GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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 **251 - 275** of **1582** in total

« First

‹ Prev

…

7

8

9

10

11

12

13

14

15

…

Next ›

Last »
Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
79660	protein phosphatase 1 regulatory subunit 3B	PPP1R3B Aliases: FLJ14005 GL PP1 subunit R4 PPP1R4 hepatic glycogen-targeting subunit, G(L)	Homo sapiens (human)	Lafora disease alcohol use disorder antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer coronary artery disease depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer major depressive disorder maturity-onset diabetes of the young melancholic depression melanoma neurotic disorder obesity obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency skin melanoma steatotic liver disease thrombophilia type 2 diabetes mellitus
5506	protein phosphatase 1 regulatory subunit 3A	PPP1R3A Aliases: GM glycogen-associated regulatory subunit of protein phosphatase-1 protein phosphatase 1 regulatory subunit GM	Homo sapiens (human)	Alzheimer's disease adult lymphoma atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative breast cancer cancer carcinoma central nervous system lymphoma childhood lymphoma chronic monocytic leukemia colorectal cancer colorectal carcinoma communication disorder congestive heart failure diabetes mellitus diabetic ketoacidosis embryoma glucose intolerance hematologic cancer hypoglycemia language disorder large intestine cancer laryngeal squamous cell carcinoma lymphoid leukemia lymphoma myeloid leukemia obsolete ymphosarcoma prediabetes syndrome prostate cancer prostate carcinoma sarcomatoid carcinoma type 2 diabetes mellitus
5504	protein phosphatase 1 regulatory inhibitor subunit 2	PPP1R2	Homo sapiens (human)
5502	protein phosphatase 1 regulatory inhibitor subunit 1A	PPP1R1A	Homo sapiens (human)
5501	protein phosphatase 1 catalytic subunit gamma	PPP1CC	Homo sapiens (human)	cancer congestive heart failure type 2 diabetes mellitus
5500	protein phosphatase 1 catalytic subunit beta	PPP1CB	Homo sapiens (human)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
5499	protein phosphatase 1 catalytic subunit alpha	PPP1CA	Homo sapiens (human)	cancer type 2 diabetes mellitus
53632	protein kinase AMP-activated non-catalytic subunit gamma 3	PRKAG3	Homo sapiens (human)	Wolff-Parkinson-White syndrome lethal congenital glycogen storage disease of heart neurodegenerative disease
51422	protein kinase AMP-activated non-catalytic subunit gamma 2	PRKAG2	Homo sapiens (human)	Wolff-Parkinson-White syndrome glycogen storage disease hypertrophic cardiomyopathy 6 lethal congenital glycogen storage disease of heart neurodegenerative disease
5563	protein kinase AMP-activated catalytic subunit alpha 2	PRKAA2 Aliases: AMPK AMPKa2	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 Chediak-Higashi syndrome Clouston syndrome Duchenne muscular dystrophy Fanconi anemia complementation group A Fanconi anemia Friedreich ataxia 1 Friedreich ataxia Gilbert syndrome Graves' disease Hermansky-Pudlak syndrome 5 Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Lown-Ganong-Levine syndrome Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pelger-Huet anomaly Peutz-Jeghers syndrome Pick's disease Reye syndrome Sjogren's syndrome T-cell acute lymphoblastic leukemia Timothy syndrome Van der Woude syndrome Werner syndrome Wolff-Parkinson-White syndrome Zollinger-Ellison syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute myocarditis adenocarcinoma adenoma adrenoleukodystrophy adult acute lymphocytic leukemia adult acute monocytic leukemia amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome 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 dominant polycystic kidney disease 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 bacterial infectious disease bacterial sepsis basal cell carcinoma bilirubin metabolic disorder bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease central nervous system cancer cerebral degeneration cerebral infarction cerebral malaria cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood leukemia childhood osteosarcoma cholestasis chondrosarcoma chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia clear cell renal cell carcinoma cleidocranial dysplasia cocaine abuse cocaine dependence colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cryptococcosis cyclic hematopoiesis cystic fibrosis cystinosis cystitis dengue disease depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diarrhea diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dissociative amnesia distal myopathy early infantile epileptic encephalopathy embryoma endocrine exophthalmos endometrial cancer endometrial carcinoma endomyocardial fibrosis esophageal cancer esophageal carcinoma essential hypertension facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial periodic paralysis fibromyalgia gallbladder disease gastric