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 **626 - 650** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
9365	klotho	KL Aliases: KLA alpha-klotho	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 Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Duchenne muscular dystrophy 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 IgA glomerulonephritis Kummell's 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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Prinzmetal angina Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Smith-McCort dysplasia Werner syndrome X-linked Aarskog syndrome X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acromegaly actinic keratosis acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adult respiratory distress syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis androgen insensitivity syndrome anemia aortic valve disease 1 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome bacterial infectious disease bacterial sepsis beta thalassemia bicuspid aortic valve disease bipolar disorder bladder carcinoma bone disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer cardiomyopathy cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cartilage disease central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma chondrocalcinosis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure connective tissue disease coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma dedifferentiated liposarcoma dementia demyelinating disease depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endomyocardial fibrosis enthesopathy epilepsy essential hypertension exostosis familial adenomatous polyposis familial hyperlipidemia familial nephrotic syndrome follicular adenoma fundus albipunctatus gastroenteritis giant cell glioblastoma glioblastoma glomerulonephritis granular cell carcinoma growth hormone secreting pituitary adenoma head and neck squamous cell carcinoma heart disease hematologic cancer hepatocellular carcinoma high grade glioma hypercalcemia hyperglycemia hyperinsulinism hyperparathyroidism hyperphosphatemia hyperphosphatemic familial tumoral calcinosis hyperpituitarism hypertension hypertrophic cardiomyopathy hypoglycemia hypophosphatemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis infertility insulinoma intellectual disability intracranial embolism invasive ductal carcinoma kidney cancer kidney disease kidney failure kidney hypertrophy kwashiorkor large intestine cancer late onset Parkinson's disease learning disability lipoid nephrosis liposarcoma liver cancer liver cirrhosis localized scleroderma lung benign neoplasm lung cancer lung carcinoma lung large cell carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma macrocytic anemia major depressive disorder marasmus melancholic depression melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia middle cerebral artery infarction monoclonal gammopathy of uncertain significance mood disorder multiple myeloma multiple sclerosis muscular dystrophy musculoskeletal system disease myelitis myocardial infarction myositis nephritis nephrocalcinosis nephrolithiasis nephrosis nephrotic syndrome nervous system disease neurodegenerative disease neurotic disorder newborn respiratory distress syndrome nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive sleep apnea osteitis fibrosa osteoarthritis osteomalacia osteonecrosis osteoporosis ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenoma papillary renal cell carcinoma parathyroid adenoma parathyroid carcinoma parathyroid gland disease periarthritis phosphorus metabolism disease placental insufficiency pleomorphic liposarcoma polycystic kidney disease 1 porphyria cutanea tarda postinflammatory pulmonary fibrosis premature menopause priapism primary hyperparathyroidism primary ovarian insufficiency primary pulmonary hypertension progeria progressive muscular atrophy prostate cancer prostate carcinoma protein-energy malnutrition pulmonary emphysema pulmonary fibrosis pulmonary large cell neuroendocrine carcinoma pyoureter reflex sympathetic dystrophy relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis pigmentosa 1 retinitis pigmentosa retinitis retrograde amnesia rheumatoid arthritis rickets sarcomatoid renal cell carcinoma schizophrenia scleroderma seborrheic keratosis secondary hyperparathyroidism sickle cell anemia silent myocardial infarction skin disease skin melanoma spondyloarthropathy spondylosis squamous cell carcinoma systemic scleroderma tendinitis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tongue squamous cell carcinoma 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 uremia ureteral obstruction uric acid nephrolithiasis urinary bladder cancer vascular dementia vascular disease
