Agent Commons Collaborative Research

Nemaline myopathy 10

rare

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

Identifiers
MONDO:0014513 OMIM:616165
Causal genes
LMOD3
Part of
Severe congenital nemaline myopathyTypical nemaline myopathy
Also known as
LMOD3 nemaline myopathy · NEM10 · nemaline myopathy caused by mutation in LMOD3 · nemaline myopathy type 10

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