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	October 29, 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

Search results for "glycoprotein metabolic process"

Displaying entries **1 - 25** of **17827** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
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
2131	exostosin glycosyltransferase 1	EXT1 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase ttv	Homo sapiens (human)	Alzheimer's disease Cenani-Lenz syndactyly syndrome Cornelia de Lange syndrome 4 Cornelia de Lange syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Legg-Calve-Perthes disease Lennox-Gastaut syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Ollier disease Pick's disease Reye syndrome Ritter's disease Werner syndrome achondroplasia acute lymphoblastic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia anaplastic astrocytoma antisocial personality disorder arthritis arthropathy autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebral degeneration cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chondroblastoma chondroma chondrosarcoma cleidocranial dysplasia clubfoot conduct disorder connective tissue disease cranial nerve disease cranial nerve palsy cribriform carcinoma cryoglobulinemia diabetes mellitus disease of mental health embryoma endometrial cancer endometrial carcinoma epilepsy exostosis familial hypercholesterolemia familial nephrotic syndrome fibrillary astrocytoma fibromyalgia frontotemporal dementia gallbladder disease gemistocytic astrocytoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma hereditary multiple exostoses high grade glioma humeroradial synostosis hydrocephalus hyperostosis hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease intellectual disability juvenile myoclonic epilepsy juvenile pilocytic astrocytoma learning disability leukemia lipoid nephrosis liver cancer liver disease lupus nephritis malignant astrocytoma membranous glomerulonephritis metachondromatosis microcephaly mixed glioma mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple myeloma myositis nephrotic syndrome osteoarthritis osteonecrosis osteopoikilosis osteoporosis osteosarcoma periarthritis personality disorder pilocytic astrocytoma progeria protoplasmic astrocytoma psychotic disorder radioulnar synostosis rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis schizophrenia scoliosis spinal cord disease subependymal giant cell astrocytoma tendinitis thrombophilia trichorhinophalangeal syndrome type II tubular adenocarcinoma type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer vasculitis vesicoureteral reflux visual epilepsy
2132	exostosin glycosyltransferase 2	EXT2 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase SOTV	Homo sapiens (human)	Alzheimer's disease Cenani-Lenz syndactyly syndrome Dent disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Marfan syndrome Ollier disease Pick's disease Reye syndrome achondroplasia adenosarcoma agnosia anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease cerebral degeneration cherubism chondrosarcoma cleidocranial dysplasia clubfoot congenital hypothyroidism congenital nystagmus connective tissue disease cranial nerve disease cranial nerve palsy craniosynostosis cryptorchidism developmental and epileptic encephalopathy 36 developmental coordination disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus epilepsy esophagitis essential hypertension exostosis familial hypercholesterolemia frontotemporal dementia gastroesophageal reflux disease hereditary multiple exostoses humeroradial synostosis hyperostosis hypertension hypertropia hypothyroidism immune system disease intellectual disability large intestine cancer learning disability lupus nephritis macrocytic anemia mechanical strabismus membranous glomerulonephritis metachondromatosis microcephaly mucopolysaccharidosis III mucopolysaccharidosis type IIIA myxedema nephroblastoma nonsyndromic congenital nail disorder 9 obsolete constipation ophthalmoplegia osteoarthritis osteonecrosis osteosarcoma parietal foramina pathologic nystagmus peptic esophagitis periarthritis radioulnar synostosis scoliosis situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus tendinitis tuberous sclerosis type 2 diabetes mellitus ventricular septal defect visual epilepsy
2134	exostosin like glycosyltransferase 1	EXTL1 Aliases: EXTL MGC70794 alpha-N-acetylglucosaminyltransferase II exostosin-L glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase glucuronyl-N-acetylglucosaminylproteoglycan alpha-1,4-N- acetylglucosaminyltransferase	Homo sapiens (human)	cancer embryoma hereditary multiple exostoses neuroblastoma
