Restrictive cardiomyopathy due to endomyocardial abnormality (Q86507): Difference between revisions
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13 August 2026
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Latest revision as of 11:55, 15 August 2026
Restrictive cardiomyopathy due to endomyocardial abnormality is restrictive cardiomyopathy related to a primary fibrosis involving the endocardial and myocardial layers of one or both ventricular chambers, with aggressive scarring obliterating the ventricular apices and subvalvar regions. Subclassification relates to the presence or not of hypereosinophilia, as well as geographic presentation (temperate versus tropical).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_612301769 |
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| English | Restrictive cardiomyopathy due to endomyocardial abnormality |
Restrictive cardiomyopathy due to endomyocardial abnormality is restrictive cardiomyopathy related to a primary fibrosis involving the endocardial and myocardial layers of one or both ventricular chambers, with aggressive scarring obliterating the ventricular apices and subvalvar regions. Subclassification relates to the presence or not of hypereosinophilia, as well as geographic presentation (temperate versus tropical). |
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CID11:ID_612301769
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dki-india-ID_612301769
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Concluído
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13 August 2026
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