DISEASES

Disease-gene associations mined from literature

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Human genes for scapuloperoneal myopathy

Scapuloperoneal myopathy [DOID:0060253]

A muscular dystrophy which begins at the lower legs and affects the shoulder region earlier and more severely than distal arm.

Synonyms:  scapuloperoneal myopathy,  DOID:0060253,  scapuloperoneal myopathies

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.