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Disease Ontology Browser
nemaline myopathy (DOID:3191)
Synonyms: Nemaline body disease; nemaline rod myopathy; rod myopathy
Alt IDs: OMIM:161800, OMIM:256030, OMIM:605355, OMIM:609273, OMIM:609284, OMIM:609285, OMIM:610687, OMIM:615348, OMIM:615731, OMIM:616165, ICD10CM:G71.2, MESH:D017696, ORDO:607, UMLS_CUI:C0206157
Definition: A congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity; certain muscle fibers show the presence of rod-like structures called nemaline bodies.

Disease References using Mouse Models (14)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory