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Summary Literature (0)
MIM:613838 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16

Xenbase Genes: myoz2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013455 - hypertrophic cardiomyopathy 16

Disease Ontology (DO):
DOID:0110322 - hypertrophic cardiomyopathy 16