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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 **5451 - 5475** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:0110555	autosomal dominant nonsyndromic deafness 25 Aliases: DFNA25 autosomal dominant deafness 25	eat-4 vglu-2 vglu-3	176291 176441 176442	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5463	cochlear disease	eat-4	176291	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9784	trichinosis Aliases: Trichinella spiralis infection	eat-4	176291	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3209	junctional epidermolysis bullosa Aliases: congenital junctional epidermolysis bullosa	epi-1 ina-1 lam-1 lam-2	176296 177292 177956 180980	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11723	Duchenne muscular dystrophy Aliases: Muscular dystrophy, Duchenne	cri-2 ina-1 timp-1	176296 179197 179199	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080000	muscular disease	ina-1	176296	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110639	congenital muscular dystrophy due to integrin alpha-7 deficiency Aliases: congenital muscular dystrophy with ITGA7 deficiency congenital muscular dystrophy with integrin alpha-7 deficiency congenital myopathy due to integrin alpha-7 deficiency	ina-1	176296	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060733	junctional epidermolysis bullosa with pyloric atresia Aliases: Carmi syndrome JEB-PA epidermolysis bullosa junctionalis with pyloric atresia junctional epidermolysis bullosa-pyloric atresia syndrome	ina-1	176296	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060737	junctional epidermolysis bullosa Herlitz type Aliases: Herlitz type epidermolysis bullosa junctionalis Herlitz-Pearson-type epidermolysis bullosa JEB-H JEB-Herlitz type epidermolysis bullosa letalis junctional epidermolysis bullosa generalisata gravis junctional epidermolysis bullosa, Herlitz-Pearson type	ina-1	176296	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12700	hyperprolactinemia Aliases: Chiari-Frommel syndrome Pregnancy-related A-G syndrome hyperprolactinaemia	dat-1 dop-2 mrp-1 mrp-2	176304 179347 180408 180409	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11119	Gilles de la Tourette syndrome Aliases: Guinon's disease Psychogenic tics Tourette syndrome motor-verbal tic disorder	dat-1 dop-2	176304 179347	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090145	dopamine beta-hydroxylase deficiency Aliases: congenital dopamine beta-hydroxylase deficiency noradrenaline deficiency norepinephrine deficiency	dat-1 tbh-1	176304 181639	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070489	classic dopamine transporter deficiency syndrome Aliases: PKDYS1 classic DTDS infantile parkinsonism-dystonia 1	dat-1	176304	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11569	neurocirculatory asthenia Aliases: Cardiovascular malfunction arising from mental factors Cardiovascular neurosis Da Costa's syndrome Krishaber's disease	dat-1	176304	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080832	mild cognitive impairment	dat-1	176304	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3659	sialuria	slc-17.2	176317	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080738	Ehlers-Danlos syndrome spondylodysplastic type 1	sqv-3	176382	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2978	carbohydrate metabolic disorder Aliases: disorder of carbohydrate transport and metabolism inborn carbohydrate metabolism disorder inborn errors of carbohydrate metabolism	ZK632.4 gly-20	176388 179562	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080554	congenital disorder of glycosylation Ib Aliases: congenital disorder of glycosylation 1b	ZK632.4	176388	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110219	Brugada syndrome 2 Aliases: BRGDA2	gpdh-2	176399	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112202	developmental and epileptic encephalopathy	unc-47	176431	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060170	generalized epilepsy with febrile seizures plus Aliases: GEFS+	unc-47	176431	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060050	autoimmune disease of blood	C38H2.2	176455	Caenorhabditis elegans	Alliance of Genome Resources
DOID:206	hereditary multiple exostoses Aliases: Multiple congenital exostosis Multiple exostosis syndromes Osteochondromatosis syndrome hereditary multiple exostoses 1 hereditary multiple exostoses 2 hereditary multiple exostoses 3 multiple ostechondromas	rib-1 rib-2	176502 178080	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050869	villous adenoma	plr-1	176575	Caenorhabditis elegans	Alliance of Genome Resources

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