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| Lang | Name | Synonyms |
|---|---|---|
| en | X-linked intellectual disability-spastic quadriparesis syndrome | |
| fr | Syndrome de déficience intellectuelle liée à l'X-quadriparésie spastique | |
| de | Syndrom der X-chromosomalen Intelligenzminderung mit spastischer Quadriparese | |
| es | Síndrome de discapacidad intelectual-cuadriparesia espástica ligado al cromosoma X | |
| it | Sindrome disabilità intellettiva legata all'X-tetraparesi spastica | |
| nl | X-gebonden intellectuele achterstand - spastische tetraparese-syndroom | |
| pt | Síndrome de perturbação do desenvolvimento intelectual ligada ao X-tetraparesia espástica | |
| pl | Niepełnosprawność intelektualna sprzężona z chromosomem X - niedowład spastyczny czterokończynowy | |
| cs | Syndrom zahrnující X-vázanou mentální retardaci a spastickou kvadruparézu | |
| uk | Х-зчеплена інтелектуальна недостатність - синдром спастичного квадрипарезу | |
| zh | X连锁智力障碍-痉挛性四肢瘫综合征 | |
| tr | X'e bağlı zihinsel yetersizlik-spastik kuadriparezi sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 309640 | E | validated |
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 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/163982
- This record as JSON: /data/d/163982.json