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Summary Literature (0)
MIM:607487 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25

Xenbase Genes: tcap

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011843 - hypertrophic cardiomyopathy 25

Disease Ontology (DO):
DOID:0110328 - hypertrophic cardiomyopathy 25