BC43.0ICD-11 MMS 2026-01
Dilated cardiomyopathy
Description
Dilated cardiomyopathy is a myocardial disorder in which there is systolic dysfunction and chamber dilation of one or both ventricles in the absence of a haemodynamic cause that can produce the existent dilation and dysfunction, including physiological (such as sepsis) or anatomic causes with either abnormal loading conditions (such as coarctation of the aorta) or ischaemia (such as coronary artery disease or anomalies). Additional information: Physiological and anatomic conditions can affect the dilated cardiomyopathy morphofunctional phenotype. If this morphofunctional phenotype is retained after appropriate intervention, then a dilated cardiomyopathy is established.
Inclusions
- Congestive cardiomyopathy
Exclusions from above levels
Child codes
Sibling codes
BC43.1– Hypertrophic cardiomyopathyBC43.2– Restrictive cardiomyopathyBC43.3– Endocardial fibroelastosisBC43.4– Cardiomyopathy due to drugs or other external agentsBC43.5– Stress-induced cardiomyopathyBC43.6– Arrhythmogenic ventricular cardiomyopathyBC43.7– Diabetic cardiomyopathyBC43.Y– Other specified cardiomyopathyBC43.Z– Cardiomyopathy, unspecified
Foundation entity
Dilated cardiomyopathy – http://id.who.int/icd/entity/1916294688
Allowed postcoordination axes
Part of: BC43: Cardiomyopathy › 11: Diseases of the circulatory system