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Infantile Hypertrophic Cardiomyopathy

Disease ID: disease_node_16927

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DbxrefMIM:500006
SubclassofDOID_11984
Data SourceDOID
Doid Labelinfantile hypertrophic cardiomyopathy
Doid DescriptionA hypertrophic cardiomyopathy characterized by isolated hypertrophic cardiomyopathy and congestive heart failure that has_material_basis_in mutation in the overlapping mitochondrial genes MTATP6 and MTATP8.
Disease Node Iddisease_node_16927
Doid IdDOID_0111753
LabelInfantile Hypertrophic Cardiomyopathy