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 **1251 - 1275** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
648791	protein phosphatase 1 regulatory subunit 3G	PPP1R3G	Homo sapiens (human)	obesity steatotic liver disease
57223	protein phosphatase 4 regulatory subunit 3B	PPP4R3B	Homo sapiens (human)
5538	palmitoyl-protein thioesterase 1	PPT1 Aliases: CLN1 INCL ceroid-lipofuscinosis, neuronal 1, infantile	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 Gaucher's disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pick's disease Reye syndrome Stargardt disease Unverricht-Lundborg syndrome actinic keratosis age related macular degeneration alternating hemiplegia of childhood amnestic disorder autonomic neuropathy basal cell carcinoma blepharospasm blindness brain disease breast cancer breast carcinoma cancer cannabis abuse cannabis dependence central nervous system disease cerebral degeneration colorectal cancer congestive heart failure degeneration of macula and posterior pole denture stomatitis depressive disorder dysthymic disorder early myoclonic encephalopathy embryoma endometriosis of uterus endometriosis epilepsy eye disease focal hand dystonia giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma hyperthyroidism intellectual disability inverted follicular keratosis keratoacanthoma large intestine cancer learning disability lingual-facial-buccal dyskinesia liver cancer lung cancer lung non-small cell carcinoma lysosomal storage disease macular degeneration major depressive disorder male infertility melancholic depression melanoacanthoma movement disease nervous system disease neuroblastoma neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder obsolete melancholia optic atrophy polycystic ovary syndrome primary immunodeficiency disease prostate adenocarcinoma prostate cancer prostate carcinoma psychotic disorder retrograde amnesia schizoaffective disorder schizophrenia schizophreniform disorder seborrheic keratosis secondary Parkinson disease skin disease stomatitis syndromic X-linked intellectual disability 94 thyrotoxicosis ulcerative stomatitis visual epilepsy
9374	palmitoyl-protein thioesterase 2	PPT2	Homo sapiens (human)	cancer cerebellar ataxia cerebellar disease embryoma histiocytosis membranous glomerulonephritis multiple myeloma multiple sclerosis neuroblastoma neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis
5553	proteoglycan 2, pro eosinophil major basic protein	PRG2 Aliases: BMPG MBP eosinophil major basic protein proMBP	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 Chagas disease Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 Pick's disease Reye syndrome allergic asthma asthma 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 breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration cholera colorectal cancer colorectal carcinoma congenital muscular dystrophy dermatophytosis dilated cardiomyopathy 1A dilated cardiomyopathy distal myopathy embryoma endometrial cancer endometrial carcinoma eosinophilic esophagitis facioscapulohumeral muscular dystrophy fungal infectious disease intrinsic asthma large intestine cancer limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma muscular dystrophy myelofibrosis myofibrillar myopathy 1 myofibrillar myopathy 3 nodular prostate 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 peritoneum cancer prostate cancer prostate carcinoma prostatic adenoma rippling muscle disease 2 uterine corpus cancer
10394	proteoglycan 3, pro eosinophil major basic protein 2	PRG3 Aliases: MBP2 MBPH	Homo sapiens (human)	brain cancer cancer cerebral infarction cerebrovascular disease embryoma
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
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
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
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
5589	PRKCSH beta subunit of glucosidase II	PRKCSH	Homo sapiens (human)	Marfan syndrome Meckel syndrome autosomal dominant polycystic kidney disease beta thalassemia breast cancer breast carcinoma cancer cerebellar ataxia, mental retardation and dysequlibrium syndrome cystic kidney disease diabetic ketoacidosis episodic ataxia type 2 esophagitis familial hemiplegic migraine 1 familial hemiplegic migraine familial hypercholesterolemia gallbladder disease gastroesophageal reflux disease hepatitis B hepatocellular carcinoma liver cancer liver disease non-congenital cyst of kidney obsolete type 1 diabetes mellitus 9 peptic esophagitis polycystic kidney disease 1 polycystic liver disease situs inversus tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
