DISEASES

Disease-gene associations mined from literature

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Human genes for dilated cardiomyopathy 1J

Dilated cardiomyopathy 1J [DOID:0110440]

A dilated cardiomyopathy that has_material_basis_in mutation in the EYA4 gene on chromosome 6q23.2.

Synonyms:  dilated cardiomyopathy 1J,  DOID:0110440,  autosomal dominant dilated cardiomyopathy with sensorineural hearing loss,  CMD1J,  neurosensory deafness with dilated cardiomyopathy ...

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.