DISEASES

Disease-gene associations mined from literature

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Human genes for dilated cardiomyopathy 1L

Dilated cardiomyopathy 1L [DOID:0110436]

A dilated cardiomyopathy that has_material_basis_in mutations in the SGCD gene on chromosome 5q33.2-q33.3.

Synonyms:  dilated cardiomyopathy 1L,  DOID:0110436,  CMD1L

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.