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Summary Literature (0)
MIM:616165 - NEMALINE MYOPATHY 10; NEM10

Xenbase Genes: lmod3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014513 - nemaline myopathy 10
MONDO:0015735 - severe congenital nemaline myopathy
MONDO:0015737 - typical nemaline myopathy

Disease Ontology (DO):
DOID:0110931 - nemaline myopathy 10