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 **26 - 50** of **1582** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
131	alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide	ADH7 Aliases: ADH-4	Homo sapiens (human)	Leber congenital amaurosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma alcohol dependence alcohol use disorder aniridia cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma cone-rod dystrophy cribriform carcinoma embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma fundus albipunctatus fundus dystrophy granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer lung cancer lung non-small cell carcinoma nicotine dependence nonpapillary renal cell carcinoma papillary renal cell carcinoma pharynx cancer renal carcinoma renal cell carcinoma retinitis pigmentosa sarcomatoid renal cell carcinoma squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma substance abuse substance-related disorder tongue squamous cell carcinoma tubular adenocarcinoma uterine corpus cancer
141	ADP-ribosylarginine hydrolase	ADPRH Aliases: ARH1 [Protein ADP-ribosylarginine] hydrolase	Homo sapiens (human)	autosomal recessive hypercholesterolemia cancer cardiomyopathy cholera endomyocardial fibrosis familial hypercholesterolemia hypertrophic cardiomyopathy ovarian cancer ovarian carcinoma
142	poly(ADP-ribose) polymerase 1	PARP1 Aliases: ARTD1 PARP PARS Poly-PARP	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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Balo concentric sclerosis Barrett's esophagus Burkitt lymphoma Chagas disease Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Down syndrome Dubowitz syndrome Duchenne muscular dystrophy Ewing sarcoma Fanconi anemia complementation group A Fanconi anemia Gilles de la Tourette syndrome Graves' disease Hailey-Hailey disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Keshan disease Langerhans-cell histiocytosis Lynch syndrome MHC class II deficiency Marinesco-Sjogren syndrome Meniere's disease 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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Patau syndrome Peyronie's disease Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Sertoli cell-only syndrome Sezary's disease Silver-Russell syndrome Stevens-Johnson syndrome T-cell acute lymphoblastic leukemia Treacher Collins syndrome Warsaw breakage syndrome Weissenbacher-Zweymuller syndrome Werner syndrome X-linked Aarskog syndrome X-linked ichthyosis Y-linked spermatogenic failure 1 Zika fever abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acrodermatitis acute biphenotypic leukemia acute leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adenosine deaminase deficiency adrenal gland cancer adrenoleukodystrophy adult fibrosarcoma adult medulloblastoma age related macular degeneration agranulocytosis alexia allergic asthma allergic rhinitis alopecia alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis anaplastic astrocytoma androgen insensitivity syndrome androgenic alopecia anemia anthrax disease anxiety disorder arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia with oculomotor apraxia type 1 atelosteogenesis atherosclerosis atrial fibrillation autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 Robinow syndrome 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 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 meningitis bacterial sepsis balanitis xerotica obliterans benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder urothelial carcinoma bone marrow cancer bone osteosarcoma borna disease botryoid rhabdomyosarcoma brachydactyly type B1 brachydactyly brain cancer brain ischemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood astrocytic tumor childhood cerebral astrocytoma childhood germ cell cancer childhood leukemia childhood medulloblastoma childhood osteosarcoma childhood pilocytic astrocytoma cholangiocarcinoma chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma chordoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic interstitial cystitis chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital muscular dystrophy congestive heart failure corneal disease coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cutis laxa deafness-dystonia-optic neuronopathy syndrome dedifferentiated liposarcoma degeneration of macula and posterior pole denture stomatitis depressive disorder dermatitis diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy differentiated thyroid gland carcinoma diffuse large B-cell lymphoma disease of metabolism dissociative amnesia distal arthrogryposis distal myopathy duodenum cancer dyslexia dysplastic nevus syndrome dysthymic disorder embryoma embryonal cancer embryonal rhabdomyosarcoma encephalitis encephalomyelitis endocrine exophthalmos endolymphatic hydrops endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy epithelioid leiomyosarcoma epithelioid malignant peripheral nerve sheath tumor epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus small cell carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia eye disease facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familiar ovarian carcinoma fibrillary