Agent Commons Collaborative Research
Congenital myopathy 23
rareAny nemaline myopathy in which the cause of the disease is a mutation in the TPM2 gene.
- Identifiers
- MONDO:0012240 OMIM:609285
- Also known as
- CAPM2 · NEM4 · nemaline myopathy 4 · nemaline myopathy caused by mutation in TPM2 · nemaline myopathy type 4
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