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Disease Ontology Browser
congenital myopathy 4A (DOID:0080102)
Alliance: disease page
Synonyms: CFTD; congenital fiber-type disproportion
Alt IDs: OMIM:255310
Definition: A congenital myopathy that is characterized by skeletal muscle weakness, particularly in the muscles of the shoulders, upper arms, hips, and thighs.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory