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Summary Literature (0)
MIM:614807 - MYOPATHY, CENTRONUCLEAR, 4; CNM4

Xenbase Genes: ccdc78

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013890 - congenital myopathy with internal nuclei and atypical cores

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