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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 **751 - 775** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:0070264	congenital disorder of glycosylation type IIl Aliases: CDG IIl CDG syndrome type IIL CDG2L CDGIIdl COG6-CGD Congenital disorder of glycosylation type 2l	COG6	57511	Homo sapiens (human)	Glyco-Disease Genes Database DisGeNET Alliance of Genome Resources
DOID:0060230	basal ganglia calcification Aliases: Fahr disease	MYORG	57462	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:7519	endocervical carcinoma Aliases: carcinoma of endocervix carcinoma of the Endocervix	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:403	mouth disease	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:0050450	Gitelman syndrome Aliases: HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:431	myofascial pain syndrome	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:9946	steroid-induced glaucoma Aliases: Corticosteroid-induced glaucoma	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:14181	calcific tendinitis	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:0111167	Dyggve-Melchior-Clausen disease Aliases: DMC disease pseudo-Morquio disease type I	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:4514	thyroid angiosarcoma Aliases: hemangiosarcoma of the Thyroid	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:0080160	Cytomegalovirus retinitis Aliases: CMV retinitis	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:12237	bile reflux	PTGS2	5743	Homo sapiens (human)	DisGeNET
DOID:0080822	aspirin-induced respiratory disease Aliases: aspirin-sensitive asthma	PTGS2	5743	Homo sapiens (human)	Alliance of Genome Resources
DOID:4492	avian influenza Aliases: avian flu bird flu	CD14 PTGS2	5743 929	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:6595	gastric tubular adenocarcinoma Aliases: tubular adenocarcinoma of stomach	CBR1 PTGS2	5743 873	Homo sapiens (human)	DisGeNET
DOID:0060777	congenital secretory sodium diarrhea 8 Aliases: DIAR8	CALR DGAT1 PTGS2	5743 811 8694	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0060781	congenital secretory sodium diarrhea 3 Aliases: congenital secretory sodium diarrhea 3 syndromic congenital secretory sodium diarrhea 3 with or without other congenital anomalies congenital secretory sodium diarrhoea 3 congenital secretory sodium diarrhoea 3 syndromic congenital secretory sodium diarrhoea 3 with or without other congenital anomalies	CALR DGAT1 PTGS2	5743 811 8694	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0111058	platelet-type bleeding disorder 12 Aliases: BDPLT12 PGHS1 deficiency platelet COX1 deficiency platelet cyclooxygenase 1 deficiency platelet prostaglandin-endoperoxide synthase 1 deficiency	PTGS1	5742	Homo sapiens (human)	DisGeNET
DOID:0050904	salivary gland carcinoma	PTGS1	5742	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111180	French Canadian Leigh disease Aliases: French Canadian type COX deficiency French Canadian type Leigh syndrome French Canadian type cytochrome c oxidase deficiency Saguenay Lac saint Jean type COX deficiency Saguenay Lac saint Jean type Leigh syndrome mitochondrial complex IV deficiency nuclear type 5	PTGS1	5742	Homo sapiens (human)	DisGeNET
DOID:2825	nose disease Aliases: disorder of the nose nasal disorder	PTGS1 PTGS2	5742 5743	Homo sapiens (human)	DisGeNET
DOID:2965	bursitis	PTGS1 PTGS2	5742 5743	Homo sapiens (human)	DisGeNET
DOID:14550	root resorption	PTGS1 PTGS2 TNF	5742 5743 7124	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0070254	congenital disorder of glycosylation type IIb Aliases: CDG IIb CDG2B CDGIIb glucosidase I deficiency	Mogs	57377	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111359	large congenital melanocytic nevus Aliases: Congenital pigmented nevus GMN Giant congenital melanocytic nevus Giant pigmented hairy nevus LCMN	PTGDS	5730	Homo sapiens (human)	DisGeNET

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