5621	prion protein (Kanno blood group)	PRNP Aliases: AltPrP CD230 Creutzfeldt-Jakob disease Gerstmann-Strausler-Scheinker syndrome PRP fatal familial insomnia p27-30	Homo sapiens (human)	3p deletion syndrome Alpers-Huttenlocher 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 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Angelman syndrome Balo concentric sclerosis Bernard-Soulier syndrome 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 Chediak-Higashi syndrome Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down syndrome Dubowitz syndrome Friedreich ataxia Gerstmann-Straussler-Scheinker syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease ITM2B-related cerebral amyloid angiopathy 1 Japanese encephalitis Kennedy's disease Lewy body dementia MYH-9 related disease Marfan syndrome NFIA-related disorder 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 Pelger-Huet anomaly Pick's disease Prader-Willi syndrome REM sleep behavior disorder Reye syndrome Robinow syndrome SATB2-associated syndrome Seckel syndrome Silver-Russell syndrome Smith-Magenis syndrome Unverricht-Lundborg syndrome Wilson disease X-linked Aarskog syndrome acoustic neuroma acquired immunodeficiency syndrome acute myocardial infarction adenocarcinoma adenoma adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy agnosia akinetic mutism alcoholic hepatitis allergic asthma alopecia alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis anaplastic astrocytoma androgenic alopecia anxiety disorder aphasia apraxia arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis attention deficit hyperactivity disorder autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cerebellar ataxia autosomal recessive Robinow syndrome bipolar disorder blepharospasm blindness bone osteosarcoma brain disease brain ischemia brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular schwannoma central nervous system cancer central nervous system disease cerebellar ataxia cerebellar disease cerebral amyloid angiopathy cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood osteosarcoma chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma choreatic disease chromophobe renal cell carcinoma chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome chronic kidney disease chronic obstructive pulmonary disease chronic wasting disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma common wart complex partial epilepsy cone-rod dystrophy congenital diarrhea 5 with tufting enteropathy congenital nystagmus conversion disorder coronary artery disease coronary thrombosis cribriform carcinoma critical illness polyneuropathy cystic fibrosis dementia demyelinating polyneuropathy dengue disease dentatorubral-pallidoluysian atrophy depressive disorder diabetic cataract diabetic retinopathy diarrhea dissociated nystagmus dissociative disorder distal 10q deletion syndrome dysthymic disorder early myoclonic encephalopathy embryoma encephalitis encephalomyelitis epilepsy essential hypertension factor VIII deficiency familial mediterranean fever familial periodic paralysis fatal familial insomnia fibrillary astrocytoma focal hand dystonia frontotemporal dementia frozen shoulder fundus albipunctatus gemistocytic astrocytoma generalized anxiety disorder giant cell glioblastoma glaucoma glioblastoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hemochromatosis hepatitis B hepatitis C hepatocellular carcinoma hereditary ataxia hereditary neuropathy with liability to pressure palsies high grade glioma human immunodeficiency virus infectious disease hydrocephalus hyperekplexia 1 hyperekplexia 2 hyperekplexia 3 hyperekplexia hyperglycemia hypertension hypothalamic disease inclusion body myositis inflammatory and toxic neuropathy inflammatory bowel disease influenza intrinsic asthma iron metabolism disease juvenile pilocytic astrocytoma juvenile rheumatoid arthritis kuru large intestine cancer lingual-facial-buccal dyskinesia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder malignant astrocytoma malignant peripheral nerve sheath tumor melancholic depression melanoma melanotic neurilemmoma meningitis meningoencephalitis mevalonic aciduria microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia migraine mixed glioma mood disorder motor peripheral neuropathy movement disease multiple sclerosis multiple system atrophy myelitis myocardial infarction myopathy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 narcolepsy neovascular glaucoma nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuropathy neurotic disorder normal pressure hydrocephalus obesity obsolete Alpers syndrome obsolete Matthew-Wood syndrome obsolete constipation obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia ocular hypotension osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma parathyroid gland disease paroxysmal nocturnal hemoglobinuria pathologic nystagmus peripheral nervous system disease pilocytic astrocytoma pityriasis rubra pilaris placental insufficiency plexiform schwannoma polyneuropathy primary cerebellar degeneration primary cutaneous amyloidosis primary open angle glaucoma prion disease progressive multifocal leukoencephalopathy progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy 4 progressive myoclonus epilepsy progressive supranuclear palsy prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder qualitative platelet defect radial nerve lesion radial neuropathy recurrent hypersomnia renal carcinoma renal cell carcinoma retinitis pigmentosa retrograde amnesia sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scrapie secondary Parkinson disease sickle cell anemia silent myocardial infarction situs inversus skin melanoma spinal muscular atrophy spinocerebellar ataxia type 31 spinocerebellar ataxia type 7 spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma sudden infant death syndrome syndromic X-linked intellectual disability type 10 synovitis tauopathy temporal lobe epilepsy tendinitis tenosynovitis tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trigeminal neuralgia tuberous sclerosis tubular adenocarcinoma vascular dementia vestibular nystagmus viral infectious disease visual epilepsy vitiligo yellow fever
