MeSH Browser

MeSH Supplementary: Idiopathic dilation cardiomyopathy
Unique ID: C536277
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536277
Entry Term(s): Cardiomyopathy, Dilated, 1h; Cardiomyopathy, Dilated, With Conduction Defect; Dilated cardiomyopathy with conduction defect
Registry Numbers: 0
Heading Mapped to: *Cardiomyopathy, Dilated
Frequency: 113
Note: Dilated cardiomyopathy that is characterized by cardiac dilatation and reduced systolic function. It is the most frequent form of cardiomyopathy and accounts for more than half of all cardiac transplantations performed in children between 1 and 10 years of age. For CMD1A, 20 to 30% of cases are heritable and show an autosomal dominant inheritance pattern. Germline mutations in the LMNA gene have been identified. OMIM: 115200
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Idiopathic dilation cardiomyopathy MeSH Supplementary Concept Data 2025