raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3056

X-linked intellectual disability, Brooks type

inactive · moved to ORPHA:528084Non-specific syndromic intellectual disability

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Non-specific syndromic intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enX-linked intellectual disability, Brooks type
frDéficience intellectuelle liée à l'X type Brooks
deIntelligenzminderung, X-chromosomale, Typ Brooks
esDiscapacidad intelectual ligada al cromosoma X tipo Brooks
itDisabilità intellettiva legata all'X, tipo Brooks
nlX-gebonden intellectuele achterstand, Brooks-type
ptPerturbação do desenvolvimento intelectual ligada ao X, tipo Brooks
plNiepełnosprawność intelektualna sprzężona z chromosomem X typu Brooksa
csX-vázaná mentální retardace, Brooksův typ
ukХ-зчеплена розумова відсталість, тип Брукса
zhX连锁智力障碍,Brooks亚型
trX'e bağlı zihinsel yetersizlik, Brooks 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