BC43.0

ICD-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

  • BC42 – Myocarditis
  • 01 – Certain infectious or parasitic diseases
  • 05 – Endocrine, nutritional or metabolic diseases
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  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 19 – Certain conditions originating in the perinatal period
  • 20 – Congenital malformations, deformations and chromosomal abnormalities
  • 22 – Injury, poisoning or certain other consequences of external causes

Child codes

  • BC43.00 – Familial-genetic dilated cardiomyopathy
  • BC43.01 – Nonfamilial dilated cardiomyopathy
  • BC43.0Z – Dilated cardiomyopathy, unspecified

Sibling codes

  • BC43.1 – Hypertrophic cardiomyopathy
  • BC43.2 – Restrictive cardiomyopathy
  • BC43.3 – Endocardial fibroelastosis
  • BC43.4 – Cardiomyopathy due to drugs or other external agents
  • BC43.5 – Stress-induced cardiomyopathy
  • BC43.6 – Arrhythmogenic ventricular cardiomyopathy
  • BC43.7 – Diabetic cardiomyopathy
  • BC43.Y – Other specified cardiomyopathy
  • BC43.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