5631	phosphoribosyl pyrophosphate synthetase 1	PRPS1 Aliases: CMTX5 DFNX1 PPRibP PRS I PRS-I ribose-phosphate diphosphokinase 1	Homo sapiens (human)	Arts syndrome 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 type X Charcot-Marie-Tooth disease Foster-Kennedy syndrome Laron syndrome Werner syndrome X-linked deafness 1 X-linked nonsyndromic deafness achondroplasia acute lymphoblastic leukemia adult acute lymphocytic leukemia agenesis of the corpus callosum with peripheral neuropathy agnosia alternating exotropia anaplastic astrocytoma blindness breast cancer breast carcinoma cancer carcinoma central sleep apnea childhood acute lymphocytic leukemia childhood cerebral astrocytoma coloboma colorectal cancer colorectal carcinoma communication disorder congenital nystagmus critical illness polyneuropathy developmental coordination disorder diabetes insipidus disease of metabolism dissociated nystagmus embryoma epilepsy exotropia fibrillary astrocytoma fundus dystrophy gemistocytic astrocytoma giant cell glioblastoma glioblastoma gout hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperuricemia inflammatory and toxic neuropathy intellectual disability juvenile pilocytic astrocytoma kidney failure kwashiorkor language disorder large intestine cancer learning disability liver cancer locked-in syndrome malignant astrocytoma marasmus meningoencephalitis monocular exotropia motor peripheral neuropathy neuroblastoma neurodegeneration with brain iron accumulation neurohypophyseal diabetes insipidus neuropathy nutrition disease nutritional optic neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum optic atrophy optic nerve disease pancreas disease paraplegia pathologic nystagmus peripheral nervous system disease phosphoribosylpyrophosphate synthetase superactivity pilocytic astrocytoma placental insufficiency polyneuropathy primary immunodeficiency disease progeria protein-energy malnutrition protoplasmic astrocytoma quadriplegia retinitis pigmentosa sarcomatoid carcinoma scoliosis sensorineural hearing loss sensory peripheral neuropathy spontaneous ocular nystagmus subependymal giant cell astrocytoma uric acid nephrolithiasis visual epilepsy visual pathway disease
221823	phosphoribosyl pyrophosphate synthetase 1 like 1	PRPS1L1 Aliases: PRPS3	Homo sapiens (human)
5634	phosphoribosyl pyrophosphate synthetase 2	PRPS2 Aliases: PRS II ribose-phosphate diphosphokinase 2	Homo sapiens (human)	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 cancer embryoma oligospermia systemic lupus erythematosus
10942	serine protease 21	PRSS21 Aliases: ESP-1 TEST1 testisin	Homo sapiens (human)	Behcet's disease Down syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder atrial fibrillation cancer cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood germ cell cancer diabetes mellitus diabetic ketoacidosis disorder of sexual development embryonal cancer germ cell and embryonal cancer germ cell cancer germinoma hepatitis B hermaphroditism human immunodeficiency virus infectious disease monoclonal gammopathy of uncertain significance monoclonal paraproteinemia ovarian cancer ovarian carcinoma plasma cell neoplasm pseudohermaphroditism type 2 diabetes mellitus
360226	serine protease 41	PRSS41	Homo sapiens (human)	ovarian cancer ovarian carcinoma
5652	serine protease 8	PRSS8 Aliases: CAP1 channel-activating serine protease 1 prostasin	Homo sapiens (human)	Bartter disease Conn's syndrome Waterhouse-Friderichsen syndrome actinic keratosis alopecia autosomal recessive congenital ichthyosis 4B bladder carcinoma bladder urothelial carcinoma breast cancer breast carcinoma cancer central nervous system cancer cholera chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma esophagus squamous cell carcinoma essential hypertension gastroenteritis gliosarcoma hepatocellular carcinoma high grade glioma hypertension ileitis ileocolitis influenza intestinal benign neoplasm intestinal cancer liver cancer lung cancer lung non-small cell carcinoma mixed glioma obsolete congenital ichthyosiform erythroderma ovarian cancer ovarian carcinoma oxyphilic adenoma papillary renal cell carcinoma placenta disease primary hyperaldosteronism prostate cancer prostate carcinoma in situ prostate carcinoma renal carcinoma renal cell carcinoma renal oncocytoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease tarsal-carpal coalition syndrome type 2 diabetes mellitus urinary bladder cancer
127281	peroxiredoxin like 2B	PRXL2B Aliases: MGC26818 prostamide/prostaglandin F synthase thioredoxin-type PGF synthase	Homo sapiens (human)
