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Summary Literature (0)
MIM:614399 - CONGENITAL MYOPATHY 10A, SEVERE VARIANT; CMYP10A

Xenbase Genes: megf10

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013731 - MEGF10-related myopathy

Disease Ontology (DO):
DOID:0111333 - early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome