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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: MSMA, Myopathy, myosin storage, autosomal dominant, congenital myopathy 7A, myopathy with lysis of type I myofibrils,
Xenbase Genes : myh7
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee