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Cardiomyopathy, Hypertrophic, Familial

Disease ID: disease_node_10938

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DbxrefMESH:D024741, MIM:PS192600, NCI:C84773, ORDO:217569, SNOMEDCT_US_2023_03_01:83978005, UMLS_CUI:C0949658
SubclassofDOID_11984
Data SourceDOID, MESH
Mesh IdD024741
Mesh LabelCardiomyopathy, Hypertrophic, Familial
Mesh SubclassofD030342, D002312
Doid Labelfamilial hypertrophic cardiomyopathy
Doid DescriptionA hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal domit inheritance of one or more gene mutations.
Disease Node Iddisease_node_10938
Doid IdDOID_0080326
LabelCardiomyopathy, Hypertrophic, Familial