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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 **201 - 225** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:0080570	congenital disorder of glycosylation It Aliases: congenital disorder of glycosylation 1t	PGM1 PGM2	853732 855131	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3307	teratoma	PCM1 PGM1 PGM2	853732 855131 856652	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080108	myoglobinuria	GPM1	853705	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111630	familial erythrocytosis 8 Aliases: BPGM deficiency DPGM deficiency ECYT8 bisphosphoglycerate mutase deficiency bisphosphoglyceromutase deficiency diphosphoglycerate mutase deficiency of erythrocyte hemolytic anemia due to diphosphoglycerate mutase deficiency	GPM1	853705	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110669	congenital myasthenic syndrome 14 Aliases: CMS14 CMSTA3 congenital myasthenic syndrome 14, with tubular aggregates congenital myasthenic syndrome with tubular aggregates 3	ALG2	85365	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0050700	cardiomyopathy Aliases: Cardiomyopathies	PMT4	853608	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9296	cleft lip Aliases: Labium leporinum cheiloschisis cleft lip, unilateral, complete complete unilateral cleft lip hare lip	PMT4	853608	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110297	autosomal recessive limb-girdle muscular dystrophy type 2K Aliases: LGMD2K MDDGC1 limb-girdle muscular dystrophy-intellectual disability syndrome muscular dystrophy limb-girdle type 2K muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1	PMT4	853608	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111237	congenital muscular dystrophy-dystroglycanopathy type A1 Aliases: MDDGA1 Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1	PMT4	853608	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050588	muscular dystrophy-dystroglycanopathy type B1 Aliases: CMD due to dystroglycanopathy Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1	PMT4	853608	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081097	Rafiq syndrome Aliases: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15	MNS1	853595	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050589	inflammatory bowel disease	KAR2	853418	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0090145	dopamine beta-hydroxylase deficiency Aliases: congenital dopamine beta-hydroxylase deficiency noradrenaline deficiency norepinephrine deficiency	KAR2	853418	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2055	post-traumatic stress disorder Aliases: PTSD traumatic neurosis	KAR2	853418	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5199	ureteral obstruction	KAR2	853418	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:224	transient cerebral ischemia Aliases: TIA TIA - Transient ischaemic attack Transient cerebral ischaemia Transient ischemic attacks transient ischemic attack	KAR2 OGG1 ZWF1	853418 854942 855480	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080507	Cornelia de Lange syndrome 3 Aliases: CDLS3 Cornelia De Lange syndrome 3 with or without midline brain defects	SMC3	853371	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11725	Cornelia de Lange syndrome Aliases: Brachmann de Lange syndrome De Lange syndrome	SMC3	853371	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050579	glycogen storage disease XV Aliases: Glycogen storage disease 15 Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency glycogen storage disease type XV	GLG1 GLG2	853304 853932	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:936	brain disease Aliases: encephalopathy	ENO1 ENO2	853169 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:12783	migraine without aura Aliases: common migraine	ENO1 ENO2	853169 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1800	neuroendocrine carcinoma	ENO1 ENO2	853169 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3459	breast carcinoma Aliases: Mammary carcinoma carcinoma of breast	ENO1 ENO2 RHO1	853169 856294 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1712	aortic valve stenosis Aliases: Aortic stenosis Rheumatic aortic stenosis rheumatic aortic valve stenosis	ENO1 ENO2 ERR1 ERR2 ERR3	853169 854575 855373 855848 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080855	Parkinsonism	ENO1 ENO2 ERR1 ERR2 ERR3	853169 854575 855373 855848 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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