Congenital myopathy 23

Any nemaline myopathy in which the cause of the disease is a mutation in the TPM2 gene.

Also known as: CAPM2, NEM4, TPM2 nemaline myopathy, nemaline myopathy 4, nemaline myopathy caused by mutation in TPM2, nemaline myopathy type 4

37 clinical trials for this condition and its sub-types.