raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:217052

OBSOLETE: Infantile non-syndromic cataract

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

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Early-onset non-syndromic cataract

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Infantile non-syndromic cataract
frOBSOLETE : Cataracte non syndromique à début précoce
deOBSOLET: Katarakt, frühmanifeste, nicht-syndromale
esOBSOLETO: Catarata no sindrómica infantil
itOBSOLETO: Cataratta non sindromica ad esordio precoce
nlOBSOLEET: Infantiel niet-syndromaal cataract
ptOBSOLETO: Catarata não-sindromática da infância
plNIEAKTUALNE: Niesyndromiczna zacma o wczesnym poczatku
csNEAKTUÁLNÍ: Dětská nesyndromická katarakta
ukЗАСТАРІЛО: Дитяча несиндромальна катаракта
zh弃用: 婴幼儿非综合征性白内障
trEski adı: İnfantil 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