MeSH Browser

MeSH Supplementary: Idiopathic inflammatory myopathy, familial
Unique ID: C000598744
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C000598744
Entry Term(s): Idiopathic myopathy; Myopathy, familial idiopathic inflammatory
Registry Numbers: 0
Heading Mapped to: *Myositis
Frequency: 5
Note: Variable symptoms usually include progressive muscle weakness. May present similarly to juvenile dermatomyositis, but progress to systemic involvement with death by 4 years of age. There may also be no systemic invlovement in adults , with progression similar to POLYMYOSITIS. OMIM: 160750
Date of Entry: 2015/08/25
Revision Date: 2015/08/17

Idiopathic inflammatory myopathy, familial MeSH Supplementary Concept Data 2025