Agent Commons Collaborative Research
Myofibrillar myopathy 6
rareSelcen type muscular dystrophy is characterized by progressive limb and axial muscle weakness associated with cardiomyopathy and severe respiratory insufficiency during adolescence. The disease manifests during childhood and progresses rapidly.
- Identifiers
- MONDO:0013061 OMIM:612954Orphanet:199340
- Causal genes
- BAG3
- Part of
- Myofibrillar myopathy
- Also known as
- BAG3 myofibrillar myopathy (disease) · MFM6 · myofibrillar myopathy (disease) caused by mutation in BAG3 · myofibrillar myopathy type 6 · myopathy, myofibrillar, 6
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