GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **9751 - 9775** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
445	argininosuccinate synthase 1	ASS1
444	aspartate beta-hydroxylase	ASPH
434	agouti signaling protein	ASIP
433	asialoglycoprotein receptor 2	ASGR2 CLEC4H2
432	asialoglycoprotein receptor 1	ASGR1 CLEC4H1	acrodermatitis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease dermatitis hepatocellular carcinoma liver cancer nutmeg liver thrombocytopenia
427	N-acylsphingosine amidohydrolase 1	ASAH1 AC ACDase FLJ21558 PHP32 acid ceramidase acylsphingosine deacylase	Albright's hereditary osteodystrophy 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 Beckwith-Wiedemann syndrome Bell's palsy CLOVES syndrome Erdheim-Chester disease Ewing sarcoma Fabry disease Farber lipogranulomatosis IGSF1 deficiency syndrome Krabbe disease Laron syndrome Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Perlman syndrome Pick's disease Reye syndrome Sotos syndrome Turner syndrome Unverricht-Lundborg syndrome Usher syndrome type 2 Usher syndrome type 3 Usher syndrome Wolman disease achondroplasia acute monocytic leukemia acute myeloid leukemia adult medulloblastoma agnosia amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy atrial fibrillation autosomal recessive distal hereditary motor neuronopathy 1 benign ependymoma benign epilepsy with centrotemporal spikes blepharospasm brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cellular ependymoma cerebral degeneration childhood ependymoma childhood medulloblastoma chylomicron retention disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined saposin deficiency congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus cystic fibrosis dementia dentatorubral-pallidoluysian atrophy developmental coordination disorder dissociated nystagmus early myoclonic encephalopathy embryoma epilepsy facial nerve disease facial paralysis focal hand dystonia gastroenteritis gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gonadal dysgenesis head and neck cancer head and neck squamous cell carcinoma herpes simplex high grade glioma hyperglycemia hypoparathyroidism hypothyroidism idiopathic generalized epilepsy idiopathic interstitial pneumonia ileitis ileocolitis intellectual disability invasive ductal carcinoma large intestine cancer lateral sclerosis learning disability lipid storage disease lung benign neoplasm lung cancer lung carcinoma lysosomal storage disease measles medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma motor neuron disease myxedema myxopapillary ependymoma neonatal diabetes neurodegenerative disease neuroectodermal tumor obesity ocular melanoma osteoporosis pancreatic cancer pancreatic carcinoma papillary carcinoma papillary ependymoma pathologic nystagmus pneumonia postinflammatory pulmonary fibrosis progressive muscular atrophy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy prostate cancer prostate carcinoma pseudohypoparathyroidism type IB pseudohypoparathyroidism pseudopseudohypoparathyroidism pulmonary fibrosis rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent corneal erosion retinitis pigmentosa-deafness syndrome retinoblastoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis sensorineural hearing loss skin melanoma speech disorder sphingolipidosis spinal muscular atrophy with progressive myoclonic epilepsy spinal muscular atrophy spontaneous ocular nystagmus tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma transient neonatal diabetes mellitus viral infectious disease
420	ADP-ribosyltransferase 4 (inactive) (Dombrock blood group)	ART4 ARTC4 CD297 DOK1 NAD(+)--protein-arginine ADP-ribosyltransferase 4	carotid artery thrombosis carotid stenosis conjunctivitis
419	ADP-ribosyltransferase 3 (inactive)	ART3 ARTC3	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
417	ADP-ribosyltransferase 1	ART1 ART2 ARTC1 CD296	arthritis arthropathy astigmatism cancer central nervous system cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liver cancer mixed glioma nasopharynx carcinoma nephritis pancreatic cancer pancreatic carcinoma squamous cell carcinoma tongue squamous cell carcinoma tuberculosis
416	arylsulfatase F	ARSF ASF	Kuhnt-Junius degeneration breast cancer cancer embryoma epithelioid sarcoma hepatocellular carcinoma inflammatory bowel disease influenza liver cancer lung benign neoplasm lung cancer lung non-small cell carcinoma multiple sclerosis myositis neuroblastoma papilloma progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma sarcoma spinal muscular atrophy spindle cell sarcoma squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma substance abuse substance-related disorder systemic lupus erythematosus tongue squamous cell carcinoma
415	arylsulfatase L	ARSL chondrodysplasia punctata 1
414	arylsulfatase D	ARSD ASD	Asperger syndrome Bannayan-Riley-Ruvalcaba syndrome Beckwith-Wiedemann syndrome CLOVES syndrome Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Cowden syndrome Down syndrome Dubowitz syndrome Lown-Ganong-Levine syndrome Marfan syndrome Mowat-Wilson 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 Perlman syndrome Prader-Willi syndrome Rett syndrome Richter's syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Sotos syndrome Williams-Beuren syndrome Wolff-Parkinson-White syndrome X-linked Aarskog syndrome acute kidney tubular necrosis acute myeloid leukemia acute promyelocytic leukemia adult respiratory distress syndrome alexia amnestic disorder aniridia anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve stenosis argininosuccinic aciduria arteriosclerotic cardiovascular disease 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 atrioventricular block atrioventricular septal defect attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bicuspid aortic valve disease breast cancer breast carcinoma buphthalmos cardiomyopathy cardiovascular system disease cerebral palsy chondrodysplasia-pseudohermaphroditism syndrome chronic lymphocytic leukemia citrullinemia communication disorder conduct disorder congenital heart disease congestive heart failure coronary artery disease depressive disorder developmental coordination disorder disease of mental health dyslexia dysthymic disorder eating disorder endocarditis endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy essential hypertension excessive tearing familial hypertrophic cardiomyopathy fragile X syndrome generalized anxiety disorder glaucoma heart disease hemiplegia hydrophthalmos hyperargininemia hypertension hypertrophic cardiomyopathy hypospadias immune system disease infective endocarditis intellectual disability juvenile glaucoma lacrimal apparatus disease language disorder learning disability major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia neurotic disorder newborn respiratory distress syndrome nicotine dependence obesity obsolete melancholia patent ductus arteriosus patent foramen ovale phobic disorder polycystic ovary syndrome post-traumatic stress disorder primary open angle glaucoma psychotic disorder pulmonary valve stenosis retrograde amnesia schizophrenia sclerocornea situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy subacute bacterial endocarditis substance abuse substance-related disorder supravalvular aortic stenosis syndromic X-linked intellectual disability 94 tuberous sclerosis ventricular septal defect visual epilepsy
412	steroid sulfatase	STS ARSC arylsulfatase C steryl-sulfatase	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Barrett's esophagus Chagas disease Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down syndrome Dubowitz syndrome Evans' syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Joubert syndrome Kallmann syndrome Kawasaki disease Klinefelter syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Mycobacterium avium complex disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Patau syndrome Pick's disease Prader-Willi syndrome Renpenning syndrome Reye syndrome Robinow syndrome Seckel syndrome Sertoli cell-only syndrome Sheehan syndrome Silver-Russell syndrome Sjogren's syndrome Sjogren-Larsson syndrome Smith-Lemli-Opitz syndrome Smith-Magenis syndrome Streptococcus pneumonia T-cell acute lymphoblastic leukemia Usher syndrome type 1 X-linked Aarskog syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 X-linked ichthyosis Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 achondroplasia achromatopsia acoustic neuroma acquired color blindness acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute biphenotypic leukemia acute leukemia acute myeloid leukemia adenocarcinoma in situ adenocarcinoma adenoma adult fibrosarcoma adult liposarcoma adult lymphoma alcoholic hepatitis allergic asthma alopecia amnestic disorder amyloidosis anaplastic astrocytoma androgen insensitivity syndrome androgenic alopecia angioimmunoblastic T-cell lymphoma angiomatous meningioma anhidrosis anogenital venereal wart antithrombin III deficiency aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve insufficiency aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ascending cholangitis asthma ataxia with oculomotor apraxia type 1 atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune thrombocytopenic purpura autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant chondrodysplasia punctata autosomal recessive Robinow syndrome 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 azoospermia bacterial infectious disease bacterial sepsis benign meningioma bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma blastomycosis blue color blindness bone osteosarcoma brain cancer brain infarction breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cataract 9 multiple types cellular schwannoma central nervous system lymphoma cerebral cavernous malformation 1 cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood cerebral astrocytoma childhood liposarcoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholangitis cholera cholesteatoma chondrodysplasia punctata chondrodysplasia-pseudohermaphroditism syndrome chorioamnionitis chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma common wart communication disorder complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital nystagmus congestive heart failure corneal dystrophy coronary artery disease cribriform carcinoma cryptorchidism cutaneous fibrous histiocytoma cystic fibrosis dedifferentiated liposarcoma dermatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma disease of metabolism dissociated nystagmus distal arthrogryposis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epidermodysplasia verruciformis epidermolysis bullosa dystrophica epidermolytic hyperkeratosis epilepsy epithelioid sarcoma esophagus adenocarcinoma essential hypertension essential thrombocythemia essential tremor eunuchism familial mediterranean fever familial nephrotic syndrome fibrillary astrocytoma fibrosarcoma fibrous meningioma gallbladder disease gastroenteritis gastrointestinal system disease gastroparesis gastroschisis gemistocytic astrocytoma generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma hemochromatosis type 1 hemochromatosis hepatic