134526	acyl-CoA thioesterase 12	ACOT12 Aliases: Cach STARD15 StAR-related lipid transfer (START) domain containing 15 THEAL	Homo sapiens (human)	hepatocellular carcinoma leukodystrophy leukoencephalopathy with vanishing white matter liver cancer
3425	alpha-L-iduronidase	IDUA Aliases: MPS1 MPSI mucopolysaccharidosis type I	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Creutzfeldt-Jakob disease Fabry disease Gaucher's disease Hartnup disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Klippel-Feil syndrome Krabbe disease Laron syndrome Loeys-Dietz syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Richter's syndrome Scheie syndrome Sly syndrome T-cell acute lymphoblastic leukemia Weissenbacher-Zweymuller syndrome achondroplasia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia adrenoleukodystrophy adult medulloblastoma agranulocytosis anemia anogenital venereal wart aortic valve disease 2 aortic valve insufficiency aortic valve stenosis autosomal recessive hypophosphatemic rickets benign mesothelioma blindness bone disease brain cancer breast cancer breast carcinoma cancer cardiomyopathy cartilage disease central nervous system disease cerebral palsy childhood medulloblastoma chromophobe renal cell carcinoma chronic lymphocytic leukemia chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart communicating hydrocephalus congenital heart disease connective tissue disease deficiency anemia dental caries dentin caries depressive disorder disease of mental health disease of metabolism dysthymic disorder embryoma endomyocardial fibrosis essential hypertension gastric ulcer giant cell glioblastoma gingival hypertrophy gingival overgrowth glaucoma glioblastoma glycogen storage disease II glycoproteinosis head and neck squamous cell carcinoma hemiplegia hepatocellular carcinoma high grade glioma hydrocephalus hypertension hypertrophic cardiomyopathy hypochromic anemia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia inherited metabolic disorder intellectual disability intracranial hypotension large intestine cancer learning disability leukopenia lipid storage disease liver cancer liver carcinoma lung benign neoplasm lung carcinoma lymphoblastic lymphoma lysosomal storage disease macrocytic anemia major depressive disorder malignant mesothelioma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma microcytic anemia mitral valve insufficiency mitral valve prolapse mucolipidosis II alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih/s mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma narcolepsy nervous system disease neurotic disorder neutropenia nonpapillary renal cell carcinoma obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus obstructive sleep apnea osteochondrodysplasia osteoporosis otitis media pancreatic ductal adenocarcinoma papillary renal cell carcinoma primary pulmonary hypertension psychotic disorder recurrent corneal erosion renal carcinoma renal cell carcinoma retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain sensorineural hearing loss severe congenital neutropenia skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy sphingolipidosis spinal cord disease spondylolisthesis stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tracheal stenosis tyrosinemia type I tyrosinemia ulcerative colitis
3607	forkhead box K2	FOXK2	Homo sapiens (human)
2331	fibromodulin	FMOD Aliases: SLRR2E fibromodulin proteoglycan	Homo sapiens (human)	B-cell lymphoma Richter's syndrome adult cystic teratoma adult lymphoma adult teratoma age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast cancer breast carcinoma cancer central nervous system cancer central nervous system lymphoma childhood leukemia childhood lymphoma chronic lymphocytic leukemia colon carcinoma colorectal cancer congestive heart failure coronary artery disease cystic teratoma degeneration of macula and posterior pole embryoma enthesopathy exostosis female stress incontinence fibromyalgia giant cell glioblastoma gingivitis glioblastoma gliosarcoma glomerulonephritis high grade glioma kidney disease leiomyoma leukemia liver cirrhosis lung small cell carcinoma lymphoma macular degeneration malignant teratoma mantle cell lymphoma mature teratoma mixed glioma myofibroma myopia neovascular inflammatory vitreoretinopathy nephritis nephrosis obsolete ymphosarcoma osteoarthritis periarthritis periodontitis prostate cancer prostate carcinoma prostate disease pyoureter tendinitis teratoma uterine fibroid
6646	sterol O-acyltransferase 1	SOAT1 Aliases: ACAT ACAT1 acyl-Coenzyme A: cholesterol acyltransferase	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 Behcet's disease Burkitt lymphoma Chagas disease Clouston syndrome Crohn's colitis Crohn's disease Down syndrome Fanconi anemia complementation group A Fanconi anemia Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Japanese encephalitis Kallmann syndrome Klinefelter syndrome Langerhans-cell histiocytosis Laron syndrome MHC class II deficiency Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Pick's disease Reye syndrome Sezary's disease Sheehan syndrome Sjogren's syndrome St. Louis encephalitis T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Zika fever achondroplasia acoustic neuroma acquired immunodeficiency syndrome acrodermatitis actinic keratosis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adenosine deaminase deficiency adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult lymphoma aggressive NK-cell leukemia allergic asthma allergic rhinitis alopecia areata alopecia amyloidosis amyotrophic lateral sclerosis anemia angiomatous meningioma ankylosing spondylitis arteriolosclerosis arteriosclerosis obliterans arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis atopic dermatitis atrial fibrillation autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant polycystic kidney disease bacterial sepsis basal cell carcinoma benign meningioma bladder carcinoma bone disease bone marrow cancer bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma brucellosis bullous pemphigoid cancer cardiac tamponade cardiovascular system disease cartilage disease central nervous system cancer central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood leukemia childhood lymphoma childhood osteosarcoma childhood type dermatomyositis chromophobe renal cell carcinoma chronic fatigue syndrome chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia chronic neutrophilic leukemia chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency cone-rod dystrophy 2 cone-rod dystrophy congenital merosin-deficient muscular dystrophy 1A congestive heart failure connective tissue disease coronary artery disease coronary thrombosis cribriform carcinoma cryptococcosis cutaneous lupus erythematosus dengue disease depressive disorder dermatitis herpetiformis dermatitis dermatomyositis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dry eye syndrome dysthymic disorder embryoma encephalitis encephalomyelitis endocrine exophthalmos endometrial cancer endometrial carcinoma eosinophilic esophagitis epithelioid malignant peripheral nerve sheath tumor esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential thrombocythemia extramedullary plasmacytoma familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial retinoblastoma fibrous meningioma gallbladder adenocarcinoma gastrointestinal stromal tumor gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance granular cell carcinoma granuloma annulare head and neck cancer head and neck squamous cell carcinoma heart disease hematologic cancer hematopoietic system disease hemiplegia hepatitis B hepatitis C hepatitis D hepatitis hepatoblastoma hepatocellular carcinoma herpes simplex high grade glioma human immunodeficiency virus infectious disease hyper IgE recurrent infection syndrome 1 hyperglycemia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease impotence inflammatory bowel disease 1 inflammatory bowel disease intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile myelomonocytic leukemia keratoconjunctivitis sicca kidney disease kidney rhabdoid cancer large intestine cancer leishmaniasis leprosy leukemia leukoencephalopathy with vanishing white matter liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma lymphoplasmacyte-rich meningioma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macrocytic anemia macroglobulinemia major depressive disorder malignant peripheral nerve sheath tumor melancholic depression melanoma meningioma meningothelial meningioma microcystic meningioma microphthalmia mitochondrial metabolism disease mitochondrial myopathy mixed glioma mood disorder multiple myeloma multiple sclerosis mumps myelitis myelodysplastic syndrome myelofibrosis myeloproliferative neoplasm myocardial infarction nasopharynx carcinoma nephritis nephrosis neurilemmoma neuroblastoma neurofibroma neurofibrosarcoma neurotic disorder non-Hodgkin lymphoma nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete lymphoplasmacytic lymphoma obsolete malignant histiocytosis obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma olfactory groove meningioma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panhypopituitarism papillary renal cell carcinoma parapsoriasis parasagittal meningioma peripheral T-cell lymphoma peripheral nervous system neoplasm phototoxic dermatitis pituitary adenoma plasmacytoma polycystic kidney disease 1 polycythemia vera polycythemia porphyria cutanea tarda postinflammatory pulmonary fibrosis prediabetes syndrome premature ejaculation primary biliary cholangitis primary cutaneous T-cell non-Hodgkin lymphoma primary immunodeficiency disease primary open angle glaucoma primary progressive multiple sclerosis progressive multifocal leukoencephalopathy progressive muscular atrophy progressive relapsing multiple sclerosis prostate cancer prostate carcinoma psammomatous