ORPHA:98694
OBSOLETE: Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly
inactive · referred to ORPHA:519341Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly | |
| fr | OBSOLETE : Dégénérescence spinocérébelleuse et paraparésie spastique avec anomalie oculomotrice | |
| de | OBSOLET: Spinozerebelläre Degeneration und spastische Paraparese mit okulomotorischer Anomalie | |
| es | OBSOLETO: Degeneración espinocerebelosa y paraparesia espástica con anomalía oculomotora | |
| it | OBSOLETO: Degenerazione spinocerebellare e paraparesi spastica con anomalia oculomotoria | |
| nl | OBSOLEET: Spinocerebellaire degenerescentie en spastische paraparese met een oculomotorische anomalie | |
| pt | OBSOLETO: Degenerescência espinocerebelosa e paraparesia espástica com anomalia oculomotora | |
| pl | NIEAKTUALNE: Zwyrodnienie rdzeniowo-mózdzkowe i parapareza spastyczna z anomalia okoruchowa | |
| cs | NEAKTUÁLNÍ: Spinocerebelární degenerace a spastické paraparézy s okohybnou anomálií | |
| uk | ЗАСТАРІЛО: Спіноцеребеллярна дегенерація та спастичний парапарез з окоруховою аномалією | |
| zh | 弃用：脊髓小脑变性和痉挛性截瘫伴眼球运动异常 | |
| tr | Eski adı: Okülomotor anomali ile seyreden spinoserebellar dejeneresan ve spastik paraparezi |
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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/98694
- This record as JSON: /data/d/98694.json