adenocarcinoma gastroenteritis gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance granular cell carcinoma gyrate atrophy head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis B hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease humeroradial synostosis hyperglycemia hyperinsulinism hyperkalemic periodic paralysis hypertension hyperthyroidism hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypokalemic periodic paralysis hypothyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease inflammatory and toxic neuropathy inflammatory bowel disease influenza invasive ductal carcinoma islet cell tumor keratoconjunctivitis sicca kidney disease kidney failure large intestine cancer laryngeal squamous cell carcinoma leishmaniasis leukemia limb-girdle muscular dystrophy liver cancer liver carcinoma liver cirrhosis liver disease long QT syndrome 8 lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lysosomal storage disease malignant pleural mesothelioma megaconial type congenital muscular dystrophy melanoma middle cerebral artery infarction mitral valve insufficiency mitral valve prolapse mixed glioma multiple myeloma muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myocardial infarction myopathy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 myxedema nasopharynx carcinoma nemaline myopathy nephritis nephrogenic diabetes insipidus nephrosis neuroblastoma neurodegenerative disease nonpapillary renal cell carcinoma nutmeg liver obesity obsolete Opitz-GBBB syndrome 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 melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive sleep apnea oculopharyngeal muscular dystrophy optic atrophy 1 optic atrophy osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma overnutrition pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma pituitary adenoma pituitary cancer pituitary carcinoma placental insufficiency polycystic kidney disease 1 polycystic ovary syndrome postinflammatory pulmonary fibrosis postural orthostatic tachycardia syndrome prediabetes syndrome primary pulmonary hypertension prion disease progeria prostate cancer prostate carcinoma pulmonary fibrosis pyoureter radioulnar synostosis renal carcinoma renal cell carcinoma retrograde amnesia rigid spine muscular dystrophy 1 sarcomatoid carcinoma sarcomatoid renal cell carcinoma sick sinus syndrome silent myocardial infarction situs inversus skin melanoma spindle cell hemangioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovitis systemic lupus erythematosus tauopathy tenosynovitis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma trigonitis tuberculosis tuberous sclerosis 1 tuberous sclerosis 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 ureteral obstruction urinary bladder cancer uterine corpus cancer vascular disease viral infectious disease visceral leishmaniasis von Hippel-Lindau disease yellow fever
5562	protein kinase AMP-activated catalytic subunit alpha 1	PRKAA1	Homo sapiens (human)	Huntington's disease Parkinson's disease breast cancer cholestasis colon cancer lung non-small cell carcinoma obesity type 2 diabetes mellitus
2923	protein disulfide isomerase family A member 3	PDIA3 Aliases: ERp57 ERp60 ERp61 GRP57 HsT17083 P58 PI-PLC	Homo sapiens (human)	Clostridium difficile colitis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Zika fever absence epilepsy acute myeloid leukemia adenocarcinoma adenoma allergic asthma amyotrophic lateral sclerosis arthritis arthropathy asphyxia neonatorum asthma autoimmune hepatitis breast cancer breast carcinoma breast ductal carcinoma cancer carcinoma central nervous system cancer cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma depressive disorder dysplastic nevus syndrome embryoma endocrine system disease endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis epilepsy essential thrombocythemia giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma inflammatory and toxic neuropathy influenza intellectual disability intrinsic asthma invasive ductal carcinoma irritable bowel syndrome large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver cirrhosis lung cancer lung non-small cell carcinoma major depressive disorder male infertility melancholic depression melanoma mixed glioma mood disorder myelodysplastic syndrome neuroblastoma neurocirculatory asthenia neurodegenerative disease neurotic disorder nonpapillary renal cell carcinoma obsolete melancholia osteoarthritis ovarian cancer ovarian carcinoma papillary renal cell carcinoma platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 post-traumatic stress disorder primary pulmonary hypertension prion disease progressive muscular atrophy prostate cancer prostate carcinoma pulmonary hypertension renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma spinocerebellar ataxia type 17 squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma tubular adenocarcinoma uterine corpus cancer visual epilepsy von Willebrand's disease
