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Disease Ontology Browser
Miyoshi muscular dystrophy (DOID:0070198)
Alliance: disease page
Synonyms: Miyoshi myopathy
Alt IDs: MESH:C537480, OMIM:PS254130, ORDO:45448
Definition: A distal myopathy that is characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood.

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