GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **12001 - 12025** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:11446	sciatic neuropathy	Ca-alpha1D Fur2 Nmdar1 Shaw Sod3 Tl htl para sgg tor	31248 32604 32619 33599 34950 35717 36232 40665 42160 43222	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:11723	Duchenne muscular dystrophy Aliases: Muscular dystrophy, Duchenne	Ca-alpha1D Dg mew	32275 34950 36773	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110810	hereditary spastic paraplegia 5A Aliases: SPG5A autosomal recessive spastic paraplegia 5A autosomal recessive spastic paraplegia type 5A	CYP7B1	9420	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111070	congenital bile acid synthesis defect 3 Aliases: CBAS3 oxysterol 7-alpha-hydroxylase deficiency	CYP7B1	9420	Homo sapiens (human)	Alliance of Genome Resources
DOID:5773	oral submucous fibrosis Aliases: Oral cavity Submucous Fibrosis Oral submucosal fibrosis Oral submucosal fibrosis, including of tongue	CYP3A5 TGFB1 TP53	1577 7040 7157	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110808	hereditary spastic paraplegia 56 Aliases: SPG56 autosomal recessive spastic paraplegia 56 autosomal recessive spastic paraplegia type 56	CYP2U1	113612	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080887	vitamin D-dependent rickets type 1B	CYP2R1	120227	Homo sapiens (human)	Alliance of Genome Resources
DOID:4248	coronary stenosis Aliases: Coronary artery stenosis	CYP2R1 EDN1 IGF1R ITGAV MDK PECAM1 TNFRSF11B	120227 1906 3480 3685 4192 4982 5175	Homo sapiens (human)	Alliance of Genome Resources
DOID:10320	asbestosis	CYP2E1 NOS2 TNC	1571 3371 4843	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080665	warfarin resistance	CYP2C9	1559	Homo sapiens (human)	Alliance of Genome Resources
DOID:4661	multiple chemical sensitivity Aliases: 20th century disease chemical AIDS environmental illness idiopathic environmental illness total allergy syndrome	CYP2C19	1557	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080886	vitamin D-dependent rickets type 1A	CYP27B1	1594	Homo sapiens (human)	Alliance of Genome Resources
DOID:10609	rickets Aliases: active rickets	CYP27B1 FAM20C	1594 56975	Homo sapiens (human)	Alliance of Genome Resources
DOID:4810	cerebrotendinous xanthomatosis Aliases: Cholestanol storage disease	CYP27A1	1593	Homo sapiens (human)	Alliance of Genome Resources
DOID:3713	ovary adenocarcinoma Aliases: Ovarian adenocarcinoma ovarian adenoacanthoma	CYP24A1	1591	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050860	colorectal adenoma	CYP24A1 EZH2 F5 FOS GPX2 GPX3 JUN PTCH1 PTGIS RAF1 SELENOP SMAD4 TNFRSF1A TTR	1591 2146 2153 2353 2877 2878 3725 4089 5727 5740 5894 6414 7132 7276	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080611	anterior segment dysgenesis 6	CYP1B1	1545	Homo sapiens (human)	Alliance of Genome Resources
DOID:11212	hydrophthalmos	CYP1B1	1545	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060673	Peters anomaly	CYP1B1	1545	Homo sapiens (human)	Alliance of Genome Resources
DOID:11211	buphthalmos Aliases: primary congenital glaucoma 3A simple buphthalmos	CYP1B1 FOXC1 TYR	1545 2296 7299	Homo sapiens (human)	Alliance of Genome Resources
DOID:11934	head and neck cancer Aliases: head and neck neoplasm head and neck tumours head/neck neoplasm tumor of head and neck	CYP1A1 KDM4C	1543 23081	Homo sapiens (human)	Alliance of Genome Resources
DOID:6196	reactive arthritis Aliases: Fiessinger Leroy Reiter syndrome Post-bacterial arthropathy Reiter disease Reiter's disease postdysenteric arthropathy	CYP1A1 HLA-B SOD2 TAP1	1543 3106 6648 6890	Homo sapiens (human)	Alliance of Genome Resources
DOID:6132	bronchitis Aliases: CI - Chest infection Chest infection acute Bronchitis chest cold chronic bronchitis recurrent wheezy bronchitis	CYP1A1 HDAC2	1543 3066	Homo sapiens (human)	Alliance of Genome Resources
DOID:11836	clubfoot Aliases: Congenital equinovarus Equinovarus deformity of foot congenital clubfoot congenital talipes equinovarus	CYP1A1 FLNB FRAS1 GLI3 GRIP1 HOXD13 PITX1 RET	1543 2317 23426 2737 3239 5307 5979 80144	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050083	Keshan disease	CYP1A1 CYP2C19 GPX1	1543 1557 2876	Homo sapiens (human)	Alliance of Genome Resources

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