raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:171860

OBSOLETE: Intellectual disability-cataracts-kyphosis syndrome

inactive · referred to ORPHA:324737SRD5A3-CDG

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 SRD5A3-CDG

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Intellectual disability-cataracts-kyphosis syndrome
frOBSOLETE : Syndrome de déficience intellectuelle-cataracte-cyphose
deOBSOLET: Intelligenzminderung-Katarakte-Kyphose-Syndrom
esOBSOLETO: Síndrome de discapacidad intelectual-cataratas-cifosis
itOBSOLETO: Sindrome deficit cognitivo-cataratta-cifosi
nlOBSOLEET: Intellectuele achterstand - cataract - kyfose-syndroom
ptOBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-cataratas-cifose
plNIEAKTUALNE: Niepełnosprawność intelektualna - zaćma - kifoza
csNEAKTUÁLNÍ: Syndrom zahrnující intelektovou nedostatečnost, kataraktu a kyfózu
ukЗАСТАРІЛО: Синдром інтелектуальної недостатності - катаракти - кіфозу
zh智力障碍-白内障-脊柱后凸综合征
trZihinsel yetersizlik-katarakt-kifoz sendromu

Definition in:

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