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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

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