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inclusion body myositis (DOID:3429)
Alliance: disease page
Synonyms: Distal Myopathy with Rimmed Vacuoles; Distal myopathy, Nonaka type; Hereditary Inclusion Body Myopathy; HIBM; IBM2; IBM-3; inclusion body myopathy 2; inclusion body myopathy 3; Nonaka Myopathy; Nonaka myopathy
Alt IDs: OMIM:147421, OMIM:605637, OMIM:605820, ICD10CM:G72.41, ICD9CM:359.71, MESH:D018979, NCI:C84786, UMLS_CUI:C0238190
Definition: A myositis that is characterized by slowly progressive weakness and wasting of both distal and proximal muscles, most apparent in the muscles of the arms and legs that can occur in a sporadic or hereditary forms.

Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory