ORPHA:100990
OBSOLETE: Autosomal dominant spastic paraplegia type 9
inactive · referred to ORPHA:100979Autosomal dominant complex spastic paraplegia
Synonyms: OBSOLETE: SPG9
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Autosomal dominant complex spastic paraplegia
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Autosomal dominant spastic paraplegia type 9 | OBSOLETE: SPG9 |
| fr | OBSOLETE : Paraplégie spastique autosomique dominante type 9 | OBSOLETE : SPG9 · OBSOLETE : Syndrome de cataracte-neuropathie motrice-petite taille-anomalies squelettiques · OBSOLETE : Syndrome de paraparésie spastique-amyopathie-cataracte-reflux gastro-oesophagien |
| de | OBSOLET: Spastische Paraplegie, autosomal-dominante, Typ 9 | OBSOLET: SPG9 |
| es | OBSOLETO: Paraplejía espástica autosómica dominante tipo 9 | OBSOLETO: SPG9 · OBSOLETO: Síndrome de paraplejía espástica-amiopatía-cataratas-reflujo gastroesofágico |
| it | OBSOLETO: Paraplegia spastica autosomica dominante, tipo 9 | OBSOLETO: SPG9 |
| nl | OBSOLEET: Autosomaal dominante spastische paraplegie type 9 | OBSOLEET: Cataracten - motorische neuropathie - kleine gestalte - skeletale anomalieën-syndroom · OBSOLEET: SPG9 · OBSOLEET: Spastische paraparese - amyopathie - cataracten - gastro-oesofageale reflux-syndroom |
| pt | OBSOLETO: Paraplegia espástica autossómica dominante tipo 9 | OBSOLETO: SPG9 |
| pl | NIEAKTUALNE: Autosomalna dominujaca paraplegia spastyczna typu 9 | NIEAKTUALNE: Parapareza spastyczna - amiopatia - zaćma - refluks żołądkowo-przełykowy · NIEAKTUALNE: SPG9 · NIEAKTUALNE: Zaćma - neuropatia ruchowa - niski wzrost - wady szkieletu |
| cs | NEAKTUÁLNÍ: Autozomálně dominantní spastická paraplegie, typ 9 | NEAKTUÁLNÍ: Syndrom zahrnující katarakta, motorickou neuropatii, nízký vzrůst a anomálie skeletu · NEAKTUÁLNÍ: SPG9 · NEAKTUÁLNÍ: Syndrom zahrnující spastickou paraparézu, amyopatii, katarakta a gastroezofageální reflux |
| uk | ЗАСТАРІЛО: Аутосомно-домінантна спастична параплегія, тип 9 | ЗАСТАРІЛО: SPG9 |
| zh | 弃用:常染色体显性遗传痉挛性截瘫9型 | SPG9 |
| tr | Eski adı: Otozomal dominant spastik parapleji tip 9 | SPG9 |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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/100990
- This record as JSON: /data/d/100990.json