ORPHA:320342
Pure or complex autosomal dominant spastic paraplegia
Synonyms: Pure or complicated autosomal dominant spastic paraplegia
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Autosomal dominant
- 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 autosomal dominant spastic paraplegia | Pure or complicated autosomal dominant spastic paraplegia |
| fr | Paraplégie spastique autosomique dominante pure ou complexe | |
| de | Spastische Paraplegie, reine oder komplexe, autosomal-dominante | Spastische Paraplegie, reine oder komplizierte, autosomal-dominante |
| es | Paraplejía espástica autosómica dominante pura o compleja | |
| it | Paraplegia spastica autosomica dominante complessa o pura | Paraplegia spastica autosomica dominante complicata o pura |
| nl | Zuivere of complexe autosomaal dominante spastische paraplegie | Zuivere of gecompliceerde autosomaal dominante spastische paraplegie |
| pt | Paraplegia espástica autossómica dominante pura ou complexa | |
| pl | Czysta lub złożona autosomalna dominująca paraplegia spastyczna | Czysta lub powikłana autosomalna dominująca paraplegia spastyczna |
| cs | Čistá nebo komplexní autozomálně dominantní spastická paraplegie | Čistá nebo komplikovaná autozomálně dominantní spastická paraplegie |
| uk | Чиста або складна аутосомно-домінантна спастична параплегія | Чиста або ускладнена аутосомно-домінантна спастична параплегія |
| zh | 单纯性或复杂性常染色体显性遗传痉挛性截瘫 | = en |
| tr | Saf veya kompleks otozomal dominant spastik parapleji | Saf veya karmaşık otozomal baskın spastik parapleji |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17914 | E | validated | |
| UMLS | C5679886 | 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
Children (11):
- ORPHA:100991Autosomal dominant spastic paraplegia type 10
- ORPHA:100994Autosomal dominant spastic paraplegia type 13
- ORPHA:100984Autosomal dominant spastic paraplegia type 3
- ORPHA:101011Autosomal dominant spastic paraplegia type 31
- ORPHA:100985Autosomal dominant spastic paraplegia type 4
- ORPHA:100988Autosomal dominant spastic paraplegia type 6
- ORPHA:100989Autosomal dominant spastic paraplegia type 8
- ORPHA:447757Autosomal dominant spastic paraplegia type 9B
- ORPHA:209951Autosomal spastic paraplegia type 18
- ORPHA:101010Autosomal spastic paraplegia type 30
- ORPHA:99013Spastic paraplegia type 7
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/320342
- This record as JSON: /data/d/320342.json