5660	prosaposin	PSAP Aliases: saposin-A saposin-B saposin-C saposin-D variant Gaucher disease and variant metachromatic leukodystrophy	Homo sapiens (human)	Farber lipogranulomatosis Gaucher's disease type I Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Krabbe disease Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Unverricht-Lundborg syndrome X-linked nonsyndromic deafness acquired immunodeficiency syndrome adult fibrosarcoma agnosia allergic asthma amnestic disorder amyotrophic lateral sclerosis anemia aortic valve disease 2 aortic valve stenosis asthma atypical Gaucher's disease due to saposin c deficiency autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness bacterial sepsis blepharospasm breast cancer breast carcinoma cancer candidiasis central nervous system cancer central sleep apnea cholecystitis choreatic disease colitis combined saposin deficiency critical illness polyneuropathy cutaneous candidiasis dementia dental caries dentin caries denture stomatitis depressive disorder dysthymic disorder dystonia early myoclonic encephalopathy embryoma epilepsy fascioliasis fibrosarcoma focal hand dystonia frontotemporal dementia gallbladder cancer gallbladder carcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma hepatitis B hepatitis E hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease ileitis ileocolitis inflammatory and toxic neuropathy inflammatory bowel disease late onset Parkinson's disease leukodystrophy lingual-facial-buccal dyskinesia lipid storage disease liver cancer lysosomal storage disease macrocytic anemia major depressive disorder malaria melancholic depression meningoencephalitis metachromatic leukodystrophy mixed glioma movement disease multiple myeloma neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neuropathy neurotic disorder obsolete autosomal recessive nonsyndromic deafness 105 obsolete melancholia optic atrophy oral candidiasis ovarian cancer ovarian carcinoma panic disorder paraplegia parapsoriasis peripheral nervous system disease phobic disorder plasma cell neoplasm polyneuropathy progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole retrograde amnesia schizophrenia situs inversus social phobia sphingolipidosis stomach cancer stomach carcinoma stomatitis syndromic X-linked intellectual disability type 10 thrombocytopenia tuberous sclerosis ulcerative stomatitis visual epilepsy vulvovaginal candidiasis vulvovaginitis
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
9791	phosphatidylserine synthase 1	PTDSS1 Aliases: KIAA0024 PSS1 PSSA	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 Bell's palsy Hailey-Hailey disease Laron syndrome Lenz-Majewski hyperostotic dwarfism Pick's disease Reye syndrome Rothmund-Thomson syndrome achondroplasia aortic disease aortic valve disease 2 aortic valve stenosis autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant osteopetrosis 2 autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive osteopetrosis 7 cerebral degeneration choanal atresia communicating hydrocephalus cryptorchidism cutis laxa dental enamel hypoplasia facial nerve disease facial paralysis humeroradial synostosis hydrocephalus hypogonadism hypospadias inguinal hernia intellectual disability lateral meningocele syndrome learning disability mal de Meleda obstructive hydrocephalus osteopetrosis osteosclerosis placental insufficiency priapism restrictive dermopathy scoliosis senile degeneration of brain sensorineural hearing loss syndactyly tongue disease
81490	phosphatidylserine synthase 2	PTDSS2 Aliases: PSS2	Homo sapiens (human)
5728	phosphatase and tensin homolog	PTEN Aliases: MMAC1 PTEN1 TEP1 mutated in multiple advanced cancers 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 B-cell adult acute lymphocytic leukemia B-cell lymphoma Balo concentric sclerosis Bannayan-Riley-Ruvalcaba syndrome Barrett's esophagus Burkitt lymphoma Carney complex Clouston syndrome Cockayne syndrome Cornelia de Lange syndrome Cowden syndrome Crohn's colitis Crohn's disease Cronkhite-Canada syndrome Dubowitz syndrome EEC syndrome Epstein-Barr virus infectious disease Evans' syndrome Ewing sarcoma Fanconi anemia complementation group A Fanconi anemia Foster-Kennedy syndrome Goodpasture syndrome Graves' disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma IgA glomerulonephritis Lafora disease Lambert-Eaton myasthenic syndrome Langerhans-cell histiocytosis Laron syndrome Li-Fraumeni syndrome 1 Li-Fraumeni syndrome Lynch syndrome MHC class II deficiency Marfan syndrome Marinesco-Sjogren syndrome Miller-Dieker lissencephaly syndrome Nijmegen breakage syndrome 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 with multiple lentigines 1 Noonan syndrome with multiple lentigines Noonan syndrome PTEN hamartoma tumor syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peutz-Jeghers syndrome Pick's disease Pitt-Hopkins syndrome Prader-Willi syndrome Proteus syndrome Reye syndrome Richter's syndrome Robinow syndrome Seckel syndrome Sezary's disease Shwachman-Diamond syndrome Silver-Russell syndrome Sjogren's syndrome Smith-McCort dysplasia T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Takayasu's arteritis VACTERL association X-linked Aarskog syndrome X-linked ichthyosis