raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:95448

Congenital aortic valve atresia

Type
Clinical subtype
Group
Subtype of disorder
Status
active

This disease is described under Congenital aortic valve stenosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCongenital aortic valve atresia
frAtrésie valvulaire aortique congénitale
deAortenklappenatresie, kongenitale
esAtresia de la válvula aórtica congénita
itAtresia della valvola aortica
nlCongenitale aortaklepatresie
ptAtresia da válvula aórtica
plArtrezja zastawki aorty
csAtrézie aortální chlopně
ukАтрезія аортального клапана
zh先天性主动脉瓣闭锁
trDoğumsal aort kapak atrezisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q23.0NTBTattributedvalidated
ICD-11LA8A.23Especificvalidated
MONDO0019808Evalidated
UMLSC0265843Evalidated
MedDRA10066801Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card