raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3091

Congenital systemic veins 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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCongenital systemic veins anomaly
frAnomalie congénitale des veines systémiques
deVenenanomalie, kongenitale sytemische
esAnomalía congénita de las venas sistémicas
itAnomalia venosa sistemica congenita
nlCongenitale anomalie van systemische venen
ptAnomalia do retorno venoso sistémico
plWrodzone anomalie żył systemowych
csVrozená anomálie systémových žil
ukВроджена вада розвитку системних вен
zh先天性体循环血管异常
trDoğumsal sistemik ven anomalisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO17710Evalidated
UMLSC5680873Evalidated

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 (5):

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