raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:263355

OBSOLETE: ATR-X-related syndrome

inactive · referred to ORPHA:847X-linked alpha-thalassemia-intellectual disability syndrome

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 Alpha-thalassemia-X-linked intellectual disability syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: ATR-X-related syndrome
frOBSOLETE : Syndrome lié à ATR-X
deOBSOLET: ATR-X-abhängiges Syndrom
esOBSOLETO: Síndrome ATR ligado al cromosoma X
itOBSOLETO: Sindrome legata ad ATR-X
nlOBSOLEET: ATR-X-gerelateerd syndroom
ptOBSOLETO: Síndrome ATR-X-relacionada
plNIEAKTUALNE: Zespół zwiazany z ATR-X
csNEAKTUÁLNÍ: ATR-X-vázaný syndrom
ukЗАСТАРІЛО: Синдром, повязаний з ATR-X
zhATR-X相关综合征
trATR-X -ilişkili sendrom
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