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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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **2976 - 3000** of **4115** in total

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Disease ID	Disease Name ▲	Gene Symbol	Gene ID	Organism	Source
DOID:0070462	mitochondrial complex V (ATP synthase) deficiency nuclear type 4B Aliases: MC5DN4B	ATP5F1A	498	Homo sapiens (human)	Alliance of Genome Resources
DOID:890	mitochondrial encephalomyopathy	TYMP	1890	Homo sapiens (human)	Alliance of Genome Resources
DOID:700	mitochondrial metabolism disease	HADHB	3032	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070540	mitochondrial short-chain enoyl-CoA hydratase 1 deficiency Aliases: ECHS1D	ECHS1	1892	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070619	mitochondrial trifunctional protein deficiency 1 Aliases: MTPD1	HADHA	3030	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060999	mitochondrial trifunctional protein deficiency 2 Aliases: MTPD2	HADHB	3032	Homo sapiens (human)	Alliance of Genome Resources
DOID:61	mitral valve disease Aliases: Mitral RH valve dis. Rheumatic mitral insufficiency Rheumatic mitral valve changes Rheumatic mitral valve regurgitation chronic rheumatic mitral valve disease of mitral valve rheumatic disease of mitral valve rheumatic mitral valve incompetence	ACE	1636	Homo sapiens (human)	Alliance of Genome Resources
DOID:988	mitral valve prolapse Aliases: Barlow's syndrome floppy mitral valve	ACE AGT DCHS1 DZIP1 FBN1 FLNA HLA-B PLAU TSHR	1636 183 2200 22873 2316 3106 5328 7253 8642	Homo sapiens (human)	Alliance of Genome Resources
DOID:3492	mixed connective tissue disease Aliases: Connective tissue disease overlap syndrome mixed collagen vascular disease	FBN1 HLA-DRB1 SNRPB SNRPC	2200 3123 6628 6631	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111166	molybdenum cofactor deficiency type C Aliases: MOCOD type C MOCODC combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C molybdenum cofactor deficiency complementation group C	GPHN	10243	Homo sapiens (human)	Alliance of Genome Resources
DOID:7442	monoclonal gammopathy of uncertain significance Aliases: MGUS Monoclonal gammopathy of undetermined significance	CTLA4 NEFH	1493 4744	Homo sapiens (human)	Alliance of Genome Resources
DOID:3324	mood disorder Aliases: episodic mood disorder	AVPR1B	553	Homo sapiens (human)	Alliance of Genome Resources
DOID:11981	morbid obesity Aliases: Severe obesity	AGER CTNNBL1 GHRL MC4R MCHR1 NPY2R NTRK2	177 2847 4160 4887 4915 51738 56259	Homo sapiens (human)	Alliance of Genome Resources
DOID:2560	morphine dependence	COMT	1312	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080141	mosaic variegated aneuploidy syndrome 1	BUB1B	701	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080142	mosaic variegated aneuploidy syndrome 2	CEP57	9702	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080689	mosaic variegated aneuploidy syndrome 3	TRIP13	9319	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080688	mosaic variegated aneuploidy syndrome	SLF2 SMC5	23137 55719	Homo sapiens (human)	Alliance of Genome Resources
DOID:231	motor neuron disease	SOD1 TARDBP	23435 6647	Homo sapiens (human)	Alliance of Genome Resources
DOID:2477	motor peripheral neuropathy Aliases: HSMN HSMN - Hereditary sensory and motor neuropathy Hereditary motor and sensory neuropathy Peripheral Motor Neuropathy neuropathic muscular atrophy	EGR2	1959	Homo sapiens (human)	Alliance of Genome Resources
DOID:480	movement disease	DRD2	1813	Homo sapiens (human)	Alliance of Genome Resources
DOID:3030	mucinous adenocarcinoma Aliases: Mucin-Secreting adenocarcinoma Mucin-Secreting carcinoma Mucous carcinoma Pseudomyxoma peritonei with unknown primary site mucin-producing adenocarcinoma	MUC1	4582	Homo sapiens (human)	Alliance of Genome Resources
DOID:9155	mucocutaneous leishmaniasis Aliases: American cutaneous leishmaniasis American mucocutaneous leishmaniasis Cutaneous leishmaniasis, American Mucocutaneous leishmaniasis, American New World cutaneous leishmaniasis	LTA TNF	4049 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:4531	mucoepidermoid carcinoma Aliases: MEC	CDH1	999	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080070	mucolipidosis II alpha/beta Aliases: I-cell disease inclusion-cell disease mucolipidosis II	GNPTAB	79158	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources

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