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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 **876 - 900** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
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
8692	hyaluronidase 2	HYAL2 Aliases: LUCA2 LuCa-2 PH-20 homolog lysosomal hyaluronidase	Homo sapiens (human)	B-cell lymphoma acute chest syndrome adenocarcinoma adenoma adult lymphoma arthritis arthropathy breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma childhood lymphoma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital heart disease cribriform carcinoma dysplastic nevus syndrome embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis gastroenteritis gliosarcoma granular cell carcinoma high grade glioma ileitis ileocolitis inflammatory bowel disease large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma lymphoma melanoma microphthalmia mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IX mucopolysaccharidosis VI mucopolysaccharidosis obsolete Matthew-Wood syndrome obsolete ymphosarcoma osteoarthritis primary pulmonary hypertension pulmonary hypertension reticulosarcoma rheumatoid arthritis sarcomatoid carcinoma skin melanoma squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma uterine corpus cancer
8681	JMJD7-PLA2G4B readthrough	JMJD7-PLA2G4B	Homo sapiens (human)	head and neck squamous cell carcinoma
8660	insulin receptor substrate 2	IRS2	Homo sapiens (human)	Alzheimer's disease amnestic disorder glucose metabolism disease intellectual disability metabolic dysfunction-associated steatotic liver disease osteoporosis type 2 diabetes mellitus
8658	tankyrase	TNKS Aliases: ARTD5 PARP-5a PARP5A TIN1 TINF1 TNKS1 TRF1-interacting ankyrin-related ADP-ribose polymerase 1 pART5	Homo sapiens (human)	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 acoustic neuroma acute myeloid leukemia adenocarcinoma adenoma adult hepatocellular carcinoma adult medulloblastoma amyotrophic lateral sclerosis anaplastic astrocytoma angiomatous meningioma arthritis arthropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome benign meningioma bladder carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cerebral convexity meningioma cerebral infarction cerebrovascular disease cherubism childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood medulloblastoma childhood osteosarcoma chondrodysplasia-pseudohermaphroditism syndrome clear cell meningioma cleft lip colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma depressive disorder embryoma exostosis familial adenomatous polyposis 1 familial adenomatous polyposis fibrillary astrocytoma fibrous meningioma gemistocytic astrocytoma giant cell glioblastoma glioblastoma granular cell carcinoma hepatocellular carcinoma herpes simplex high grade glioma inflammatory liposarcoma inherited metabolic disorder insulinoma intraorbital meningioma intraventricular meningioma islet cell tumor juvenile pilocytic astrocytoma large intestine cancer liver cancer lung acinar adenocarcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma major depressive disorder malignant astrocytoma medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma meningioma meningothelial meningioma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma monoclonal gammopathy of uncertain significance multiple myeloma neuroblastoma neurotic disorder obesity obsolete melancholia olfactory groove meningioma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma parasagittal meningioma pilocytic astrocytoma pituitary adenoma progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma sarcomatoid carcinoma sclerosing liposarcoma secretory meningioma spinal meningioma stomach cancer stomach carcinoma subependymal giant cell astrocytoma tarsal-carpal coalition syndrome transitional cell carcinoma transitional meningioma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma urinary bladder cancer well-differentiated liposarcoma
