ORPHA:320350
Pure or complex X-linked spastic paraplegia
Synonyms: Pure or complicated X-linked spastic paraplegia
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pure or complex X-linked spastic paraplegia | Pure or complicated X-linked spastic paraplegia |
| fr | Paraplégie spastique liée à l'X pure ou complexe | |
| de | Spastische Paraplegie, reine oder komplexe, X-chromosomale | Spastische Paraplegie, reine oder komplizierte, X-chromosomale |
| es | Paraplejía espástica ligada al cromosoma X pura o compleja | |
| it | Paraplegia spastica legata all'X complessa o pura | Paraplegia spastica legata all'X complicata o pura |
| nl | Zuivere of complexe X-gebonden spastische paraplegie | Zuivere of gecompliceerde X-gebonden spastische paraplegie |
| pt | Paraplegia espástica ligada ao X pura ou complexa | |
| pl | Czysta lub złożona paraplegia spastyczna sprzężona z chromosomem X | Czysta lub powikłana paraplegia spastyczna sprzężona z chromosomem X |
| cs | Čistá nebo komplexní X-vázaná spastická paraplegie | Čistá nebo komplikovaná X-vázaná spastická paraplegie |
| uk | Чиста або складна Х-зчеплена спастична параплегія | Чиста або ускладнена Х-зчеплена спастична параплегія |
| zh | 单纯性或复杂性X连锁痉挛性截瘫 | = en |
| tr | Saf veya karmaşık X'e bağlı spastik parapleji | Saf veya karmaşık X'e bağlı spastik parapleji |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17916 | E | validated | |
| UMLS | C5679888 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:320335Pure or complex hereditary spastic paraplegia
rare genetic diseases; rare neurological diseases
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/320350
- This record as JSON: /data/d/320350.json