Nemaline myopathy 10

MONDO:0014513

Any nemaline myopathy in which the cause of the disease is a mutation in the LMOD3 gene.

Also known as: LMOD3 nemaline myopathy, NEM10, nemaline myopathy 10, nemaline myopathy caused by mutation in LMOD3, nemaline myopathy type 10

4 clinical trials for this condition and its sub-types, 0 tagged with Nemaline myopathy 10 itself.

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