raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:519357

OBSOLETE: Syndromic malformation of the optic disc

inactive · referred to ORPHA:519345Rare disorder with optic disc malformation

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 optic disc malformation

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Syndromic malformation of the optic disc
frOBSOLETE : Syndromic malformation of the optic disc
deOBSOLET: Syndromale Fehlbildung der Sehnervenpapille
esOBSOLETO: Malformación sindrómica del disco óptico
itOBSOLETO: Malformazione del disco ottico sindromica
nlOBSOLEET: Syndromale malformatie van papil
ptOBSOLETO: Malformação síndrómica do disco óptico
plNIEAKTUALNE: Zespól malformacji tarczy nerwu wzrokowego
csNEAKTUÁLNÍ: Syndromická malformace terče zrakového nervu
ukЗАСТАРІЛО: Синдромальна вада розвитку диска зорового нерва
zh弃用:综合征性视神经盘畸形
trEski adı: Optik diskin sendromik malformasyonu
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