raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:95499

Congenital anomaly of the inferior vena cava

Synonyms: Congenital anomaly of the IVC · Congenital anomaly of the inferior caval vein

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCongenital anomaly of the inferior vena cavaCongenital anomaly of the IVC · Congenital anomaly of the inferior caval vein
frAnomalie congénitale de la veine cave inférieure
deVena cava inferior, kongenitale Anomalie derKongenitale Anomalie der unteren Hohlvene
esAnomalía congénita de la vena cava inferiorIVC
itAnomalia congenita della vena cava inferioreAnomalia congenita della IVC
nlCongenitale anomalie van vena cava inferiorCongenitale anomalie van VCI · Congenitale anomalie van onderste holle ader
ptAnomalia congénita da veia cava inferiorAnomalia congénita da VCI
plWada wrodzona żyły głównej dolnejWada wrodzona IVC · Wrodzona anomalia żyły głównej dolnej
csVrozené anomálie dolní duté žílyVrozené anomálie VCI · Vrozené anomálie vena cava inferior
ukВроджена аномалія нижньої порожнистої вениВроджена аномалія нижньої порожнистої вени · Вроджена аномалія внутрішньої порожнистої вени
zh先天性下腔静脉异常先天性下腔静脉异常
trİnferior vena kavanın doğumsal anomalisiIVC'nin doğumsal anomalisi · İnferior kaval venin doğumsal anomalisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-11LA86.YNTBTindexvalidated
MONDO0019830Evalidated
UMLSC0265932Evalidated

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):

Children (6):

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