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Summary Literature (0)
MIM:613876 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20

Xenbase Genes: nexn

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013477 - hypertrophic cardiomyopathy 20

Disease Ontology (DO):
DOID:0110326 - hypertrophic cardiomyopathy 20