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Summary Literature (0)
MIM:611705 - CONGENITAL MYOPATHY 5 WITH CARDIOMYOPATHY; CMYP5

Xenbase Genes: ttn

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012714 - early-onset myopathy with fatal cardiomyopathy

Disease Ontology (DO):
DOID:0081341 - congenital myopathy 5