raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:101033

OBSOLETE: Peters anomaly-cataract syndrome

inactive · referred to ORPHA:708Peters anomaly

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Peters anomaly

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Peters anomaly-cataract syndrome
frOBSOLETE : Syndrome d'anomalie de Peters-cataracte
deOBSOLET: Peters Anomalie-Katarakt-Syndrom
esOBSOLETO: Síndrome de anomalía de Peters-catarata
itOBSOLETO: Anomalia di Peters - cataratta
nlOBSOLEET: Peters-anomalie - cataract-syndroom
ptOBSOLETO: Síndrome de anomalia de Peters-catarata
plNIEAKTUALNE: Anomalia Petersa z zacma
csNEAKTUÁLNÍ: Syndrom zahrnující Petersovu anomálii a kataraktu
ukЗАСТАРІЛО: Синдром аномалії Петерса-катаракти
zh弃用:彼得斯异常白内障综合征
trEski adı: Peters anomali-katarakt sendromu
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