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autosomal recessive hyaline body myopathy (DOID:0111268)
Alliance: disease page
Synonyms: congenital myopathy 7B; MSMB; Myopathy, myosin storage, autosomal recessive
Alt IDs: OMIM:255160
Definition: A hyaline body myopathy that has_material_basis_in compound heterozygous or homozygous mutation in MYH7 on 14q11.2.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory