Dilated cardiomyopathy due to congenital anomaly of coronary artery

Description

Dilated cardiomyopathy due to a congenital anomaly of one or more coronary arteries, such as anomalous left coronary artery from pulmonary artery (ALCAPA), coronary ostial stenosis or atresia, right ventricular dependent coronary circulation in pulmonary atresia with an intact ventricular septum. It is a form of ischaemic cardiomyopathy causing systolic ventricular dysfunction that relates to a spectrum of perfusion contraction matching and mismatching, including myocardial infarction, stunning, hibernation and scarring.

Index terms

Dilated cardiomyopathy due to congenital anomaly of coronary artery

Exclusions from above levels

01 – Certain infectious or parasitic diseases
05 – Endocrine, nutritional or metabolic diseases
18 – Complications of pregnancy, childbirth and the puerperium

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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

Sibling codes

BA51.Y – Other specified ischaemic cardiomyopathy
BA51.Z – Ischaemic cardiomyopathy, unspecified

Foundation entity

Dilated cardiomyopathy due to congenital anomaly of coronary artery – http://id.who.int/icd/entity/167155244

Part of: BA51: Ischaemic cardiomyopathy › 11: Diseases of the circulatory system