astrocytoma fibrosarcoma follicular adenoma frozen shoulder gastroenteritis gastrointestinal system disease gemistocytic astrocytoma generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glycogen storage disease II goiter granular cell carcinoma granular corneal dystrophy 2 head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematologic cancer hepatitis A hepatitis B hepatitis hepatoblastoma hepatocellular carcinoma hereditary breast ovarian cancer syndrome hidradenoma high grade glioma human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperglycemia hypersensitivity vasculitis hypertension hyperthyroidism hypertrophic cardiomyopathy hypoparathyroidism-deafness-renal disease syndrome idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma intellectual disability intermediate coronary syndrome interstitial cystitis intestinal disease intracranial aneurysm intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma keratoconus kidney disease kidney failure large cell medulloblastoma large intestine cancer laryngeal squamous cell carcinoma learning disability leiomyoma leiomyosarcoma leukemia leukopenia limb-girdle muscular dystrophy liposarcoma liver cancer liver carcinoma liver cirrhosis luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma lupus erythematosus lymphangioleiomyomatosis lymphoma macrocytic anemia macular degeneration major depressive disorder mal de Meleda malignant astrocytoma malignant mesothelioma malignant peripheral nerve sheath tumor malignant pleural mesothelioma mantle cell lymphoma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningitis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia middle cerebral artery infarction mitochondrial DNA depletion syndrome mixed glioma monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis muscular dystrophy myelitis myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myxoid leiomyosarcoma narcolepsy nasopharynx carcinoma nephritis nephroblastoma nephrosis nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neurofibrosarcoma neuronal ceroid lipofuscinosis 1 neurotic disorder neutropenia nodular nonsuppurative panniculitis non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood 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 precursor B lymphoblastic lymphoma/leukemia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy oligospermia osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panniculitis papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma paraganglioma parapsoriasis patent ductus arteriosus perinatal necrotizing enterocolitis peritoneal carcinoma pheochromocytoma phobic disorder phototoxic dermatitis pilocytic astrocytoma pleomorphic liposarcoma pneumonia premature menopause primary cerebellar degeneration primary cutaneous amyloidosis primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension proctitis progeria progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma prune belly syndrome psoriasis pulmonary emphysema pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma respiratory failure restrictive dermopathy reticulosarcoma retinal disease retinitis retrograde amnesia rhabdomyosarcoma rheumatic fever rheumatoid arthritis rippling muscle disease 2 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma secondary Parkinson disease senile cataract severe combined immunodeficiency severe congenital neutropenia silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag small intestine cancer spindle cell sarcoma sporadic breast cancer squamous cell carcinoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma stomatitis subependymal giant cell astrocytoma syringoma systemic lupus erythematosus systemic scleroderma teratocarcinoma thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transient cerebral ischemia trigeminal neuralgia trypanosomiasis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ulcerative stomatitis uremia ureteral obstruction urinary bladder cancer uterine corpus cancer uterine fibroid uveal melanoma vasomotor rhinitis vertebrobasilar insufficiency viral infectious disease viral meningitis vitiligo xeroderma pigmentosum group A
143	poly(ADP-ribose) polymerase family member 4	PARP4 Aliases: ARTD4 VAULT3 VPARP VWA5C p193 vault poly(ADP-ribose) polymerase von Willebrand factor A domain containing 5C	Homo sapiens (human)	Down syndrome breast cancer breast carcinoma cancer central nervous system lymphoma childhood leukemia colon cancer colonic benign neoplasm colorectal cancer embryoma esophagus squamous cell carcinoma goiter intracranial hypertension large intestine cancer leukemia lymphoma obsolete ymphosarcoma pancreatic cancer pancreatic carcinoma pseudotumor cerebri thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease
155	adrenoceptor beta 3	ADRB3	Homo sapiens (human)	Alzheimer's disease colitis congestive heart failure coronary artery disease cystic fibrosis diabetic retinopathy dilated cardiomyopathy 1H endometrial cancer gout hypertension metabolic dysfunction-associated steatotic liver disease obesity polycystic ovary syndrome rheumatoid arthritis type 2 diabetes mellitus