8644	aldo-keto reductase family 1 member C3	AKR1C3 Aliases: 3-alpha hydroxysteroid dehydrogenase, type II DDX HAKRB KIAA0119 PGFS dihydrodiol dehydrogenase X prostaglandin F synthase	Homo sapiens (human)	B-cell lymphoma B-lymphoblastic leukemia/lymphoma Langerhans-cell histiocytosis T-cell acute lymphoblastic leukemia Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acrodermatitis acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adult acute lymphocytic leukemia alcohol dependence alcohol use disorder anaplastic astrocytoma androgen insensitivity syndrome anxiety disorder aortic valve insufficiency atopic dermatitis benign mesothelioma bladder carcinoma breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma castration-resistant prostate carcinoma cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood germ cell cancer childhood leukemia choriocarcinoma chromophobe renal cell carcinoma chronic myeloid leukemia cicatricial pemphigoid clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer cribriform carcinoma dermatitis dermoid cyst of ovary dermoid cyst disease of metabolism disorder of sexual development ductal carcinoma in situ embryoma embryonal cancer endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of ovary endometriosis of uterus endometriosis epilepsy esophageal cancer esophageal carcinoma essential hypertension fibrillary astrocytoma gemistocytic astrocytoma generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma glaucoma granular cell carcinoma hepatocellular carcinoma hermaphroditism high grade glioma hyperandrogenism hyperinsulinism hypertension juvenile pilocytic astrocytoma kidney cancer large intestine cancer leukemia liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma malignant astrocytoma malignant mesothelioma nephroblastoma non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete ymphosarcoma ovarian cancer ovarian carcinoma panic disorder papillary renal cell carcinoma papillary transitional carcinoma parapsoriasis parathyroid adenoma parathyroid carcinoma phobic disorder pilocytic astrocytoma placenta cancer polycystic ovary syndrome pre-eclampsia prostate adenocarcinoma prostate cancer prostate carcinoma protoplasmic astrocytoma pseudohermaphroditism psoriasis pustulosis of palm and sole renal carcinoma renal cell carcinoma reticulosarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin squamous cell carcinoma squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma tongue squamous cell carcinoma tubular adenocarcinoma urinary bladder cancer uterine corpus cancer
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
8613	phospholipid phosphatase 3	PLPP3 Aliases: LPP3 PAP-2b	Homo sapiens (human)	acute myocardial infarction aortic valve disease 1 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bicuspid aortic valve disease cancer cardiovascular system disease cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congestive heart failure coronary artery disease coronary thrombosis embryoma giant cell glioblastoma glioblastoma heart disease high grade glioma myocardial infarction nutmeg liver silent myocardial infarction
8612	phospholipid phosphatase 2	PLPP2 Aliases: LPP2 PAP-2c	Homo sapiens (human)	cancer carcinoma embryoma sarcoma sarcomatoid carcinoma squamous cell carcinoma tongue squamous cell carcinoma
8611	phospholipid phosphatase 1	PLPP1 Aliases: LPP1 PAP-2a	Homo sapiens (human)	breast cancer breast carcinoma cancer cervical adenocarcinoma cervical cancer cervix carcinoma embryoma giant cell glioblastoma glioblastoma hepatitis B high grade glioma ovarian cancer ovarian carcinoma prostate adenocarcinoma schizophrenia stomach cancer stomach carcinoma
8605	phospholipase A2 group IVC	PLA2G4C Aliases: cPLA2-gamma	Homo sapiens (human)	adult oligodendroglioma allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis autism spectrum disorder autistic disorder breast cancer cancer central nervous system cancer childhood oligodendroglioma chronic obstructive pulmonary disease gliosarcoma hepatitis C high grade glioma intrinsic asthma mixed glioma mixed oligodendroglioma-astrocytoma oligodendroglioma schizophrenia
8604	solute carrier family 25 member 12	SLC25A12	Homo sapiens (human)	Asperger syndrome autism spectrum disorder autistic disorder citrullinemia common bile duct disease developmental and epileptic encephalopathy 39 intrahepatic cholestasis
8574	aldo-keto reductase family 7 member A2	AKR7A2	Homo sapiens (human)	Alzheimer's disease pancreatic ductal adenocarcinoma
