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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 .

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 "hydrolase activity, acting on glycosyl bonds"

Displaying entries **26 - 50** of **16787** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
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
2760	ganglioside GM2 activator	GM2A Aliases: GM2-AP GM2-activator protein GM2AP SAP-3 cerebroside sulfate activator protein sphingolipid activator protein 3	Homo sapiens (human)	Clostridium difficile colitis GM2 gangliosidosis, AB variant GM2 gangliosidosis Laron syndrome Sandhoff disease Schimke immuno-osseous dysplasia Tay-Sachs disease achondroplasia alcohol dependence alcohol use disorder anxiety disorder blindness breast cancer breast carcinoma cancer cerebral degeneration choreatic disease chronic obstructive pulmonary disease dementia dystonia embryoma epilepsy generalized anxiety disorder neurodegenerative disease neuroendocrine carcinoma nicotine dependence perinatal necrotizing enterocolitis progressive muscular atrophy retinal disease retinitis spinal muscular atrophy syndromic X-linked intellectual disability type 10 visual epilepsy vulvovaginal candidiasis
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
3073	hexosaminidase subunit alpha	HEXA Aliases: GM2 gangliosidosis Tay Sachs disease beta-hexosaminidase subunit alpha	Homo sapiens (human)	GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Sandhoff disease Tay-Sachs disease Werdnig-Hoffmann disease acquired immunodeficiency syndrome adult lymphoma amyotrophic lateral sclerosis blindness cancer central nervous system cancer central nervous system lymphoma childhood lymphoma childhood spinal muscular atrophy cystic fibrosis dementia diffuse scleroderma embryoma epilepsy gangliosidosis gliosarcoma glycoproteinosis high grade glioma human immunodeficiency virus infectious disease inherited metabolic disorder intellectual disability juvenile spinal muscular atrophy learning disability lingual-facial-buccal dyskinesia lymphoma lysosomal storage disease mixed glioma movement disease mucolipidosis type IV neurodegenerative disease obesity obsolete ymphosarcoma progressive muscular atrophy rheumatoid arthritis sensorineural hearing loss sickle cell anemia spinal muscular atrophy visual epilepsy
3074	hexosaminidase subunit beta	HEXB Aliases: beta-hexosaminidase subunit beta	Homo sapiens (human)	GM2 gangliosidosis, AB variant GM2 gangliosidosis HCL-V Sandhoff disease Schimke immuno-osseous dysplasia Tay-Sachs disease Unverricht-Lundborg syndrome acquired immunodeficiency syndrome acute kidney failure allergic asthma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anhidrosis anterior horn cell disease asthma autosomal recessive distal hereditary motor neuronopathy 1 blindness central nervous system cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital nystagmus dissociated nystagmus early myoclonic encephalopathy epilepsy gangliosidosis gliosarcoma hairy cell leukemia high grade glioma human immunodeficiency virus infectious disease hypohidrosis impotence inherited metabolic disorder intrinsic asthma kidney disease large intestine cancer lateral sclerosis liver cirrhosis lysosomal storage disease mixed glioma motor neuron disease multiple system atrophy neurodegenerative disease pathologic nystagmus postural orthostatic tachycardia syndrome premature ejaculation psychologic dyspareunia retinal disease retinitis rheumatoid arthritis spinal muscular atrophy spontaneous ocular nystagmus visual epilepsy
3373	hyaluronidase 1	HYAL1 Aliases: HYAL-1 LUCA1	Homo sapiens (human)	Laron syndrome achondroplasia arthritis arthropathy bladder carcinoma breast cancer breast carcinoma cancer carcinoma central nervous system cancer chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma embryoma endometrial cancer endometrial carcinoma gliosarcoma head and neck cancer head and neck squamous cell carcinoma high grade glioma juvenile rheumatoid arthritis large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer lung benign neoplasm lung cancer lung non-small cell carcinoma lung small cell carcinoma lysosomal storage disease mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IX mucopolysaccharidosis VI mucopolysaccharidosis osteoarthritis osteochondrodysplasia ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma primary pulmonary hypertension prostate cancer prostate carcinoma pulmonary hypertension sarcomatoid carcinoma skin disease squamous cell carcinoma tongue squamous cell carcinoma urinary bladder cancer uterine corpus cancer
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
