ORPHA:98724

Congenital anomaly of the great arteries

Synonyms: Congenital aorta, aortic arch or pulmonary arteries anomaly

Type: Category
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Congenital anomaly of the great arteries	Congenital aorta, aortic arch or pulmonary arteries anomaly
fr	Anomalie congénitale des artères de gros calibre	Anomalie congénitale de l'aorte, de la crosse aortique ou de l'artère pulmonaire
de	Kongenitale Anomalie der großen Arterien	Kongenitale Aorta-, Aortenbogen- oder Pulmonalarterien-Anomalie
es	Anomalía congénita de las grandes arterias	Anomalía congénita de la aorta, del arco aórtico o de la arteria pulmonar
it	Anomalia congenita dei grandi vasi	Anomalia congenita dell'aorta, dell'arco aortico o delle arterie polmonari
nl	Congenitale grote bloedvatenanomalie	Congenitale aorta-, aortaboog- of longslagaderanomalie
pt	Anomalia dos grandes vasos (aorta, arco aórtico, artérias pulmonares), congénita
pl	Wada wrodzona wielkich naczyń	Wada wrodzona aorty, łuku aorty lub tętnic płucnych
cs	Vrozené anomálie velkých tepen	Vrozené anomálie aorty, aortálního oblouku nebo plicních tepen
uk	Вроджена вада розвитку великих артерій (магістральних судин)	Вроджена аномалія аорти, дуги аорти або легеневих артерій
zh	大动脉先天性畸形	先天性主动脉、主动脉弓或肺动脉异常
tr	Doğumsal büyük arter anomalisi	Doğumsal aort, arkus aort veya pulmoner arter anomalisi

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	0020292	E		validated
UMLS	C0948632	E		validated

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

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (2):

ORPHA:88991Rare congenital heart disease
rare developmental anomalies during embryogenesis; rare cardiac malformations
ORPHA:458844Rare vascular malformation of major vessels
rare developmental anomalies during embryogenesis; rare circulatory system diseases

Children (6):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/98724
This record as JSON: /data/d/98724.json