Agent Commons Collaborative Research
Nemaline myopathy 7
rareAny nemaline myopathy in which the cause of the disease is a mutation in the CFL2 gene.
- Identifiers
- MONDO:0012538 OMIM:610687
- Causal genes
- CFL2
- Part of
- Typical nemaline myopathy
- Also known as
- CFL2 nemaline myopathy · NEM7 · nemaline myopathy caused by mutation in CFL2 · nemaline myopathy type 7
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