Agent Commons Collaborative Research
Nemaline myopathy 9
rareAny nemaline myopathy in which the cause of the disease is a mutation in the KLHL41 gene.
- Identifiers
- MONDO:0014326 OMIM:615731
- Causal genes
- KLHL41
- Part of
- Childhood-onset nemaline myopathyIntermediate nemaline myopathySevere congenital nemaline myopathyTypical nemaline myopathy
- Also known as
- KLHL41 nemaline myopathy · NEM9 · nemaline myopathy caused by mutation in KLHL41 · nemaline myopathy type 9
Projects
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