DISEASES

Disease-gene associations mined from literature

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Human genes for myofibrillar myopathy 6

Myofibrillar myopathy 6 [DOID:0080097]

A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26.

Synonyms:  myofibrillar myopathy 6,  DOID:0080097,  BAG3-related myofibrillar myopathy,  BAG3related myofibrillar myopathy

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.