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Disease Ontology Browser
nemaline myopathy (DOID:3191)
Alliance: disease page
Synonyms: Nemaline body disease; nemaline rod myopathy; rod body disease; rod myopathy
Alt IDs: ICD10CM:G71.21, MESH:D017696, OMIM:PS161800, ORDO:607, UMLS_CUI:C0206157
Definition: A congenital myopathy characterized by generally non-progressive muscle weakness of varying severity and problems with the tone and contraction of skeletal muscles. The muscle cells contain abnormal clumps of threadlike material called nemaline bodies.

Disease References using Mouse Models (20)
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
11/19/2024
MGI 6.24 		The Jackson Laboratory