29954	protein O-mannosyltransferase 2	POMT2 Aliases: Dolichyl-phosphate-mannose--protein mannosyltransferase LGMD2N	Homo sapiens (human)	Axenfeld-Rieger syndrome Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome X-linked dilated cardiomyopathy agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 bilateral optic nerve hypoplasia blindness buphthalmos campomelic dysplasia cancer cataract cleft lip cleft palate coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A2 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cryptorchidism cystic kidney disease 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 distal myopathy embryoma epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hyperopia hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly mechanical strabismus megalocornea meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy peripheral retinal degeneration pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type tuberous sclerosis visual epilepsy
10585	protein O-mannosyltransferase 1	POMT1 Aliases: LGMD2K dolichyl-phosphate-mannose-protein mannosyltransferase	Homo sapiens (human)	Axenfeld-Rieger syndrome Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 bilateral optic nerve hypoplasia blindness brain cancer brain disease buphthalmos campomelic dysplasia cardiomyopathy cataract centronuclear myopathy cleft lip cleft palate clubfoot coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus albipunctatus fundus dystrophy glaucoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hypertrophic cardiomyopathy hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly locked-in syndrome mechanical strabismus megaconial type congenital muscular dystrophy megalocornea meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy-dystroglycanopathy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myositis nemaline myopathy neuromuscular disease 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy oligohydramnios ophthalmoplegia optic atrophy peripheral retinal degeneration placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 quadriplegia recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type tuberous sclerosis visual epilepsy
84197	protein O-mannose kinase	POMK Aliases: FLJ23356 SgK196	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 bilateral optic nerve hypoplasia blindness cardiomyopathy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type C12 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopia 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
84892	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	POMGNT2 Aliases: AGO61 FLJ14566 protein O-mannose beta-1,4-N-acetylglucosaminyltransferase 2	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome acute myeloid leukemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly malaria microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type C8 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
55624	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	POMGNT1 Aliases: FLJ20277 LGMD2O MGAT1.2 protein O-mannose beta-1,2-N-acetylglucosaminyltransferase	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Unverricht-Lundborg syndrome Walker-Warburg syndrome Zollinger-Ellison syndrome adult medulloblastoma agnosia autism spectrum disorder autistic disorder autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 bilateral optic nerve hypoplasia blepharospasm blindness buphthalmos cardiomyopathy cataract centronuclear myopathy childhood medulloblastoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A3 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness congenital structural myopathy cornea plana corneal disease cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder diabetes mellitus dissociated nystagmus distal myopathy early myoclonic encephalopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal hand dystonia fundus albipunctatus fundus dystrophy giant cell glioblastoma glaucoma glioblastoma high grade glioma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hyperinsulinism hypertrophic cardiomyopathy hypertropia hypogonadism intellectual disability isolated elevated serum creatine phosphokinase levels keratoconus learning disability limb-girdle muscular dystrophy lissencephaly mechanical strabismus medulloblastoma medullomyoblastoma megaconial type congenital muscular dystrophy megalocornea melanotic medulloblastoma meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia nemaline myopathy neuroblastoma night blindness obesity obsolete asthenopia 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment retinal disease retinitis pigmentosa retinitis rigid spine muscular dystrophy 1 rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type type 2 diabetes mellitus visual epilepsy
143888	protein O-glucosyltransferase 3	POGLUT3 Aliases: MGC33424	Homo sapiens (human)	chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma myofibroma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma uterine fibroid
79070	protein O-glucosyltransferase 2	POGLUT2 Aliases: EP58 MGC5302	Homo sapiens (human)	bipolar disorder
56983	protein O-glucosyltransferase 1	POGLUT1 Aliases: 9630046K23Rik KDELC family like 1 KDELCL1 MDS010 MDSRP MGC32995 Rumi hCLP46	Homo sapiens (human)	Dowling-Degos disease Duchenne muscular dystrophy T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia acute myeloid leukemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 type 2Z autosomal recessive limb-girdle muscular dystrophy cancer childhood T-cell acute lymphoblastic leukemia childhood leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy embryoma essential thrombocythemia facioscapulohumeral muscular dystrophy hematopoietic system disease isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leukemia limb-girdle muscular dystrophy lung cancer lung non-small cell carcinoma mongolian spot muscular dystrophy myelodysplastic syndrome myofibrillar myopathy 1 myofibrillar myopathy 3 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 oculopharyngeal muscular dystrophy primary biliary cholangitis pseudoxanthoma elasticum reticulate acropigmentation of Kitamura rippling muscle disease 2
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
23509	protein O-fucosyltransferase 1	POFUT1 Aliases: FUT12 GDP-fucose protein O-fucosyltransferase 1 KIAA0180 O-FUT O-Fuc-T peptide-O-fucosyltransferase	Homo sapiens (human)	Dowling-Degos disease acrodermatitis actinic keratosis acute myocardial infarction bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery anomaly coronary thrombosis dermatitis gallbladder disease hepatocellular carcinoma invasive ductal carcinoma large intestine cancer liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcephaly myeloproliferative neoplasm myocardial infarction reticulate acropigmentation of Kitamura schizophrenia seborrheic keratosis silent myocardial infarction skin disease
5716	proteasome 26S subunit, non-ATPase 10	PSMD10	Homo sapiens (human)	B-cell lymphoma T-cell acute lymphoblastic leukemia West Nile fever acute myocardial infarction adenocarcinoma adenoma adult T-cell leukemia/lymphoma adult cystic teratoma adult teratoma autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer childhood osteosarcoma childhood testicular germ cell tumor cholangiocarcinoma cholesteatoma of middle ear cholesteatoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary thrombosis cystic teratoma dedifferentiated liposarcoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis ehrlichiosis embryoma embryonal cancer embryonal carcinoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis epilepsy esophageal cancer esophageal carcinoma exudative vitreoretinopathy 1 exudative vitreoretinopathy familial adenomatous polyposis 1 familial adenomatous polyposis familial retinoblastoma follicular adenoma gastroenteritis germ cell and embryonal cancer germ cell cancer germinoma gliosarcoma head and neck squamous cell carcinoma hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma high grade glioma ileitis ileocolitis immune system disease inflammatory bowel disease influenza intrahepatic cholangiocarcinoma invasive ductal carcinoma islet cell tumor large intestine cancer liposarcoma liver cancer liver carcinoma liver cirrhosis lung cancer lung non-small cell carcinoma malignant teratoma mature teratoma melanoma microcystic adenoma mixed glioma multiple myeloma multiple sclerosis myelitis myocardial infarction myopia nonpapillary renal cell carcinoma normal pressure hydrocephalus obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma pleomorphic liposarcoma polyp of middle ear prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinoblastoma retinopathy of prematurity sarcomatoid renal cell carcinoma schizophrenia seminoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma teratoma testicular cancer testicular germ cell cancer testicular malignant germ cell cancer testis seminoma thymic carcinoma thymoma tongue squamous cell carcinoma trilateral retinoblastoma type 2 diabetes mellitus uterine corpus cancer viral infectious disease visual epilepsy
5743	prostaglandin-endoperoxide synthase 2	PTGS2 Aliases: COX2 cyclooxygenase 2 prostaglandin G/H synthase 2	Homo sapiens (human)	46,XY sex reversal Aicardi-Goutieres syndrome 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Barrett's adenocarcinoma Barrett's esophagus Bartter disease Burkitt lymphoma Chagas 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 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 3 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 Clostridium difficile colitis Clouston syndrome Conn's syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Cytomegalovirus retinitis Down syndrome Dyggve-Melchior-Clausen disease Ehlers-Danlos syndrome Evans' syndrome Ewing sarcoma Friedreich ataxia Gitelman syndrome Guillain-Barre syndrome Hantavirus hemorrhagic fever with renal 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 Japanese encephalitis Kaposi's sarcoma Kawasaki disease Langerhans-cell histiocytosis Lewy body dementia Leydig cell tumor Liddle syndrome Lyme disease Lynch syndrome MHC class II deficiency Marfan syndrome Marinesco-Sjogren syndrome Meckel syndrome Miller Fisher syndrome Netherton syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Parkinsonism Peutz-Jeghers syndrome Pick's disease Plasmodium falciparum malaria Q fever Reye syndrome Richter's syndrome Shwachman-Diamond syndrome Stevens-Johnson syndrome Stickler syndrome Streptococcus pneumonia Van der Woude syndrome Wernicke encephalopathy abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acne acoustic neuroma acquired hyperkeratosis acquired immunodeficiency syndrome acrodermatitis actinic keratosis acute chest syndrome acute interstitial pneumonia acute kidney failure acute kidney tubular necrosis acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute myocarditis acute pancreatitis acute pericementitis acute promyelocytic leukemia acute pyelonephritis adenocarcinoma adenoid cystic carcinoma adenoma adenosarcoma adenosine deaminase deficiency adrenal gland cancer adult fibrosarcoma adult hepatocellular carcinoma adult lymphoma adult medulloblastoma adult oligodendroglioma adult respiratory distress syndrome agenesis of the corpus callosum with peripheral neuropathy aggressive periodontitis agnosia allergic asthma allergic rhinitis alopecia alternating hemiplegia of childhood ameloblastoma amnestic disorder ampulla of Vater carcinoma amyloidosis amyotrophic lateral sclerosis-parkinsonism/dementia complex 1 amyotrophic lateral sclerosis anaplastic astrocytoma anemia angioedema angiomatous meningioma ankyloblepharon-ectodermal defects-cleft lip/palate syndrome ankylosing spondylitis anorexia nervosa anthracosilicosis anthracosis anxiety disorder aortic aneurysm aortic atherosclerosis aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis asphyxia neonatorum aspirin-induced respiratory disease asthma atherosclerosis atopic dermatitis atrial fibrillation atrophic gastritis atypical chronic myeloid leukemia, BCR-ABL1 negative atypical teratoid rhabdoid tumor autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis autonomic neuropathy autosomal dominant polycystic kidney disease avian influenza bacterial infectious disease bacterial sepsis bagassosis basal cell carcinoma benign ependymoma benign meningioma benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma bile reflux biliary tract cancer bipolar disorder bladder carcinoma bladder neck obstruction bladder urothelial carcinoma bone cancer bone marrow disease bone osteosarcoma brain cancer brain disease brain ischemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma breast ductal carcinoma breast fibroadenosis breast fibrocystic disease bronchus cancer bronchus carcinoma bursitis calcific tendinitis calcinosis calcium metabolism disease cancer cannabis abuse cannabis dependence carcinoma cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease carotid stenosis carpal tunnel syndrome cat-scratch disease cataract catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cellular ependymoma cellular schwannoma central nervous system cancer central nervous system disease central nervous system lymphoma cerebral artery occlusion cerebral cavernous malformation 1 cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral malaria cerebral palsy cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood leukemia childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma childhood type dermatomyositis cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholesteatoma of middle ear cholesteatoma chondroblastoma chondrocalcinosis chondrosarcoma chorioamnionitis chromophobe renal cell carcinoma chromosome 10q23 deletion syndrome chronic fatigue syndrome chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy chronic interstitial cystitis chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma clitoris cancer colitis collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart complement deficiency complex partial epilepsy congenital central hypoventilation syndrome congenital heart disease congenital hypothyroidism congenital secretory sodium diarrhea 3 congenital secretory sodium diarrhea 8 congestive heart failure corneal ulcer coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma cutaneous fibrous histiocytoma cyclic hematopoiesis cystic fibrosis cystitis cytochrome-c oxidase deficiency disease decubitus ulcer degenerative disc disease dementia demyelinating disease demyelinating polyneuropathy dengue disease depressive disorder dermatitis dermatomyositis dermoid cyst diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy diarrhea differentiated thyroid gland carcinoma diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health disease