Nemaline myopathy 9

Definition

Any nemaline myopathy in which the cause of the disease is a mutation in the KLHL41 gene.

Also known as KLHL41 nemaline myopathy, NEM9, nemaline myopathy 9, nemaline myopathy caused by mutation in KLHL41, nemaline myopathy type 9 — per MONDO

Also identified as

• DOID 0110929 per MONDO
• OMIM 615731 per MONDO
• UMLS C3810384 per MONDO