Zollinger-Ellison syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 achondroplasia acinar cell carcinoma acoustic neuroma acquired immunodeficiency syndrome acral lentiginous melanoma actinic keratosis acute interstitial pneumonia acute lymphoblastic leukemia acute megakaryocytic leukemia acute myeloid leukemia acute myocardial infarction acute pancreatitis acute promyelocytic leukemia adenocarcinoma in situ adenocarcinoma adenoid cystic carcinoma adenoma adenosarcoma adenosine deaminase deficiency adenosquamous carcinoma adenosquamous lung carcinoma adiposis dolorosa adrenal cortex cancer adrenal gland cancer adrenoleukodystrophy adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult cystic teratoma adult epithelioid sarcoma adult liposarcoma adult lymphoma adult medulloblastoma adult oligodendroglioma adult respiratory distress syndrome adult teratoma age related macular degeneration agnosia allergic asthma alternating hemiplegia of childhood amnestic disorder ampulla of Vater adenocarcinoma amyotrophic lateral sclerosis anal carcinoma anal margin carcinoma anal margin squamous cell carcinoma anal squamous cell carcinoma anaplastic astrocytoma androgen insensitivity syndrome anemia angioid streaks angiokeratoma angioma serpiginosum angiomatous meningioma angiomyolipoma angiosarcoma anisometropia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome ankylosing spondylitis anthracosilicosis antithrombin III deficiency anxiety disorder aortic aneurysm aortic valve insufficiency aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arteriovenous malformation arthritis arthropathy asbestosis asthma astroblastoma atherosclerosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atrophic gastritis attention deficit hyperactivity disorder atypical chronic myeloid leukemia, BCR-ABL1 negative autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial infectious disease bacterial sepsis basal cell carcinoma benign breast phyllodes tumor benign ependymoma benign meningioma benign mesothelioma bilateral breast cancer bile duct adenocarcinoma bile duct cancer bile duct carcinoma biliary atresia biliary tract cancer bladder carcinoma bladder neck obstruction bladder squamous cell carcinoma bladder urothelial carcinoma bone osteosarcoma botryoid rhabdomyosarcoma brain cancer brain disease brain stem infarction breast adenocarcinoma breast adenoid cystic carcinoma breast adenoma breast cancer breast carcinoma breast disease breast ductal carcinoma breast fibroadenoma breast fibroadenosis breast fibrocystic disease bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma buphthalmos cancer capillary disease capillary hemangioma carbamoyl phosphate synthetase I deficiency disease carcinoma of supraglottis carcinoma carcinosarcoma cardiomyopathy cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cavernous hemangioma celiac disease cellular ependymoma cellular schwannoma central nervous system cancer central nervous system disease central nervous system lymphoma cerebellum cancer cerebral artery occlusion cerebral cavernous malformation 1 cerebral cavernous malformation cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervical endometrioid adenocarcinoma cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood angiosarcoma childhood astrocytic tumor childhood cerebral astrocytoma childhood ependymoma childhood epithelioid sarcoma childhood kidney cell carcinoma childhood leukemia childhood liposarcoma childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma childhood ovarian germ cell tumor childhood pilocytic astrocytoma childhood testicular germ cell tumor cholangiocarcinoma cholangiolocellular carcinoma cholera chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma chordoid meningioma chordoma chorioangioma choriocarcinoma chromophobe renal cell carcinoma chromosome 10q23 deletion syndrome chromosome 17p13.1 deletion syndrome chronic eosinophilic leukemia chronic fatigue syndrome chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell adenocarcinoma clear cell meningioma clear cell renal cell carcinoma clear cell sarcoma clitoris cancer clubfoot colitis collagenous colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart communicating hydrocephalus communication disorder cone-rod dystrophy 2 cone-rod dystrophy congenital central hypoventilation syndrome congenital heart disease congenital hypothyroidism congenital ptosis congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cranial nerve disease cranial nerve palsy craniosynostosis cribriform carcinoma cutaneous fibrous histiocytoma cystadenoma cystic fibrosis cystic kidney disease cystic teratoma dedifferentiated liposarcoma degeneration of macula and posterior pole degenerative disc disease dental caries dentin caries depressive disorder dermatofibrosarcoma protuberans dermoid cyst of ovary developmental coordination disorder diabetes insipidus diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy diastrophic dysplasia differentiated thyroid gland carcinoma diffuse large B-cell lymphoma diffuse scleroderma dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health disease of metabolism distal