ORPHA:1167
OBSOLETE: Facial asymmetry-temporal seizures syndrome
inactive · referred to ORPHA:98259Childhood-onset epilepsy syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Childhood-onset epilepsy syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Facial asymmetry-temporal seizures syndrome | |
| fr | OBSOLETE : Syndrome d'asymétrie faciale-épilepsie temporale | |
| de | OBSOLET: Gesichtsasymmetrie-temporäre Anfälle-Syndrom | |
| es | OBSOLETO: Síndrome de asimetría facial-epilepsia temporal | |
| it | OBSOLETO: Asimmetria facciale - epilessia temporale | |
| nl | OBSOLEET: Faciale asymmetrie - temporele aanvallen-syndroom | |
| pt | OBSOLETO: Síndrome de assimetria facial-epilepsia temporal | |
| pl | NIEAKTUALNE: Asymetria twarzy - napady skroniowe | |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující asymetrii obličeje a temporální záchvaty | |
| uk | ЗАСТАРІЛО: Синдром асиметрії обличчя та скроневих судом | |
| zh | 弃用：面部不对称-颞叶癫痫综合征 | |
| tr | Eski adı: Fasiyal asimetrisi-temporal nöbet sendromu |
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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/1167
- This record as JSON: /data/d/1167.json