ORPHA:306762
OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature
inactive · referred to ORPHA:98261Progressive myoclonic epilepsy
- 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 Progressive myoclonic epilepsy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature | |
| fr | OBSOLETE : Epilepsie et/ou ataxie progressive avec myoclonie comme manifestation majeure | |
| de | OBSOLET: Progressive Epilepsie und/oder Ataxie mit Myoklonie als Hauptmerkmal | |
| es | OBSOLETO: Epilepsia progresiva y/o ataxia con mioclonos como característica principal | |
| it | OBSOLETO: Epilessia progressiva e/o atassia con mioclono come segno cardinale | |
| nl | OBSOLEET: Progressieve epilepsie en/of ataxie met myoclonus als hoofdkenmerk | |
| pt | OBSOLETO: Epilepsia progressiva e/ou ataxia com mioclonia como característica principal | |
| pl | NIEAKTUALNE: Postepujaca padaczka i(lub) ataksja, w której mioklonus jest objawem glównym | |
| cs | NEAKTUÁLNÍ: Progresivní epilepsie a/nebo ataxie s myoklonem jako hlavním příznakem | |
| uk | ЗАСТАРІЛО: Прогресуюча епілепсія та/або атаксія з міоклонусом як основною ознакою | |
| zh | 弃用：肌阵挛为主要特征进行性癫痫和/或共济失调 | |
| tr | Eski adı: Esas klinik özelliği miyoklonus olan ilerleyici epilepsi ve/veya ataksi |
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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/306762
- This record as JSON: /data/d/306762.json