coma hepatic encephalopathy hepatitis C hepatocellular carcinoma hidradenoma high grade glioma human immunodeficiency virus infectious disease hydranencephaly hyperandrogenism hypercalcemia hypertension hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypohidrosis hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism hypopituitarism ichthyosis vulgaris ichthyosis ileitis ileocolitis in situ carcinoma inflammatory bowel disease inherited metabolic disorder intellectual disability intestinal disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma keratoconjunctivitis sicca keratosis follicularis kidney disease kidney failure language disorder large intestine cancer laryngeal squamous cell carcinoma learning disability leprosy lipoid nephrosis liposarcoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphoma malignant astrocytoma malignant peripheral nerve sheath tumor melanoma melanotic neurilemmoma melioidosis meningioma meningothelial meningioma metachromatic leukodystrophy mevalonic aciduria microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma middle cerebral artery infarction migraine mixed glioma mixed oligodendroglioma-astrocytoma mongolian spot mood disorder mucosulfatidosis myelitis myelodysplastic syndrome myelofibrosis nephritis nephrocalcinosis nephronophthisis 1 nephrosis nephrotic syndrome neurilemmoma neurodegenerative disease nodular prostate non-suppurative otitis media non-syndromic X-linked intellectual disability nonpapillary renal cell carcinoma obesity obsolete congenital ichthyosiform erythroderma obsolete ymphosarcoma ocular albinism 1 olfactory groove meningioma oligospermia osteoarthritis osteosarcoma otitis media ovarian cancer ovarian carcinoma palindromic rheumatism pancreatic adenocarcinoma panhypopituitarism papillary renal cell carcinoma papilloma paracoccidioidomycosis parapsoriasis parasagittal meningioma patent ductus arteriosus pathologic nystagmus periodontitis peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma placental choriocarcinoma pleomorphic adenoma pleomorphic liposarcoma plexiform schwannoma pneumocystosis pneumonia polycystic ovary syndrome polyp of middle ear pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postpartum depression primary sclerosing cholangitis prostate cancer prostate carcinoma prostatic adenoma protein C deficiency protein S deficiency protoplasmic astrocytoma psammomatous meningioma pseudohypoparathyroidism pseudoxanthoma elasticum psoriasis pustulosis of palm and sole pyoureter recessive dystrophic epidermolysis bullosa recurrent corneal erosion red color blindness red-green color blindness renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinal disease retinitis retrograde amnesia rheumatoid arthritis rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sclerosing cholangitis seborrheic keratosis secretory meningioma seminoma septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin disease skin melanoma skin papilloma skin tag speech disorder spinal meningioma spindle cell sarcoma spontaneous ocular nystagmus squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma suppurative cholangitis syndromic X-linked intellectual disability Najm type syringoma testicular cancer testicular germ cell cancer testis seminoma thrombophilia tick-borne encephalitis tongue squamous cell carcinoma transitional meningioma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trypanosomiasis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer varicose veins vasculitis visual epilepsy
411	arylsulfatase B	ARSB ASB	Balo concentric sclerosis Fabry disease Laron syndrome Machado-Joseph disease Scheie syndrome abdominal obesity-metabolic syndrome 1 achondroplasia adrenoleukodystrophy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer cardiomyopathy carotid artery disease central nervous system disease chondrodysplasia punctata chronic obstructive pulmonary disease chylomicron retention disease colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease cystic fibrosis embryoma endomyocardial fibrosis essential hypertension glaucoma glycogen storage disease II hydrocephalus hypertension hypertrichosis hypertrophic cardiomyopathy inguinal hernia large intestine cancer lipid storage disease lung benign neoplasm lysosomal storage disease melanoma metachromatic leukodystrophy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myocarditis narcolepsy nervous system disease obstructive hydrocephalus omphalocele osteochondrodysplasia osteonecrosis prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophreniform disorder senile degeneration of brain sensorineural hearing loss skin melanoma spinal cord disease tuberculosis umbilical hernia
410	arylsulfatase A	ARSA ASA metachromatic leucodystrophy	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Behcet's disease 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 Clostridium difficile colitis Clouston syndrome Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease DiGeorge syndrome Down syndrome Dubowitz syndrome Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Gaucher's disease Klatskin's tumor Krabbe disease Landau-Kleffner syndrome Lynch syndrome Niemann-Pick disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Phelan-McDermid syndrome Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Sandhoff disease Seckel syndrome Silver-Russell syndrome Sneddon syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia Tay-Sachs disease Unverricht-Lundborg syndrome Wilson disease X-linked Aarskog syndrome X-linked ichthyosis X-linked nonsyndromic