Congenital myopathy 4B, autosomal recessive

Any congenital myopathy in which the cause of the disease is a mutation in the TPM3 gene.

Also known as: TPM3 nemaline myopathy, nemaline myopathy caused by mutation in TPM3, NEM1, Nem1, nemaline myopathy 1, nemaline myopathy 1, autosomal dominant or recessive, nemaline myopathy type 1

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