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GlyCosmos Diseases

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

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

Displaying entries **6751 - 6775** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:693	dental enamel hypoplasia Aliases: enamel hypoplasia	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9563	bronchiectasis Aliases: Polynesian bronchiectasis	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10808	gastric ulcer Aliases: acute gastric ulcer with haemorrhage and perforation acute gastric ulcer with hemorrhage AND with perforation but without obstruction acute gastric ulcer with hemorrhage and obstruction acute gastric ulcer with hemorrhage and perforation acute gastric ulcer with hemorrhage and perforation, with obstruction acute gastric ulcer with hemorrhage and perforation, without mention of obstruction acute gastric ulcer with hemorrhage, with obstruction acute gastric ulcer with hemorrhage, with perforation AND with obstruction acute gastric ulcer with perforation acute gastric ulcer with perforation AND obstruction acute gastric ulcer with perforation, with obstruction acute gastric ulcer without hemorrhage and without perforation acute gastric ulcer without hemorrhage, without perforation AND without obstruction acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction bleeding acute gastric ulcer chronic gastric ulcer without hemorrhage AND without perforation chronic gastric ulcer without hemorrhage AND without perforation but with obstruction chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080526	bronchiectasis 1	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11132	prostatic hypertrophy	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13316	exocrine pancreatic insufficiency Aliases: EPI	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111862	congenital bilateral absence of vas deferens Aliases: CAVD CBAVD congenital bilateral agenesis of vas deferens congenital bilateral aplasia of vas deferens	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111864	autosomal recessive congenital bilateral absence of vas deferens	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13166	allergic bronchopulmonary aspergillosis Aliases: pulmonary aspergillus disease	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060643	primary sclerosing cholangitis	NFT1 STE6	853671 853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1724	duodenal ulcer Aliases: Curling Ulcer Curling's ulcers Stress Ulcer	NFT1 SMF3 TRE1 TRE2 VPS70	850721 853590 853978 854430 855927	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070425	combined oxidative phosphorylation deficiency 52 Aliases: COXPD52	NFS1	9054	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081152	common variable immunodeficiency 10	NFKB2	4791	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081154	common variable immunodeficiency 12	NFKB1	4790	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050340	opportunistic bacterial infectious disease	NFKB1 NFKB2 SMARCA2 SMARCA4 SMARCC1 SMARCC2	4790 4791 6595 6597 6599 6601	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112102	Sotos syndrome 2 Aliases: SOTOS2	NFIX	4784	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050858	Marshall-Smith syndrome	NFIX	4784	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060409	NFIA-related disorder Aliases: 1p31p32 microdeletion syndrome Chromosome 1, Monosomy 1p32 brain malformations with or without urinary tract defects chromosome 1p32-p31 deletion syndrome	NFIA	4774	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070483	Watson syndrome	NF1	4763	Homo sapiens (human)	Alliance of Genome Resources
DOID:8712	neurofibromatosis	NF1	4763	Homo sapiens (human)	Alliance of Genome Resources
DOID:4992	optic nerve glioma Aliases: glioma of the optic nerve	NF1	4763	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111683	neurofibromatosis-Noonan syndrome Aliases: NFNS Noonan neurofibromatosis syndrome neurofibromatosis type 1-Noonan syndrome neurofibromatosis with Noonan phenotype	NF1	4763	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070482	spinal neurofibromatosis Aliases: FNSF SNF familial spinal neurofibromatosis	NF1	4763	Homo sapiens (human)	Alliance of Genome Resources
DOID:5151	plexiform neurofibroma	NF1	4763	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111253	neurofibromatosis 1 Aliases: NF1 Peripheral Neurofibromatosis Recklinghausen's neurofibromatosis neurofibromatosis type I von Recklinghausen Disease	NF1 VEGFA	4763 7422	Homo sapiens (human)	Alliance of Genome Resources

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