raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:217049

OBSOLETE: Rare non-syndromic cataract

inactive · referred to ORPHA:91492Early onset non-syndromic cataract

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 Early-onset non-syndromic cataract

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Rare non-syndromic cataract
frOBSOLETE : Cataracte rare non syndromique
deOBSOLET: Katarakt, seltene, nicht-syndromale
esOBSOLETO: Catarata rara no sindrómica
itOBSOLETO: Cataratta non sindromica rara
nlOBSOLEET: Zeldzaam niet-syndromaal cataract
ptOBSOLETO: Catarata não-sindromática rara
plNIEAKTUALNE: Rzadka niesyndromiczna zacma
csNEAKTUÁLNÍ: Vzácná nesyndromická katarakta
ukЗАСТАРІЛО: Рідкісна несиндромальна катаракта
zh弃用: 罕见非综合征性白内障
trEski adı: Nadir, sendromik olmayan katarakt
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