ORPHA:401825
Autosomal recessive spastic paraplegia type 68
inactive · moved to ORPHA:320406Spastic paraplegia-optic atrophy-neuropathy syndrome
Synonyms: SPG68
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Spastic paraplegia-optic atrophy-neuropathy syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Autosomal recessive spastic paraplegia type 68 | SPG68 |
| fr | Paraplégie spastique autosomique récessive type 68 | = en |
| de | Spastische Paraplegie, autosomal-rezessive, Typ 68 | = en |
| es | Paraplejía espástica autosómica recesiva tipo 68 | = en |
| it | Paraplegia spastica autosomica recessiva, tipo 68 | = en |
| nl | Autosomaal recessieve spastische paraplegie type 68 | = en |
| pt | Paraplegia espástica autossómica recessiva tipo 68 | |
| pl | Autosomalna recesywna paraplegia spastyczna typu 68 | = en |
| cs | Autozomálně recesivní spastická paraplegie, typ 68 | = en |
| uk | Аутосомно-рецесивна спастична параплегія, тип 68 | = en |
| zh | 常染色体隐性遗传痉挛性截瘫68型 | = en |
| tr | Otozomal resesif spastik parapleji tip 68 | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/401825
- This record as JSON: /data/d/401825.json