3554	interleukin 1 receptor type 1	IL1R1 Aliases: CD121A D2S1473 interleukin-1 receptor, type I	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 Balkan nephropathy Behcet's disease Bloch-Sulzberger syndrome COVID-19 Crohn's colitis Crohn's disease Evans' syndrome Gilles de la Tourette syndrome Hantavirus hemorrhagic fever with renal syndrome Kawasaki disease Loeffler syndrome Paget's disease of bone Pick's disease Reye syndrome Wilson disease abdominal aortic aneurysm acrodermatitis actinic keratosis acute myeloid leukemia acute pericementitis adult lymphoma adult malignant schwannoma adult respiratory distress syndrome aggressive periodontitis alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma allergic disease ankylosing spondylitis arthritis arthropathy articular cartilage disease ascending cholangitis asthma atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura benign ependymoma bipolar disorder bone disease bone osteosarcoma breast cancer breast carcinoma cancer cardiovascular system disease cartilage disease cellular ependymoma central nervous system lymphoma cerebral degeneration cerebral infarction cerebral malaria cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood lymphoma childhood malignant schwannoma childhood osteosarcoma cholangitis cholesteatoma of middle ear chondromalacia choriocarcinoma chronic fatigue syndrome chronic recurrent multifocal osteomyelitis colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer complex regional pain syndrome connective tissue benign neoplasm connective tissue disease coronary artery disease cyclic hematopoiesis dengue hemorrhagic fever depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis endometriosis of ovary endometriosis of uterus endometriosis eosinophilic pneumonia epithelioid leiomyosarcoma epithelioid malignant peripheral nerve sheath tumor esophagitis essential hypertension familial nephrotic syndrome focal segmental glomerulosclerosis gastroenteritis gastroesophageal reflux disease gestational diabetes glomerulonephritis glucose intolerance gout heart disease heart valve disease hemochromatosis hepatitis C hepatitis high grade glioma hyperglycemia hypertension hypomelanosis of Ito ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease inflammatory myofibroblastic tumor intrinsic asthma iron metabolism disease juvenile myelomonocytic leukemia kidney disease large intestine cancer leiomyosarcoma lepromatous leprosy leukemia lipoid nephrosis liver cirrhosis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 major depressive disorder malaria malignant fibrous histiocytoma malignant peripheral nerve sheath tumor melancholic depression myelitis myxoid leiomyosarcoma myxopapillary ependymoma nephritis nephrosis nephrotic syndrome neurilemmoma neurofibrosarcoma neurogenic arthropathy neurotic disorder newborn respiratory distress syndrome obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma panic disorder papillary adenocarcinoma papillary ependymoma papillary renal cell carcinoma parapsoriasis peptic esophagitis periodontitis periodontosis placenta cancer pneumonia polycystic ovary syndrome prediabetes syndrome primary sclerosing cholangitis psoriasis pterygium pulmonary eosinophilia pulmonary tuberculosis pulpitis pustulosis of palm and sole pyoureter rhabdomyosarcoma rheumatoid arthritis schizophrenia scleroderma sclerosing cholangitis seborrheic keratosis severe acute respiratory syndrome skin disease suppurative cholangitis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tanycytic ependymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tuberculosis tuberculous pneumothorax 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
3556	interleukin 1 receptor accessory protein	IL1RAP Aliases: C3orf13 IL-1RAcP IL1R3	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 Kawasaki disease Pick's disease Reye syndrome X-linked adrenal hypoplasia congenita acute monocytic leukemia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder autistic disorder bacterial infectious disease cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma chronic myeloid leukemia chronic obstructive pulmonary disease ciliary body disease colitis coronary artery disease endometriosis of uterus endometriosis gallbladder disease gastroenteritis head and neck squamous cell carcinoma hepatocellular carcinoma ileitis ileocolitis intellectual disability iris disease learning disability liver cancer liver disease obesity pancreatic adenocarcinoma panuveitis parapsoriasis premenstrual tension psoriasis pustulosis of palm and sole rheumatoid arthritis scleroderma skin disease systemic lupus erythematosus systemic scleroderma uveitis
3906	lactalbumin alpha	LALBA Aliases: HAMLET LYZG LYZL7 lactose synthase B lysozyme G	Homo sapiens (human)	breast cancer breast carcinoma cancer deficiency anemia embryoma eosinophilic esophagitis fibromyalgia gastroenteritis hypochromic anemia liver cirrhosis microcytic anemia milk allergy mitral valve stenosis multiple sclerosis myositis obesity polycystic ovary syndrome steatotic liver disease
