DISEASES

Disease-gene associations mined from literature

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Human genes for congenital disorder of glycosylation type IIl

Congenital disorder of glycosylation type IIl [DOID:0070264]

A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of COG6 on chromosome 13q14.11.

Synonyms:  congenital disorder of glycosylation type IIl,  congenital disorder of glycosylation type IIls,  DOID:0070264,  CDG2L,  CDGIIdl ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.