175	aspartylglucosaminidase	AGA Aliases: ASRG N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase glycosylasparaginase	Homo sapiens (human)	Clostridium difficile colitis Down syndrome Fabry disease Klippel-Feil syndrome Laron syndrome abdominal obesity-metabolic syndrome 1 achalasia achondroplasia acne acrodermatitis agranulocytosis alcoholic hepatitis allergic bronchopulmonary aspergillosis alopecia androgenic alopecia arthritis arthropathy aspartylglucosaminuria attention deficit hyperactivity disorder cancer cataract celiac disease cerebral degeneration cervical squamous cell carcinoma cholecystitis chylomicron retention disease clubfoot common wart congenital disorder of glycosylation craniosynostosis dental caries dentin caries dermatitis herpetiformis diabetes mellitus diabetic ketoacidosis diarrhea dystonia encephalitis encephalomyelitis enterocele eosinophilic esophagitis epilepsy esophageal disease familial isolated hypoparathyroidism fucosidosis functional diarrhea gestational diabetes gingival hypertrophy gingival overgrowth goiter hepatitis C hepatocellular carcinoma hypoparathyroidism immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease influenza inguinal hernia intellectual disability irritable bowel syndrome learning disability lingual-facial-buccal dyskinesia lipid storage disease livedoid vasculitis liver cancer liver cirrhosis lupus nephritis lysosomal storage disease megaesophagus microcephaly mitral valve insufficiency mitral valve prolapse mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple sclerosis myelitis neurocirculatory asthenia neutropenia obsolete dyspepsia obsolete type 1 diabetes mellitus 9 omphalocele otitis media peroxisome biogenesis disorder 10A placental insufficiency primary sclerosing cholangitis schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis scoliosis selective IgA deficiency disease severe congenital neutropenia skeletal tuberculosis speech disorder spondylolisthesis spondylolysis stomach cancer stomach carcinoma stomach disease thyroid gland disease tropical sprue tuberculosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis umbilical hernia vascular skin disease visual epilepsy
176	aggrecan	ACAN Aliases: CSPGCP aggrecan proteoglycan	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Lyme disease Marfan syndrome SADDAN Silverman-Handmaker type dyssegmental dysplasia Werner syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia actinic keratosis amyloidosis anthracosilicosis aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis atherosclerosis autism spectrum disorder autistic disorder 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 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 bagassosis bicuspid aortic valve disease bone disease cancer cardiovascular system disease carpal tunnel syndrome cartilage disease cerebral infarction cerebrovascular disease cherubism chondroblastoma chondromalacia chondrosarcoma chordoma chorioamnionitis chronic interstitial cystitis ciliary body disease colon cancer colonic benign neoplasm colorectal cancer congestive heart failure connective tissue disease coronary artery disease degenerative disc disease dental fluorosis developmental and epileptic encephalopathy 39 diabetic ketoacidosis distal myopathy enterocele epithelioid sarcoma exostosis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy heart disease hepatocellular carcinoma hereditary multiple exostoses hypochondroplasia hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease infantile myofibromatosis interstitial cystitis iris disease juvenile rheumatoid arthritis large intestine cancer laryngeal carcinoma laryngeal disease larynx cancer limb-girdle muscular dystrophy lipoma liver cancer mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia multiple sclerosis multiple symmetric lipomatosis muscular dystrophy neurogenic arthropathy nicotine dependence obesity obsessive-compulsive disorder obsessive-compulsive personality disorder 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 type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoarthritis osteochondritis dissecans osteochondrodysplasia osteogenesis imperfecta panuveitis periarthritis peroxisome biogenesis disorder 5A pleomorphic lipoma pneumoconiosis polycystic ovary syndrome progeria progressive pseudorheumatoid arthropathy of childhood prune belly syndrome pseudoachondroplasia reticulate acropigmentation of Kitamura rheumatoid arthritis sarcoma schizophrenia scoliosis septic arthritis siderosis situs inversus spindle cell sarcoma spondylitis spondyloarthropathy spondyloepiphyseal dysplasia Kimberley type spondyloepiphyseal dysplasia congenita spondylosis status epilepticus tendinitis tracheal disease tropical spastic paraparesis 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 uveitis
