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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	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **3876 - 3900** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism
DOID:3314	angiomyolipoma	Ogg1	18294	Mus musculus (house mouse)
DOID:5520	head and neck squamous cell carcinoma Aliases: carcinoma of the head and neck squamous cell carcinoma of the head and neck squamous cell carcinomas of head and neck	Ogg1	18294	Mus musculus (house mouse)
DOID:9669	senile cataract	Ogg1	18294	Mus musculus (house mouse)
DOID:678	progressive supranuclear palsy Aliases: Steele-Richardson-Olszewski syndrome progressive supranuclear ophthalmoplegia	Ogg1	18294	Mus musculus (house mouse)
DOID:2237	hepatitis Aliases: acute and subacute liver necrosis acute hepatitis acute/subac. necrosis of liver animal hepatitis chronic hepatitis chronic persistent hepatitis	Abo Ogg1	18294 80908	Mus musculus (house mouse)
DOID:2513	basal cell carcinoma Aliases: Basal cell cancer Basal cell carcinoma of skin Basal cell neoplasm Basal cell tumor Epithelioma basal cell Rodent ulcer malignant Basal cell neoplasm malignant basal cell tumor	Ogg1 Trp53	18294 22059	Mus musculus (house mouse)
DOID:0002116	pterygium Aliases: surfer's eye	Ogg1 Trp53	18294 22059	Mus musculus (house mouse)
DOID:0070468	Yoon-Bellen neurodevelopmental syndrome Aliases: YOBELN	Ogdh	18293	Mus musculus (house mouse)
DOID:0081326	oxoglutarate dehydrogenase deficiency Aliases: Oxoglutaric aciduria alpha-ketoglutarate dehydrogenase deficiency	Ogdh	18293	Mus musculus (house mouse)
DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13 Aliases: MDDGA13 Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13	bgnt-1.4 bgnt-1.5	182795 3565692	Caenorhabditis elegans
DOID:0080555	congenital disorder of glycosylation Ic Aliases: congenital disorder of glycosylation 1c	algn-6	182392	Caenorhabditis elegans
DOID:0080411	familial adenomatous polyposis 3	Nthl1	18207	Mus musculus (house mouse)
DOID:1825	childhood absence epilepsy Aliases: petit mal seizure pyknolepsy	Npy1r	18166	Mus musculus (house mouse)
DOID:2030	anxiety disorder Aliases: anxiety anxiety state	Manea Npy1r	18166 242362	Mus musculus (house mouse)
DOID:3328	temporal lobe epilepsy Aliases: epilepsy, temporal lobe	Npy1r Pgf	18166 18654	Mus musculus (house mouse)
DOID:3633	beta-mannosidosis Aliases: Beta-D-mannosidosis beta-mannosidase deficiency lysosomal beta-mannosidase deficiency	C33G3.4	181517	Caenorhabditis elegans
DOID:0070113	Niemann-Pick disease type C1 Aliases: NPC1	Npc1	18145	Mus musculus (house mouse)
DOID:14504	Niemann-Pick disease Aliases: Sphingomyelinase Deficiency Disease lipoid histiocytosis sphingomyelin lipidosis	Npc1 Smpd1	18145 20597	Mus musculus (house mouse)
DOID:9538	multiple myeloma Aliases: myeloma	cht-1	180628	Caenorhabditis elegans
DOID:0050685	small cell carcinoma Aliases: Small cell carcinoma - intermediate cell Small cell carcinoma, intermediate cell intermediate cell small cell carcinoma	cht-1	180628	Caenorhabditis elegans
DOID:0080199	colorectal carcinoma	cht-1	180628	Caenorhabditis elegans
DOID:7148	rheumatoid arthritis Aliases: Arthritis or polyarthritis, rheumatic atrophic Arthritis	cht-1	180628	Caenorhabditis elegans
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	cht-1	180628	Caenorhabditis elegans
DOID:3068	glioblastoma Aliases: GBM adult glioblastoma multiforme glioblastoma multiforme grade IV adult Astrocytic tumor primary glioblastoma multiforme spongioblastoma multiforme	cht-1	180628	Caenorhabditis elegans
DOID:13375	temporal arteritis Aliases: Horton's disease giant cell arteritis	cht-1	180628	Caenorhabditis elegans

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