MeSH Browser

MeSH Supplementary: Inclusion body myopathy autosomal recessive
Unique ID: C538329
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538329
Entry Term(s): Inclusion Body Myopathy, Autosomal Recessive; Inclusion Body Myopathy, Quadriceps-Sparing; Inclusion body myopathy 2, autosomal recessive; Inclusion body myopathy quadriceps sparing
Registry Number: 0
Heading Mapped to: Myositis, Inclusion Body / *congenital
Frequency: 11
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Inclusion body myopathy autosomal recessive MeSH Supplementary Concept Data 2024