3938	lactase	LCT	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 Clostridium difficile colitis Crohn's colitis Crohn's disease EEC syndrome Gilles de la Tourette syndrome Leydig cell tumor Pick's disease Reye syndrome Sertoli cell-only syndrome T-cell acute lymphoblastic leukemia Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 acute myocardial infarction acute retinal necrosis syndrome adult T-cell leukemia/lymphoma adult respiratory distress syndrome allergic asthma antiphospholipid syndrome antithrombin III deficiency asthma autoimmune polyendocrine syndrome bullous congenital ichthyosiform erythroderma cancer celiac disease cerebral degeneration colitis colorectal cancer colorectal carcinoma congenital lactase deficiency coronary artery disease coronary thrombosis cystic fibrosis diarrhea dysentery ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 embryoma eosinophilic esophagitis essential hypertension extraosseous Ewing sarcoma extraosseous Ewings sarcoma-primitive neuroepithelial tumor familial adenomatous polyposis 1 familial adenomatous polyposis gastritis gastroenteritis gastrointestinal system disease gestational diabetes gingival recession hypertension ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intestinal infectious disease intrinsic asthma irritable bowel syndrome islet cell tumor kidney disease kwashiorkor lactic acidosis lactose intolerance large intestine cancer lupus erythematosus marasmus myocardial infarction neurocirculatory asthenia newborn respiratory distress syndrome nutrition disease obesity obsessive-compulsive disorder oligospermia osteomyelitis osteoporosis pneumonia polycystic ovary syndrome prostate cancer prostate carcinoma protein C deficiency protein S deficiency protein-energy malnutrition schizophrenia silent myocardial infarction systemic lupus erythematosus testicular cancer thrombophilia transthyretin amyloidosis tropical sprue ulcerative colitis
4069	lysozyme	LYZ Aliases: renal amyloidosis	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 Behcet's disease Burkitt lymphoma Crohn's colitis Crohn's disease Graves' disease Langerhans-cell histiocytosis Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Pick's disease Reye syndrome Shwachman-Diamond syndrome Sjogren's syndrome abdominal obesity-metabolic syndrome 1 acinar cell carcinoma acne acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia adenocarcinoma adenoid cystic carcinoma adenoma alcohol dependence alcohol use disorder allergic rhinitis alternating hemiplegia of childhood amyloidosis anorexia nervosa aphthous stomatitis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome autonomic neuropathy bacterial infectious disease bacterial vaginosis biliary tract disease breast cancer breast carcinoma cancer candidiasis celiac disease central nervous system cancer central nervous system disease cerebral degeneration childhood leukemia cholestasis chronic ethmoiditis chronic monocytic leukemia chronic myelomonocytic leukemia chronic sphenoidal sinusitis colitis common cold complement deficiency congestive heart failure coronary artery disease craniosynostosis cribriform carcinoma dacryoadenitis dacryocystitis diabetes mellitus diabetic ketoacidosis diarrhea dysentery egg allergy endocrine exophthalmos essential hypertension exanthem familial hyperlipidemia familial mediterranean fever familial nephrotic syndrome familial visceral amyloidosis follicular adenoma gallbladder disease gastritis gastroduodenal Crohn's disease gastroenteritis gastrointestinal stromal tumor gastrointestinal system disease gingivitis gliosarcoma glomerulonephritis granular cell carcinoma hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypertension hyperthyroidism hypohidrotic ectodermal dysplasia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease intestinal disease intestinal infectious disease jejunoileitis juvenile myelomonocytic leukemia juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease kidney failure leukemia lipoid nephrosis liver cancer liver disease malignant fibrous histiocytoma mastitis meningitis mevalonic aciduria microcystic adenoma mixed glioma myeloid sarcoma nephritis nephrosis nephrotic syndrome nervous system disease neuropathy nodular prostate non-Langerhans-cell histiocytosis obsolete malignant histiocytosis obsolete ymphosarcoma obstructive jaundice oral candidiasis oral mucosa leukoplakia papillary adenoma parapsoriasis periodontal disease peripheral nervous system disease polyneuropathy post-traumatic stress disorder proctitis prostatic adenoma proteinuria psoriasis pulmonary tuberculosis purpura pustulosis of palm and sole pyoureter reticulohistiocytic granuloma rheumatoid arthritis salivary gland adenoid cystic carcinoma sarcoidosis seborrheic keratosis shigellosis sickle cell anemia skin disease spiradenoma stomach cancer stomach carcinoma systemic lupus erythematosus thyrotoxicosis tuberculosis tuberculous pneumothorax tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uremia ureteral obstruction uveoparotid fever vaginitis vasomotor rhinitis vulvitis vulvovaginitis white sponge nevus
