raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3061

OBSOLETE: X-linked intellectual disability, Raynaud type

inactive · referred to ORPHA:777X-linked non-syndromic intellectual disability

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 X-linked non-syndromic intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: X-linked intellectual disability, Raynaud type
frOBSOLETE : Déficience intellectuelle liée à l'X type Raynaud
deOBSOLET: X-chromosomale Intelligenzminderung Typ Raynaud
esOBSOLETO: Discapacidad intelectual ligada al cromosoma X tipo Raynaud
itOBSOLETO: Ritardo mentale legato all'X, tipo Raynaud
nlOBSOLEET: Intellectuele achterstand, X-gebonden, Raynaud-type
ptOBSOLETO: Perturbação do desenvolvimento intelectual ligada ao X, tipo Raynaud
plNIEAKTUALNE: Niepelnosprawnosc intelektualna sprzezona z chromosomem X typu Raynauda
csNEAKTUÁLNÍ: X-vázaná mentální retardace, typ Raynaudové
ukЗАСТАРІЛО: Х-зчеплена розумова відсталість, тип Рейно
zh弃用:X连锁智力障碍,Raynaud亚型
trEski adı: X'e bağlı zihinsel yetersizlik, Raynaud 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