178	amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase	AGL Aliases: GDE glycogen debranching enzyme glycogen storage disease type III	Homo sapiens (human)	Duchenne muscular dystrophy Laron syndrome achondroplasia acute promyelocytic leukemia atrichia with papular lesions 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 bladder carcinoma cancer cardiomyopathy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital muscular dystrophy cystinuria disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hyperlipidemia familial partial lipodystrophy familial periodic paralysis galactosemia giardiasis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis C hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy liver cirrhosis lung cancer lung non-small cell carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy nodular nonsuppurative panniculitis 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 panniculitis primary immunodeficiency disease rippling muscle disease 2 uremia urinary bladder cancer
189	alanine--glyoxylate aminotransferase	AGXT Aliases: AGT AGT1 AGXT1 L-alanine: glyoxylate aminotransferase 1 PH1 SPT Ser-PyrAT TLH6 glycolicaciduria oxalosis I primary hyperoxaluria type 1	Homo sapiens (human)	Foster-Kennedy syndrome Laurin-Sandrow syndrome Raynaud disease Senior-Loken syndrome acrodermatitis allergic asthma allergic rhinitis alopecia androgenic alopecia anemia angioedema arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrioventricular block autosomal recessive osteopetrosis 7 beriberi calcinosis calcium metabolism disease cancer carcinoma cerebral infarction cerebrovascular disease chronic kidney disease coronary artery disease cystinuria dermatitis disease of metabolism distal arthrogryposis eosinophilic esophagitis essential hypertension extraosseous Ewing sarcoma extraosseous Ewings sarcoma-primitive neuroepithelial tumor galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory neuropathy high grade glioma hypercalcemia hypertension inherited metabolic disorder intermittent claudication intrinsic asthma kidney failure lactic acidosis liver cancer macrocytic anemia middle cerebral artery infarction nephrocalcinosis nephrolithiasis nephronophthisis neuropathy optic atrophy optic nerve disease osteopetrosis osteosclerosis parasitic helminthiasis infectious disease peripheral nervous system disease peripheral vascular disease phosphorus metabolism disease primary hyperoxaluria type 1 primary hyperoxaluria retinal disease retinitis riboflavin deficiency sarcomatoid carcinoma sensory peripheral neuropathy skin disease subacute bacterial endocarditis thiamine deficiency disease uremia uric acid nephrolithiasis urinary tract obstruction urticaria vasomotor rhinitis visual pathway disease
202	crystallin beta-gamma domain containing 1	CRYBG1 Aliases: suppression of tumorigenicity 4	Homo sapiens (human)	allergic asthma asthma cancer intrinsic asthma melanoma multiple myeloma patent ductus arteriosus prostate cancer prostate carcinoma skin melanoma
207	AKT serine/threonine kinase 1	AKT1	Homo sapiens (human)	Cowden syndrome 6 Parkinson's disease Proteus syndrome alcohol use disorder autosomal recessive polycystic kidney disease bipolar disorder brain ischemia breast cancer cancer chronic myeloid leukemia colon cancer colorectal cancer diabetic retinopathy esophageal cancer esophagus squamous cell carcinoma hepatocellular carcinoma hypertension idiopathic pulmonary fibrosis impotence in situ carcinoma intermediate coronary syndrome invasive ductal carcinoma lung non-small cell carcinoma malignant astrocytoma myocardial infarction ovarian cancer pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paraplegia prostate adenocarcinoma prostate cancer pulmonary tuberculosis renal cell carcinoma schizophrenia type 2 diabetes mellitus ureteral obstruction urinary bladder cancer vulva cancer
208	AKT serine/threonine kinase 2	AKT2	Homo sapiens (human)	Parkinson's disease alcohol use disorder cancer colorectal cancer endometrial cancer hepatocellular carcinoma high grade glioma hypertension hypoglycemia hypoinsulinemic hypoglycemia with hemihypertrophy ischemia malignant astrocytoma obesity ovarian carcinoma polycystic ovary syndrome prostate adenocarcinoma prostate cancer prostate carcinoma type 2 diabetes mellitus
217	aldehyde dehydrogenase 2 family member	ALDH2	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 Cockayne syndrome Fanconi anemia complementation group A Fanconi anemia Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Pick's disease Prinzmetal angina Reye syndrome Weissenbacher-Zweymuller syndrome Wernicke-Korsakoff syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adrenoleukodystrophy agnosia agranulocytosis alcohol dependence alcohol use disorder alcoholic cardiomyopathy alcoholic hepatitis alcoholic liver cirrhosis alcoholic neuropathy alcoholic pancreatitis allergic asthma amnestic disorder anemia antisocial personality disorder anxiety disorder aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation atrophic gastritis atrophy of testis attention deficit hyperactivity disorder autistic disorder bacterial sepsis bipolar disorder bladder carcinoma brain infarction brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease carotid artery disease central sleep apnea cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease chronic interstitial cystitis chronic kidney disease chronic obstructive pulmonary disease cleidocranial dysplasia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma conduct disorder congenital heart disease 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 