Myofibrillar Myopathy 6

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant subtype of myofibrillar myopathy caused by mutation(s) in the BAG3 gene, encoding BAG family molecular chaperone regulator 3.

**Synonyms:** - BAG3-Related Myofibrillar Myopathy - MFM6 - Muscular Dystrophy, Selcen Type