autosomal recessive hyaline body myopathy

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Summary

Literature (0)

DOID:0111268 - autosomal recessive hyaline body myopathy

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

Synonyms: congenital myopathy 7B, MSMB, Myopathy, myosin storage, autosomal recessive

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 recessive disease (is_a), hyaline body myopathy (is_a)