raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:716455

Rare progressive retinal vasculopathy

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

9 of 12 languages
LangNameSynonyms
enRare progressive retinal vasculopathy
frVasculopathie rétinienne progressive rare
deSeltene progrediente retinale Vaskulopathie
esVasculopatía retiniana progresiva rara
itVasculopatia retinica rara progressiva
nlZeldzame progressieve retinale vasculopathie
ptRare progressive retinal vasculopathy
plRzadka postępująca waskulopatia siatkówki
csRare progressive retinal vasculopathy
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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