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Summary Literature (0)
MIM:192600 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1

Xenbase Genes: myh6, myh7l, actc1, tnnc1, cav3, cav3.2, calr3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008647 - hypertrophic cardiomyopathy 1

Disease Ontology (DO):
DOID:0110307 - hypertrophic cardiomyopathy 1