meningioma pseudosarcomatous fibromatosis psoriasis psychologic dyspareunia pulmonary alveolar proteinosis pulmonary emphysema pulmonary fibrosis pulmonary tuberculosis pustulosis of palm and sole pyoderma gangrenosum pyoureter rabies renal carcinoma renal cell carcinoma reticulosarcoma retinoblastoma rheumatoid arthritis sarcoidosis sarcomatoid renal cell carcinoma scleroderma seborrheic keratosis secondary progressive multiple sclerosis secretory meningioma severe combined immunodeficiency silent myocardial infarction skin disease skin melanoma skin squamous cell carcinoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal meningioma spondyloarthropathy spondylosis squamous cell carcinoma stomach cancer stomach carcinoma subacute delirium synovitis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tauopathy tenosynovitis thrombocytopenia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma tongue squamous cell carcinoma transitional meningioma trilateral retinoblastoma trypanosomiasis tuberculous pneumothorax 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 urinary bladder cancer uterine corpus cancer uveoparotid fever vascular disease vasomotor rhinitis ventricular septal defect viral infectious disease visceral leishmaniasis vitiligo xanthomatosis xerophthalmia yellow fever
148003	galectin 16	LGALS16	Homo sapiens (human)	congestive heart failure diffuse large B-cell lymphoma thyroid adenoma thyroid cancer thyroid gland carcinoma
2932	glycogen synthase kinase 3 beta	GSK3B	Homo sapiens (human)	Alzheimer's disease Parkinson's disease acute myocardial infarction amyotrophic lateral sclerosis bipolar disorder colon cancer colorectal adenocarcinoma degenerative disc disease depressive disorder diabetic encephalopathy endometrial carcinoma heart disease hypertension middle cerebral artery infarction myocardial infarction oral squamous cell carcinoma schizophrenia sciatic neuropathy status epilepticus substance-related disorder type 2 diabetes mellitus vascular dementia
80255	solute carrier family 35 member F5	SLC35F5 Aliases: FLJ22004	Homo sapiens (human)	Kawasaki disease cancer
9468	phosphate cytidylyltransferase 1B, choline	PCYT1B Aliases: CCT-beta CCTbeta CTB CTP:phosphocholine cytidylyltransferase-beta choline-phosphate cytidylyltransferase beta phosphorylcholine transferase beta	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 Clouston syndrome Leber congenital amaurosis 1 Pick's disease Reye syndrome adult respiratory distress syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma breast ductal carcinoma cancer cerebral degeneration cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease juvenile rheumatoid arthritis large intestine cancer liver cancer liver carcinoma newborn respiratory distress syndrome progressive muscular atrophy prostate cancer prostate carcinoma type 2 diabetes mellitus ulcerative colitis urinary tract obstruction vasomotor rhinitis
148641	solute carrier family 35 member F3	SLC35F3 Aliases: FLJ37712	Homo sapiens (human)	acute myeloid leukemia beriberi chronic obstructive pulmonary disease dry beriberi essential hypertension hypertension intracranial aneurysm pellagra thiamine deficiency disease
22854	netrin G1	NTNG1 Aliases: KIAA0976 Lmnt1 Netrin-G1 netrin G1f	Homo sapiens (human)	Rett syndrome anorexia nervosa autistic disorder bipolar disorder brain disease cancer cerebral infarction cerebrovascular disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma epilepsy esophagitis gastroesophageal reflux disease head and neck squamous cell carcinoma hydrocephalus intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia microcephaly morphine dependence movement disease nephrolithiasis neuroendocrine carcinoma neuroendocrine tumor neuropathy patent ductus arteriosus peptic esophagitis peripheral nervous system disease polyneuropathy schizophrenia sensorineural hearing loss uric acid nephrolithiasis visual epilepsy
84992	phosphatidylinositol glycan anchor biosynthesis class Y	PIGY Aliases: MGC14156 PIG-Y Phosphatidylinositol N-acetylglucosaminyltransferase subunit Y	Homo sapiens (human)	Cogan syndrome Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome blepharospasm capillary disease craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 6 hypertropia inguinal hernia isolated elevated serum creatine phosphokinase levels mechanical strabismus microcephaly monocular esotropia oligohydramnios ophthalmoplegia polyhydramnios scoliosis situs inversus strabismus syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis visual epilepsy
8760	CDP-diacylglycerol synthase 2	CDS2 Aliases: phosphatidate cytidylyltransferase 2	Homo sapiens (human)	cancer congestive heart failure eye disease
10434	lysophospholipase 1	LYPLA1 Aliases: APT-1 LPL1 acyl-protein thioesterase 1	Homo sapiens (human)	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome cancer carcinoma diabetes mellitus embryoma lung cancer lung non-small cell carcinoma melanoma pancreatic cancer prostate cancer prostate carcinoma sarcomatoid carcinoma skin melanoma type 2 diabetes mellitus
23275	protein O-fucosyltransferase 2	POFUT2 Aliases: FUT13 GDP-fucose protein O-fucosyltransferase 2 KIAA0958 peptide-O-fucosyltransferase	Homo sapiens (human)	Down syndrome Peters plus syndrome congenital disorder of glycosylation malaria popliteal pterygium syndrome schizophrenia
9517	serine palmitoyltransferase long chain base subunit 2	SPTLC2 Aliases: KIAA0526 LCB2 LCB2A hLCB2a	Homo sapiens (human)	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 acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anhidrosis cancer coronary thrombosis diarrhea hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 1C hereditary sensory and autonomic neuropathy type 2 hereditary sensory neuropathy hypohidrosis liver cancer motor peripheral neuropathy myocardial infarction neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum osteomyelitis parapsoriasis peripheral nervous system disease psoriasis pustulosis of palm and sole sensory peripheral neuropathy silent myocardial infarction teratocarcinoma
3032	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta	HADHB Aliases: MTPB mitochondrial trifunctional protein, beta subunit	Homo sapiens (human)	Alzheimer's 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 Norum disease Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy agnosia beta-ketothiolase deficiency breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease cholestasis choreaacanthocytosis clubfoot colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure critical illness polyneuropathy developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy embryoma endomyocardial fibrosis epilepsy familial hyperlipidemia familial periodic paralysis fibromyalgia fundus albipunctatus heart disease hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hypercalcemia hypertrophic cardiomyopathy hypolipoproteinemia hypoparathyroidism inflammatory and toxic neuropathy intellectual disability lactic acidosis large intestine cancer learning disability lipid metabolism disorder melanoma meningoencephalitis mitochondrial metabolism disease mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse motor peripheral neuropathy myoglobinuria myopathy myositis nephrocalcinosis neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease phosphorus metabolism disease placental insufficiency polydactyly polyneuropathy prostate adenocarcinoma prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinitis pigmentosa sick sinus syndrome skin melanoma steatotic liver disease tricuspid valve insufficiency urea cycle disorder visual epilepsy
51805	coenzyme Q3, methyltransferase	COQ3	Homo sapiens (human)
249	alkaline phosphatase, biomineralization associated	ALPL Aliases: TNALP TNAP TNSALP tissue non-specific alkaline phosphatase	Homo sapiens (human)	ARC syndrome Ehlers-Danlos syndrome Laron syndrome Loeffler syndrome Werner syndrome achondroplasia acoustic neuroma adult hypophosphatasia allergic asthma anemia angiomatous meningioma ankylosing spondylitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthrogryposis, renal dysfunction, and cholestasis 1 arthropathy asthma atherosclerosis autosomal recessive osteopetrosis 7 benign meningioma bone disease bone osteosarcoma breast cancer breast carcinoma calcinosis calcium metabolism disease campomelic dysplasia cancer cartilage disease cerebral convexity meningioma childhood hypophosphatasia chondrocalcinosis clear cell meningioma colitis connective tissue disease coronary artery disease craniosynostosis dental caries dentin caries depressive disorder diabetes mellitus dysthymic disorder embryoma embryonal carcinoma enophthalmos eosinophilic pneumonia epilepsy familial combined hyperlipidemia fibrous meningioma focal epilepsy gastroenteritis generalized anxiety disorder glomerulonephritis hereditary elliptocytosis hypercalcemia hyperostosis hyperphosphatemic familial tumoral calcinosis hypophosphatasia ileitis ileocolitis in situ carcinoma infantile hypophosphatasia inherited metabolic disorder intraorbital meningioma intraventricular meningioma intrinsic asthma keratosis follicularis kidney disease macrocytic anemia major depressive disorder melancholic depression meningioma meningothelial meningioma microcystic meningioma mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia musculoskeletal system disease nephritis nephrocalcinosis nephrolithiasis nephrosis neurotic disorder nutmeg liver obesity obsolete exophthalmos obsolete melancholia olfactory groove meningioma orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteomalacia osteopetrosis osteoporosis osteosarcoma osteosclerosis parasagittal meningioma partial motor epilepsy phobic disorder phosphorus metabolism disease pituitary adenoma polyhydramnios progeria prostate cancer prostate carcinoma psammomatous meningioma pseudoxanthoma elasticum pulmonary eosinophilia pyoureter rickets schizophrenia 10 schizophrenia secondary hyperparathyroidism secretory meningioma spinal meningioma steatotic liver disease transitional meningioma type 2 diabetes mellitus uremia uric acid nephrolithiasis visual epilepsy
