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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 **576 - 600** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
63917	polypeptide N-acetylgalactosaminyltransferase 11	GALNT11 Aliases: GalNAc-T11 polypeptide GalNAc transferase 11	Homo sapiens (human)	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
79695	polypeptide N-acetylgalactosaminyltransferase 12	GALNT12 Aliases: GalNAc-T12 polypeptide GalNAc transferase 12	Homo sapiens (human)	adenocarcinoma adenoma bilateral breast cancer cancer colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma islet cell tumor large intestine cancer microcystic adenoma papillary adenoma
114805	polypeptide N-acetylgalactosaminyltransferase 13	GALNT13 Aliases: GalNAc-T13 KIAA1918 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 13 polypeptide GalNAc transferase 13	Homo sapiens (human)	cancer chronic obstructive pulmonary disease lung benign neoplasm lung carcinoma sickle cell anemia
79623	polypeptide N-acetylgalactosaminyltransferase 14	GALNT14 Aliases: FLJ12691 GalNac-T10 GalNac-T14 polypeptide GalNAc transferase 14	Homo sapiens (human)	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
117248	polypeptide N-acetylgalactosaminyltransferase 15	GALNT15 Aliases: GALNT7 polypeptide GalNAc transferase 15 pp-GalNAc-T15	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
57452	polypeptide N-acetylgalactosaminyltransferase 16	GALNT16 Aliases: GalNAc-T16 KIAA1130 polypeptide GalNAc transferase 16	Homo sapiens (human)	breast cancer breast carcinoma idiopathic scoliosis
64409	polypeptide N-acetylgalactosaminyltransferase 17	GALNT17 Aliases: GALNTL3 GalNAc-T17 GalNAc-T19 GalNAc-T5L polypeptide GalNAc transferase 3 polypeptide N-acetylgalactosaminyltransferase-like 3 ppGalNAc-T17	Homo sapiens (human)	allergic asthma asthma autism spectrum disorder autistic disorder intrinsic asthma
374378	polypeptide N-acetylgalactosaminyltransferase 18	GALNT18 Aliases: GALNT15 GalNAc-T18 MGC71806 polypeptide GalNAc transferase 18	Homo sapiens (human)	gastric adenocarcinoma rheumatoid arthritis
2590	polypeptide N-acetylgalactosaminyltransferase 2	GALNT2 Aliases: GalNAc-T2 polypeptide GalNAc transferase 2	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 achondroplasia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital disorder of glycosylation type II coronary artery disease diabetes mellitus embryoma essential hypertension familial hyperlipidemia gastric adenocarcinoma gliosarcoma hepatocellular carcinoma high grade glioma hyperalphalipoproteinemia 1 hyperglycemia hypertension hypochondroplasia inflammatory bowel disease 1 inflammatory bowel disease liver cancer mixed glioma nutmeg liver obesity papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma type 2 diabetes mellitus ulcerative colitis
2591	polypeptide N-acetylgalactosaminyltransferase 3	GALNT3 Aliases: GalNAc-T3 HFTC HHS polypeptide GalNAc transferase 3	Homo sapiens (human)	CHARGE syndrome X-linked dyskeratosis congenita adenocarcinoma adenoma angioid streaks arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive hypophosphatemic rickets bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cerebral infarction cerebrovascular disease chondrocalcinosis chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma dental enamel hypoplasia dental pulp calcification dentin dysplasia diabetes mellitus diabetic ketoacidosis disease of metabolism dyskeratosis congenita embryoma endometriosis of uterus endometriosis gallbladder cancer gallbladder carcinoma granular cell carcinoma hypercalcemia hyperostosis hyperphosphatemia hyperphosphatemic familial tumoral calcinosis hypotrichosis 1 hypotrichosis large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma microphthalmia musculoskeletal system disease nephrocalcinosis nodular prostate nutmeg liver obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 osteoarthritis osteoporosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma phosphorus metabolism disease prostate cancer prostate carcinoma prostatic adenoma pulp degeneration renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin disease skin melanoma squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus viral infectious disease
