DISEASES

Disease-gene associations mined from literature

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Human genes for X-linked dilated cardiomyopathy

X-linked dilated cardiomyopathy [DOID:0110461]

A dilated cardiomyopathy that has_material_basis_in mutation in the gene encoding dystrophin (DMD) on chromosome Xp21, without skeletal muscle weakness or wasting.

Synonyms:  X-linked dilated cardiomyopathy,  DOID:0110461,  Xlinked dilated cardiomyopathy,  X-linked dilated cardiomyopathies,  CMD3B ...

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.