deafness abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acoustic neuroma acute chest syndrome acute intermittent porphyria acute interstitial pneumonia acute kidney tubular necrosis acute myocardial infarction adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy agnosia alcohol dependence alcohol use disorder allergic asthma alternating hemiplegia of childhood amnestic disorder amyloidosis anemia angioedema ankylosing spondylitis anterior spinal artery syndrome anxiety disorder argininosuccinic aciduria arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia 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 autism spectrum disorder autistic disorder autoimmune hepatitis autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 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 dominant osteopetrosis 2 autosomal recessive Robinow syndrome 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 autosomal recessive osteopetrosis 7 bacterial sepsis benign epilepsy with centrotemporal spikes blood coagulation disease brain cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cataract cellular schwannoma central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood T-cell acute lymphoblastic leukemia cholangiocarcinoma cholecystitis chondrodysplasia-pseudohermaphroditism syndrome choreatic disease chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease chylomicron retention disease colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism coronary artery disease coronary thrombosis craniosynostosis critical illness polyneuropathy dementia demyelinating disease demyelinating polyneuropathy dentatorubral-pallidoluysian atrophy depressive disorder diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism diverticulitis dysthymic disorder dystonia early myoclonic encephalopathy embryoma encephalitis encephalomyelitis enterocele epilepsy esophageal cancer esophageal carcinoma esophagitis essential hypertension essential thrombocythemia familial hyperlipidemia female stress incontinence follicular adenoma gallbladder cancer gastroenteritis gastroesophageal reflux disease generalized anxiety disorder generalized atherosclerosis giant cell glioblastoma glioblastoma glomerulonephritis glycogen storage disease Ia heart disease hemiplegia hemochromatosis hepatitis B hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 herpes zoster high grade glioma hyperglycemia hypertension hypothyroidism ichthyosis idiopathic interstitial pneumonia ileitis ileocolitis inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intermediate coronary syndrome intrahepatic cholangiocarcinoma intrinsic asthma iron metabolism disease irritable bowel syndrome keratitis keratoconjunctivitis kidney disease kidney failure large intestine cancer late onset Parkinson's disease learning disability leukodystrophy lipid storage disease locked-in syndrome lung benign neoplasm lung cancer lung carcinoma lung disease lysosomal storage disease macrocytic anemia major depressive disorder malignant peripheral nerve sheath tumor malignant pleural mesothelioma mediastinitis medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanotic neurilemmoma meningoencephalitis metachromatic leukodystrophy microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia mitochondrial metabolism disease mitochondrial myopathy motor peripheral neuropathy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis multiple sclerosis myelitis myelomeningocele myocardial infarction myxedema nasopharynx carcinoma nephritis nephrosis nervous system disease neurilemmoma neuroblastoma neurocirculatory asthenia neurodegenerative disease neuropathy neurotic disorder nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete autosomal recessive nonsyndromic deafness 105 obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete inherited blood coagulation disease obsolete melancholia obstructive sleep apnea optic atrophy osteoarthritis osteopetrosis osteoporosis osteosclerosis pancreatic adenocarcinoma pancreatic ductal adenocarcinoma papillary adenoma patent foramen ovale peptic esophagitis peripheral artery disease peripheral nervous system disease phobic disorder plexiform schwannoma pneumonia polyneuropathy primary immunodeficiency disease primary pulmonary hypertension primary sclerosing cholangitis progressive bulbar palsy progressive myoclonus epilepsy 1A progressive myoclonus epilepsy psychotic disorder pyoureter quadriplegia rectal benign neoplasm rectum adenocarcinoma rectum cancer red-green color blindness retrograde amnesia sarcomatoid carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis silent myocardial infarction spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy sphingolipidosis spina bifida spinal cancer superior mesenteric artery syndrome syndromic X-linked intellectual disability type 10 systemic lupus erythematosus tethered spinal cord syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma tuberculosis type 2 diabetes mellitus ulcerative colitis urethral stricture urticaria vascular dementia velocardiofacial syndrome ventricular septal defect visual epilepsy
408	arrestin beta 1	ARRB1
406	basic helix-loop-helix ARNT like 1	BMAL1
405	aryl hydrocarbon receptor nuclear translocator	ARNT
403	ARF like GTPase 3	ARL3
397	Rho GDP dissociation inhibitor beta	ARHGDIB
393	Rho GTPase activating protein 4	ARHGAP4
391	ras homolog family member G	RHOG
389	ras homolog family member C	RHOC
388	ras homolog family member B	RHOB
387	ras homolog family member A	RHOA RHOH12 Rho12

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