raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:163982

X-linked intellectual disability-spastic quadriparesis syndrome

inactive · moved to ORPHA:59Allan-Herndon-Dudley syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Allan-Herndon-Dudley syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enX-linked intellectual disability-spastic quadriparesis syndrome
frSyndrome de déficience intellectuelle liée à l'X-quadriparésie spastique
deSyndrom der X-chromosomalen Intelligenzminderung mit spastischer Quadriparese
esSíndrome de discapacidad intelectual-cuadriparesia espástica ligado al cromosoma X
itSindrome disabilità intellettiva legata all'X-tetraparesi spastica
nlX-gebonden intellectuele achterstand - spastische tetraparese-syndroom
ptSíndrome de perturbação do desenvolvimento intelectual ligada ao X-tetraparesia espástica
plNiepełnosprawność intelektualna sprzężona z chromosomem X - niedowład spastyczny czterokończynowy
csSyndrom zahrnující X-vázanou mentální retardaci a spastickou kvadruparézu
ukХ-зчеплена інтелектуальна недостатність - синдром спастичного квадрипарезу
zhX连锁智力障碍-痉挛性四肢瘫综合征
trX'e bağlı zihinsel yetersizlik-spastik kuadriparezi sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM309640Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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