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

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

Synonyms: cardiomyopathy, familial hypertrophic 1, CMH1, hypertrophic cardiomyopathy 19

Xenbase Genes : actc1, tnnc1, cav3, myh6, myh7l, cav3.2, calr3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008647 - hypertrophic cardiomyopathy 1

MIM:
MIM:192600 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): familial hypertrophic cardiomyopathy (is_a), hypertrophic cardiomyopathy (is_a)