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

Referenced Disease Ontology:
DOID:0110307 - hypertrophic cardiomyopathy 1

Human Disease Resources: OMIM

Xenbase Genes: myh6, myh7, actc1, tnnc1, cav3.1, cav3.2, calr3

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