raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:99079

Cervical aortic arch

Type
Morphological anomaly
Group
Disorder
Status
active

A rare, congenital anomaly of the great arteries characterized by cranially situated aortic arch ascending into the neck above the clavicles. Most patients remain asymptomatic, some present with a murmur and a pulsatile neck mass, stridor, dyspnea, recurrent bronchitis, dysphagia or signs and symptoms of a stenosis/aneurism of the aortic arch. Other congenital heart anomalies are frequently associated, including abnormalities of arch laterality and branching, aortic coarctation or aneurysm.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCervical aortic arch
frAorte cervicaleCrosse aortique cervicale
deAortenbogen, zervikaler
esArco aórtico cervical
itArco aortico cervicaleSindrome dell'arco aortico
nlCervicale aortaboog
ptArco aórtico cervical
plŁuk aorty szyjnejZespół łuku aorty
csCervikální aortální obloukSyndrom aortálního oblouku
ukВисоке (шийне) розташування дуги аорти
zh颈型主动脉弓
trServikal aort ark

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q25.4NTBTattributedvalidated
ICD-11LA8B.2YNTBTindexvalidated
UMLSC0345065Evalidated

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