of metabolism distal arthrogryposis double outlet right ventricle dry eye syndrome ductal carcinoma in situ duodenal ulcer duodenum cancer duodenum disease dysplastic nevus syndrome dysthymic disorder eclampsia embryoma encephalitis encephalomyelitis endemic goiter endocervical carcinoma endocrine exophthalmos endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometrioid ovary carcinoma endometriosis of ovary endometriosis of uterus endometriosis endometritis endomyocardial fibrosis enthesopathy eosinophilic esophagitis epidermodysplasia verruciformis epilepsy epithelioid leiomyosarcoma epithelioid sarcoma esophageal cancer esophageal carcinoma esophageal disease esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension exanthem exfoliation syndrome exostosis extrahepatic bile duct carcinoma extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial hypocalciuric hypercalcemia 1 familial nephrotic syndrome familial periodic paralysis familial retinoblastoma fasciitis fibrillary astrocytoma fibromyalgia fibrosarcoma fibrous dysplasia fibrous meningioma focal epilepsy follicular adenoma frozen shoulder gallbladder cancer gallbladder carcinoma gallbladder disease gastric adenocarcinoma gastric cardia adenocarcinoma gastric lymphoma gastric tubular adenocarcinoma gastric ulcer gastritis gastroenteritis gastroesophageal junction adenocarcinoma gastroesophageal reflux disease gastrointestinal stromal tumor gastrointestinal system cancer gastrointestinal system disease gemistocytic astrocytoma generalized anxiety disorder gestational diabetes giant cell glioblastoma gingivitis glioblastoma gliosarcoma glomerulonephritis goiter gonorrhea granular cell carcinoma granuloma annulare granulosa cell tumor growth hormone secreting pituitary adenoma head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematologic cancer hemiplegia hemolytic anemia hemopericardium hepatitis A hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma hepatopulmonary syndrome hereditary neuropathy with liability to pressure palsies hereditary spherocytosis type 1 hereditary spherocytosis herpes simplex hidradenoma high grade glioma human immunodeficiency virus infectious disease hydronephrosis hypercalcemia hypereosinophilic syndrome hyperglycemia hyperhomocysteinemia hyperparathyroidism hypertension hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia hypothyroidism hypotrichosis 7 hypotrichosis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis ileus immune system disease in situ carcinoma inclusion conjunctivitis inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma inflammatory myofibroblastic tumor influenza intermediate coronary syndrome interstitial cystitis intestinal benign neoplasm intestinal cancer intestinal disease intestinal obstruction intracranial aneurysm intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma invasive ductal carcinoma invasive lobular carcinoma inverted follicular keratosis irritable bowel syndrome ischemia ischemic colitis islet cell tumor isovaleric acidemia juvenile pilocytic astrocytoma juvenile polyposis syndrome keratoacanthoma keratosis follicularis kidney cancer kidney disease kidney failure kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease laryngeal squamous cell carcinoma larynx cancer late onset Parkinson's disease leiomyoma leiomyosarcoma leprosy leukemia leukopenia lichen disease lichen planus lipoid nephrosis liver cancer liver carcinoma liver cirrhosis liver disease lobular neoplasia localized scleroderma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma lupus erythematosus lupus nephritis lymphangioleiomyomatosis lymphoid leukemia lymphoma lymphoplasmacyte-rich meningioma macrocytic anemia major depressive disorder malaria malignant astrocytoma malignant conjunctival melanoma malignant fibrous histiocytoma malignant mesothelioma malignant peripheral nerve sheath tumor malignant pleural mesothelioma marasmus mast-cell leukemia mastocytosis meconium aspiration syndrome medulloblastoma medulloepithelioma medullomyoblastoma melancholic depression melanoacanthoma melanoma melanotic medulloblastoma melanotic neurilemmoma melorheostosis meningioma meningothelial meningioma microcystic adenoma microcystic meningioma microglandular adenosis microinvasive gastric cancer microphthalmia middle cerebral artery infarction migraine mixed glioma mixed oligodendroglioma-astrocytoma mixed sleep apnea mongolian spot mood disorder motor peripheral neuropathy mouth disease mucoepidermoid carcinoma mucositis multidrug-resistant tuberculosis multiple myeloma multiple sclerosis musculoskeletal system disease mycosis fungoides myelitis myeloid leukemia myocardial infarction myocarditis myofascial pain syndrome myofibroma myopathy myositis myxedema myxoid leiomyosarcoma myxopapillary ependymoma nasopharynx carcinoma nephritis nephroblastoma nephrocalcinosis nephrogenic diabetes insipidus nephrosis nephrotic syndrome nervous system