8693	polypeptide N-acetylgalactosaminyltransferase 4	GALNT4 Aliases: GalNAc-T4 polypeptide GalNAc transferase 4	Homo sapiens (human)	acute chest syndrome arteriosclerotic cardiovascular disease atherosclerosis breast cancer cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease large intestine cancer prostate cancer prostate carcinoma
11227	polypeptide N-acetylgalactosaminyltransferase 5	GALNT5 Aliases: GalNAc-T5 polypeptide GalNAc transferase 5	Homo sapiens (human)	breast cancer cancer embryoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma stomach cancer stomach carcinoma
11226	polypeptide N-acetylgalactosaminyltransferase 6	GALNT6 Aliases: GalNAc-T6 polypeptide GalNAc transferase 6	Homo sapiens (human)	adenocarcinoma adenoma breast cancer breast carcinoma cancer carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis granular cell carcinoma large intestine cancer lung adenocarcinoma lung cancer ovarian cancer ovarian carcinoma sarcomatoid carcinoma serous cystadenocarcinoma stomach cancer stomach carcinoma tubular adenocarcinoma uterine corpus cancer
51809	polypeptide N-acetylgalactosaminyltransferase 7	GALNT7 Aliases: GALNAC-T7 polypeptide GalNAc transferase 7	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma colorectal cancer colorectal carcinoma coronary artery disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma gliosarcoma high grade glioma large intestine cancer laryngeal squamous cell carcinoma mixed glioma nasopharynx carcinoma
26290	polypeptide N-acetylgalactosaminyltransferase 8	GALNT8 Aliases: GALNAC-T8 polypeptide GalNAc transferase 8	Homo sapiens (human)	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C
50614	polypeptide N-acetylgalactosaminyltransferase 9	GALNT9 Aliases: GALNAC-T9 polypeptide GalNAc transferase 9	Homo sapiens (human)	breast cancer breast carcinoma cancer neuroblastoma
168391	polypeptide N-acetylgalactosaminyltransferase like 5	GALNTL5 Aliases: GalNAc-T5L polypeptide GalNAc transferase-like 5	Homo sapiens (human)	actinic keratosis gastric adenocarcinoma male infertility seborrheic keratosis skin disease
442117	polypeptide N-acetylgalactosaminyltransferase like 6	GALNTL6 Aliases: GALNT17 GalNAc-T6L polypeptide GalNAc transferase-like 6	Homo sapiens (human)	nicotine dependence
2592	galactose-1-phosphate uridylyltransferase	GALT	Homo sapiens (human)	acquired immunodeficiency syndrome agnosia androgen insensitivity syndrome bacterial sepsis blood coagulation disease cancer cataract cerebellar ataxia cerebellar disease classic galactosemia cystinuria diabetic cataract diarrhea disease of metabolism endometriosis of uterus endometriosis galactokinase deficiency galactose epimerase deficiency galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatocellular carcinoma human immunodeficiency virus infectious disease hypoglycemia hypogonadism inherited metabolic disorder intellectual disability kwashiorkor lactic acidosis learning disability liver cancer liver cirrhosis liver disease marasmus neonatal jaundice nutrition disease osteoporosis ovarian cancer ovarian carcinoma premature menopause primary ovarian insufficiency protein-energy malnutrition proteinuria speech-language disorder-1 trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
23193	glucosidase II alpha subunit	GANAB Aliases: G2AN GIIA GluII KIAA0088 neutral alpha-glucosidase AB	Homo sapiens (human)	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
2595	glucosidase alpha, neutral C	GANC	Homo sapiens (human)	congenital dyserythropoietic anemia panic disorder
2597	glyceraldehyde-3-phosphate dehydrogenase	GAPDH	Homo sapiens (human)	ACTH-secreting pituitary adenoma 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 Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Down syndrome Dubowitz syndrome Ewing sarcoma HELLP 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 IgA glomerulonephritis Japanese encephalitis Kawasaki disease Kennedy's disease Keshan disease Laron syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Sertoli cell-only syndrome Silver-Russell syndrome Turner syndrome X-linked Aarskog syndrome X-linked spermatogenic failure 1 Zika fever achondroplasia acidophil adenoma acoustic neuroma acute lymphoblastic leukemia acute megakaryocytic leukemia acute poststreptococcal glomerulonephritis adenosarcoma adrenal adenoma adrenal cortex cancer alcohol dependence alcohol use disorder alcoholic cardiomyopathy alcoholic hepatitis allergic asthma amyloidosis amyotrophic lateral sclerosis angioimmunoblastic T-cell lymphoma angiomatous meningioma aortic aneurysm aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arthritis arthropathy asthma autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial sepsis basal cell carcinoma benign meningioma bicuspid aortic valve disease bladder carcinoma bone osteosarcoma brain glioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cerebral convexity meningioma cerebral degeneration cervical cancer cervix carcinoma childhood osteosarcoma chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease dengue disease dentatorubral-pallidoluysian atrophy developmental and epileptic encephalopathy 2 diabetes mellitus diabetic cataract diabetic retinopathy diffuse large B-cell lymphoma dysplastic nevus syndrome early infantile epileptic encephalopathy embryoma encephalitis encephalomyelitis endocrine exophthalmos endomyocardial fibrosis epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fasciitis fibrous meningioma follicular lymphoma ganglioneuroblastoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gonadal dysgenesis granuloma annulare hepatitis B hepatitis C hepatitis D hepatocellular carcinoma hereditary spherocytosis high grade glioma hypertrophic cardiomyopathy hypopharynx cancer immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal schistosomiasis intraorbital meningioma intraventricular meningioma intrinsic asthma kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease leishmaniasis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioleiomyomatosis malaria melanoma membranous glomerulonephritis meningioma meningothelial meningioma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma microphthalmia middle cerebral artery infarction mixed glioma multiple endocrine neoplasia type 1 multiple myeloma multiple sclerosis myelitis nephritis nephroblastoma neuroblastoma neurodegenerative disease neuroectodermal tumor nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete infantile epileptic encephalopathy obsolete ymphosarcoma olfactory groove meningioma oral squamous cell carcinoma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma pituitary adenoma placental insufficiency pre-eclampsia progressive muscular atrophy progressive myoclonus epilepsy prolactinoma prostate cancer prostate carcinoma psammomatous meningioma psoriasis pustulosis of palm and sole reflex sympathetic dystrophy renal carcinoma renal cell carcinoma rheumatic heart disease sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia secretory meningioma sickle cell anemia skin melanoma sleeping sickness spinal meningioma spinal muscular atrophy status epilepticus stomach cancer stomach carcinoma tarsal-carpal coalition syndrome thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma transitional meningioma trypanosomiasis tuberculosis type 2 diabetes mellitus ulcerative colitis urinary bladder cancer viral infectious disease visceral leishmaniasis yellow fever
26330	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	GAPDHS Aliases: GAPD2 GAPDH-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 Creutzfeldt-Jakob disease Pick's disease Reye syndrome cancer cerebral degeneration diabetes mellitus diabetic ketoacidosis embryoma melanoma skin melanoma
2619	growth arrest specific 1	GAS1	Homo sapiens (human)	Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Kallmann syndrome Laron syndrome Marfan syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Potter's syndrome Sakati-Nyhan syndrome Sheehan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia allergic asthma asthma bilateral renal aplasia bladder carcinoma bone osteosarcoma branchiootic syndrome breast cancer breast carcinoma cancer cavernous hemangioma central nervous system cancer childhood osteosarcoma choanal atresia chorioangioma chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate collecting duct carcinoma coloboma colorectal cancer colorectal carcinoma congenital hypothyroidism degenerative disc disease diabetes mellitus diabetic ketoacidosis disorder of sexual development duodenal atresia embryoma epilepsy gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor hemangioma hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory neuropathy hermaphroditism high grade glioma histiocytoid hemangioma holoprosencephaly 1 holoprosencephaly hypertropia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothyroidism intellectual disability intramuscular hemangioma intrinsic asthma isolated cleft palate 