2135	exostosin like glycosyltransferase 2	EXTL2 Aliases: alpha-1,4-N-acteylhexosaminyltransferase	Homo sapiens (human)	autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer chronic kidney disease hereditary multiple exostoses mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis osteopetrosis osteosclerosis
2137	exostosin like glycosyltransferase 3	EXTL3 Aliases: REG receptor REGR botv glucuronyl-galactosyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase	Homo sapiens (human)	MHC class II deficiency acute myeloid leukemia adenosine deaminase deficiency agnosia arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 bacterial sepsis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cherubism chondrodysplasia punctata ciliary body disease cocaine abuse cocaine dependence colorectal cancer colorectal carcinoma coronary artery disease developmental coordination disorder endometriosis of uterus endometriosis epithelioid sarcoma exostosis giant cell glioblastoma glioblastoma head and neck cancer head and neck squamous cell carcinoma hereditary multiple exostoses hypereosinophilic syndrome intellectual disability iris disease large intestine cancer learning disability liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia morphine dependence mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis multiple epiphyseal dysplasia nutmeg liver osteochondrodysplasia osteopetrosis osteosclerosis panuveitis periarthritis pulmonary embolism sarcoma scoliosis secondary syphilis severe combined immunodeficiency spindle cell sarcoma tendinitis tuberculosis uveitis
2530	fucosyltransferase 8	FUT8 Aliases: alpha (1,6) fucosyltransferase	Homo sapiens (human)	Laron syndrome achondroplasia adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma buphthalmos cancer chronic fatigue syndrome chronic myeloid leukemia chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congenital disorder of glycosylation coronary artery disease embryoma encephalitis encephalomyelitis epilepsy follicular adenoma glaucoma hepatitis A hepatitis C hepatitis hepatocellular carcinoma hydrophthalmos idiopathic interstitial pneumonia intellectual disability juvenile glaucoma large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma microcephaly microcystic adenoma myelitis ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm papillary adenoma papillary carcinoma placental insufficiency polyhydramnios postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pseudomyxoma peritonei pulmonary emphysema pulmonary fibrosis schizophrenia scoliosis skin melanoma visual epilepsy
2595	glucosidase alpha, neutral C	GANC	Homo sapiens (human)	congenital dyserythropoietic anemia panic disorder
2650	glucosaminyl (N-acetyl) transferase 1	GCNT1 Aliases: C2GNT NAGCT2 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N--acetylglucosaminyltransferase core 2 beta1,6 N-acetylglucosaminyltransferase-I	Homo sapiens (human)	adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma embryoma granular cell carcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma neuroblastoma pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma seminoma testicular cancer testicular germ cell cancer tubular adenocarcinoma
2720	galactosidase beta 1	GLB1 Aliases: EBP elastin binding protein	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Balo concentric sclerosis Behcet's disease Burkitt lymphoma Clostridium difficile colitis Cockayne syndrome Cornelia de Lange syndrome Costello syndrome Crohn's colitis Crohn's disease Dubowitz syndrome Duchenne muscular dystrophy Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM1 gangliosidosis GM2 gangliosidosis Gaucher's disease Kawasaki disease Krabbe disease Laron 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 Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Sandhoff disease Seckel syndrome Silver-Russell syndrome Silverman-Handmaker type dyssegmental dysplasia X-linked Aarskog syndrome X-linked dilated cardiomyopathy X-linked ichthyosis X-linked spondyloepiphyseal dysplasia tarda Zollinger-Ellison syndrome achondroplasia acquired immunodeficiency syndrome acute promyelocytic leukemia adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma adult lymphoma allergic asthma anaplastic astrocytoma anogenital venereal wart aortic valve disease 2 aortic valve stenosis arthritis arthropathy aspartylglucosaminuria asthma atopic dermatitis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 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 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 benign mesothelioma bladder carcinoma bladder urothelial carcinoma bone disease brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer carcinoma cardiomyopathy cartilage disease celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood astrocytic tumor childhood cerebral astrocytoma childhood leukemia childhood lymphoma cholera chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma chronic kidney disease chronic lymphocytic leukemia chronic obstructive pulmonary disease chylomicron retention disease collagen disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital muscular dystrophy congestive heart failure connective tissue disease contact dermatitis corneal neovascularization cutaneous fibrous histiocytoma cystic fibrosis dental caries dentin caries depressive disorder dermatitis diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy dysostosis dystonia embryoma endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hypercholesterolemia familial hyperlipidemia familial hypertrophic cardiomyopathy familial retinoblastoma fibrillary astrocytoma fibrosarcoma filariasis focal hand dystonia fucosidosis galactosialidosis gangliosidosis gemistocytic astrocytoma generalized dystonia giant cell glioblastoma giant cell reparative granuloma gingival hypertrophy gingival overgrowth glioblastoma gliosarcoma glycoproteinosis head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatoblastoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies herpes simplex hidradenoma high grade glioma human immunodeficiency virus infectious disease hydrocephalus hyperinsulinism hypertrichosis hypertrophic cardiomyopathy hypotrichosis 7 hypotrichosis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia inherited metabolic disorder intellectual disability intracranial hypertension intrinsic asthma irritable bowel syndrome islet cell tumor juvenile pilocytic astrocytoma kwashiorkor lactose intolerance large intestine cancer learning disability leiomyoma leukemia limb-girdle muscular dystrophy lipid storage disease liver cancer liver cirrhosis localized scleroderma locked-in syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung large cell carcinoma lung small cell carcinoma lymphoma lysosomal storage disease major depressive disorder malignant astrocytoma malignant mesothelioma marasmus measles melancholic depression melanoma metachromatic leukodystrophy microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mixed glioma mucolipidosis III alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myofibroma narcolepsy nervous system disease neuroblastoma neurocirculatory asthenia neurodegeneration with brain iron accumulation neurodegenerative disease neurohypophyseal diabetes insipidus nevoid basal cell carcinoma syndrome nutrition disease 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 melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma occupational dermatitis oculopharyngeal muscular dystrophy optic atrophy osteoarthritis osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma pancytopenia papilloma parasitic helminthiasis infectious disease patent ductus arteriosus pilocytic astrocytoma postinflammatory pulmonary fibrosis primary biliary cholangitis primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma pseudotumor cerebri pulmonary fibrosis quadriplegia recurrent corneal erosion retinoblastoma rhabdomyosarcoma rheumatoid arthritis rippling muscle disease 2 sarcomatoid carcinoma scleroderma scoliosis sea-blue histiocytosis secondary Parkinson disease sensorineural hearing loss skin melanoma skin papilloma skin squamous cell carcinoma skin tag sphingolipidosis spondyloepiphyseal dysplasia congenita squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma synovial sarcoma syringoma systemic scleroderma tarsal-carpal coalition syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma transthyretin amyloidosis trilateral retinoblastoma 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 uterine fibroid viral infectious disease visual epilepsy