disease neurilemmoma neuroblastoma neurocirculatory asthenia neurodegenerative disease neuroectodermal tumor neurofibromatosis neurogenic arthropathy neurotic disorder newborn respiratory distress syndrome nodular prostate non-Hodgkin lymphoma nonpapillary renal cell carcinoma nose disease nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete dyspepsia obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive sleep apnea olfactory groove meningioma oligodendroglioma open-angle glaucoma oral mucosa leukoplakia oral submucous fibrosis osteitis fibrosa osteoarthritis 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 osteomyelitis osteosarcoma ovarian cancer ovarian carcinoma ovarian cyst ovarian hyperstimulation syndrome ovary adenocarcinoma ovary serous adenocarcinoma oxyphilic adenoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis papillary adenocarcinoma papillary adenoma papillary carcinoma papillary ependymoma papillary renal cell carcinoma papilloma paraganglioma parasagittal meningioma partial motor epilepsy patent ductus arteriosus peptic esophagitis peptic ulcer disease periapical granuloma pericardial effusion perinatal necrotizing enterocolitis periodontal disease periodontitis periodontosis peripheral artery disease peritoneal mesothelioma pharyngitis pheochromocytoma phobic disorder phosphorus metabolism disease photosensitivity disease phototoxic dermatitis pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma placental insufficiency pleomorphic adenoma pleurisy plexiform schwannoma pneumoconiosis pneumonia pneumothorax polycystic kidney disease 1 polycystic kidney disease polycystic ovary syndrome polyp of corpus uteri polyp of middle ear portal hypertension post-traumatic stress disorder postinflammatory pulmonary fibrosis pre-eclampsia primary biliary cholangitis primary cerebellar degeneration primary cutaneous T-cell non-Hodgkin lymphoma primary cutaneous amyloidosis primary hyperaldosteronism primary hyperparathyroidism primary hypertrophic osteoarthropathy primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension primary sclerosing cholangitis prion disease progressive muscular atrophy prolactinoma prostate adenocarcinoma prostate cancer prostate carcinoma in situ prostate carcinoma prostatic adenoma prostatic hypertrophy prostatitis protein-energy malnutrition proteinuria protoplasmic astrocytoma prune belly syndrome psammomatous meningioma pseudomyxoma peritonei pseudosarcomatous fibromatosis pseudoxanthoma elasticum psoriatic arthritis psychotic disorder pterygium pulmonary emphysema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis pyoureter reactive arthritis rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal oncocytoma renal osteodystrophy renovascular hypertension respiratory syncytial virus infectious disease reticulosarcoma retinal disease retinitis retinoblastoma retrograde amnesia rhabdoid cancer rhabdomyosarcoma rheumatoid arthritis rickets root resorption salivary gland adenoid cystic carcinoma sarcoidosis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma sclerosing cholangitis sebaceous carcinoma seborrheic keratosis secondary Parkinson disease secondary hyperparathyroidism secondary hypertrophic osteoarthropathy secretory meningioma sensorineural hearing loss serous cystadenocarcinoma severe combined immunodeficiency sick sinus syndrome siderosis silent myocardial infarction silicosis situs inversus skin benign neoplasm skin cancer skin carcinoma skin disease skin melanoma skin papilloma skin squamous cell carcinoma skin tag sleep apnea small intestine cancer spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal cord disease spinal meningioma spinal muscular atrophy spinal stenosis spindle cell hemangioma spindle cell sarcoma spondyloarthropathy spondylosis squamous cell carcinoma squamous cell neoplasm squamous cell papilloma squamous papillomatosis status epilepticus steatotic liver disease steroid-induced glaucoma stomach cancer stomach carcinoma stomach disease stomatitis subacute bacterial endocarditis subependymal giant cell astrocytoma substernal goiter supratentorial primitive neuroectodermal tumor sweat gland cancer synovial sarcoma syringoma syringomyelia systemic lupus erythematosus systemic scleroderma systolic heart failure tanycytic ependymoma tarsal-carpal coalition syndrome tauopathy temporal arteritis temporal lobe epilepsy teratocarcinoma thromboangiitis obliterans thrombocytopenia thrombosis thrombotic thrombocytopenic purpura thymic carcinoma thymoma thyroid adenoma thyroid angiosarcoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland follicular carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue cancer tongue squamous cell carcinoma tracheal disease transient cerebral ischemia transitional cell carcinoma transitional meningioma transthyretin amyloidosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency trigonitis trilateral retinoblastoma trypanosomiasis tuberculosis tuberculous peritonitis tuberous sclerosis 1 tuberous sclerosis 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 type C thymoma typhus ulcerative colitis uremia ureteral obstruction uric acid nephrolithiasis urinary bladder cancer urinary tract obstruction urticaria uterine corpus cancer uterine fibroid uveoparotid fever varicose veins vascular dementia vascular disease vasomotor rhinitis vertebrobasilar insufficiency vestibular schwannomatosis viral infectious disease visual epilepsy vitiligo von Hippel-Lindau disease vulva cancer vulva carcinoma white sponge nevus xeroderma pigmentosum group A xeroderma pigmentosum group C xerophthalmia yellow fever