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 kidney disease large intestine cancer learning disability lymphangioma mechanical strabismus melanoma microcephaly mixed glioma myxedema nephritis nephrosis neuroblastoma neuropathy nevoid basal cell carcinoma syndrome nonpapillary renal cell carcinoma ophthalmoplegia orofaciodigital syndrome I orofaciodigital syndrome X osteosarcoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease placental insufficiency primary open angle glaucoma pseudohermaphroditism pyoureter rabies renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma scoliosis sensorineural hearing loss sensory peripheral neuropathy situs inversus skin melanoma solitary median maxillary central incisor stomach cancer stomach carcinoma strabismus tetralogy of Fallot thymus gland disease thyroid gland papillary carcinoma tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer visual epilepsy
2629	glucosylceramidase beta 1	GBA1 Aliases: glucocerebrosidase	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 Canavan disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Cogan syndrome DiGeorge syndrome Fabry disease Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Lafora disease Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Netherton syndrome Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease type C2 Niemann-Pick disease PCWH syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease REM sleep behavior disorder Reye syndrome Sjogren-Larsson syndrome Tay-Sachs disease Unverricht-Lundborg syndrome West Nile fever Wolman disease abdominal obesity-metabolic syndrome 1 achondroplasia acquired hyperkeratosis actinic keratosis adult lymphoma agenesis of the corpus callosum with peripheral neuropathy agnosia alternating hemiplegia of childhood amyotrophic lateral sclerosis anemia arthritis arthropathy atypical Gaucher's disease due to saposin c deficiency autonomic neuropathy autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis autosomal recessive osteopetrosis 7 blepharospasm brain disease cancer cardiac arrest central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma chylomicron retention disease communicating hydrocephalus congestive heart failure dementia dentatorubral-pallidoluysian atrophy depressive disorder developmental coordination disorder diffuse interstitial keratitis diffuse large B-cell lymphoma dissociated nystagmus dysthymic disorder dystonia early myoclonic encephalopathy ectropion embryoma endometriosis of uterus endometriosis esotropia essential hypertension essential tremor female stress incontinence fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome focal hand dystonia follicular lymphoma glucose intolerance hemopericardium hepatitis B hepatopulmonary syndrome hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hydrocephalus hypertension hypomyelinating leukodystrophy 2 hypomyelinating leukodystrophy 3 hypomyelinating leukodystrophy 4 hypomyelinating leukodystrophy 6 hypomyelinating leukodystrophy 9 ichthyosis interstitial lung disease intracranial aneurysm keratosis follicularis late onset Parkinson's disease leukoencephalopathy with vanishing white matter leukopenia lingual-facial-buccal dyskinesia lipid storage disease liver cirrhosis lymphoma lysosomal storage disease macrocytic anemia major depressive disorder melancholic depression metachromatic leukodystrophy microcephaly mitral valve stenosis mongolian spot monocular esotropia motor peripheral neuropathy movement disease multiple myeloma nervous system disease neuroblastoma neurodegenerative disease neurotic disorder non-Hodgkin lymphoma obsolete congenital ichthyosiform erythroderma obsolete constipation obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus ophthalmoplegia osteoarthritis osteonecrosis osteopetrosis osteosclerosis pancytopenia pathologic nystagmus pericardial effusion placental insufficiency polyhydramnios prediabetes syndrome primary pulmonary hypertension progressive muscular atrophy progressive myoclonus epilepsy 4 progressive myoclonus epilepsy progressive supranuclear palsy proteinuria pseudoxanthoma elasticum psoriasis reticulosarcoma schizophrenia seborrheic keratosis secondary Parkinson disease senile degeneration of brain sensorineural hearing loss skin disease speech disorder sphingolipidosis spontaneous ocular nystagmus thrombocytopenia velocardiofacial syndrome

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