artery vasospasm coronary stenosis coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic retinopathy disease of mental health dissociative amnesia dysthymic disorder embryoma endocrine exophthalmos endomyocardial fibrosis esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension female breast carcinoma follicular adenoma gallbladder disease generalized anxiety disorder glucose intolerance granular cell carcinoma granuloma annulare head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis type 1 hemochromatosis hemorrhoid hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma heroin dependence humeroradial synostosis hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hyperuricemia hypopharynx cancer interstitial cystitis intrinsic asthma kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer late onset Parkinson's disease leukopenia liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lymphopenia macrocytic anemia major depressive disorder male infertility marasmus megaconial type congenital muscular dystrophy melancholic depression metabolic dysfunction-associated steatotic liver disease microcystic adenoma middle cerebral artery infarction mitochondrial metabolism disease mitochondrial myopathy morphine dependence muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myocardial infarction nasopharynx carcinoma nemaline myopathy neurodegenerative disease neurotic disorder neutropenia nutmeg liver nutrition disease obesity obsolete asthenopia obsolete melancholia obsolete type 1 diabetes mellitus 9 opiate dependence oral mucosa leukoplakia oropharynx cancer osteonecrosis osteoporosis ovarian cancer ovarian carcinoma pancreas disease pancreatic cancer pancreatic carcinoma pancreatitis pancytopenia papillary adenoma parapsoriasis perinatal necrotizing enterocolitis personality disorder phobic disorder placental insufficiency prediabetes syndrome primary pulmonary hypertension protein-energy malnutrition prune belly syndrome psoriasis psychotic disorder pustulosis of palm and sole radioulnar synostosis rectal benign neoplasm rectum adenocarcinoma rectum cancer retinal disease retinitis rigid spine muscular dystrophy 1 sarcomatoid carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sick sinus syndrome silent myocardial infarction situs inversus speech-language disorder-1 squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder tetralogy of Fallot tongue squamous cell carcinoma tracheal disease tuberculosis 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 urinary bladder cancer vascular disease viral infectious disease white sponge nevus
218	aldehyde dehydrogenase 3 family member A1	ALDH3A1 Aliases: aldehyde dehydrogenase, dimeric NADP-preferring	Homo sapiens (human)	Sjogren-Larsson syndrome allergic asthma arteriosclerosis asthma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cataract colon cancer colon carcinoma colonic benign neoplasm colorectal cancer depressive disorder dysthymic disorder embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma intrinsic asthma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression melanoma mucoepidermoid carcinoma neurotic disorder obsolete congenital ichthyosiform erythroderma obsolete melancholia placental insufficiency pleomorphic adenoma prostate cancer prostate carcinoma pterygium sarcomatoid carcinoma schizophrenia skin melanoma stomach cancer
219	aldehyde dehydrogenase 1 family member B1	ALDH1B1 Aliases: ALDHX	Homo sapiens (human)	adenocarcinoma adenoma alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis bone osteosarcoma breast cancer breast carcinoma cancer childhood osteosarcoma cholestasis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma gallbladder disease granular cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer liver cirrhosis liver disease lung cancer lung non-small cell carcinoma obesity osteosarcoma pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma steatotic liver disease succinic semialdehyde dehydrogenase deficiency tubular adenocarcinoma
220	aldehyde dehydrogenase 1 family member A3	ALDH1A3 Aliases: RALDH3 retinaldehyde dehydrogenase 3	Homo sapiens (human)	Marfan syndrome Meckel syndrome 1 Meckel syndrome acoustic neuroma adenocarcinoma adenoma angiomatous meningioma autism spectrum disorder autistic disorder benign meningioma bilateral optic nerve hypoplasia bile duct adenocarcinoma bile duct carcinoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral convexity meningioma choanal atresia cholangiocarcinoma clear cell meningioma coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma distal arthrogryposis embryoma familial adenomatous polyposis 1 familial adenomatous polyposis fibrous meningioma gallbladder cancer gallbladder carcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma high grade glioma intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor isolated microphthalmia 1 isolated microphthalmia 2 isolated microphthalmia 3 isolated microphthalmia 4 isolated microphthalmia 6 isolated microphthalmia 7 isolated microphthalmia 8 large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma malignant pleural mesothelioma melanoma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma neuroblastoma olfactory groove meningioma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma pituitary adenoma polycystic ovary syndrome prostate cancer prostate carcinoma psammomatous meningioma rheumatoid arthritis secretory meningioma seminoma situs inversus skin melanoma spinal meningioma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testicular germ cell cancer thyroid gland papillary carcinoma transitional meningioma transthyretin amyloidosis tuberous sclerosis tubular adenocarcinoma
221	aldehyde dehydrogenase 3 family member B1	ALDH3B1 Aliases: aldehyde dehydrogenase 3B1 aldehyde dehydrogenase 7	Homo sapiens (human)	Sjogren-Larsson syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma delusional disorder papillary renal cell carcinoma paranoid schizophrenia renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
222	aldehyde dehydrogenase 3 family member B2	ALDH3B2	Homo sapiens (human)	Sjogren-Larsson syndrome alcohol dependence alcohol use disorder
223	aldehyde dehydrogenase 9 family member A1	ALDH9A1 Aliases: E3	Homo sapiens (human)	cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hemolytic anemia kidney cancer nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
224	aldehyde dehydrogenase 3 family member A2	ALDH3A2 Aliases: FALDH fatty aldehyde dehydrogenase	Homo sapiens (human)	Cogan syndrome Laron syndrome Senior-Loken syndrome Sjogren-Larsson syndrome X-linked adrenal hypoplasia congenita achondroplasia acquired hyperkeratosis acrodermatitis age related macular degeneration allergic asthma alternating hemiplegia of childhood angioedema asthma autonomic neuropathy autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis central nervous system disease cerebral palsy cone-rod dystrophy corneal disease degeneration of macula and posterior pole dental enamel hypoplasia dermatitis diabetic ketoacidosis epilepsy ethylmalonic encephalopathy fundus albipunctatus granuloma annulare hepatitis B ichthyosis intellectual disability intrinsic asthma keratoconus keratosis follicularis learning disability lipid metabolism disorder localized scleroderma locked-in syndrome lung cancer lung non-small cell carcinoma macular degeneration microcephaly mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia myopia nephronophthisis nervous system disease normal pressure hydrocephalus obsolete asthenopia obsolete congenital ichthyosiform erythroderma obsolete type 1 diabetes mellitus 9 osteochondrodysplasia papilloma paraplegia pseudoxanthoma elasticum quadriplegia retinal disease retinitis pigmentosa retinitis scleroderma scoliosis spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy squamous cell papilloma squamous papillomatosis systemic scleroderma 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 urticaria visual epilepsy
226	aldolase, fructose-bisphosphate A	ALDOA	Homo sapiens (human)	Laron syndrome abdominal obesity-metabolic syndrome 1 achondroplasia arthritis arthropathy bile duct adenocarcinoma bile duct cancer bile duct carcinoma bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma childhood osteosarcoma cholangiocarcinoma cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital hemolytic anemia congenital ptosis coronary artery disease cystinuria embryoma favism galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemoglobinopathy hemolytic anemia hepatocellular carcinoma hereditary elliptocytosis intrahepatic cholangiocarcinoma invasive ductal carcinoma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma nonpapillary renal cell carcinoma normocytic anemia obstructive sleep apnea osteoarthritis osteosarcoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma ptosis renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma spondyloarthropathy spondylosis
229	aldolase, fructose-bisphosphate B	ALDOB	Homo sapiens (human)	Gilbert syndrome autoimmune hepatitis bilirubin metabolic disorder blood coagulation disease cancer cataract chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma diabetes mellitus diarrhea epilepsy hepatitis hepatocellular carcinoma hereditary fructose intolerance syndrome hyperglycemia hyperuricemia hypoglycemia hypophosphatemia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability kwashiorkor lactic acidosis large intestine cancer learning disability liver benign neoplasm liver cancer liver cirrhosis marasmus nonpapillary renal cell carcinoma nutrition disease obesity obsolete constipation obsolete inherited blood coagulation disease papillary renal cell carcinoma peritonitis protein-energy malnutrition rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal tubular acidosis sarcomatoid renal cell carcinoma steatotic liver disease stomach cancer stomach carcinoma type 2 diabetes mellitus ulcerative colitis visual epilepsy
230	aldolase, fructose-bisphosphate C	ALDOC	Homo sapiens (human)	autoimmune disease of the nervous system borna disease hepatoblastoma hepatocellular carcinoma liver cancer neuroblastoma schizophrenia
231	aldo-keto reductase family 1 member B	AKR1B1 Aliases: AR aldose reductase	Homo sapiens (human)	46,XY sex reversal Alzheimer's disease Clostridium difficile colitis Cockayne syndrome Leber hereditary optic neuropathy Schwartz-Jampel syndrome 1 Stevens-Johnson syndrome X-linked adrenal hypoplasia congenita abdominal obesity-metabolic syndrome 1 acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland hyperfunction adrenocortical carcinoma adrenoleukodystrophy adult acute lymphocytic leukemia adult fibrosarcoma adult respiratory distress syndrome alcoholic hepatitis alcoholic liver cirrhosis allergic asthma allergic disease allergic rhinitis anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative breast adenocarcinoma breast cancer breast carcinoma in situ breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease carotid artery disease cataract central nervous system cancer cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood cerebral astrocytoma chronic kidney disease chronic monocytic leukemia ciliary body disease colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease cystinuria deafness-dystonia-optic neuronopathy syndrome diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy embryoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis essential hypertension familial hyperlipidemia fibrillary astrocytoma fibrosarcoma follicular adenoma frozen shoulder galactokinase deficiency galactosemia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease heart disease hemochromatosis type 1 hemochromatosis hepatitis C hepatobiliary disease hepatoblastoma hepatocellular carcinoma hereditary lymphedema I hereditary lymphedema IA hereditary lymphedema herpes simplex high grade glioma hyperglycemia hypertension hypokalemia intrinsic asthma iris disease irritable bowel syndrome juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure large intestine cancer leiomyoma leukopenia liver cancer liver cirrhosis low tension glaucoma lung cancer lung carcinoma lung small cell carcinoma lymphedema lymphoid leukemia malignant astrocytoma membranous glomerulonephritis microcystic adenoma mixed glioma mongolian spot multiple epiphyseal dysplasia multiple sclerosis myeloid leukemia nephritis nephrosis neuroblastoma neurocirculatory asthenia neuropathy newborn respiratory distress syndrome nutmeg liver nutritional optic neuropathy obesity obsolete Cushing's syndrome obsolete type 1 diabetes mellitus 9 ocular hypertension open-angle glaucoma osteochondrodysplasia osteoporosis pancreatic cancer pancreatic carcinoma panuveitis papillary adenoma peripheral nervous system disease pilocytic astrocytoma placental insufficiency pneumonia polycystic ovary syndrome polyneuropathy primary hyperaldosteronism primary open angle glaucoma proliferative diabetic retinopathy protoplasmic astrocytoma pseudoxanthoma elasticum pyoureter retinal disease retinitis sarcomatoid carcinoma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma temporal arteritis tuberculosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uremia uterine corpus cancer uterine fibroid uveitis vascular disease vasculitis vasomotor rhinitis
239	arachidonate 12-lipoxygenase, 12S type	ALOX12 Aliases: 12S-LOX Arachidonate 12-lipoxygenase, 12S-type platelet 12-LOX	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 Becker muscular dystrophy Crohn's disease Duchenne muscular dystrophy Pick's disease Reye syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult lymphoma amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 bacterial sepsis benign mesothelioma bipolar disorder bone marrow cancer breast cancer breast carcinoma cancer cardiovascular system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood lymphoma chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy congenital toxoplasmosis congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis distal myopathy embryoma endomyocardial fibrosis esophagus squamous cell carcinoma essential hypertension facioscapulohumeral muscular dystrophy follicular adenoma gastroenteritis glomerulonephritis granular cell carcinoma heart disease hepatocellular carcinoma hypertension ileitis ileocolitis juvenile rheumatoid arthritis kidney disease kidney hypertrophy large intestine cancer leech infestation limb-girdle muscular dystrophy liver cancer lymphoma malignant mesothelioma melanoma microcystic adenoma muscular dystrophy myeloproliferative neoplasm myiasis myocardial infarction nephritis nephrosis neuroblastoma neurodegenerative disease neuropathy nodular prostate nonpapillary renal cell carcinoma obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy osteoporosis ovarian cancer ovarian carcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis peripheral nervous system disease pneumonia post-traumatic stress disorder prostate cancer prostate carcinoma prostatic adenoma psoriasis pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal disease retinitis rheumatoid arthritis sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis silent myocardial infarction skin benign neoplasm skin cancer skin disease skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma toxoplasmosis tuberculosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis urinary bladder cancer vitelliform macular dystrophy vitiligo

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