raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98464

OBSOLETE: X-linked syndromic intellectual disability

inactive · referred to ORPHA:102369Rare syndromic intellectual disability

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 Rare syndromic intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: X-linked syndromic intellectual disability
frOBSOLETE : Déficience intellectuelle liée à l'X syndromique
deOBSOLET: Intelligenzminderung, X-chromosomale, syndromale
esOBSOLETO: Discapacidad intelectual sindrómica ligada al cromosoma X
itOBSOLETO: Disabilità intellettiva sindromica legata all’X
nlOBSOLEET: X-gebonden syndromale intellectuele achterstand
ptOBSOLETO: Perturbação do desenvolvimento intelectual sindromático ligado ao X
plNIEAKTUALNE: Syndromiczna niepełnosprawność intelektualna sprzężona z chromosomem X
csNEAKTUÁLNÍ: X-vázané syndromické mentální retardace
ukЗАСТАРІЛО: Зчеплена з Х-хромосомою синдромна розумова відсталість
zhX连锁智力障碍综合征
trX'e bağlı sendromik zihinsel yetersizlik
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