DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for mitochondrial myopathy

Mitochondrial myopathy [DOID:699]

A myopathy that is characterized by mitochondrial dysfunction.

Synonyms:  mitochondrial myopathy,  DOID:699,  mitochondrial myopathies,  mitochondrial cytopathy,  mitochondrial cytopathies

Linkouts:  OMIM #1 #2 #3

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.