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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: CMH6, cardiomyopathy, familial hypertrophic 6,
Echinobase Genes :
MIM:600858 - cardiomyopathy, familial hypertrophic, 6; cmh6 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypertrophic cardiomyopathy (is_a)