raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1455

OBSOLETE: Autosomal dominant coarctation of aorta

inactive · referred to ORPHA:1457Coarctation of aorta

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Autosomal dominant coarctation of aorta
frOBSOLETE : Coarctation de l'aorte autosomique dominante
deOBSOLET: Aortenisthmusstenose, dominante
esOBSOLETO: Coartación de aorta autosómica dominante
itOBSOLETO: coartazione dell'aorta autosomica dominante
nlOBSOLEET: Autosomaal dominante coarctatie van aorta
ptOBSOLETO: Coartação da aorta autossómica dominante
plNIEAKTUALNE: Autosomalnie dominująca koarktacja aorty
csNEAKTUÁLNÍ: Autozomálně dominantní koarktace aorty
ukЗАСТАРІЛО: Аутосомно-домінантна коарктація аорти
zh常染色体显性主动脉缩窄
trOtozomal dominant aort koarktasyonu
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