arthrogryposis double outlet right ventricle duodenum cancer duodenum disease dysgerminoma of ovary dysgerminoma dysplastic nevus syndrome dysthymic disorder dystonia ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 elephantiasis embryoma embryonal cancer embryonal carcinoma embryonal rhabdomyosarcoma encephalitis encephalomyelitis endemic goiter endocrine gland cancer endodermal sinus tumor endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometrial serous adenocarcinoma endometrioid ovary carcinoma endometriosis of ovary endometriosis of uterus endometriosis endometritis endometrium carcinoma in situ endomyocardial fibrosis enophthalmos epidermal nevus epidermodysplasia verruciformis epilepsy episodic kinesigenic dyskinesia 1 epithelioid leiomyosarcoma epithelioid malignant peripheral nerve sheath tumor epithelioid sarcoma esophageal atresia esophageal cancer esophageal carcinoma esophageal disease esophagus adenocarcinoma esophagus small cell carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exanthem exfoliation syndrome exostosis extrahepatic bile duct carcinoma extramedullary plasmacytoma familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial meningioma familial periodic paralysis familial retinoblastoma female breast carcinoma female reproductive endometrioid cancer fetal alcohol spectrum disorder fibrillary astrocytoma fibrosarcoma fibrous meningioma filarial elephantiasis fissured tongue flat ductal epithelial atypia focal epilepsy follicular adenoma follicular lymphoma fragile X syndrome fundus albipunctatus galactosemia gallbladder cancer gallbladder carcinoma gallbladder disease gangliocytoma ganglioglioma ganglioneuroma gastric adenocarcinoma gastroenteritis gastroesophageal junction adenocarcinoma gastrointestinal stromal tumor gastrointestinal system cancer gemistocytic astrocytoma generalized anxiety disorder geographic tongue germ cell and embryonal cancer germ cell cancer germinoma gestational diabetes gestational trophoblastic neoplasm giant cell glioblastoma glaucoma glioblastoma gliomatosis cerebri gliosarcoma glomerulonephritis glomus tumor goiter granular cell carcinoma granular cell tumor granulomatosis with polyangiitis granulosa cell tumor gynecomastia head and neck cancer head and neck squamous cell carcinoma heart cancer hemangioblastoma hemangioma hemangiopericytoma hematologic cancer hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma hepatopulmonary syndrome hereditary breast ovarian cancer syndrome hereditary hemorrhagic telangiectasia hereditary lymphedema I hereditary lymphedema IA hereditary lymphedema hidradenoma high grade glioma histiocytoid hemangioma human immunodeficiency virus infectious disease hydrocephalus hydrophthalmos hypereosinophilic syndrome hyperglycemia hyperinsulinism hyperostosis hypertension hyperthyroidism hypertrophic cardiomyopathy hypertrophy of breast hypertropia hypoglycemia hypothyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease immunoglobulin alpha deficiency in situ carcinoma inclusion body myositis infant gynecomastia inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma influenza insulinoma intellectual disability intermediate coronary syndrome intermediate uveitis intestinal pseudo-obstruction intracranial aneurysm intracranial hypertension intrahepatic cholangiocarcinoma intramuscular hemangioma intraorbital meningioma intraventricular meningioma intrinsic asthma intussusception invasive ductal carcinoma inverted papilloma islet cell tumor juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma juvenile polyposis syndrome keratoconjunctivitis sicca keratosis follicularis kidney cancer kidney disease lactocele large intestine cancer laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer larynx squamous papilloma lateral meningocele syndrome learning disability leiomyoma leiomyosarcoma leprosy leptomeninges sarcoma leukemia leukocyte adhesion deficiency 1 leukocyte adhesion deficiency lingual-facial-buccal dyskinesia lipoma lipomatosis liposarcoma lissencephaly livedoid vasculitis liver angiosarcoma liver cancer liver carcinoma liver cirrhosis liver disease long QT syndrome low tension glaucoma luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lung squamous cell carcinoma lupus nephritis lymphadenitis lymphangioma lymphedema lymphoblastic lymphoma lymphocytic colitis lymphoid leukemia lymphoma lymphoplasmacyte-rich meningioma macrocephaly-autism syndrome macrocytic anemia macular degeneration major depressive disorder male breast cancer malignant adult ependymoma malignant astrocytoma malignant fibrous histiocytoma malignant mesothelioma malignant peripheral nerve sheath tumor malignant teratoma mature teratoma mechanical strabismus medulloblastoma medulloepithelioma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma melanotic neurilemmoma membranoproliferative glomerulonephritis meninges sarcoma meningioma meningothelial meningioma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly microcystic adenoma microcystic meningioma microglandular adenosis microinvasive gastric cancer microphthalmia microscopic colitis middle cerebral artery infarction migraine