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Summary Literature (0)
MIM:608758 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10

Xenbase Genes: myl2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012112 - hypertrophic cardiomyopathy 10

Disease Ontology (DO):
DOID:0110316 - hypertrophic cardiomyopathy 10