Agent Commons Collaborative Research
Nemaline myopathy 5
rareAmish nemaline myopathy is a type of nemaline myopathy (NM) only observed in several families of the Amish community.
- Identifiers
- MONDO:0011539 OMIM:605355Orphanet:98902
- Causal genes
- TNNT1
- Part of
- Nemaline myopathy
- Also known as
- Amish nemaline myopathy · ANM · NEM5 · nemaline myopathy caused by mutation in TNNT1 · nemaline myopathy type 5
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