5742	prostaglandin-endoperoxide synthase 1	PTGS1 Aliases: COX1 PGHS-1 PTGHS cyclooxygenase-1	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 Barrett's esophagus Creutzfeldt-Jakob disease Evans' syndrome French Canadian Leigh disease Guillain-Barre syndrome Hantavirus hemorrhagic fever with renal syndrome Leigh disease Lyme disease Marfan syndrome Meckel syndrome Miller Fisher syndrome Pick's disease Reye syndrome Streptococcus pneumonia acoustic neuroma acquired immunodeficiency syndrome actinic keratosis acute chest syndrome acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma amnestic disorder amyloidosis angiomatous meningioma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis autism spectrum disorder autistic disorder autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autosomal dominant polycystic kidney disease basal cell carcinoma benign meningioma bipolar disorder bladder carcinoma blood coagulation disease brain ischemia brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma bursitis cancer carcinoma cardiac arrest cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood type dermatomyositis chorioamnionitis chromophobe renal cell carcinoma chronic ethmoiditis chronic kidney disease 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 congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cytochrome-c oxidase deficiency disease depressive disorder dermatomyositis diabetes mellitus diabetic ketoacidosis dysthymic disorder eclampsia embryoma endometrial carcinoma epilepsy erythromelalgia esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue eyelid disease familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia fibrous meningioma follicular adenoma frozen shoulder gastric lymphoma gastric ulcer gastritis gastroenteritis gastroesophageal reflux disease gastrointestinal system cancer gastrointestinal system disease giant cell glioblastoma glaucoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemiplegia hepatic coma hepatic encephalopathy hepatitis hepatocellular carcinoma high grade glioma histiocytosis human immunodeficiency virus infectious disease hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal disease intracranial vasospasm intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor isovaleric acidemia keratoacanthoma kidney disease kidney failure lactic acidosis large intestine cancer leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphoplasmacyte-rich meningioma major depressive disorder meconium aspiration syndrome melancholic depression melanoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma mixed glioma mood disorder mucoepidermoid carcinoma multiple myeloma myocardial infarction myositis nephritis nephrosis neurogenic arthropathy neuromuscular disease neurotic disorder nonpapillary renal cell carcinoma nose disease nutmeg liver obesity obsolete dyspepsia obsolete inherited blood coagulation disease obsolete melancholia obstructive sleep apnea olfactory groove meningioma osteoarthritis ovarian cancer ovarian carcinoma ovarian cyst oxyphilic adenoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma peptic esophagitis peptic ulcer disease peripheral artery disease pituitary adenoma platelet-type bleeding disorder 12 pneumonia pneumothorax polycystic kidney disease portal hypertension pre-eclampsia primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension prostate cancer prostate carcinoma psammomatous meningioma psoriasis psoriatic arthritis pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renovascular hypertension retrograde amnesia rheumatoid arthritis root resorption salivary gland carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia secretory meningioma silent myocardial infarction situs inversus skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal meningioma spindle cell hemangioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombosis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma tongue squamous cell carcinoma transient cerebral ischemia transitional meningioma tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uremia urinary bladder cancer urinary tract obstruction viral infectious disease visual epilepsy xanthomatosis

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements