raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:68362

Rare vascular disease

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 vascular disease
frMaladie vasculaire rare
deGefäßkrankheit, seltene
esEnfermedad vascular rara
itMalattia vascolare rara
nlZeldzame vasculaire ziekte
ptDoença vascular rara
plRzadkie choroby naczyń
csVzácná vaskulární nemoc
ukРідкісне судинне захворювання
zh罕见血管疾病
trNadir vasküler hastalık
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO19048Evalidated
UMLSC5681327Evalidated

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 (2):

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