DISEASES

Disease-gene associations mined from literature

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Human genes for autosomal dominant hyaline body myopathy

Autosomal dominant hyaline body myopathy [DOID:0111269]

A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2.

Synonyms:  autosomal dominant hyaline body myopathy,  autosomal dominant hyaline body myopathies,  DOID:0111269,  MSMA,  Myopathy, myosin storage, autosomal dominant ...

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.