raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1376

OBSOLETE: Congenital cataract-ichthyosis syndrome

inactive · referred to ORPHA:281244Autosomal ichthyosis syndrome with other associated signs

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 Autosomal ichthyosis syndrome with other associated signs

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital cataract-ichthyosis syndrome
frOBSOLETE : Syndrome de cataracte-ichtyose
deOBSOLET: Katarakt, kongenitale - Ichthyose
esOBSOLETO: Síndrome de catarata congénita-ictiosis
itOBSOLETO: Cataratta congenita - ittiosi
nlOBSOLEET: Congenitaal cataract - ichthyosis-syndroom
ptOBSOLETO: Síndrome de catarata congénita-ictiose
plNIEAKTUALNE: Zacma wrodzona - rybia luska
csNEAKTUÁLNÍ: Syndrom zahrnující vrozenou kataraktu a ichtyózu
ukЗАСТАРІЛО: Синдром вродженої катаракти - іхтіозу
zh弃用:先天性白内障-鱼鳞病综合征
trEski adı: Doğumsal katarakt-iktiyoz 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