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Hypertrophic Cardiomyopathy 6

Disease ID: disease_node_16943

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DbxrefMIM:600858
SubclassofDOID_0080326
Data SourceDOID
SynonymsCMH6, cardiomyopathy, familial hypertrophic 6
Doid Labelhypertrophic cardiomyopathy 6
Doid DescriptionA 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).
Disease Node Iddisease_node_16943
Doid IdDOID_0110312
LabelHypertrophic Cardiomyopathy 6