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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 **1551 - 1575** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:5534	renal pelvis squamous cell carcinoma Aliases: Epidermoid carcinoma of the kidney Pelvis	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:10986	discitis	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:0060670	cerebral cavernous malformation 2	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:5292	mediastinum leiomyosarcoma Aliases: leiomyosarcoma of mediastinum	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:6345	malignant melanocytic neoplasm of the peripheral nerve sheath Aliases: Melanotic malignant nerve sheath tumor Melanotic malignant peripheral nerve sheath tumor Melanotic malignant peripheral nerve sheath tumour melanocytic MPNST	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:9768	heart aneurysm Aliases: cardiac aneurysm	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:11824	multicentric reticulohistiocytosis Aliases: Lipoid dermatoarthritis	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:4889	lymph node tuberculosis Aliases: Tuberculous adenitis Tuberculous lymphadenopathy king's evil scrofula	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:5042	malignant granular cell myoblastoma Aliases: granular cell tumor, malignant malignant granular cell neoplasm malignant granular cell tumor	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:0060317	lung abscess	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:4415	fibrous histiocytoma Aliases: Fibroxanthoma benign fibrous histiocytoma	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:3241	lipid pneumonia Aliases: Exogenous lipoid pneumonia Lipoid pneumonitis	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:0080507	Cornelia de Lange syndrome 3 Aliases: CDLS3 Cornelia De Lange syndrome 3 with or without midline brain defects	SMC3	9126	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:11372	megacolon Aliases: Dilatation of colon	SMC3	9126	Homo sapiens (human)	DisGeNET
DOID:11766	blind hypotensive eye	SMC3	9126	Homo sapiens (human)	DisGeNET
DOID:1770	toxic megacolon	SMC3	9126	Homo sapiens (human)	DisGeNET
DOID:0080506	Cornelia de Lange syndrome 2	SMC3	9126	Homo sapiens (human)	DisGeNET
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:0080507	Cornelia de Lange syndrome 3 Aliases: CDLS3 Cornelia De Lange syndrome 3 with or without midline brain defects	SMC3	32627	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:11725	Cornelia de Lange syndrome Aliases: Brachmann de Lange syndrome De Lange syndrome	SMC3	32627	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080899	lung pleomorphic carcinoma	SLC3A2	6520	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080587	congenital myasthenic syndrome 22	SLC3A1	6519	Homo sapiens (human)	DisGeNET
DOID:0060858	hypotonia-cystinuria syndrome Aliases: cystinuria with mitochondrial disease	SLC3A1	6519	Homo sapiens (human)	DisGeNET
DOID:0070266	congenital disorder of glycosylation type IIn Aliases: CDG IIn CDG syndrome type IIn CDG2N CDGIIdn Carbohydrate deficient glycoprotein syndrome type IIn Congenital disorder of glycosylation type 2n SLC39A8-CDG	SLC39A8	64116	Homo sapiens (human)	DisGeNET Alliance of Genome Resources

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