MeSH Browser

MeSH Supplementary: Filaminopathy, autosomal dominant
Unique ID: C537932
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537932
Entry Term(s): Filamin C-related myofibrillar myopathy; Mfm, Filamin C-Related; Myofibrillar myopathy, filamin C-related; Myopathy, Myofibrillar, Filamin C-Related
Registry Number: 0
Heading Mapped to: *Muscular Dystrophies
Frequency: 13
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Filaminopathy, autosomal dominant MeSH Supplementary Concept Data 2023