2817	glypican 1	GPC1 Aliases: glypican glypican proteoglycan 1	Homo sapiens (human)	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 Duchenne muscular dystrophy ITM2B-related cerebral amyloid angiopathy 1 ITM2B-related cerebral amyloid angiopathy 2 Kallmann syndrome Niemann-Pick disease type C1 Niemann-Pick disease Pick's disease Reye syndrome Sheehan syndrome Simpson-Golabi-Behmel syndrome type 1 adenocarcinoma adenoma ameloblastoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma biliary atresia borderline personality disorder breast cancer breast carcinoma cancer central nervous system cancer cerebral amyloid angiopathy cerebral degeneration cervical cancer cholangiocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism craniosynostosis cribriform carcinoma embryoma epilepsy esophagus squamous cell carcinoma eyelid disease fibrodysplasia ossificans progressiva gallbladder cancer gallbladder carcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothyroidism intermittent explosive disorder intrahepatic cholangiocarcinoma 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 large intestine cancer liver cancer lung adenocarcinoma lung cancer malignant epithelial mesothelioma malignant mesothelioma microphthalmia mixed glioma muscular dystrophy myositis ossificans myxedema nodular prostate obsolete Matthew-Wood syndrome ophthalmoplegia ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panhypopituitarism placental insufficiency prostate cancer prostate carcinoma prostatic adenoma pseudohypoparathyroidism pseudopseudohypoparathyroidism rheumatoid arthritis schizophrenia squamous cell carcinoma thymus gland disease tongue squamous cell carcinoma tubular adenocarcinoma visual epilepsy xanthomatosis
2990	glucuronidase beta	GUSB	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Clouston syndrome Crohn's colitis Crohn's disease De Quervain disease Fabry disease Laron syndrome Pick's disease Reye syndrome Richter's syndrome Sly syndrome Werner syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adrenal gland cancer alcohol dependence alcohol use disorder alternating hemiplegia of childhood arteriosclerotic cardiovascular disease arteriovenous malformation arthritis arthropathy atherosclerosis autonomic neuropathy bladder carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system disease cerebral degeneration cholecystolithiasis choledocholithiasis cholelithiasis chondrodysplasia punctata chronic lymphocytic leukemia chronic myeloid leukemia chylomicron retention disease clubfoot colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease cystic fibrosis diabetes mellitus diabetic ketoacidosis diarrhea duodenum cancer elephantiasis embryoma endomyocardial fibrosis factor VIII deficiency familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma gallbladder disease gastroenteritis gastrointestinal system disease gingival hypertrophy gingival overgrowth glycoproteinosis head and neck cancer head and neck squamous cell carcinoma heart cancer hepatitis B hepatitis C hepatitis hepatocellular carcinoma herpes simplex hydrocephalus hyperglycemia hypertrichosis hypertrophic cardiomyopathy ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intestinal disease islet cell tumor large intestine cancer learning disability lipid storage disease liver cancer liver disease lung adenocarcinoma lung cancer lung carcinoma lymphedema lysosomal storage disease microcystic adenoma mucolipidosis II alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myeloproliferative neoplasm nasopharynx carcinoma nephroblastoma nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus omphalocele ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma paraganglioma peritonitis pheochromocytoma progeria prostate cancer prostate carcinoma proteinuria pulmonary tuberculosis recurrent corneal erosion retinal disease retinitis rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss shigellosis small intestine cancer stomach cancer stomach carcinoma subacute thyroiditis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis umbilical hernia urinary bladder cancer
3340	N-deacetylase and N-sulfotransferase 1	NDST1 Aliases: N-Deacetylase-N-sulfotransferase 1 NST1 [Heparan sulfate]-glucosamine N-sulfotransferase 1 heparan sulfate/heparin GlcNAc N-deacetylase/GlcN N-sulfotransferase 1	Homo sapiens (human)	DiGeorge syndrome Treacher Collins syndrome acute myocardial infarction adult respiratory distress syndrome agnosia autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia breast cancer breast carcinoma cancer cerebral degeneration chikungunya choreatic disease chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma congenital diaphragmatic hernia coronary thrombosis dengue hemorrhagic fever depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia embryoma encephalitis encephalomyelitis epilepsy focal epilepsy gastrointestinal stromal tumor giant cell glioblastoma glioblastoma glomerulonephritis hiatus hernia high grade glioma hypereosinophilic syndrome intellectual disability kidney disease learning disability lingual-facial-buccal dyskinesia liver cirrhosis major depressive disorder melancholic depression microcephaly microphthalmia myelitis myocardial infarction nephritis nephrosis neurotic disorder newborn respiratory distress syndrome nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary renal cell carcinoma partial motor epilepsy pyoureter renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma silent myocardial infarction stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus velocardiofacial syndrome visual epilepsy
