raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:95449

OBSOLETE: Congenital aortic valve insufficiency

inactive · referred to ORPHA:98718Aortic malformation

Type
Morphological anomaly
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Aortic malformation

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital aortic valve insufficiency
frOBSOLETE : Insuffisance aortique congénitale
deOBSOLET: Aortenklappeninsuffizienz, kongenitale
esOBSOLETO: Insuficiencia congénita de la válvula aórtica
itOBSOLETO: Insufficienza della valvola aortica
nlOBSOLEET: Congenitale aortaklepinsufficiëntie
ptOBSOLETO: Insuficiência da válvula aórtica, congénita
plNIEAKTUALNE: Wrodzona niedomykalnosc zastawki aorty
csNEAKTUÁLNÍ: Vrozená nedostatečnost aortální chlopně
ukЗАСТАРІЛО: Вроджена недостатність аортального клапана
zh弃用:先天性主动脉瓣关闭不全
trEski adı: Doğumsal aort kapağı yetersizliği
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

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