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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 **5326 - 5350** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:0050574	L-2-hydroxyglutaric aciduria Aliases: L-2-HYDROXYGLUTARIC ACIDEMIA	L2HGDH	79944	Homo sapiens (human)
DOID:1407	anterior uveitis	LACC1 TLR2 TLR4 TNF	144811 7097 7099 7124	Homo sapiens (human)
DOID:4376	milk allergy Aliases: milk allergic reaction	LALBA	3906	Homo sapiens (human)
DOID:0111242	congenital muscular dystrophy-dystroglycanopathy type A6 Aliases: MDDGA6 Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6	LARGE1	9215	Homo sapiens (human)
DOID:3611	acute retinal necrosis syndrome Aliases: acute retinal necrosis	LCT	3938	Homo sapiens (human)
DOID:0111646	congenital lactase deficiency Aliases: CLD congenital alactasia congenital alactasia syndrome congenital lactose intolerance congenital lactose malabsorption disaccharide intolerance II	LCT	3938	Homo sapiens (human)
DOID:5139	cellular leiomyoma	LDHA	3939	Homo sapiens (human)
DOID:7910	maxillary sinus squamous cell carcinoma Aliases: Epidermoid carcinoma of the Maxillofacial sinus	LDHB MICA PNP	100507436 3945 4860	Homo sapiens (human)
DOID:10605	short bowel syndrome Aliases: acquired short bowel syndrome short gut syndrome	LEP LEPR	3952 3953	Homo sapiens (human)
DOID:0060611	abdominal obesity-metabolic syndrome	LEP NEIL1 PPARGC1A	10891 3952 79661	Homo sapiens (human)
DOID:0111334	congenital leptin deficiency Aliases: LEPD leptin deficiency or dysfunction obesity due to congenital leptin deficiency	LEP	3952	Homo sapiens (human)
DOID:0050568	spondylocostal dysostosis Aliases: Jarcho-Levin syndrome costovertebral dysplasia spondylothoracic dysostosis spondylothoracic dysplasia	LFNG SLC35A3	23443 3955	Homo sapiens (human)
DOID:0112361	spondylocostal dysostosis 3 Aliases: SCDO3 autosomal recessive spondylocostal dysostosis 3	LFNG	3955	Homo sapiens (human)
DOID:1687	neovascular glaucoma Aliases: secondary angle-closure glaucoma with rubeosis	LGALS1 PRNP	3956 5621	Homo sapiens (human)
DOID:3277	thymus cancer Aliases: Thymic tumor neoplasm of thymus thymic neoplasm	LGALS1 PTEN	3956 5728	Homo sapiens (human)
DOID:11563	retinal vasculitis	LGALS1	3956	Homo sapiens (human)
DOID:0111120	nephronophthisis 9 Aliases: NPHP9	LGALS1	3956	Homo sapiens (human)
DOID:0050256	angiostrongyliasis	LGALS2	3957	Homo sapiens (human)
DOID:4151	skull base chordoma Aliases: Chordoma of the Skull Base	LGALS3 LGALS9 PIK3CA PIK3CB PIK3CD PIK3CG	3958 3965 5290 5291 5293 5294	Homo sapiens (human)
DOID:3951	acute myocarditis	LGALS3 LGALS9 PRKAA2 PTGS2 SMUG1 SULT1E1	23583 3958 3965 5563 5743 6783	Homo sapiens (human)
DOID:5757	endocervicitis	LGALS3 MSLN	10232 3958	Homo sapiens (human)
DOID:2568	cervicitis	LGALS3 MSLN	10232 3958	Homo sapiens (human)
DOID:4400	dermatosis papulosa nigra	LGALS3 NTHL1 PIK3CA PIK3CB PIK3CD PIK3CG	3958 4913 5290 5291 5293 5294	Homo sapiens (human)
DOID:467	venous hemangioma	LGALS3 PIK3CA PIK3CB PIK3CD PIK3CG TM7SF2	3958 5290 5291 5293 5294 7108	Homo sapiens (human)
DOID:0050784	primary progressive multiple sclerosis Aliases: PPMS Primary-progressive MS	LGALS3 RGMA SOAT1	3958 56963 6646	Homo sapiens (human)

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