GlyCosmos Portal

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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **901 - 925** of **1582** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
3292	hydroxysteroid 17-beta dehydrogenase 1	HSD17B1 Aliases: Estradiol 17-beta-dehydrogenase-1 HSD17 MGC138140 SDR28C1 short chain dehydrogenase/reductase family 28CE, member 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 Pick's disease Reye syndrome Sertoli-Leydig cell tumor T-cell acute lymphoblastic leukemia adenocarcinoma adenoma breast cancer breast carcinoma breast disease breast fibrocystic disease bronchus cancer bronchus carcinoma cancer cerebral degeneration cholera choriocarcinoma colorectal cancer colorectal carcinoma congenital adrenal hyperplasia cribriform carcinoma cystic kidney disease embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis follicular adenoma granular cell carcinoma hepatocellular carcinoma hereditary breast ovarian cancer syndrome infertility invasive ductal carcinoma lactocele large intestine cancer leiomyoma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease male breast cancer microcystic adenoma microglandular adenosis myofibroma nodular prostate non-congenital cyst of kidney obesity osteoporosis ovarian cancer ovarian carcinoma papillary adenoma placenta cancer placental insufficiency polycystic ovary syndrome prostate cancer prostate carcinoma prostatic adenoma sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma tubular adenocarcinoma uterine corpus cancer uterine disease uterine fibroid
51144	hydroxysteroid 17-beta dehydrogenase 12	HSD17B12 Aliases: 3-ketoacyl-CoA reductase KAR SDR12C1 short chain dehydrogenase/reductase family 12C, member 1	Homo sapiens (human)	breast cancer breast carcinoma cancer carcinoma cardiovascular system disease diabetes mellitus disease of mental health embryoma head and neck squamous cell carcinoma heart disease idiopathic scoliosis intellectual disability invasive ductal carcinoma learning disability melanoma neuroblastoma obesity ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma psychotic disorder sarcomatoid carcinoma schizophrenia skin melanoma type 2 diabetes mellitus
3294	hydroxysteroid 17-beta dehydrogenase 2	HSD17B2 Aliases: HSD17 SDR9C2 short chain dehydrogenase/reductase family 9C, member 2	Homo sapiens (human)	breast cancer breast carcinoma cancer cavernous hemangioma chorioangioma colorectal cancer colorectal carcinoma dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis glomus tumor hemangioma hepatocellular carcinoma histiocytoid hemangioma intramuscular hemangioma large intestine cancer leiomyoma liver cancer lymphangioma myofibroma nodular prostate osteoporosis ovarian cancer ovarian carcinoma polycystic ovary syndrome prostate cancer prostate carcinoma prostatic adenoma rectal benign neoplasm rectum adenocarcinoma rectum cancer sporadic breast cancer stomach cancer stomach carcinoma uterine corpus cancer uterine fibroid
3293	hydroxysteroid 17-beta dehydrogenase 3	HSD17B3 Aliases: SDR12C2 short chain dehydrogenase/reductase family 12C, member 2	Homo sapiens (human)	17-beta hydroxysteroid dehydrogenase 3 deficiency Alzheimer's disease Kallmann syndrome Sheehan syndrome acne androgen insensitivity syndrome autoimmune hepatitis cancer congenital adrenal hyperplasia congenital hypothyroidism cryptorchidism diabetes mellitus disorder of sexual development endometriosis of uterus endometriosis gynecomastia hepatitis hermaphroditism hypertrophy of breast hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 23 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 hypospadias hypothyroidism infant gynecomastia infertility 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 myxedema nicotine dependence nodular prostate obesity panhypopituitarism premature menopause prostate cancer prostate carcinoma prostatic adenoma pseudohermaphroditism type 2 diabetes mellitus
3295	hydroxysteroid 17-beta dehydrogenase 4	HSD17B4 Aliases: 17-beta-HSD IV 17-beta-hydroxysteroid dehydrogenase 4 17beta-estradiol dehydrogenase type IV 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase D-3-hydroxyacyl-CoA dehydratase D-bifunctional protein, peroxisomal DBP MFE-2 SDR8C1 beta-hydroxyacyl dehydrogenase beta-keto-reductase peroxisomal multifunctional protein 2 short chain dehydrogenase/reductase family 8C, member 1	Homo sapiens (human)	Addison's disease 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 D-bifunctional protein deficiency Friedreich ataxia Laron syndrome Perrault syndrome Pick's disease Refsum disease Reye syndrome Stiff-Person syndrome Turner syndrome