8560	delta 4-desaturase, sphingolipid 1	DEGS1 Aliases: DEGS-1 DES1 Des-1 FADS7 MLD dihydroceramide desaturase 1 sphingolipid delta(4)-desaturase 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 Graves' disease Krabbe disease Pick's disease Reye syndrome acute intermittent porphyria acute interstitial pneumonia acute myocardial infarction alternating hemiplegia of childhood amyloidosis autonomic neuropathy autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer cardiovascular system disease central nervous system disease cerebral degeneration chronic fatigue syndrome colorectal cancer colorectal carcinoma congenital nystagmus coronary thrombosis critical illness polyneuropathy depressive disorder diabetes mellitus diabetic ketoacidosis disease of mental health dissociated nystagmus dysthymic disorder dystonia embryoma encephalitis encephalomyelitis epilepsy esophageal cancer esophageal carcinoma esophagitis essential hypertension gastroesophageal reflux disease giant cell glioblastoma glioblastoma heart disease high grade glioma hyperglycemia hypertension hyperthyroidism hypomyelinating leukodystrophy 18 hypomyelinating leukodystrophy idiopathic interstitial pneumonia inflammatory and toxic neuropathy kidney failure large intestine cancer leukodystrophy locked-in syndrome major depressive disorder melancholic depression meningoencephalitis metachromatic leukodystrophy myelitis myocardial infarction nervous system disease neurodegenerative disease neuropathy neurotic disorder obesity obsolete melancholia osteopetrosis osteosclerosis pathologic nystagmus peptic esophagitis peripheral nervous system disease pneumonia polyneuropathy prostate cancer prostate carcinoma psychotic disorder quadriplegia scoliosis silent myocardial infarction spontaneous ocular nystagmus substance abuse substance-related disorder thyrotoxicosis type 2 diabetes mellitus uremia visual epilepsy
8547	ficolin 3	FCN3 Aliases: FCNH HAKA1 Hakata antigen	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal aortic aneurysm acute myocardial infarction amyotrophic lateral sclerosis anogenital venereal wart arteriosclerotic cardiovascular disease atherosclerosis bacterial infectious disease cancer common wart complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency coronary artery disease coronary thrombosis diabetes mellitus essential hypertension gestational diabetes hepatocellular carcinoma hypertension inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease leprosy liver cancer lupus nephritis myocardial infarction ovarian cancer ovarian carcinoma placental insufficiency primary immunodeficiency disease progressive muscular atrophy sarcoidosis scleroderma silent myocardial infarction systemic lupus erythematosus systemic scleroderma tuberculosis type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis
8540	alkylglycerone phosphate synthase	AGPS Aliases: ADAP-S ADAS ADHAPS ADPS ALDHPSY	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 X-linked chondrodysplasia punctata 1 Zellweger syndrome agammaglobulinemia amyloidosis autosomal dominant chondrodysplasia punctata cancer central nervous system cancer cerebral degeneration chondrodysplasia punctata congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy dementia embryoma epilepsy essential hypertension gliosarcoma hepatocellular carcinoma high grade glioma hypertension liver cancer lymphopenia mixed glioma peroxisome biogenesis disorder 1A photoallergic dermatitis rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 rhizomelic chondrodysplasia punctata thyroid adenoma thyroid cancer thyroid gland carcinoma visual epilepsy
8534	carbohydrate sulfotransferase 1	CHST1 Aliases: C6ST KSGal6ST Keratan sulfotransferase	Homo sapiens (human)	cataract mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia
8529	cytochrome P450 family 4 subfamily F member 2	CYP4F2	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 acute myocardial infarction adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adrenoleukodystrophy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation brain stem infarction cancer cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis embryoma essential hypertension heart disease hepatocellular carcinoma hypertension inflammatory bowel disease 1 inflammatory bowel disease liver cancer myocardial infarction nutmeg liver obesity pancreatic ductal adenocarcinoma patent ductus arteriosus silent myocardial infarction steatotic liver disease thrombophilia ulcerative colitis varicose veins vascular disease
