(Q41516644)
English
infantile histiocytoid cardiomyopathy
intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has material basis in a mutation in the gene encoding mitochondrial cytochrome b
- Oncocytic cardiomyopathy
- Infantile xanthomatous cardiomyopathy
- Cardiomyopathy, Oncocytic
- Arachnocytosis of the Myocardium
- Histiocytoid cardiomyopathy
- Congenital Cardiomyopathy
- Myocardial Hamartoma
- Focal lipid cardiomyopathy
- Purkinje Cell Hamartoma
- CARDIOMYOPATHY, INFANTILE HISTIOCYTOID
- Infantile cardiomyopathy with histiocytoid change
- Isolated Cardiac Lipidosis
- Cardiomyopathy, Infantile Xanthomatous
- Foamy Myocardial Transformation of Infancy
- Infantile histiocytoid cardiomyopathy
- Cardiomyopathy, Focal Lipid
Statements
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C45745
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