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Hypertrophic Cardiomyopathy 13

Disease ID: disease_node_16936

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DbxrefMIM:613243
SubclassofDOID_0080326
Data SourceDOID
SynonymsCMH13, cardiomyopathy familial hypertrophic 13
Doid Labelhypertrophic cardiomyopathy 13
Doid DescriptionA familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.
Disease Node Iddisease_node_16936
Doid IdDOID_0110319
LabelHypertrophic Cardiomyopathy 13