West syndrome Zellweger syndrome achondroplasia adrenal carcinoma adrenal cortex cancer adrenal cortical hypofunction adrenocortical carcinoma adrenoleukodystrophy alpha-methylacyl-CoA racemase deficiency androgen insensitivity syndrome beta-ketothiolase deficiency blindness breast cancer breast carcinoma cancer carnitine palmitoyltransferase I deficiency cerebellar ataxia cerebellar disease cerebral degeneration cholestasis clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital bile acid synthesis defect 4 congenital nystagmus craniosynostosis cystic kidney disease diabetic ketoacidosis dissociated nystagmus endometrial cancer endometrial carcinoma epilepsy essential hypertension gonadal dysgenesis hepatocellular carcinoma hereditary ataxia hydrocephalus hypertension hypertropia infantile Refsum disease large intestine cancer leukodystrophy lipid metabolism disorder liver cancer liver carcinoma mechanical strabismus non-congenital cyst of kidney obesity obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 ophthalmoplegia osteoporosis pathologic nystagmus peroxisomal disease peroxisome biogenesis disorder 1A polycystic ovary syndrome polyhydramnios premature menopause primary cerebellar degeneration primary ovarian insufficiency prostate cancer prostate carcinoma rhizomelic chondrodysplasia punctata type 1 scoliosis seminoma sensorineural hearing loss spontaneous ocular nystagmus steatotic liver disease strabismus testicular cancer testicular germ cell cancer 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 uterine corpus cancer visual epilepsy
8630	hydroxysteroid 17-beta dehydrogenase 6	HSD17B6 Aliases: 3(alpha->beta)-hydroxysteroid epimerasel 3-hydroxysteroid epimerase HSE NAD+ -dependent 3 alpha-hydroxysteroid dehydrogenase RODH SDR9C6 oxidative 3-alpha-hydroxysteroid-dehydrogenase oxidoreductase retinol dehydrogenase short chain dehydrogenase/reductase family 9C, member 6	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 Coffin-Lowry syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Leber congenital amaurosis Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sjogren-Larsson syndrome autoimmune hepatitis autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer cerebral degeneration chromophobe renal cell carcinoma chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy congenital adrenal hyperplasia dengue disease diabetes mellitus embryoma endometrial cancer endometrial carcinoma exocrine pancreatic insufficiency fundus albipunctatus fundus dystrophy gallbladder disease hepatitis ichthyosis keratosis follicularis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melioidosis mitochondrial metabolism disease mitochondrial myopathy mongolian spot multiple sclerosis neuroblastoma neurofibromatosis 1 neurofibromatosis nonpapillary renal cell carcinoma obsolete congenital ichthyosiform erythroderma optic atrophy papillary renal cell carcinoma paraplegia polycystic ovary syndrome prostate cancer prostate carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinitis pigmentosa rheumatoid arthritis sarcomatoid renal cell carcinoma shigellosis spinocerebellar ataxia type 1 systemic lupus erythematosus tuberculosis type 2 diabetes mellitus uterine corpus cancer viral infectious disease yellow fever
51478	hydroxysteroid 17-beta dehydrogenase 7	HSD17B7 Aliases: PRAP SDR37C1 short chain dehydrogenase/reductase family 37C, member 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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Zellweger syndrome adenocarcinoma adenoma adrenal gland cancer androgen insensitivity syndrome basal cell carcinoma breast cancer breast carcinoma breast ductal carcinoma cancer carcinoma cerebral degeneration choriocarcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis disorder of sexual development duodenum cancer duodenum disease embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis esophageal disease follicular adenoma gallbladder cancer gallbladder carcinoma glaucoma goiter heart cancer hereditary breast ovarian cancer syndrome hermaphroditism hyperandrogenism hypogonadotropic hypogonadism 23 with or without anosmia hypospadias invasive ductal carcinoma large intestine cancer leiomyoma microcystic adenoma multiple sclerosis myofibroma nodular prostate ovarian cancer ovarian carcinoma papillary adenoma peroxisomal disease peroxisome biogenesis disorder 1A pheochromocytoma placenta cancer polycystic ovary syndrome primary immunodeficiency disease prolactinoma prostate cancer prostate carcinoma prostatic adenoma pseudohermaphroditism sebaceous carcinoma small intestine cancer sporadic breast cancer steatotic liver disease steroid inherited metabolic disorder stomach cancer stomach carcinoma stomach disease sweat gland cancer thymic carcinoma thymoma thyroid gland disease type 2 diabetes mellitus uterine corpus cancer uterine fibroid
7923	hydroxysteroid 17-beta dehydrogenase 8	HSD17B8 Aliases: D6S2245E H2-KE6 HKE6 KE6 RING2 SDR30C1 short chain dehydrogenase/reductase family 30C, member 1	Homo sapiens (human)	breast cancer breast carcinoma cancer hepatitis B rheumatoid arthritis tuberculosis
3251	hypoxanthine phosphoribosyltransferase 1	HPRT1 Aliases: HGPRT Lesch-Nyhan syndrome hypoxanthine guanine phosphoribosyl transferase	Homo sapiens (human)	Alzheimer's disease Borjeson-Forssman-Lehmann syndrome CD40 ligand deficiency Creutzfeldt-Jakob disease Duchenne muscular dystrophy Ewing sarcoma Fanconi anemia complementation group A Fanconi anemia Guillain-Barre syndrome HRPT-related hyperuricemia Laron syndrome Lesch-Nyhan syndrome Marfan syndrome Miller Fisher syndrome Rett syndrome Simpson-Golabi-Behmel syndrome type 1 T-cell acute lymphoblastic leukemia X-linked dilated cardiomyopathy X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 achondroplasia acoustic neuroma acquired polycythemia acute biphenotypic leukemia acute kidney failure acute leukemia acute lymphoblastic leukemia acute myeloid leukemia acute promyelocytic leukemia adult acute lymphocytic leukemia adult fibrosarcoma agnosia alternating hemiplegia of childhood anemia angiomatous meningioma arthritis arthropathy aspartylglucosaminuria ataxia telangiectasia atrophy of testis attention deficit hyperactivity disorder autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy bacterial sepsis basal ganglia disease benign meningioma blepharospasm bone disease bone marrow cancer bone marrow disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence cartilage disease central nervous system disease central nervous system lymphoma cerebral convexity meningioma cerebral palsy childhood acute lymphocytic leukemia childhood leukemia childhood type dermatomyositis choriocarcinoma chronic fatigue syndrome chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy chronic myeloid leukemia clear cell meningioma colitis collagen disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer connective tissue disease demyelinating disease dermatomyositis developmental coordination disorder diabetic ketoacidosis dilated cardiomyopathy 1A 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 dysplastic nevus syndrome dystonia embryoma encephalitis encephalomyelitis endometrial stromal sarcoma endometriosis of uterus endometriosis epilepsy epithelioid sarcoma erythropoietin polycythemia esophageal cancer esophageal carcinoma familial erythrocytosis 2 fibrosarcoma fibrous meningioma focal hand dystonia frozen shoulder fucosidosis galactosialidosis gastroenteritis giardiasis glomerulonephritis glycoproteinosis gout hematopoietic system disease hemiplegia hepatoblastoma hepatocellular carcinoma herpes simplex histiocytosis hyperglycemia hyperuricemia ileitis ileocolitis immune system disease inflammatory bowel disease inherited metabolic disorder intellectual disability intrahepatic cholestasis of pregnancy intraorbital meningioma intraventricular meningioma kidney disease kidney failure large intestine cancer learning disability leukemia leukopenia lingual-facial-buccal dyskinesia liver cancer lobular neoplasia lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphoma lymphoplasmacyte-rich meningioma macrocytic anemia malaria measles megaloblastic anemia melanoma meningioma meningothelial meningioma microcystic meningioma middle cerebral artery infarction movement disease multiple sclerosis muscular dystrophy myelitis myeloproliferative neoplasm myositis neovascular inflammatory vitreoretinopathy nephritis nephrolithiasis nephrosis nervous system disease neuroblastoma non-syndromic X-linked intellectual disability obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculocerebrorenal syndrome olfactory groove meningioma osteoarthritis osteoporosis ovarian cancer papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma paroxysmal nocturnal hemoglobinuria pituitary adenoma placenta cancer pleomorphic adenoma polycythemia prostate cancer prostate carcinoma psammomatous meningioma purine-pyrimidine metabolic disorder pyoureter relapsing-remitting multiple sclerosis rheumatoid arthritis sarcoma scleroderma secretory meningioma situs inversus skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal cord disease spinal meningioma spindle cell sarcoma stress polycythemia syringomyelia systemic lupus erythematosus systemic scleroderma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma transitional meningioma tropical spastic paraparesis tuberculosis 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 uric acid nephrolithiasis uterine corpus sarcoma visual epilepsy xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
