GlyCosmos Portal

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Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1951 - 1975** of **4621** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism
DOID:0090105	autosomal recessive hypercholesterolemia Aliases: ARH ARH1 ARH2 FHCB1 FHCB2 autosomal recessive hypercholesterolemia 1 autosomal recessive hypercholesterolemia 2 familial autosomal recessive hypercholesterolemia	ADH1A ADPRH ADPRS CD14 LPL MPI	124 141 4023 4351 54936 929	Homo sapiens (human)
DOID:0050167	autoimmune polyendocrine syndrome type 1 Aliases: Autoimmune Polyglandular Syndrome I Whitaker syndrome autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy	ADH1A CD1D CLEC7A CYP1A2 CYP2B6 DLAT FCGR3B LYZ VCAM1	124 1544 1555 1737 2215 4069 64581 7412 912	Homo sapiens (human)
DOID:4810	cerebrotendinous xanthomatosis Aliases: Cholestanol storage disease	B4GALNT2 CYP27A1 CYP27B1 CYP2B6 CYP3A4 HSD11B1 HSD11B2 PTGDS	124872 1555 1576 1593 1594 3290 3291 5730	Homo sapiens (human)
DOID:8557	oropharynx cancer Aliases: Oropharyngeal carcinoma malignant Oropharyngeal tumor malignant tumor of oropharynx malignant tumour of mesopharynx oropharyngeal cancer	ADH1B ADH1C ADH5 ALDH2 CD44 MTAP NEIL2 PIK3CA PIK3CB PIK3CD PIK3CG SMUG1 TYMP	125 126 128 1890 217 23583 252969 4507 5290 5291 5293 5294 960	Homo sapiens (human)
DOID:6841	flat ductal epithelial atypia	ADH1B ADH4 PTEN	125 127 5728	Homo sapiens (human)
DOID:9976	heroin dependence	ABAT ADH1B ALDH2 COMT CYP2B6 CYP2C19 ENO2 GAD1 GAD2 HPGDS ICAM1 MDH2 NCAM1 NPY1R PARP9 PIK3CA PIK3CB PIK3CD PIK3CG RGMA	125 1312 1555 1557 18 2026 217 2571 2572 27306 3383 4191 4684 4886 5290 5291 5293 5294 56963 83666	Homo sapiens (human)
DOID:2560	morphine dependence	ABAT ADH1B ALDH2 COMT CYP2B6 ENO2 EXTL3 FDFT1 GAD1 GAD2 MANEA MDH2 NCAM1 NTNG1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG RGMA SMUG1 UMOD	125 1312 1555 18 2026 2137 217 2222 22854 23583 2571 2572 4191 4684 5290 5291 5293 5294 56963 7369 79694 83666	Homo sapiens (human)
DOID:2559	opiate dependence Aliases: Opioid type dependence	ABAT ADH1B ALDH2 COMT CYP2B6 ENO2 GAD1 MDH2 NCAM1 NPY1R PARP9 PIK3CA PIK3CB PIK3CD PIK3CG RGMA	125 1312 1555 18 2026 217 2571 4191 4684 4886 5290 5291 5293 5294 56963 83666	Homo sapiens (human)
DOID:10939	antisocial personality disorder Aliases: Asocial personality Dissocial personality disorder Psychopath.personality Psychopathic personality Psychopathic personality disorder sociopathic personality	ACE ADH1B ALDH2 CAT COMT CYP2E1 EXT1 GAD1 IMPA1	125 1312 1571 1636 2131 217 2571 3612 847	Homo sapiens (human)
DOID:8618	oral cavity cancer Aliases: malignant neoplasm of floor of mouth	ADH1B CYP1A1 CYP2E1 PIK3CA PTEN	125 1543 1571 5290 5728	Homo sapiens (human)
DOID:1510	personality disorder Aliases: character disorder	ACE ADH1B ALDH2 CAT CYP2E1 EXT1 GAD1	125 1571 1636 2131 217 2571 847	Homo sapiens (human)
DOID:0050459	hyperphosphatemia	ADH1B CYP11B2 CYP24A1 CYP27B1 GALNT3 KL PGAP2 PIK3C2A SHMT1 SMPD3	125 1585 1591 1594 2591 27315 5286 55512 6470 9365	Homo sapiens (human)
DOID:14183	alcoholic neuropathy Aliases: Alcohol-related polyneuropathy Alcoholic polyneuropathy	ADH1B ALDH2 IGF2	125 217 3481	Homo sapiens (human)
DOID:204	enthesopathy	ACLY ADH1B CALR CD14 CD22 CD44 ENPP1 FMOD FOLR2 HSPG2 KL KLRC1 KLRD1 LGALS8 NT5E PTGS2 SELL VCAM1	125 2331 2350 3339 3821 3824 3964 47 4907 5167 5743 6402 7412 811 929 933 9365 960	Homo sapiens (human)