8527	diacylglycerol kinase delta	DGKD Aliases: DGKdelta KIAA0145 diglyceride kinase	Homo sapiens (human)	Lennox-Gastaut syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease cancer diabetes mellitus embryoma epilepsy hyperglycemia nephrolithiasis obsessive-compulsive disorder open-angle glaucoma primary open angle glaucoma type 2 diabetes mellitus uric acid nephrolithiasis visual epilepsy
8526	diacylglycerol kinase epsilon	DGKE Aliases: DAGK6 DGK	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease acute kidney failure allergic asthma asthma atypical hemolytic-uremic syndrome breast cancer cancer capillary disease cardiovascular system disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy embryoma epilepsy familial nephrotic syndrome fundus albipunctatus glomerulonephritis heart disease hemolytic anemia hemolytic-uremic syndrome hereditary hemorrhagic telangiectasia intrinsic asthma kidney disease kidney failure large intestine cancer lipoid nephrosis liver cirrhosis membranoproliferative glomerulonephritis mitochondrial DNA depletion syndrome nephritis nephrosis nephrotic syndrome type 7 nephrotic syndrome obesity proteinuria pyoureter retinitis pigmentosa telangiectasis thrombocytopenia thrombotic thrombocytopenic purpura uremia visual epilepsy
8525	diacylglycerol kinase zeta	DGKZ Aliases: DAGK5 DAGK6 DGK-ZETA hDGKzeta	Homo sapiens (human)	Clouston syndrome acute myocardial infarction adenocarcinoma adenoma adult lymphoma aplastic anemia bone osteosarcoma cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis cribriform carcinoma diabetes mellitus embryoma giant cell glioblastoma glioblastoma granular cell carcinoma high grade glioma large intestine cancer myocardial infarction osteosarcoma pancytopenia prostate cancer prostate carcinoma pure red-cell aplasia schizophrenia silent myocardial infarction tubular adenocarcinoma type 2 diabetes mellitus
8513	lipase F, gastric type	LIPF Aliases: HGL HLAL gastric triacylglycerol lipase	Homo sapiens (human)	Wolman disease lipid storage disease lysosomal acid lipase deficiency stomach cancer stomach carcinoma
8509	N-deacetylase and N-sulfotransferase 2	NDST2 Aliases: HSST2 NST2	Homo sapiens (human)	autism spectrum disorder azoospermia intellectual disability prostate cancer prostate carcinoma
8505	poly(ADP-ribose) glycohydrolase	PARG	Homo sapiens (human)	acute myeloid leukemia autoimmune disease autoimmune lymphoproliferative syndrome bone osteosarcoma borna disease brain infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood leukemia childhood osteosarcoma colon carcinoma colorectal cancer embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma herpes simplex high grade glioma immune system disease leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma microphthalmia obsolete Matthew-Wood syndrome osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma stress-induced childhood-onset neurodegeneration with variable ataxia and seizures thyroid gland papillary carcinoma
8482	semaphorin 7A (JohnMiltonHagen blood group)	SEMA7A Aliases: CD108 H-Sema K1 H-Sema-L John Milton Hagen blood group	Homo sapiens (human)	Kallmann syndrome Kaposi's sarcoma Sheehan syndrome Sjogren's syndrome St. Louis encephalitis alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy autosomal dominant polycystic kidney disease breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system disease cerebral infarction cerebrovascular disease chronic fatigue syndrome complex partial epilepsy congenital myasthenic syndrome coronary artery disease embryoma encephalitis encephalomyelitis epilepsy essential hypertension eunuchism gliosarcoma high grade glioma hypertension 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 idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease 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 keratoconjunctivitis sicca lung adenocarcinoma lung cancer melanoma mixed glioma multiple sclerosis myelitis nervous system disease pancreatic cancer pancreatic carcinoma panhypopituitarism pneumonia polycystic kidney disease 1 postinflammatory pulmonary fibrosis progressive familial intrahepatic cholestasis pterygium pulmonary fibrosis rheumatoid arthritis septooptic dysplasia skin melanoma systemic lupus erythematosus temporal lobe epilepsy visual epilepsy

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