ORPHA:98717

Transposition of the great arteries and conotruncal cardiac 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	Transposition of the great arteries and conotruncal cardiac anomaly
fr	Transposition des gros vaisseaux et anomalie conotroncale du coeur
de	Transposition der großen Gefäße - konotrunkale Herzanomalie
es	Transposición de los grandes vasos-anomalía conotruncal cardíaca
it	Trasposizione dei grandi vasi - anomalia cardiaca troncoconale
nl	Transpositie van grote slagaders en conotruncale hartanomalie
pt	Transposição das grandes artérias - anomalia cardíaca conotruncal
pl	Przełożenie wielkich tętnic i wada stożka tętniczego
cs	Transpozice velkých tepen a konotrunkální srdeční anomálie
uk	Транспозиція великих артерій (магістральних судин) і конотрункальні дефекти
zh	大血管和心脏圆锥动脉干畸形错位
tr	Büyük arterlerin transpozisyonu ve konotrunkal kalp anomalisi

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5681688	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 (1):

ORPHA:88991Rare congenital heart disease
rare developmental anomalies during embryogenesis; rare cardiac malformations

Children (4):

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/98717
This record as JSON: /data/d/98717.json