Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Childhood-onset nemaline myopathy · TPM3-related myopathy · Intermediate nemaline myopathy
Congenital myopathy 4B, autosomal recessive
Any congenital myopathy in which the cause of the disease is a mutation in the TPM3 gene.
This condition has no sub-types.