raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:519306

OBSOLETE: Isolated progressive inherited retinal disorder

inactive · referred to ORPHA:522572Rare genetic retinal disorder

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare genetic retinal disorder

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Isolated progressive inherited retinal disorder
frOBSOLETE : Maladie rétinienne héréditaire progressive isolée
deOBSOLET: Isolierte vererbte progressive Störung der Retina
esOBSOLETO: Trastorno retiniano hereditario progresivo aislado
itOBSOLETO: Patologia retinica ereditaria isolata progressiva
nlOBSOLEET: Geïsoleerde progressieve erfelijke aandoening van retinaNIET ZELDZAME ZIEKTE IN EUROPA: Geïsoleerde progressieve erfelijke aandoening van netvlies
ptOBSOLETO: Doença retiniana progressiva isolada hereditária
plNIEAKTUALNE: Izolowana postępująca dziedziczna choroba siatkówki
csNEAKTUÁLNÍ: Izolovaná progresivní dědičná porucha sítnice
ukІзольоване прогресуюче спадкове захворювання сітківки
zh孤立性进行性遗传性视网膜病变
trİzole ilerleyici kalıtsal retina bozukluğu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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