raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:108987

OBSOLETE: Syndromic developmental defect of the eye

inactive · referred to ORPHA:519272Structural developmental eye defect

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 Structural developmental eye defect

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Syndromic developmental defect of the eye
frOBSOLETE : Anomalie syndromique du développement de l'oeilOBSOLETE : Anomalie syndromique du développement des yeux
deOBSOLET: Entwicklungsstörung der Augen, syndromale
esOBSOLETO: Defecto sindrómico en el desarrollo del ojo
itOBSOLETO: Difetto sindromico dello sviluppo oculare
nlOBSOLEET: Syndromaal ontwikkelingsdefect van oog
ptOBSOLETO: Anomalia do desenvolvimento do olho sindromática
plNIEAKTUALNE: Syndromiczne zaburzenie rozwojowe oka
csNEAKTUÁLNÍ: Syndromické vývojové defekty oka
ukЗАСТАРІЛО: Синдромальна вада розвитку ока
zh弃用:综合征性眼部发育缺陷
trEski adı: Gözün sendromik gelişimsel defekti
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