MeSH Browser

MeSH Supplementary: Inclusion Body Myopathy 3, Autosomal Dominant
Unique ID: C565311
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565311
Entry Term(s): Myopathy with Congenital Joint Contractures, Ophthalmoplegia, and Rimmed Vacuoles
Registry Number: 0
Heading Mapped to: *Contracture; *Ophthalmoplegia; Myositis, Inclusion Body / *congenital
Frequency: 1
Note: mutation in MYHC2A
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Inclusion Body Myopathy 3, Autosomal Dominant MeSH Supplementary Concept Data 2024