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Familial Restrictive Cardiomyopathy 3

Disease ID: disease_node_16871

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DbxrefMIM:612422
SubclassofDOID_397
Data SourceDOID
SynonymsRCM3, restrictive cardiomyopathy 3
Doid Labelfamilial restrictive cardiomyopathy 3
Doid DescriptionA restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNT2 gene on chromosome 1q32.1.
Disease Node Iddisease_node_16871
Doid IdDOID_0111427
LabelFamilial Restrictive Cardiomyopathy 3