Term Name:	autosomal dominant hyaline body myopathy
Synonyms:	congenital myopathy 7A, MSMA, myopathy with lysis of type I myofibrils, Myopathy, myosin storage, autosomal dominant
Definition:	A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2.
Ontology:	Human Disease [DOID:0111269]   ( DOID:0111269 )