Aortic valvar atresia (Q46195): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Revision as of 14:37, 13 August 2026
A congenital cardiovascular malformation in which there is no orifice of the aortic valve. Additional information: aortic valvar atresia will most often not be coded independently, as it is frequently included within the 'Hypoplastic left heart syndrome' code as part of this spectrum of cardiovascular malformations. However, there is a small subset of patients with aortic valve atresia who have a well developed left ventricle and mitral valve and a large ventricular septal defect (nonrestrictive or restrictive).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA8A.23 |
||
| English | Aortic valvar atresia |
A congenital cardiovascular malformation in which there is no orifice of the aortic valve. Additional information: aortic valvar atresia will most often not be coded independently, as it is frequently included within the 'Hypoplastic left heart syndrome' code as part of this spectrum of cardiovascular malformations. However, there is a small subset of patients with aortic valve atresia who have a well developed left ventricle and mitral valve and a large ventricular septal defect (nonrestrictive or restrictive). |
Statements
CID11:LA8A.23
0 references
dki-india-LA8A.23
0 references
Concluído
0 references
13 August 2026
0 references
