raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:459548

Rare genetic venous malformation

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
enRare genetic venous malformation
frMalformation veineuse génétique rare
deSeltene venöse Fehlbildung, genetisch bedingte
esMalformación venosa genética rara
itMalformazione venosa genetica rara
nlZeldzame genetische veneuze malformatie
ptMalformação venosa genética rara
plRzadka malformacja żylna uwarunkowana genetycznie
csVzácné geneticky podmíněné venózní malformace
ukРідкісна генетично обумовлена венозна вада розвитку
zh遗传性罕见静脉畸形
trNadir genetik venöz malformasyon
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18730Evalidated
UMLSC5681113Evalidated

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 (4):

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