raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98615

OBSOLETE: Pigmented conjunctival lesion

inactive · referred to ORPHA:98610Rare disorder with conjunctival involvement as a major feature

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 disorder with conjunctival involvement as a major feature

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Pigmented conjunctival lesion
frOBSOLETE : Lésion pigmentée de la conjonctive
deOBSOLET: Bindehautläsion, pigmentierte
esOBSOLETO: Lesión pigmentada de la conjuntiva
itOBSOLETO: Lesione congiuntivale pigmentata
nlOBSOLEET: Gepigmenteerde conjunctivale laesie
ptOBSOLETO: Lesão pigmentada da conjuntiva
plNIEAKTUALNE: Zmiana barwnikowa spojówki
csNEAKTUÁLNÍ: Pigmentové léze spojivky
ukЗАСТАРІЛО: Пігментне ураження конюнктиви
zh弃用:色素结膜损伤
trEski adı: Pigmentli konjunktival lezyon
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