raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98983

OBSOLETE: Congenital cataract, Volkmann type

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

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 Early-onset non-syndromic cataract

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital cataract, Volkmann type
frOBSOLETE : Cataracte congénitale de Volkmann
deOBSOLET: Katarakt, kongenitale, Typ Volkmann
esOBSOLETO: Catarata congénita tipo Volkmann
itOBSOLETO: Cataratta congenita, tipo Volkmann
nlOBSOLEET: Congenitaal cataract, Volkmann-type
ptOBSOLETO: Catarata congénita, tipo Volkmann
plNIEAKTUALNE: Zacma wrodzona, typ Volkmanna
csNEAKTUÁLNÍ: Vrozená katarakta, typ Volkmann
ukЗАСТАРІЛО: Вроджена катаракта, тип Фолькмана
zh弃用:先天性白内障Volkmann型
trEski adı: Doğumsal katarakt, Volkmann tipi
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