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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4351 - 4375** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:0111128	focal segmental glomerulosclerosis 1 Aliases: FSGS1	ACE	1636	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0111132	focal segmental glomerulosclerosis 7 Aliases: FSGS7	ACE	1636	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0060550	ablepharon macrostomia syndrome	ACE	1636	Homo sapiens (human)	DisGeNET
DOID:0111129	focal segmental glomerulosclerosis 2 Aliases: FSGS2	ACE	1636	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:4331	burning mouth syndrome Aliases: Orodynia Stomatopyrosis	ACE CD14	1636 929	Homo sapiens (human)	DisGeNET
DOID:0050662	bestrophinopathy Aliases: autosomal recessive bestrophinopathy	ACE CAT SLC33A1	1636 847 9197	Homo sapiens (human)	DisGeNET
DOID:10272	left bundle branch hemiblock Aliases: Left bundle branch block	ACE CALR	1636 811	Homo sapiens (human)	DisGeNET
DOID:4449	macular retinal edema Aliases: macular edema macular oedema macular retinal oedema	ACE CALR CAT	1636 811 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:4447	cystoid macular edema	ACE CALR CAT	1636 811 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0050851	glomerulosclerosis	ACE PLA2G7	1636 7941	Homo sapiens (human)	Alliance of Genome Resources
DOID:13452	scleritis	ACE TNF	1636 7124	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0060071	pre-malignant neoplasm	ACE SFTPD TP53	1636 6441 7157	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110916	hereditary spherocytosis type 1 Aliases: HS1 SPH1 hereditary spherocytosis 1	ACE CAT PTGS2	1636 5743 847	Homo sapiens (human)	DisGeNET
DOID:5511	dysgerminoma of ovary Aliases: Ovarian Dysgerminoma	ACE PTEN	1636 5728	Homo sapiens (human)	DisGeNET
DOID:790	ocular hypotension Aliases: Hypotony of eye	ACE PRNP	1636 5621	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:2972	renal artery obstruction	ACE CMAS FIG4 SDHB SDHD	1636 55907 6390 6392 9896	Homo sapiens (human)	DisGeNET
DOID:397	restrictive cardiomyopathy Aliases: Cardiomyopathy, constrictive primary restrictive cardiomyopathy	ACE ENPP1 PIGT SCD5 SCD XYLT1 XYLT2	1636 51604 5167 6319 64131 64132 79966	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:3500	gallbladder adenocarcinoma Aliases: adenocarcinoma of the gallbladder	ACE NT5E OGG1 SOAT1	1636 4907 4968 6646	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:10024	migraine with aura Aliases: classic migraine	ACE ATP1A2 CAT PMM2	1636 477 5373 847	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:5845	anterolateral myocardial infarction	ACE CAT LGALS3 SLC2A4	1636 3958 6517 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:5855	anteroseptal myocardial infarction	ACE CAT LGALS3 SLC2A4	1636 3958 6517 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12720	cerebral atherosclerosis	ACE ACHE IMPA1	1636 3612 43	Homo sapiens (human)	DisGeNET DisGeNET
DOID:13097	intracranial arteriosclerosis	ACE ACHE IMPA1	1636 3612 43	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0060257	dyschromatosis symmetrica hereditaria Aliases: reticulate acropigmentation of Dohi	ACE ARSH	1636 347527	Homo sapiens (human)	DisGeNET
DOID:8886	chorioretinitis Aliases: retinochoroiditis	ACE ICAM1	1636 3383	Homo sapiens (human)	DisGeNET

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