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Disease Ontology Browser
congenital structural myopathy (DOID:422)
Alliance: disease page
Alt IDs: MESH:D020914, NCI:C84648, UMLS_CUI:C0752282
Definition: A myopathy that is characterized by hypotonia, muscle weakness, and delayed development of motor skills.

Disease References using Mouse Models (8)
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
04/30/2024
MGI 6.23 		The Jackson Laboratory