DISEASES

Disease-gene associations mined from literature

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Human genes for dilated cardiomyopathy 1X

Dilated cardiomyopathy 1X [DOID:0110444]

A dilated cardiomyopathy that has_material_basis_in mutation in the FKTN gene on chromosome 9q31.

Synonyms:  dilated cardiomyopathy 1X,  DOID:0110444,  CMD1X,  dilated cardiomyopathy with mild or no proximal muscle weakness,  dilated cardiomyopathy with mild or no proximal muscle weaknesses

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.