MeSH Browser

MeSH Supplementary: Inclusion body myopathy, autosomal dominant
Unique ID: C538330
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538330
Entry Term(s): Inclusion body myopathy 3
Registry Numbers: 0
Heading Mapped to: Contracture / congenital; *Ophthalmoplegia; Myositis, Inclusion Body / congenital
Frequency: 7
Note: Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Inclusion body myopathy, autosomal dominant MeSH Supplementary Concept Data 2025