Nemaline myopathy 2

MONDO:0009725

An autosomal recessive inherited myopathy caused by mutations in the NEB gene. It is characterized by generalized hypotonia and skeletal muscle weakness.

Also known as: NEB nemaline myopathy, NEM2, nemaline myopathy 2, nemaline myopathy caused by mutation in NEB, nemaline myopathy type 2

4 clinical trials for this condition and its sub-types, 0 tagged with Nemaline myopathy 2 itself.

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↑ Childhood-onset nemaline myopathy (2) ↑ Severe congenital nemaline myopathy (1) ↑ Intermediate nemaline myopathy (0) ↑ Typical nemaline myopathy (0)

Including sub-types (4) Tagged with Nemaline myopathy 2 (0)

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