Congenital myopathy 4B, autosomal recessive

MONDO:0012239

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

4 clinical trials for this condition and its sub-types, 0 tagged with Congenital myopathy 4B, autosomal recessive itself.

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Part of

↑ Childhood-onset nemaline myopathy (2) ↑ TPM3-related myopathy (1) ↑ Intermediate nemaline myopathy (0)

Including sub-types (4) Tagged with Congenital myopathy 4B, autosomal recessive (0)

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