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Summary Literature (0)
MIM:608751 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8

Xenbase Genes: myl3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012111 - hypertrophic cardiomyopathy 8

Disease Ontology (DO):
DOID:0110314 - hypertrophic cardiomyopathy 8