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Summary Literature (0)
DOID:0110307 - hypertrophic cardiomyopathy 1

Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12.

Synonyms: CMH1, cardiomyopathy, familial hypertrophic 1

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hypertrophic cardiomyopathy (is_a)

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