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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 **5151 - 5175** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:9206	Barrett's esophagus Aliases: Barrett esophagus Barrett's esophagus with esophagitis Barrett's oesophagus Barrett's ulcer of esophagus Barretts syndrome ulcerative esophagitis	dbl-1 gpx-3 gpx-5 sqv-8 zmp-3	174517 178748 179068 181178 182513	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080575	Larsen-like syndrome B3GAT3 type Aliases: Larsen-like syndrome, B3GAT3 type multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome	sqv-8	174517	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050570	congenital disorder of glycosylation type I	F52B11.2 ZK632.4 algn-12 algn-1 algn-5 algn-6 algn-8 algn-9 dpm-1	174542 174633 175920 176388 176874 178364 178822 179185 182392	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080560	congenital disorder of glycosylation Ih Aliases: congenital disorder of glycosylation 1h	algn-8	174542	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050827	rheumatic heart disease Aliases: rheumatic carditis	W01F3.2 gpd-1 gpd-3 gpd-4 scav-2 scav-3 zmp-4	174578 174603 176673 176787 179991 180351 180601	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3319	lymphangioleiomyomatosis Aliases: lung lymphangioleiomyomatosis lymphangiomyomatosis pulmonary lymphangioleiomyomatosis	W01F3.2 gpd-1 gpd-3 gpd-4 zmp-4	174578 174603 179991 180351 180601	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3827	congenital diaphragmatic hernia Aliases: Diaphragmatic Hernia	acn-1 dbl-1 hst-1 myrf-1 myrf-2 ver-1	174614 175182 177675 179068 180780 181229	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080634	nanophthalmos	myrf-1 myrf-2	174614 181229	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5614	eye disease	myrf-1 myrf-2	174614 181229	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9834	hyperopia Aliases: Far-sightedness farsightedness hypermetropia	myrf-1 myrf-2	174614 181229	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080564	congenital disorder of glycosylation Il Aliases: congenital disorder of glycosylation 1l	algn-9	174633	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2018	hyperinsulinism Aliases: hyperinsulinemia	dsc-4 pfkb-1.2 ptp-3	174685 176852 177363	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050425	restless legs syndrome Aliases: WED Willis-Ekbom disease Wittmaack-Ekbom syndrome	dop-2 ptp-3 smf-1 smf-2 smf-3	174685 177044 179347 180939 191766	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14227	azoospermia	hst-1 ptp-3	174685 177675	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070134	autosomal recessive cutis laxa type IIA Aliases: ARCL2A	vha-5 vha-6 vha-7	174743 177626 178219	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112171	wrinkly skin syndrome Aliases: WSS	vha-5 vha-6 vha-7	174743 177626 178219	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110942	autosomal recessive osteopetrosis 1 Aliases: OPTB1 autosomal recessive Albers-Schonberg disease infantile malignant osteopetrosis 1	vha-5 vha-6 vha-7	174743 177626 178219	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070390	developmental and epileptic encephalopathy 104 Aliases: DEE104 early infantile epileptic encephalopathy 104	vha-5 vha-6 vha-7	174743 177626 178219	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090118	congenital amegakaryocytic thrombocytopenia Aliases: CAMT congenital amegakaryocytic thrombocytopenic purpura	Mpl	17480	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1485	cystic fibrosis Aliases: CF mucoviscidosis	C47E12.3 W01F3.2 clh-1 cri-2 mec-10 mec-4 pgp-1 pgp-3 pxn-1 pxn-2 zmp-4	174821 177857 178215 179197 179991 180351 181101 181288 181326 181728 191484	Caenorhabditis elegans	Alliance of Genome Resources
DOID:446	primary hyperaldosteronism Aliases: Cushing syndrome Cushing's syndrome hyperaldosteronism	asp-1 clh-1 dop-2 srp-6 srp-7	174821 179125 179195 179347 180251	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0081336	Thomsen disease Aliases: Congenital myotonia, autosomal dominant form Thomsen's disease	clh-1	174821	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10579	leukodystrophy	clh-1	174821	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0081335	Becker disease	clh-1	174821	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111312	idiopathic generalized epilepsy 11 Aliases: EIG11	clh-1	174821	Caenorhabditis elegans	Alliance of Genome Resources

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