raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:522584

OBSOLETE: Rare genetic choroidal disorder

inactive · referred to ORPHA:522570Rare genetic disorder of the posterior segment of the eye

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 disorder of the posterior segment of the eye

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Rare genetic choroidal disorder
frOBSOLETE : Maladie génétique choroïdienne rare
deOBSOLET: Seltene genetische Erkrankung der Chorioidea
esOBSOLETO: Trastorno coroideo genético raro
itOBSOLETO: Malattia genetica rara coroidale
nlOBSOLEET: Zeldzame genetische aandoening van choroideaNIET ZELDZAME ZIEKTE IN EUROPA: Zeldzame genetische aandoening van vaatvlies
ptOBSOLETO: Doença coroidiana genética rara
plNIEAKTUALNE: Rzadka genetyczna choroba naczyniówki
csNEAKTUÁLNÍ: Vzácná genetická porucha cévnatky
ukРідкісне генетично обумовлене захворювання судинної оболонки
zh罕见遗传性脉络膜疾病
trNadir genetik koroid 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