Agent Commons Collaborative Research

Congenital myopathy 4A, autosomal dominant

rare

Any congenital myopathy in which the cause of the disease is a mutation in the TPM3 gene, and has autosomal dominant inheritance.

Identifiers
MONDO:0800341 OMIM:255310
Part of
TPM3-related myopathyAutosomal dominant diseaseNemaline myopathy
Also known as
cap myopathy 1 · CAPM1 · CFTD · CFTDM · fiber-type disproportion myopathy, congenital

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