2760	ganglioside GM2 activator	GM2A Aliases: GM2-AP GM2-activator protein GM2AP SAP-3 cerebroside sulfate activator protein sphingolipid activator protein 3	Homo sapiens (human)	Clostridium difficile colitis GM2 gangliosidosis, AB variant GM2 gangliosidosis Laron syndrome Sandhoff disease Schimke immuno-osseous dysplasia Tay-Sachs disease achondroplasia alcohol dependence alcohol use disorder anxiety disorder blindness breast cancer breast carcinoma cancer cerebral degeneration choreatic disease chronic obstructive pulmonary disease dementia dystonia embryoma epilepsy generalized anxiety disorder neurodegenerative disease neuroendocrine carcinoma nicotine dependence perinatal necrotizing enterocolitis progressive muscular atrophy retinal disease retinitis spinal muscular atrophy syndromic X-linked intellectual disability type 10 visual epilepsy vulvovaginal candidiasis
8707	beta-1,3-galactosyltransferase 2	B3GALT2 Aliases: beta3Gal-T2	Homo sapiens (human)
2137	exostosin like glycosyltransferase 3	EXTL3 Aliases: REG receptor REGR botv glucuronyl-galactosyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase	Homo sapiens (human)	MHC class II deficiency acute myeloid leukemia adenosine deaminase deficiency agnosia arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 bacterial sepsis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cherubism chondrodysplasia punctata ciliary body disease cocaine abuse cocaine dependence colorectal cancer colorectal carcinoma coronary artery disease developmental coordination disorder endometriosis of uterus endometriosis epithelioid sarcoma exostosis giant cell glioblastoma glioblastoma head and neck cancer head and neck squamous cell carcinoma hereditary multiple exostoses hypereosinophilic syndrome intellectual disability iris disease large intestine cancer learning disability liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia morphine dependence mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis multiple epiphyseal dysplasia nutmeg liver osteochondrodysplasia osteopetrosis osteosclerosis panuveitis periarthritis pulmonary embolism sarcoma scoliosis secondary syphilis severe combined immunodeficiency spindle cell sarcoma tendinitis tuberculosis uveitis
117248	polypeptide N-acetylgalactosaminyltransferase 15	GALNT15 Aliases: GALNT7 polypeptide GalNAc transferase 15 pp-GalNAc-T15	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
4669	N-acetyl-alpha-glucosaminidase	NAGLU Aliases: NAG Sanfilippo disease IIIB	Homo sapiens (human)	Alzheimer's disease Burkitt lymphoma Charcot-Marie-Tooth disease axonal type 2V Clouston syndrome Dent disease Fanconi syndrome Glanzmann's thrombasthenia Kluver-Bucy syndrome Legg-Calve-Perthes disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma amnestic disorder amyloidosis appendicitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrophic gastritis autistic disorder cancer cardiovascular system disease cholera chronic kidney disease chronic pyelonephritis cone-rod dystrophy congestive heart failure coronary artery disease cribriform carcinoma cystinosis cystitis dementia dentatorubral-pallidoluysian atrophy diabetes mellitus diabetic ketoacidosis diarrhea embryoma epilepsy essential thrombocythemia focal segmental glomerulosclerosis follicular adenoma fundus albipunctatus glomerulonephritis granular cell carcinoma gray platelet syndrome heart disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy 1 intellectual disability kidney disease kidney failure learning disability lipoid nephrosis liver cirrhosis lysosomal storage disease malignant pleural mesothelioma microcystic adenoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma myelodysplastic syndrome nephritis nephrosis neuroblastoma neurodegenerative disease oculocerebrorenal syndrome oculocutaneous albinism type IA osteochondrodysplasia otitis media panic disorder papillary adenoma parapsoriasis platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 progressive familial intrahepatic cholestasis 1 progressive myoclonus epilepsy prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole pyoureter qualitative platelet defect renal osteodystrophy retinitis pigmentosa retrograde amnesia sensorineural hearing loss spondyloepimetaphyseal dysplasia, Sponastrime type stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 trigonitis tubular adenocarcinoma type 2 diabetes mellitus viral infectious disease visual epilepsy

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