raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:519300

OBSOLETE: Isolated chorioretinal dystrophy

inactive · referred to ORPHA:716290Rare predominantly chorioretinal 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 predominantly chorioretinal disorder

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Isolated chorioretinal dystrophy
frOBSOLETE : Dystrophie choriorétinienne isolée
deOBSOLET: Isolierte chorioretinale Dystrophie
esOBSOLETO: Distrofia coriorretiniana aislada
itOBSOLETO: Distrofia corioretinica isolata
nlOBSOLEET: Geïsoleerde chorioretinale dystrofie
ptOBSOLETO: Distrofia coriorretiniana isolada
plNIEAKTUALNE: Izolowana dystrofia naczyniówki i siatkówki
csNEAKTUÁLNÍ: Izolovaná chorioretinální dystrofie
ukІзольована хоріоретинальна дистрофія
zh孤立性脉络膜视网膜营养不良
trİzole koryoretinal distrofi
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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.

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Sources for this card