3423	iduronate 2-sulfatase	IDS Aliases: Hunter syndrome ID2S	Homo sapiens (human)	Balo concentric sclerosis Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Fabry disease Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Griscelli syndrome Laron syndrome Marfan syndrome Sveinsson chorioretinal atrophy Waardenburg syndrome type 3 X-linked ichthyosis achondroplasia adrenoleukodystrophy agammaglobulinemia allergic asthma alternating hemiplegia of childhood amnestic disorder antiphospholipid syndrome asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer brain disease breast cancer breast carcinoma cancer central nervous system disease centronuclear myopathy X-linked centronuclear myopathy cerebral infarction cerebrovascular disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital adrenal hyperplasia congenital central hypoventilation syndrome congenital ptosis congenital structural myopathy congestive heart failure craniosynostosis cystinuria depressive disorder diarrhea dysthymic disorder embryoma epilepsy fragile X syndrome galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease glycoproteinosis heart valve disease hydrocephalus hypercalcemia hypertrichosis hypoglycemia inguinal hernia intellectual disability intrinsic asthma learning disability lipid storage disease lung benign neoplasm lung carcinoma lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myeloproliferative neoplasm myocarditis myotonic disease myotonic dystrophy type 2 narcolepsy nephrocalcinosis nervous system disease neurotic disorder obsolete intestinal pseudo-obstruction obsolete melancholia obstructive hydrocephalus obstructive sleep apnea ocular albinism with sensorineural deafness oculocutaneous albinism omphalocele optic papillitis osteochondrodysplasia ovarian cancer ovarian carcinoma pancytopenia papilledema paralytic ileus phosphorus metabolism disease post-traumatic stress disorder ptosis retinal edema retrograde amnesia rumination disorder senile degeneration of brain sensorineural hearing loss sick sinus syndrome situs inversus sleep apnea sudden infant death syndrome trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis umbilical hernia visual epilepsy
3425	alpha-L-iduronidase	IDUA Aliases: MPS1 MPSI mucopolysaccharidosis type I	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Creutzfeldt-Jakob disease Fabry disease Gaucher's disease Hartnup disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Klippel-Feil syndrome Krabbe disease Laron syndrome Loeys-Dietz syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Richter's syndrome Scheie syndrome Sly syndrome T-cell acute lymphoblastic leukemia Weissenbacher-Zweymuller syndrome achondroplasia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia adrenoleukodystrophy adult medulloblastoma agranulocytosis anemia anogenital venereal wart aortic valve disease 2 aortic valve insufficiency aortic valve stenosis autosomal recessive hypophosphatemic rickets benign mesothelioma blindness bone disease brain cancer breast cancer breast carcinoma cancer cardiomyopathy cartilage disease central nervous system disease cerebral palsy childhood medulloblastoma chromophobe renal cell carcinoma chronic lymphocytic leukemia chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart communicating hydrocephalus congenital heart disease connective tissue disease deficiency anemia dental caries dentin caries depressive disorder disease of mental health disease of metabolism dysthymic disorder embryoma endomyocardial fibrosis essential hypertension gastric ulcer giant cell glioblastoma gingival hypertrophy gingival overgrowth glaucoma glioblastoma glycogen storage disease II glycoproteinosis head and neck squamous cell carcinoma hemiplegia hepatocellular carcinoma high grade glioma hydrocephalus hypertension hypertrophic cardiomyopathy hypochromic anemia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia inherited metabolic