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
8870	immediate early response 3	IER3	Homo sapiens (human)	T-cell non-Hodgkin lymphoma
3612	inositol monophosphatase 1	IMPA1 Aliases: myo-inositol monophosphatase 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 Duchenne muscular dystrophy Lewy body dementia Pick's disease Reye syndrome alcohol dependence alcohol use disorder antisocial personality disorder aplastic anemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive intellectual developmental disorder 59 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 avoidant personality disorder bipolar disorder brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral atherosclerosis cerebral degeneration cerebral infarction cerebrovascular disease chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy congenital muscular dystrophy conjunctivitis cryptosporidiosis cystitis delusional disorder dermatophytosis diabetes mellitus distal myopathy embryoma epilepsy essential hypertension facioscapulohumeral muscular dystrophy focal epilepsy fundus albipunctatus fungal infectious disease gallbladder disease gliosarcoma glycogen storage disease IV glycogen storage disease VI glycogen storage disease VII heart disease high grade glioma hypertension intellectual disability intracranial arteriosclerosis large intestine cancer learning disability limb-girdle muscular dystrophy liver disease lung benign neoplasm lung cancer lung carcinoma mixed glioma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcissistic personality disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy ovarian cancer ovarian carcinoma paranoid schizophrenia partial motor epilepsy primary pulmonary hypertension retinitis pigmentosa rippling muscle disease 2 sickle cell anemia syndromic X-linked intellectual disability 94 systemic primary carnitine deficiency disease trigonitis type 2 diabetes mellitus visual epilepsy
3613	inositol monophosphatase 2	IMPA2 Aliases: myo-inositol monophosphatase 2	Homo sapiens (human)	bipolar disorder borderline personality disorder cancer cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder dysthymic disorder embryoma endometriosis of ovary endometriosis of uterus endometriosis intermittent explosive disorder major depressive disorder melancholic depression mood disorder neurotic disorder nonpapillary renal cell carcinoma obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
253430	inositol polyphosphate multikinase	IPMK	Homo sapiens (human)	Alzheimer's disease Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease cancer hepatitis idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease ovarian cancer ovarian carcinoma parapsoriasis psoriasis pustulosis of palm and sole ulcerative colitis
3636	inositol polyphosphate phosphatase like 1	INPPL1 Aliases: 51C protein SH2 domain-containing inositol 5'-phosphatase 2 SHIP2 phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2	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 Laron syndrome Pick's disease Reye syndrome Richter's syndrome Turner syndrome abdominal obesity-metabolic syndrome 1 achondroplasia alternating hemiplegia of childhood amnestic disorder atrial fibrillation autonomic neuropathy bone disease breast cancer breast carcinoma cancer cartilage disease central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease chronic lymphocytic leukemia chronic myeloid leukemia cleft palate colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure connective tissue disease cryptorchidism depressive disorder diabetes mellitus diabetic ketoacidosis disease of metabolism dysthymic disorder elephantiasis embryoma essential hypertension giant cell glioblastoma glioblastoma glucose intolerance gonadal dysgenesis gonorrhea hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension insulinoma isolated cleft palate isolated growth hormone deficiency large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung cancer lung non-small cell carcinoma lymphedema major depressive disorder melancholic depression multiple myeloma nervous system disease neurodegenerative disease neurotic disorder obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoporosis-pseudoglioma syndrome papillary adenocarcinoma papillary renal cell carcinoma polyhydramnios prediabetes syndrome retrograde amnesia schneckenbecken dysplasia scoliosis stomach cancer stomach carcinoma thyroid gland papillary carcinoma 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
3628	inositol polyphosphate-1-phosphatase	INPP1	Homo sapiens (human)	bipolar disorder cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer obsolete major affective disorder 2
3631	inositol polyphosphate-4-phosphatase type I A	INPP4A Aliases: Type I inositol 3,4-bisphosphate 4-phosphatase	Homo sapiens (human)	Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma autosomal dominant dyskeratosis congenita 1 bladder carcinoma cancer early myoclonic encephalopathy embryoma intrinsic asthma lung cancer lung non-small cell carcinoma pancreatic cancer pancreatic carcinoma situs inversus tuberous sclerosis urinary bladder cancer
8821	inositol polyphosphate-4-phosphatase type II B	INPP4B	Homo sapiens (human)	Goodpasture syndrome Takayasu's arteritis acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma adult lymphoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 6 benign breast phyllodes tumor bladder carcinoma bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma breast fibroadenosis breast fibrocystic disease breast malignant phyllodes tumor bronchus cancer bronchus carcinoma cancer carcinoma central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood lymphoma childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma embryoma goiter granular cell carcinoma granulomatosis with polyangiitis hepatocellular carcinoma inflammatory breast carcinoma large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma lymphoma melanoma microglandular adenosis multiple sclerosis nasopharynx carcinoma nonpapillary renal cell carcinoma obsolete ymphosarcoma osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma polyarteritis nodosa prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma tubular adenocarcinoma urinary bladder cancer
3632	inositol polyphosphate-5-phosphatase A	INPP5A Aliases: 43 kDa inositol polyphosphate 5-phophatase 5PTASE CTCL tumor antigen HD-CL-02 InsP3 5-phosphatase inositol polyphosphate 5-phophatase, 40kDa type I inositol-1,4,5-trisphosphate 5-phosphatase	Homo sapiens (human)	actinic keratosis ascending cholangitis cancer cholangitis inverted follicular keratosis keratoacanthoma melanoacanthoma oculocerebrorenal syndrome primary sclerosing cholangitis schizophrenia sclerosing cholangitis seborrheic keratosis skin benign neoplasm skin cancer skin disease skin squamous cell carcinoma squamous cell carcinoma suppurative cholangitis tongue squamous cell carcinoma
3633	inositol polyphosphate-5-phosphatase B	INPP5B Aliases: type II inositol 1,4,5-trisphosphate 5-phosphatase	Homo sapiens (human)	Dent disease Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome amyotrophic lateral sclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy congenital hypothyroidism congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy giant cell glioblastoma glaucoma glioblastoma hypothyroidism limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myxedema obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy progressive muscular atrophy rippling muscle disease 2
3635	inositol polyphosphate-5-phosphatase D	INPP5D Aliases: SH2 domain-containing inositol 5'-phosphatase 1 SHIP SHIP1 hp51CN	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 Burkitt lymphoma Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Down syndrome Marfan syndrome Paget's disease of bone Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adult lymphoma allergic disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood lymphoma chronic interstitial cystitis chronic myeloid leukemia chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease cystic fibrosis dementia dermatitis diabetic ketoacidosis diffuse large B-cell lymphoma embryoma essential thrombocythemia gastroenteritis glomerulonephritis gout hematologic cancer hepatocellular carcinoma idiopathic interstitial pneumonia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease interstitial cystitis interstitial keratitis juvenile myelomonocytic leukemia kidney disease large intestine cancer leukemia liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphoma melanoma microphthalmia multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm nephritis nephrosis obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculocerebrorenal syndrome oral candidiasis osteoarthritis periodontitis postinflammatory pulmonary fibrosis primary cutaneous amyloidosis pulmonary fibrosis pyoureter rheumatoid arthritis situs inversus skin melanoma steatotic liver disease stuttering systemic lupus erythematosus 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 ulcerative colitis viral infectious disease visceral leishmaniasis
