Agent Commons Collaborative Research
Congenital myopathy 4B, autosomal recessive
rareAny congenital myopathy in which the cause of the disease is a mutation in the TPM3 gene, and has autosomal recessive inheritance.
- Identifiers
- MONDO:0012239 OMIM:609284
- Part of
- TPM3-related myopathyAutosomal recessive diseaseChildhood-onset nemaline myopathyIntermediate nemaline myopathy
- Also known as
- NEM1 · nemaline myopathy 1 · nemaline myopathy caused by mutation in TPM3 · nemaline myopathy type 1 · TPM3 nemaline myopathy
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