DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for restrictive cardiomyopathy 2

Restrictive cardiomyopathy 2 [DOID:0111426]

A restrictive cardiomyopathy that has_material_basis_in variation in a region on chromosome 10q23.3.

Synonyms:  restrictive cardiomyopathy 2,  DOID:0111426,  familial restrictive cardiomyopathy 2,  RCM2,  hereditary restrictive cardiomyopathy 2

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.