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Summary Literature (0)
MIM:613873 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17

Xenbase Genes: jph2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013474 - hypertrophic cardiomyopathy 17

Disease Ontology (DO):
DOID:0110323 - hypertrophic cardiomyopathy 17