autosomal dominant hyaline body myopathy

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Summary

Literature (0)

DOID:0111269 - autosomal dominant hyaline body myopathy

Disease Ontology Definition:A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2.

Synonyms: congenital myopathy 7A, MSMA, Myopathy, myosin storage, autosomal dominant, myopathy with lysis of type I myofibrils

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: myh7l

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), hyaline body myopathy (is_a)