ORPHA:320332
X-linked pure 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 | X-linked pure spastic paraplegia | |
| fr | Paraplégie spastique pure liée à l'X | |
| de | Spastische Paraplegie, reine, X-chromosomale | |
| es | Paraplejía espástica pura ligada al cromosoma X | |
| it | Paraplegia spastica pura legata all'X | |
| nl | X-gebonden zuivere spastische paraplegie | |
| pt | Paraplegia espástica pura ligada ao X | |
| pl | Czysta paraplegia spastyczna sprzężona z chromosomem X | |
| cs | X-vázaná čistě spastická paraplegie | |
| uk | Х-зчеплена чиста спастична параплегія | |
| zh | X连锁单纯性痉挛性截瘫 | |
| tr | X'e bağlı saf spastik parapleji |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17912 | E | validated | |
| UMLS | C5680963 | 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:102012Pure hereditary spastic paraplegia
rare genetic diseases; rare neurological diseases
Children (1):
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/320332
- This record as JSON: /data/d/320332.json