LA8A.20

ICD-11 MMS 2026-01

Congenital aortic valvar stenosis

Description

A congenital cardiovascular malformation of the aortic valve in which there is narrowing or stricture (obstruction to flow). Additional information: 'Congenital aortic valvar stenosis' arises most commonly as a result of partial or complete fusion of one or more commissures, or is due to dysplasia of one or more aortic cusps. These congenital malformations of the aortic valve may not be initially obstructive but may become stenotic later in life due to leaflet thickening, poor relative growth and-or calcification. It is not until the congenitally malformed aortic valve is or becomes stenotic that this term should be used.

Index terms

  • Congenital aortic valvar stenosis
  • Congenital aortic valve stenosis
  • congenital aortic valve stricture
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  • congenital stenosis of aortic valve
  • congenital valvular aortic stenosis

Excludes

  • LA89.3 – that in hypoplastic left heart syndrome
  • LA8A.5 – Congenital subaortic stenosis

Exclusions from above levels

  • LA85.4 – Common arterial trunk
  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

  • LA8A.21 – Congenital aortic regurgitation
  • LA8A.22 – Bicuspid aortic valve
  • LA8A.23 – Aortic valvar atresia
  • LA8A.24 – Unicuspid aortic valve
  • LA8A.2Y – Other specified congenital anomaly of aortic valve
  • LA8A.2Z – Congenital anomaly of aortic valve, unspecified

Foundation entity

Congenital aortic valvar stenosis – http://id.who.int/icd/entity/1824398514

Part of: LA8A.2: Congenital anomaly of aortic valve › LA8A: Congenital anomaly of a ventriculo-arterial valve or adjacent regions › 20: Developmental anomalies