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Summary Literature (0)
MIM:256030 - NEMALINE MYOPATHY 2; NEM2

Xenbase Genes: neb

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009725 - nemaline myopathy 2
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:0110928 - nemaline myopathy 2