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
4123	mannosidase alpha class 2C member 1	MAN2C1	Homo sapiens (human)	alpha-mannosidosis breast cancer breast carcinoma carcinoma esophageal cancer esophageal carcinoma intellectual disability learning disability post-traumatic stress disorder prostate cancer prostate carcinoma sarcomatoid carcinoma
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
4350	N-methylpurine DNA glycosylase	MPG Aliases: MDG alkyladenine DNA glycosylase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Barrett's esophagus Bloch-Sulzberger syndrome IgA glomerulonephritis Pick's disease Reye syndrome adenocarcinoma adenoma anal carcinoma in situ anemia aortic valve disease 2 aortic valve stenosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ chikungunya colorectal cancer colorectal carcinoma common wart dengue hemorrhagic fever depressive disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder embryoma eosinophilic esophagitis esophagus adenocarcinoma familial retinoblastoma follicular adenoma gallbladder cancer gallbladder carcinoma giant cell glioblastoma glioblastoma gliosarcoma hepatitis C hepatocellular carcinoma high grade glioma hyperglycemia hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer leishmaniasis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia major depressive disorder male infertility melancholic depression melanoma microcystic adenoma mixed glioma multiple myeloma neurotic disorder obsolete melancholia papillary adenoma polycystic ovary syndrome postinflammatory pulmonary fibrosis pulmonary fibrosis retinoblastoma rheumatoid arthritis sarcomatoid carcinoma skin melanoma trilateral retinoblastoma tuberculosis type 2 diabetes mellitus ulcerative colitis visceral leishmaniasis xeroderma pigmentosum group C
4595	mutY DNA glycosylase	MUTYH Aliases: MYH	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Hantavirus hemorrhagic fever with renal syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lynch syndrome Muir-Torre syndrome Peutz-Jeghers syndrome acoustic neuroma adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma age related macular degeneration anal carcinoma in situ angiomatous meningioma arthritis arthropathy benign meningioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral convexity meningioma cervical squamous cell carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia cholangiocarcinoma chromosome 10q23 deletion syndrome clear cell meningioma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic ketoacidosis distal arthrogryposis dysthymic disorder embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis 2 familial adenomatous polyposis female breast carcinoma fibrous meningioma follicular adenoma gastroenteritis gastrointestinal system cancer gastrointestinal system disease gliosarcoma granular cell carcinoma hair follicle neoplasm head and neck cancer head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor juvenile polyposis syndrome large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma macular degeneration major depressive disorder melancholic depression melanoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma mixed glioma myeloproliferative neoplasm nervous system cancer neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neurotic disorder obsolete melancholia olfactory groove meningioma osteoarthritis ovarian cancer pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenoma parasagittal meningioma pilomatrixoma pituitary adenoma primary open angle glaucoma proctitis prostate cancer prostate carcinoma psammomatous meningioma rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis sarcomatoid carcinoma sebaceous adenocarcinoma secretory meningioma skin melanoma spinal meningioma stomach cancer stomach carcinoma in situ stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma transitional meningioma transthyretin amyloidosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer von Hippel-Lindau disease
4668	alpha-N-acetylgalactosaminidase	NAGA Aliases: D22S674 alpha-galactosidase B	Homo sapiens (human)	Clouston syndrome Fabry disease Kanzaki disease Schindler disease type 1 Unverricht-Lundborg syndrome acquired hyperkeratosis alternating hemiplegia of childhood angiokeratoma autistic disorder autonomic neuropathy blepharospasm cancer cardiomyopathy cataract central nervous system disease central nervous system origin vertigo cerebral degeneration chylomicron retention disease congenital nystagmus dissociated nystagmus early myoclonic encephalopathy elephantiasis embryoma endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy focal hand dystonia gallbladder disease hypertrophic cardiomyopathy hypertropia influenza intellectual disability learning disability lipid storage disease liver disease lymphedema mechanical strabismus nervous system disease neuroaxonal dystrophy neurodegeneration with brain iron accumulation 2a neuropathy ophthalmoplegia optic atrophy pathologic nystagmus peripheral nervous system disease sensorineural hearing loss spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 trichomoniasis 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
4758	neuraminidase 1	NEU1 Aliases: sialidase-1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Crohn's colitis Crohn's disease Ewing sarcoma of bone GM1 gangliosidosis type 1 GM1 gangliosidosis IgA glomerulonephritis Laron syndrome Marfan syndrome Paget's disease of bone Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia acquired hyperkeratosis adenocarcinoma adenoma allergic rhinitis anaplastic astrocytoma arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease aspartylglucosaminuria atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma biliary tract cancer bladder urothelial carcinoma blepharospasm bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cataract cerebral degeneration childhood cerebral astrocytoma childhood osteosarcoma cholangiocarcinoma chondrodysplasia punctata chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease cribriform carcinoma cutaneous Paget's disease dentatorubral-pallidoluysian atrophy dermoid cyst of ovary dissociated nystagmus early myoclonic encephalopathy embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma endomyocardial fibrosis enterocele epilepsy fibrillary astrocytoma focal hand dystonia fucosidosis galactosialidosis gastroesophageal junction adenocarcinoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance glycoproteinosis granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hyperglycemia hypertrophic cardiomyopathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza inguinal hernia intellectual disability intrahepatic cholangiocarcinoma invasive ductal carcinoma juvenile pilocytic astrocytoma kidney disease large intestine cancer learning disability livedoid vasculitis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease malignant astrocytoma mammary Paget's disease melanoma meningitis microphthalmia mucolipidosis mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia nephritis nervous system cancer nonpapillary renal cell carcinoma osteochondrodysplasia osteosarcoma ovarian cancer ovarian carcinoma ovary adenocarcinoma papillary carcinoma papillary renal cell carcinoma pathologic nystagmus pilocytic astrocytoma postinflammatory pulmonary fibrosis prediabetes syndrome progressive myoclonus epilepsy 1A progressive myoclonus epilepsy 4 progressive myoclonus epilepsy prostate cancer prostate carcinoma proteinuria protoplasmic astrocytoma pulmonary fibrosis recurrent corneal erosion renal carcinoma renal cell carcinoma retinal disease retinitis rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scoliosis sebaceous carcinoma sensorineural hearing loss serous cystadenocarcinoma situs inversus skin melanoma speech disorder spontaneous ocular nystagmus steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma sweat gland cancer systemic lupus erythematosus tarsal-carpal coalition syndrome transitional cell carcinoma tuberous sclerosis tubular adenocarcinoma ulcerative colitis uterine corpus cancer vascular skin disease vasomotor rhinitis visual epilepsy vitiligo
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
4913	nth like DNA glycosylase 1	NTHL1 Aliases: NTH1 OCTS3	Homo sapiens (human)	B-cell lymphoma Fanconi anemia complementation group D2 Fanconi anemia Langerhans-cell histiocytosis acoustic neuroma actinic keratosis adenocarcinoma adenoma angiomatous meningioma autosomal recessive intellectual developmental disorder basal cell carcinoma benign meningioma breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cerebral convexity meningioma clear cell meningioma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma dermatosis papulosa nigra duodenum adenocarcinoma embryoma endometrial cancer endometrial carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis 3 familial adenomatous polyposis fibrous meningioma follicular adenoma intraorbital meningioma intraventricular meningioma inverted follicular keratosis islet cell tumor large intestine cancer laryngeal carcinoma larynx cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma melanoacanthoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma non-Hodgkin lymphoma obsolete ymphosarcoma olfactory groove meningioma ovarian cyst pancreatic adenocarcinoma papillary adenoma parasagittal meningioma pituitary adenoma psammomatous meningioma rectal benign neoplasm rectum cancer reticulosarcoma sarcomatoid carcinoma seborrheic dermatitis seborrheic keratosis secretory meningioma skin benign neoplasm skin cancer skin disease spinal meningioma squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tongue squamous cell carcinoma transitional meningioma tuberous sclerosis 2 tuberous sclerosis urinary bladder cancer uterine corpus cancer

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