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GlyCosmos Diseases

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

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **3801 - 3825** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism
DOID:8527	monocytic leukemia Aliases: Schilling's leukaemia Schilling's leukemia monocytic leukaemia	DLD ICAM1 IDH1 KLRK1 MACROD1 VCAM1	1738 22914 28992 3383 3417 7412	Homo sapiens (human)
DOID:12550	hepatic coma Aliases: Hepatocerebral intoxication	CD14 DLD G6PD GLUL ISYNA1 PCK1 PTGS1 SMUG1 STS	1738 23583 2539 2752 412 5105 51477 5742 929	Homo sapiens (human)
DOID:13413	hepatic encephalopathy Aliases: Portal-systemic encephalopathy	CD14 DLD G6PD GLUL ISYNA1 PCK1 PTGS1 SMUG1 STS	1738 23583 2539 2752 412 5105 51477 5742 929	Homo sapiens (human)
DOID:0060350	adenine phosphoribosyltransferase deficiency Aliases: 2,8-dihydroxyadenine urolithiasis APRT deficiency	APRT DLD GALNS UMOD	1738 2588 353 7369	Homo sapiens (human)
DOID:2033	communication disorder	ARSD DLD GPD2 PPP1R3A PRPS1 PTEN STS	1738 2820 412 414 5506 5631 5728	Homo sapiens (human)
DOID:93	language disorder	ARSD DLD GPD2 PPP1R3A PRPS1 STS	1738 2820 412 414 5506 5631	Homo sapiens (human)
DOID:0080154	short chain acyl-CoA dehydrogenase deficiency	ACADS ACADSB DLD	1738 35 36	Homo sapiens (human)
DOID:5847	posterior myocardial infarction	DLD	1738	Homo sapiens (human)
DOID:0110912	leukocyte adhesion deficiency 3 Aliases: IADD LAD1 variant LAD1V LAD3 integrin activation deficiency disease leukocyte adhesion deficiency 1 variant leukocyte adhesion deficiency type III	DLD	1738	Homo sapiens (human)
DOID:0110669	congenital myasthenic syndrome 14 Aliases: CMS14 CMSTA3 congenital myasthenic syndrome 14, with tubular aggregates congenital myasthenic syndrome with tubular aggregates 3	algn-2	173912	Caenorhabditis elegans
DOID:0080561	congenital disorder of glycosylation Ii Aliases: congenital disorder of glycosylation 1i	algn-2	173912	Caenorhabditis elegans
DOID:10763	hypertension Aliases: HTN hyperpiesia vascular hypertensive disorder	cgt-1 cgt-2 cgt-3 cht-1 enol-1	174001 174423 180628 181790 188169	Caenorhabditis elegans
DOID:14504	Niemann-Pick disease Aliases: Sphingomyelinase Deficiency Disease lipoid histiocytosis sphingomyelin lipidosis	asm-1 asm-2 asm-3	174131 176879 181323	Caenorhabditis elegans
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	asm-1 asm-2 asm-3	174131 176879 181323	Caenorhabditis elegans
DOID:0070112	Niemann-Pick disease type B	asm-1 asm-2 asm-3	174131 176879 181323	Caenorhabditis elegans
DOID:0070111	Niemann-Pick disease type A	asm-1 asm-2 asm-3	174131 176879 181323	Caenorhabditis elegans
DOID:0050775	schneckenbecken dysplasia	sqv-7	174145	Caenorhabditis elegans
DOID:0070311	oligoasthenoteratozoospermia Aliases: OAT oligoasthenoteratospermia	B0495.5	174243	Caenorhabditis elegans
DOID:0060713	autosomal recessive congenital ichthyosis 4B Aliases: ARCI4B harlequin ichthyosis harlequin type ichthyosis congenita harlequin type ichthyosis fetalis	piga-1	174386	Caenorhabditis elegans
DOID:0060284	paroxysmal nocturnal hemoglobinuria	piga-1	174386	Caenorhabditis elegans
DOID:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2 Aliases: developmental and epileptic encephalopathy 20 early infantile epileptic encephalopathy 20 glycosylphosphatidylinositol biosynthesis defect 4	piga-1	174386	Caenorhabditis elegans
DOID:10652	Alzheimer's disease Aliases: Alzheimer disease Alzheimers dementia	enol-1 gpd-1 gpd-3 gpd-4 gsto-1 parp-1	174423 174578 174603 180601 183000 266823	Caenorhabditis elegans
DOID:1712	aortic valve stenosis Aliases: Aortic stenosis Rheumatic aortic stenosis rheumatic aortic valve stenosis	enol-1 ogt-1	174423 176000	Caenorhabditis elegans
DOID:0080855	Parkinsonism	enol-1 gba-3 gba-4	174423 177314 178535	Caenorhabditis elegans
DOID:936	brain disease Aliases: encephalopathy	enol-1	174423	Caenorhabditis elegans

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