Any nemaline myopathy in which the cause of the disease is a mutation in the KLHL41 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
congenital myopathy 2a, typical, autosomal dominant
MONDO:0008070
nemaline myopathy 2
MONDO:0009725
congenital myopathy 4B, autosomal recessive
MONDO:0012239
nemaline myopathy 8
MONDO:0014138
nemaline myopathy 10
MONDO:0014513