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

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

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