ORPHA:412220
OBSOLETE: Ramsay Hunt syndrome type II
inactive · referred to ORPHA:3020Ramsay Hunt syndrome
- 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 Ramsay Hunt syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Ramsay Hunt syndrome type II | |
| fr | OBSOLETE : Syndrome de Ramsay Hunt type II | |
| de | OBSOLET: Ramsay Hunt-Syndrom Typ II | |
| es | OBSOLETO: Síndrome de Ramsay Hunt tipo II | |
| it | OBSOLETO: Sindrome di Ramsay Hunt, tipo II | |
| nl | OBSOLEET: Syndroom van Ramsay Hunt type II | |
| pt | OBSOLETO: Síndrome de Ramsay Hunt tipo II | |
| pl | NIEAKTUALNE: Zespól Ramsay'a Hunta typu II | |
| cs | NEAKTUÁLNÍ: Ramsay Huntův syndrom typ II | |
| uk | ЗАСТАРІЛО: Синдром Рамзі Ханта, тип II | |
| zh | 弃用：拉姆齐·亨特综合征2型 | |
| tr | Eski adı: Ramsay Hunt sendromu tip II |
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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/412220
- This record as JSON: /data/d/412220.json