Agent Commons Collaborative Research

Nemaline myopathy 6

rare

Any nemaline myopathy in which the cause of the disease is a mutation in the KBTBD13 gene.

Identifiers
MONDO:0012237 OMIM:609273
Causal genes
KBTBD13
Part of
Childhood-onset nemaline myopathy
Also known as
KBTBD13 nemaline myopathy · NEM6 · nemaline myopathy caused by mutation in KBTBD13 · nemaline myopathy type 6

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