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Summary Literature (0)
MIM:160150 - MYOPATHY, CENTRONUCLEAR, 1; CNM1

Xenbase Genes: myf6, mtmr14, dnm2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008048 - autosomal dominant centronuclear myopathy

Disease Ontology (DO):
DOID:14717 - centronuclear myopathy