Filaminopathy, autosomal dominant [Supplementary Concept]
Date introduced: August 25, 2010
MeSH Unique ID: C537932
Heading Mapped to:
Entry Terms:
- Myopathy, Myofibrillar, Filamin C-Related
- Mfm, Filamin C-Related
- Filamin C-related myofibrillar myopathy
- Myofibrillar myopathy, filamin C-related