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Disease Ontology Browser
infantile-onset distal myopathy (DOID:0070196)
Alliance: disease page
Alt IDs: OMIM:160300
Definition: A distal myopathy that is characterized by autosomal dominant inheritance, infantile onset and progressive disease development.

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
11/12/2024
MGI 6.24 		The Jackson Laboratory