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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 **5176 - 5200** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:2106	myotonia congenita Aliases: Batten Turner congenital myopathy Thomsen and Becker disease	clh-1	174821	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2747	glycogen storage disease Aliases: glycogenosis	C14B9.8 gsy-1 gyg-2 pfk-1.1 pfk-1.2	174924 176149 179335 180119 180583	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1287	cardiovascular system disease Aliases: disease of subdivision of hemolymphoid system	C27A7.3 Y43C5A.2 enpl-1 enpp-1 gpx-3 gpx-5 gsy-1 pxn-1 pxn-2	174924 177911 178014 179663 179665 181178 181288 182513 191484	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3534	Lafora disease Aliases: Lafora Progressive Myoclonic Epilepsy Lafora's disease MYOCLONIC EPILEPSY OF LAFORA	gsy-1	174924	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3211	lysosomal storage disease Aliases: disorder of lysosomal enzyme inborn lysosomal enzyme disorder lysosomal storage metabolism disorder	AGA CTSA GGA2 GGA3 GLA HEXB MITF PSAP PSAPL1 SLC17A5 SLC66A1 TFE3 TFEB VPS16	175 23062 23163 26503 2717 3074 4286 5476 54896 5660 64601 7030 768239 7942	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050461	aspartylglucosaminuria Aliases: aspartylglucosaminidase deficiency aspartylglycosaminuria glycosylasparaginase deficiency	AGA	175	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources
DOID:0070473	Zaki syndrome	mig-14	175020	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10754	otitis media	C27A7.3 K09E4.4 cpl-1 cpr-3 cpr-4 cpr-6 enpp-1 nep-2	175063 179053 179663 179665 180033 180111 180931 188090	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110178	Charcot-Marie-Tooth disease axonal type 2V Aliases: CMT2V Charcot-Marie-Tooth neuropathy type 2V autosomal dominant Charcot-Marie-Tooth disease type 2V autosomal dominant axonal Charcot-Marie-Tooth disease type 2V	K09E4.4	175063	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12801	mucopolysaccharidosis III Aliases: Mucopolysaccharidosis, MPS-III N-sulphoglucosamine sulphohydrolase deficiency Sanfilippo's syndrome heparan sulfate sulfatase deficiency	K09E4.4	175063	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111394	mucopolysaccharidosis type IIIB Aliases: MPS3B MPSIIIB Mucopoly-saccharidosis type 3B Mucopolysaccharidosis type 3B N-acetyl-alpha-glucosaminidase deficiency NAGLU deficiency Sanfilippo syndrome type B mucopolysaccharidosis type IIIB (Sanfilippo B)	K09E4.4	175063	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5212	congenital disorder of glycosylation Aliases: carbohydrate-deficient glycoprotein syndrome	F52B11.2 algn-1 algn-3 bre-4	175065 175920 178364 190668	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080556	congenital disorder of glycosylation Id Aliases: congenital disorder of glycosylation 1d	algn-3	175065	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2377	multiple sclerosis Aliases: Generalized multiple sclerosis insular sclerosis	W01F3.2 ace-1 ace-3 bre-4 clr-1 cpi-1 cpr-3 cpr-4 cpr-6 drag-1 glp-1 grd-2 lin-12 mgl-1 smf-1 smf-2 smf-3 wrt-6 zmp-3 zmp-4	175076 176282 176286 177044 177372 178748 179053 179991 180033 180349 180351 180638 180931 180939 181706 190602 190668 191707 191766 3565419	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9974	drug dependence	ace-1 ace-3 ncam-1 pgp-1 pgp-3	175076 178215 180418 181326 181706	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1849	cannabis dependence	ace-1 ace-3 pgp-1 pgp-3	175076 178215 181326 181706	Caenorhabditis elegans	Alliance of Genome Resources
DOID:437	myasthenia gravis	ace-1 ace-3 gar-3	175076 179962 181706	Caenorhabditis elegans	Alliance of Genome Resources
DOID:8645	subacute delirium	ace-1 ace-3	175076 181706	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9266	cystinuria	atgp-1 atgp-2	175125 178504	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3407	carotid artery disease Aliases: disorder of carotid artery	W01F3.2 Y43C5A.2 lron-5 unc-52 zmp-3 zmp-4	175126 177911 178748 179991 180351 184307	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060770	dextro-looped transposition of the great arteries Aliases: D-TGA DTGA1 congenitally uncorrected transposition of the great arteries congenitally uncorrected transposition of the great vessels isolated ventriculoarterial discordance ventriculoarterial discordance with atrioventricular concordance	folt-1 unc-52	175126 179544	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090005	Schwartz-Jampel syndrome 1 Aliases: Aberfeld syndrome Burton skeletal dysplasia Burton syndrome Catel-Hempel syndrome Catel-Hempel type dysostosis enchondralis metaepiphysaria Schwartz-Jampel syndrome type 1 Schwartz-Jampel-Aberfeld syndrome myotonic chondrodystrophy myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies osteochondromuscular dystrophy	unc-52	175126	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13481	thanatophoric dysplasia	unc-52	175126	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia	unc-52	175126	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9253	gastrointestinal stromal tumor Aliases: GANT GIST Stromal tumor of gastrointestinal tract Stromal tumour of gastrointestinal tract gastrointestinal stromal tumour	F47E1.2 grd-2 stim-1 ver-1 ver-4 wrt-6	175182 175201 180349 180638 181145 186632	Caenorhabditis elegans	Alliance of Genome Resources

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