestinal system cancer giant cell glioblastoma glioblastoma granular cell carcinoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma large intestine cancer leprosy liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma microcystic adenoma microphthalmia nasopharynx carcinoma neurodegeneration with brain iron accumulation 2a neurodegeneration with brain iron accumulation 2b neurodegeneration with brain iron accumulation 3 neurodegeneration with brain iron accumulation 4 neurodegeneration with brain iron accumulation 5 neurodegeneration with brain iron accumulation 6 neurodegeneration with brain iron accumulation newborn respiratory distress syndrome nicotine dependence nodular prostate obsolete Matthew-Wood syndrome occupational dermatitis pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis pantothenate kinase-associated neurodegeneration papillary adenoma parapsoriasis primary immunodeficiency disease prostate cancer prostate carcinoma prostatic adenoma psoriasis pustulosis of palm and sole sarcomatoid carcinoma seborrheic keratosis skin disease skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer varicose veins
5322	phospholipase A2 group V	PLA2G5	Homo sapiens (human)	acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer coronary artery disease essential hypertension eye disease familial benign fleck retina gallbladder disease gliosarcoma high grade glioma hypereosinophilic syndrome hypertension liver disease mixed glioma neurodegenerative disease nutmeg liver obesity pneumonia schizophrenia
2819	glycerol-3-phosphate dehydrogenase 1	GPD1	Homo sapiens (human)	Laron syndrome Refsum disease Zellweger syndrome achondroplasia breast cancer breast carcinoma cancer central nervous system cancer diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma infantile Refsum disease inherited metabolic disorder liver cancer liver cirrhosis maturity-onset diabetes of the young mixed glioma obesity obstructive sleep apnea peroxisome biogenesis disorder 1A steatotic liver disease type 2 diabetes mellitus
79143	membrane bound O-acyltransferase domain containing 7	MBOAT7 Aliases: BB1 LPIAT1 LPLAT LPLAT11 hMBOA-7 lysophosphatidylinositol acyltransferase lysophosphatidylinositol acyltransferase 1 lysophospholipid acyltransferase 11 lysophospholipid acyltransferase 7	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 adrenoleukodystrophy agnosia alcoholic hepatitis alcoholic liver cirrhosis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autosomal recessive intellectual developmental disorder 57 cardiovascular system disease cerebral degeneration choreatic disease chronic kidney disease communicating hydrocephalus depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease major depressive disorder melancholic depression microcephaly neurotic disorder obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus partial motor epilepsy senile degeneration of brain steatotic liver disease stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy

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