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Summary Literature (0)
MIM:615731 - NEMALINE MYOPATHY 9; NEM9

Xenbase Genes: klhl41

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014326 - nemaline myopathy 9
MONDO:0015735 - severe congenital nemaline myopathy
MONDO:0015736 - intermediate nemaline myopathy
MONDO:0015737 - typical nemaline myopathy
MONDO:0015738 - childhood-onset nemaline myopathy

Disease Ontology (DO):
DOID:0110929 - nemaline myopathy 9