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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	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **8426 - 8450** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0080588	agammaglobulinemia 5	LRRC8A	56262	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060371	Parkinson's disease 8 Aliases: autosomal dominant Parkinson disease 8 autosomal dominant Parkinson's disease 8	LRRK1 LRRK2	120892 79705	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081111	osteosclerotic metaphyseal dysplasia	LRRK1	79705	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110169	Charcot-Marie-Tooth disease axonal type 2P Aliases: CMT2P Charcot-Marie-Tooth disease type 2P Charcot-Marie-Tooth neuropathy type 2P	LRSAM1	90678	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110515	autosomal recessive nonsyndromic deafness 63 Aliases: DFNB63 autosomal recessive deafness 63	LRTOMT	220074	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080950	alopecia-mental retardation syndrome 4	LSS	4047	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110267	cataract 44 Aliases: CTRCT44 total early-onset cataract	LSS	4047	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080582	hypotrichosis 14	LSS	4047	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:4398	pustulosis of palm and sole Aliases: Acropustulosis Palmoplantar Pustulosis Pustular psoriasis of the palms and/or soles	LTA TNF	4049 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060305	megalocornea Aliases: anterior megalophthalmos congenital anterior megalophthalmia	LTBP2	4053	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090143	brachyolmia-amelogenesis imperfecta syndrome Aliases: DASS STHAG6 dental anomalies and short stature platyspondyly with amelogenesis imperfecta selective tooth agenesis 5	LTBP3	4054	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111727	geleophysic dysplasia 3 Aliases: GPHYSD3	LTBP3	4054	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070139	autosomal recessive cutis laxa type IC Aliases: ARCL1C autosomal recessive cutis laxa type 1C	LTBP4	8425	Homo sapiens (human)	Alliance of Genome Resources
DOID:13689	prostate calculus Aliases: Prostatic lithiasis Prostatic stone Stone of prostate calculus of prostate	LTF	4057	Homo sapiens (human)	Alliance of Genome Resources
DOID:2935	Chediak-Higashi syndrome Aliases: CHS Chediak - Steinbrinck anomaly	LYST WDFY3	1130 23001	Homo sapiens (human)	Alliance of Genome Resources
DOID:2326	gastroenteritis Aliases: cholera morbus infectious colitis, enteritis and gastroenteritis	Lalba Tgfa	16770 21802	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2326	gastroenteritis Aliases: cholera morbus infectious colitis, enteritis and gastroenteritis	Lalba Tgfa	24528 24827	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110636	congenital merosin-deficient muscular dystrophy 1A Aliases: CMD1A MDC1A Merosin-negative congenital muscular dystrophy congenital muscular dystrophy due to laminin alpha2 deficiency	Lama2	16773	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110438	dilated cardiomyopathy 1JJ Aliases: CMD1JJ	Lama4	16775	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2975	cystic kidney disease Aliases: renal Cyst	Lama5 Robo1	140433 58946	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2590	familial nephrotic syndrome Aliases: Congenital nephrotic syndrome	Lama5	140433	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112230	lissencephaly 5 Aliases: LIS5	Lamb1	16777	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060852	Pierson syndrome Aliases: microcoria-congenital nephrosis syndrome	Lamb2 Tns2	16779 209039	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080380	nephrotic syndrome type 5 Aliases: nephrotic syndrome type 5, with or without ocular abnormalities	Lamb2	16779	Mus musculus (house mouse)	Alliance of Genome Resources

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