mitochondrial trifunctional protein deficiency mixed glioma mixed oligodendroglioma-astrocytoma mixed sleep apnea mongolian spot motor neuritis movement disease mucinous adenocarcinoma mucopolysaccharidosis IV multilocular clear cell renal cell carcinoma multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A multiple epiphyseal dysplasia multiple myeloma multiple symmetric lipomatosis mycosis fungoides myelitis myelodysplastic syndrome myeloid leukemia myocardial infarction myofibrillar myopathy myofibroma myopathy myopia myxedema myxoid leiomyosarcoma myxopapillary ependymoma narcolepsy nasopharynx carcinoma nephritis nephroblastoma nephrosis nervous system cancer nervous system disease neurilemmoma neuritis neuroblastoma neurodegenerative disease neuroectodermal tumor neuroendocrine carcinoma neuroendocrine tumor neurofibroma neurofibromatosis 1 neurofibromatosis neurofibrosarcoma neurohypophyseal diabetes insipidus neuropathy neurotic disorder nicotine dependence nodular prostate non-Hodgkin lymphoma non-congenital cyst of kidney nonepidermolytic palmoplantar keratoderma nonpapillary renal cell carcinoma nontoxic goiter nutmeg liver nutritional optic neuropathy obesity obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete constipation obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete exophthalmos obsolete extraskeletal myxoid chondrosarcoma obsolete intestinal pseudo-obstruction obsolete malignant histiocytosis obsolete melancholia obsolete multiple symmetrical lipomatosis obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive hydrocephalus obstructive sleep apnea oculocerebrorenal syndrome oculocutaneous albinism olfactory groove meningioma oligodendroglioma ophthalmoplegia optic nerve disease oral cavity cancer oral squamous cell carcinoma orbital disease osteoarthritis osteochondrodysplasia osteoglophonic dysplasia osteoporosis osteosarcoma otitis media ovarian cancer ovarian carcinoma ovarian cyst ovarian germ cell cancer ovarian germ cell teratoma ovarian mucinous neoplasm ovarian papillary neoplasm ovarian serous carcinoma oxyphilic adenoma palmoplantar keratosis pancreas disease pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm pancreatitis pancytopenia papillary adenocarcinoma papillary adenoma papillary carcinoma papillary ependymoma papillary renal cell carcinoma papillary transitional carcinoma papilloma paraganglioma paralytic ileus parapsoriasis parasagittal meningioma parathyroid adenoma parathyroid carcinoma partial motor epilepsy patent ductus arteriosus patent foramen ovale penis squamous cell carcinoma periarthritis perineurioma peripheral nerve sheath neoplasm peripheral nervous system disease peripheral nervous system neoplasm peritoneal carcinoma peritoneal mesothelioma persistent fetal circulation syndrome pheochromocytoma pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma placenta cancer placental insufficiency plasma cell leukemia plasma cell neoplasm plasmacytoma pleomorphic adenoma pleomorphic lipoma pleomorphic liposarcoma plexiform neurofibroma plexiform schwannoma polyarteritis nodosa polycystic ovary syndrome polycythemia vera polydactyly polyneuropathy polyp of corpus uteri porphyria cutanea tarda portal hypertension postinflammatory pulmonary fibrosis premature menopause primary cerebellar degeneration primary cutaneous T-cell non-Hodgkin lymphoma primary cutaneous amyloidosis primary immunodeficiency disease primary open angle glaucoma primary ovarian insufficiency primary pulmonary hypertension progressive muscular atrophy progressive supranuclear palsy prostate adenocarcinoma prostate cancer prostate carcinoma prostate disease prostatic adenoma protein C deficiency protein S deficiency protein-losing enteropathy protoplasmic astrocytoma psammomatous meningioma pseudotumor cerebri pseudoxanthoma elasticum psoriasis psychotic disorder pterygium ptosis pulmonary embolism pulmonary emphysema pulmonary fibrosis pulmonary sclerosing hemangioma pustulosis of palm and sole pyoureter rectal benign neoplasm rectal prolapse rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma respiratory failure reticulosarcoma retinal detachment retinitis pigmentosa 1 retinitis pigmentosa retinoblastoma retrograde amnesia rhabdomyosarcoma rheumatic fever rheumatoid arthritis salivary gland adenoid cystic carcinoma sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma scoliosis sebaceous adenocarcinoma sebaceous carcinoma seborrheic keratosis secondary Parkinson disease secondary hypertrophic osteoarthropathy secretory meningioma selective IgA deficiency disease seminoma senile angioma senile degeneration of brain sensorineural hearing loss serous cystadenocarcinoma severe combined immunodeficiency signet ring cell adenocarcinoma silent myocardial infarction silicosis situs inversus skin benign neoplasm skin cancer skin disease skin melanoma skin papilloma skin squamous cell carcinoma skin tag sleep apnea small intestine adenocarcinoma small intestine cancer small intestine carcinoma speech disorder spinal meningioma spinal muscular atrophy spindle cell sarcoma spindle cell thymoma sporadic breast cancer squamous cell