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Summary Literature (0)
DOID:0110312 - hypertrophic cardiomyopathy 6

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2).

Synonyms: cardiomyopathy, familial hypertrophic 6, CMH6

Xenbase Genes : prkag2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010946 - hypertrophic cardiomyopathy 6


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)