disorder intellectual disability intracranial hypotension large intestine cancer learning disability leukopenia lipid storage disease liver cancer liver carcinoma lung benign neoplasm lung carcinoma lymphoblastic lymphoma lysosomal storage disease macrocytic anemia major depressive disorder malignant mesothelioma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma microcytic anemia mitral valve insufficiency mitral valve prolapse mucolipidosis II alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih/s mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma narcolepsy nervous system disease neurotic disorder neutropenia nonpapillary renal cell carcinoma obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus obstructive sleep apnea osteochondrodysplasia osteoporosis otitis media pancreatic ductal adenocarcinoma papillary renal cell carcinoma primary pulmonary hypertension psychotic disorder recurrent corneal erosion renal carcinoma renal cell carcinoma retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain sensorineural hearing loss severe congenital neutropenia skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy sphingolipidosis spinal cord disease spondylolisthesis stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tracheal stenosis tyrosinemia type I tyrosinemia ulcerative colitis
3952	leptin	LEP	Homo sapiens (human)	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acute pancreatitis adult respiratory distress syndrome alcohol dependence alcoholic liver cirrhosis asthma breast cancer chronic obstructive pulmonary disease congenital leptin deficiency cystic fibrosis end stage renal disease familial hyperlipidemia gestational diabetes glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma hyperinsulinism hypertension hypogonadism lipid metabolism disorder lung non-small cell carcinoma metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoarthritis osteoporosis pre-eclampsia primary biliary cholangitis renal cell carcinoma rhinitis short bowel syndrome steatotic liver disease type 2 diabetes mellitus
4121	mannosidase alpha class 1A member 1	MAN1A1	Homo sapiens (human)	Gaucher's disease acquired immunodeficiency syndrome breast cancer cancer congenital disorder of glycosylation Ih congenital disorder of glycosylation type I congenital disorder of glycosylation diabetes mellitus human immunodeficiency virus infectious disease ovarian cancer ovarian carcinoma type 2 diabetes mellitus
4122	mannosidase alpha class 2A member 2	MAN2A2 Aliases: HsT19662 MANA2X	Homo sapiens (human)	attention deficit hyperactivity disorder schizophrenia
4124	mannosidase alpha class 2A member 1	MAN2A1 Aliases: GOLIM7 golgi integral membrane protein 7	Homo sapiens (human)	autoimmune disease autoimmune lymphoproliferative syndrome cancer childhood acute lymphocytic leukemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia diabetes mellitus embryoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma immune system disease liver cancer prostate cancer prostate carcinoma schizophrenia systemic lupus erythematosus type 2 diabetes mellitus
4125	mannosidase alpha class 2B member 1	MAN2B1 Aliases: LAMAN lysosomal alpha-mannosidase	Homo sapiens (human)	IgA glomerulonephritis Klippel-Feil syndrome age related macular degeneration alpha-mannosidosis aspartylglucosaminuria cerebral degeneration congenital nystagmus degeneration of macula and posterior pole dissociated nystagmus fucosidosis gingival hypertrophy gingival overgrowth glycogen storage disease II hypertrichosis inguinal hernia intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease macular degeneration methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis pathologic nystagmus retinal degeneration sensorineural hearing loss spondylolisthesis spontaneous ocular nystagmus
4126	mannosidase beta	MANBA Aliases: beta-mannosidase A	Homo sapiens (human)	Fabry disease allergic asthma allergic disease alternating hemiplegia of childhood angiokeratoma ascending cholangitis asthma attention deficit hyperactivity disorder autonomic neuropathy beta-mannosidosis central nervous system disease cholangitis chronic kidney disease chylomicron retention disease colorectal cancer colorectal carcinoma complement deficiency congenital nystagmus dissociated nystagmus epilepsy intellectual disability intrinsic asthma large intestine cancer learning disability lipid storage disease lysosomal storage disease multiple sclerosis nervous system disease obsolete constipation pathologic nystagmus primary biliary cholangitis primary sclerosing cholangitis sarcoidosis sclerosing cholangitis sensorineural hearing loss speech disorder spontaneous ocular nystagmus suppurative cholangitis uveoparotid fever visual epilepsy