carcinoma squamous cell neoplasm squamous cell papilloma squamous papillomatosis status epilepticus steatotic liver disease stomach cancer stomach carcinoma stomach disease strabismus subependymal giant cell astrocytoma substance abuse substance-related disorder substernal goiter superficial urinary bladder cancer supraglottis squamous cell carcinoma supratentorial primitive neuroectodermal tumor sweat gland cancer synovial sarcoma syringoma systemic lupus erythematosus systemic scleroderma tanycytic ependymoma tarsal-carpal coalition syndrome telangiectasis temporal arteritis tendinitis teratoma testicular cancer testicular germ cell cancer testis seminoma thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia thrombophlebitis thymic carcinoma thymoma thymus cancer thymus lymphoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyroiditis thyrotoxicosis tongue cancer tongue squamous cell carcinoma tonsil cancer transient cerebral ischemia transitional cell carcinoma transitional meningioma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trilateral retinoblastoma tuberous sclerosis 1 tuberous sclerosis 2 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 ulcerative colitis urinary bladder cancer uterine cancer uterine carcinosarcoma uterine corpus cancer uterine corpus sarcoma uterine fibroid uterus leiomyosarcoma uveal melanoma varicocele vascular disease vascular skin disease venous insufficiency verrucous carcinoma vertebrobasilar insufficiency vestibular schwannomatosis viral infectious disease visual epilepsy visual pathway disease von Hippel-Lindau disease vulva cancer vulva carcinoma xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
5730	prostaglandin D2 synthase	PTGDS Aliases: L-PGDS PGDS lipocalin-type prostaglandin D synthase	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 Axenfeld-Rieger syndrome Crohn's colitis Crohn's disease Fabry disease Graves' disease Guillain-Barre syndrome Loeffler syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome Parkinson's disease Pendred Syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acrodermatitis acute myocardial infarction acute promyelocytic leukemia adult lymphoma adult medulloblastoma allergic asthma alopecia anaplastic astrocytoma androgenic alopecia angiomatous meningioma aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atopic dermatitis attention deficit hyperactivity disorder autoimmune thyroiditis benign meningioma bipolar disorder brain cancer breast cancer breast carcinoma bronchiolitis bronchitis cancer carcinoma cardiovascular system disease carotid artery disease central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cerebrotendinous xanthomatosis childhood cerebral astrocytoma childhood lymphoma childhood medulloblastoma cholestasis chronic ethmoiditis chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniosynostosis cryptorchidism depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma disease of mental health dry eye syndrome dyshormonogenic goiter dysthymic disorder egg allergy embryoma encephalitis encephalomyelitis enterocele eosinophilic pneumonia essential hypertension fibrillary astrocytoma fibrous meningioma gastritis gastroenteritis gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis goiter heart disease high grade glioma hypereosinophilic syndrome hyperglycemia hyperinsulinism hypertension hyperthyroidism hypertrichosis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer intraorbital meningioma intraventricular meningioma intrinsic asthma juvenile pilocytic astrocytoma kidney disease large congenital melanocytic nevus large intestine cancer late onset Parkinson's disease lipid storage disease liver cirrhosis lung benign neoplasm lupus nephritis lymphoma lymphoplasmacyte-rich meningioma major depressive disorder malignant astrocytoma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma meningothelial meningioma microcystic meningioma myelitis myocardial infarction nephritis nephrosclerosis nephrosis neurofibromatosis neurotic disorder nontoxic goiter nutmeg liver obesity obsolete dyspepsia obsolete melancholia obsolete ymphosarcoma obstructive sleep apnea olfactory groove meningioma open-angle glaucoma osteoarthritis ovarian cancer ovarian carcinoma pancytopenia papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma periodontitis pigment dispersion syndrome pilocytic astrocytoma pituitary adenoma pneumonia post-traumatic stress disorder pre-eclampsia prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma psychotic disorder pyoureter respiratory syncytial virus infectious disease rhinitis sarcomatoid carcinoma schizophrenia secretory meningioma sensorineural hearing loss silent myocardial infarction sinusitis situs inversus skin melanoma skin squamous cell carcinoma spinal meningioma squamous cell carcinoma stomach cancer stomach carcinoma stuttering subependymal giant cell astrocytoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transitional meningioma tuberous sclerosis type 2 diabetes mellitus ulcerative colitis ureteral obstruction vestibular schwannomatosis xerophthalmia

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