56623	inositol polyphosphate-5-phosphatase E	INPP5E Aliases: CORS1 PPI5PIV Phosphatidylinositol polyphosphate 5-phosphatase type IV pharbin	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 13 Bardet-Biedl syndrome 14 Bardet-Biedl syndrome 15 Bardet-Biedl syndrome 16 Bardet-Biedl syndrome 17 Bardet-Biedl syndrome 18 Bardet-Biedl syndrome 19 Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 2 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 4 Bardet-Biedl syndrome 5 Bardet-Biedl syndrome 6 Bardet-Biedl syndrome 7 Bardet-Biedl syndrome 8 Bardet-Biedl syndrome 9 Bardet-Biedl syndrome Cogan syndrome Hirschsprung's disease Joubert syndrome 1 Joubert syndrome Kartagener syndrome Klippel-Feil syndrome Laurence-Moon syndrome Meckel syndrome 1 Meckel syndrome adult medulloblastoma autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease blindness cancer cataract central sleep apnea childhood medulloblastoma cleft palate clubfoot coloboma of optic nerve coloboma communicating hydrocephalus congenital nystagmus congenital ptosis cystic kidney disease dextrocardia diffuse interstitial keratitis dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 fundus dystrophy glomerulonephritis hepatocellular carcinoma hydrocephalus hypertropia inguinal hernia intellectual disability interstitial lung disease isolated cleft palate kidney disease kidney failure learning disability leukoplakia of penis liver cancer liver cirrhosis mechanical strabismus medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma nephritis nephrosis non-congenital cyst of kidney obesity obstructive hydrocephalus oculocerebrorenal syndrome ophthalmoplegia patent ductus arteriosus pathologic nystagmus polycystic kidney disease 4 polydactyly portal hypertension primary ciliary dyskinesia 1 primary ciliary dyskinesia ptosis pyoureter scoliosis senile degeneration of brain skin melanoma spondylolisthesis spontaneous ocular nystagmus strabismus viral infectious disease visual epilepsy visual pathway disease
22876	inositol polyphosphate-5-phosphatase F	INPP5F Aliases: KIAA0966 Phosphatidylinositide phosphatase SAC2 SAC2 Sac domain-containing inositol phosphatase 2 Sac domain-containing phosphoinositide 4-phosphatase 2 hSac2	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease breast cancer diabetes mellitus diabetic ketoacidosis familial hyperlipidemia hyperglycemia type 2 diabetes mellitus
27124	inositol polyphosphate-5-phosphatase J	INPP5J Aliases: INPP5 PIPP	Homo sapiens (human)	breast cancer breast carcinoma cancer
51763	inositol polyphosphate-5-phosphatase K	INPP5K Aliases: SKIP skeletal muscle and kidney enriched inositol phosphatase	Homo sapiens (human)	Aicardi-Goutieres syndrome Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Duchenne muscular dystrophy Gaucher's disease Laron syndrome Legg-Calve-Perthes disease Marinesco-Sjogren syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia agnosia anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bladder carcinoma breast cancer breast carcinoma cancer cardiovascular system disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral degeneration cerebrovascular disease congenital muscular dystrophy with cataracts and intellectual disability congenital muscular dystrophy congenital nystagmus coronary artery disease dementia depressive disorder developmental coordination disorder disease of mental health disease of metabolism dissociated nystagmus distal myopathy dysplastic nevus syndrome dysthymic disorder dystonia epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fragile X syndrome generalized anxiety disorder giant cell glioblastoma glioblastoma heart disease hepatocellular carcinoma high grade glioma hypertropia hypogonadism intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer major depressive disorder mechanical strabismus melancholic depression melanoma microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy neuropathy neurotic disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia oculocerebrorenal syndrome oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pathologic nystagmus peripheral nervous system disease phobic disorder phototoxic dermatitis primary cerebellar degeneration psychotic disorder rippling muscle disease 2 scoliosis skin benign neoplasm skin cancer skin carcinoma skin melanoma spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus tauopathy urinary bladder cancer

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