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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 **7676 - 7700** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism
DOID:1168	familial hyperlipidemia Aliases: familial hyperlipoproteinemia hyperlipemia	YBR053C	852342	Saccharomyces cerevisiae S288C
DOID:0110658	congenital myasthenic syndrome 15 Aliases: CMS15 congenital myasthenic syndrome 15 without tubular aggregates	ALG14	852362	Saccharomyces cerevisiae S288C
DOID:0080563	congenital disorder of glycosylation Ik Aliases: congenital disorder of glycosylation 1k	ALG1	852407	Saccharomyces cerevisiae S288C
DOID:10579	leukodystrophy	YDC1 YPC1	852481 856018	Saccharomyces cerevisiae S288C
DOID:0080547	metabolic dysfunction-associated steatohepatitis Aliases: MASH NASH non-alcoholic steatohepatitis nonalcoholic steatohepatitis	YDC1 YPC1	852481 856018	Saccharomyces cerevisiae S288C
DOID:1059	intellectual disability	PGI1 SMC3	852495 853371	Saccharomyces cerevisiae S288C
DOID:114	heart disease	PGI1	852495	Saccharomyces cerevisiae S288C
DOID:589	congenital hemolytic anemia Aliases: congenital hemolytic anaemia hereditary hemolytic anaemia hereditary hemolytic anemia	PGI1	852495	Saccharomyces cerevisiae S288C
DOID:440	neuromuscular disease	PGI1	852495	Saccharomyces cerevisiae S288C
DOID:3651	pyruvate carboxylase deficiency disease Aliases: deficiency of pyruvic carboxylase	PYC1 PYC2	852519 852818	Saccharomyces cerevisiae S288C
DOID:0080322	polycystic kidney disease	ALG5 ROT2	852530 855874	Saccharomyces cerevisiae S288C
DOID:0110860	polycystic kidney disease 3 Aliases: Apkd3 Pkd3 Polycystic Kidney Disease, Adult, Type III	ROT2	852530	Saccharomyces cerevisiae S288C
DOID:0110676	congenital myasthenic syndrome 13 Aliases: CMS13 CMSTA2 congenital myasthenic syndrome 13 with tubular aggregates congenital myasthenic syndrome with tubular aggregates 2	ALG7	852545	Saccharomyces cerevisiae S288C
DOID:0080562	congenital disorder of glycosylation Ij Aliases: Congenital disorder of glycosylation 1j	ALG7	852545	Saccharomyces cerevisiae S288C
DOID:3021	acute kidney failure	GPX1 GPX2	852546 853842	Saccharomyces cerevisiae S288C
DOID:0112298	spondylometaphyseal dysplasia Sedaghatian type Aliases: SMDS Sedaghatian chondrodysplasia congenital lethal metaphyseal chondrodysplasia	GPX1 GPX2	852546 853842	Saccharomyces cerevisiae S288C
DOID:3717	gastric adenocarcinoma Aliases: adenocarcinoma of stomach stomach adenocarcinoma	GPX1 GPX2	852546 853842	Saccharomyces cerevisiae S288C
DOID:0050861	colorectal adenocarcinoma	GPX1 GPX2	852546 853842	Saccharomyces cerevisiae S288C
DOID:1184	nephrotic syndrome	GPX1 GPX2	852546 853842	Saccharomyces cerevisiae S288C
DOID:219	colon cancer	GPX1 GPX2	852546 853842	Saccharomyces cerevisiae S288C
DOID:0080388	nephrotic syndrome type 7 Aliases: Ig-mediated MPGN Ig-mediated membranoproliferative glomerulonephritis Immunoglobulin-mediated MPGN immunoglobulin-mediated membranoproliferative glomerulonephritis nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis	DGKE	8526	Homo sapiens (human)
DOID:9266	cystinuria	IMA1 IMA2 IMA3 IMA4 IMA5 MAL12 MAL32	852602 853204 853209 853214 853235 854008 854635	Saccharomyces cerevisiae S288C
DOID:0112216	developmental and epileptic encephalopathy 80 Aliases: DEE80 GPIBD20 early infantile epileptic encephalopathy 80 glycosylphosphatidylinositol biosynthesis defect 20	GPI10	852735	Saccharomyces cerevisiae S288C
DOID:10112	sleeping sickness Aliases: African sleeping sickness African trypanosomiasis	GPI10	852735	Saccharomyces cerevisiae S288C
DOID:0060644	chondrodysplasia-pseudohermaphroditism syndrome Aliases: Nivelon-Nivelon-Mabille syndrome chondrodysplasia-disorder of sex development syndrome	GUP1	852796	Saccharomyces cerevisiae S288C

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