4669	N-acetyl-alpha-glucosaminidase	NAGLU Aliases: NAG Sanfilippo disease IIIB	Homo sapiens (human)	Alzheimer's disease Burkitt lymphoma Charcot-Marie-Tooth disease axonal type 2V Clouston syndrome Dent disease Fanconi syndrome Glanzmann's thrombasthenia Kluver-Bucy syndrome Legg-Calve-Perthes disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma amnestic disorder amyloidosis appendicitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrophic gastritis autistic disorder cancer cardiovascular system disease cholera chronic kidney disease chronic pyelonephritis cone-rod dystrophy congestive heart failure coronary artery disease cribriform carcinoma cystinosis cystitis dementia dentatorubral-pallidoluysian atrophy diabetes mellitus diabetic ketoacidosis diarrhea embryoma epilepsy essential thrombocythemia focal segmental glomerulosclerosis follicular adenoma fundus albipunctatus glomerulonephritis granular cell carcinoma gray platelet syndrome heart disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy 1 intellectual disability kidney disease kidney failure learning disability lipoid nephrosis liver cirrhosis lysosomal storage disease malignant pleural mesothelioma microcystic adenoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma myelodysplastic syndrome nephritis nephrosis neuroblastoma neurodegenerative disease oculocerebrorenal syndrome oculocutaneous albinism type IA osteochondrodysplasia otitis media panic disorder papillary adenoma parapsoriasis platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 progressive familial intrahepatic cholestasis 1 progressive myoclonus epilepsy prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole pyoureter qualitative platelet defect renal osteodystrophy retinitis pigmentosa retrograde amnesia sensorineural hearing loss spondyloepimetaphyseal dysplasia, Sponastrime type stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 trigonitis tubular adenocarcinoma type 2 diabetes mellitus viral infectious disease visual epilepsy
4759	neuraminidase 2	NEU2 Aliases: N-acetyl-alpha-neuraminidase 2 SIAL2	Homo sapiens (human)	allergic rhinitis cancer pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma prostate cancer prostate carcinoma rhabdomyosarcoma stomach cancer stomach carcinoma vasomotor rhinitis
5589	PRKCSH beta subunit of glucosidase II	PRKCSH	Homo sapiens (human)	Marfan syndrome Meckel syndrome autosomal dominant polycystic kidney disease beta thalassemia breast cancer breast carcinoma cancer cerebellar ataxia, mental retardation and dysequlibrium syndrome cystic kidney disease diabetic ketoacidosis episodic ataxia type 2 esophagitis familial hemiplegic migraine 1 familial hemiplegic migraine familial hypercholesterolemia gallbladder disease gastroesophageal reflux disease hepatitis B hepatocellular carcinoma liver cancer liver disease non-congenital cyst of kidney obsolete type 1 diabetes mellitus 9 peptic esophagitis polycystic kidney disease 1 polycystic liver disease situs inversus tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
6448	N-sulfoglucosamine sulfohydrolase	SGSH Aliases: HSS MPS3A SFMD mucopolysaccharidosis type IIIA sulfamidase	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 Balo concentric sclerosis Kearns-Sayre syndrome Kluver-Bucy syndrome Pick's disease Reye syndrome Schwartz-Jampel syndrome 1 Stevens-Johnson syndrome adrenoleukodystrophy ankylosing spondylitis anorexia nervosa arthritis arthropathy beta-mannosidosis cancer cardiomyopathy central nervous system disease central nervous system origin vertigo cerebral degeneration chronic obstructive pulmonary disease cone-rod dystrophy congenital nystagmus depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dissociated nystagmus embryoma endomyocardial fibrosis eosinophilic esophagitis epilepsy fundus albipunctatus fundus dystrophy hypertrichosis hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease major depressive disorder melancholic depression movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis mucosulfatidosis multiple epiphyseal dysplasia narcolepsy nervous system disease neurodegeneration with brain iron accumulation neurodegenerative disease obsolete melancholia osteoarthritis osteochondrodysplasia pathologic nystagmus retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus visual epilepsy

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