DOID:0110307	hypertrophic cardiomyopathy 1 Aliases: CMH1 cardiomyopathy, familial hypertrophic 1 hypertrophic cardiomyopathy 19	ACE APRT CALR3 GLA GNS HGSNAT ICAM1 NAGLU PKD1 PNPLA3 PRKAA2 SGSH	125972 138050 1636 2717 2799 3383 353 4669 5310 5563 6448 80339	Homo sapiens (human)
DOID:0060892	late onset Parkinson's disease Aliases: late onset Parkinson disease	ACSBG1 ADH1C ALDH2 ARSA B3GALT4 CAT COMT FH GALC GAPDH GBA1 GLA KL NTM OGG1 PAFAH1B1 PLA2G6 PSAP PTGDS PTGS2 SARM1 SLC17A5 SMPD1 ST3GAL2 VCAM1	126 1312 217 2271 23098 23205 2581 2597 2629 26503 2717 410 4968 5048 50863 5660 5730 5743 6483 6609 7412 8398 847 8705 9365	Homo sapiens (human)
DOID:9746	hemorrhoid Aliases: hemorrhoidal disease	ADH1C ALDH2 CYP1A1 ENO1	126 1543 2023 217	Homo sapiens (human)
DOID:0070322	childhood hepatocellular carcinoma Aliases: pediatric hepatocellular carcinoma	ABO ACAT1 ADH1C APRT CYP2B6 ENPP2 G6PD GPC3 LDHA PNPLA3 PTGS2 ST6GAL1 SULF1 TNKS UGT1A7 UGT1A9 VCAM1	126 1555 23213 2539 2719 28 353 38 3939 5168 54577 54600 5743 6480 7412 80339 8658	Homo sapiens (human)
DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome Aliases: CAMRQ Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 (CAMRQ1) Uner Tan syndrome VLDLR Cerebellar Hypoplasia	ADH1C HPGDS HSD11B1 PKD2 PRKCSH SFTPC	126 27306 3290 5311 5589 6440	Homo sapiens (human)
DOID:10487	Hirschsprung's disease Aliases: Hirschsprung disease aganglionic megacolon congenital megacolon macrocolon pelvirectal achalasia total intestinal aganglionosis	ABO ACHE B3GALT6 CD14 CNTN5 CNTN6 COMT CSGALNACT2 CYP2B6 ENO2 FH GFRA1 GFRA2 GFRA4 ICAM1 IL1RL2 INPP5E ITPKC L1CAM PGAP2 PGAP3 PGP PIGA PIGL PIGN PIGO PIGV PIGW PIGY PIK3CG PLCB1 PTGES SIGLEC8 SLC2A1	126792 1312 1555 2026 2271 23236 23556 2674 2675 27181 27255 27315 28 283871 284098 3383 3897 43 5277 5294 53942 55454 55650 56623 64096 6513 80271 84720 84992 8808 929 93210 9487 9536	Homo sapiens (human)
DOID:11502	mitral valve insufficiency Aliases: Congenital insufficiency of mitral valve Mitral valve incompetence congenital mitral insufficiency congenital mitral regurgitation mitral regurgitation	ABO ACE AGA B3GALT6 B3GAT3 CHST3 DSE ENPP1 G6PC3 GLA HADHA HADHB IDUA PLD1 PRKAA2 SCD XYLT1 XYLT2	126792 1636 175 26229 2717 28 29940 3030 3032 3425 5167 5337 5563 6319 64131 64132 92579 9469	Homo sapiens (human)
DOID:988	mitral valve prolapse Aliases: Barlow's syndrome floppy mitral valve	ABO ACE AGA B3GALT6 B3GAT3 CHST3 DSE ENPP1 G6PC3 GLA HADHA HADHB IDUA PLD1 PRKAA2 SCD XYLT1 XYLT2	126792 1636 175 26229 2717 28 29940 3030 3032 3425 5167 5337 5563 6319 64131 64132 92579 9469	Homo sapiens (human)
DOID:0080332	bicuspid aortic valve disease Aliases: Familial bicuspid aortic valve	ACAN ACE ARSD ATP6V0A2 B3GALT6 B3GAT3 CD44 CHST3 ENPP1 GAPDH ICAM1 KL NT5E PLA2G7 PLPP3 STS	126792 1636 176 23545 2597 26229 3383 412 414 4907 5167 7941 8613 9365 9469 960	Homo sapiens (human)
DOID:0080333	aortic valve disease 1	ACAN ACE ARSD ATP6V0A2 B3GALT6 B3GAT3 CD44 CHST3 ENPP1 GAPDH ICAM1 KL NT5E PLA2G7 PLPP3 STS	126792 1636 176 23545 2597 26229 3383 412 414 4907 5167 7941 8613 9365 9469 960	Homo sapiens (human)
DOID:319	spinal cord disease	ARSB B3GALT6 CD38 CNTN2 CNTN3 ERLEC1 EXT1 GNPTAB HMGCS1 HPRT1 IDUA IL18RAP MINPP1 PTGS2 SLC26A2 SMUG1 TMTC1	126792 1836 2131 23583 27248 3157 3251 3425 411 5067 5743 6900 79158 83857 8807 952 9562	Homo sapiens (human)

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