ORPHA:93566
OBSOLETE: Pediatric Sjögren syndrome
inactive · referred to ORPHA:289390Primary Sjögren disease
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Primary Sjögren syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Pediatric Sjögren syndrome | |
| fr | OBSOLETE : Syndrome de Gougerot-Sjögren de l'enfant | |
| de | OBSOLET: Sjögren-Syndrom des Kindesalters | |
| es | OBSOLETO: Síndrome de Sjögren pediátrica | |
| it | OBSOLETO: Sindrome di Sjögren a esordio infantile | |
| nl | OBSOLEET: Pediatrisch Sjögrensyndroom | |
| pt | OBSOLETO: Síndrome Sjögren pediátrica | |
| pl | NIEAKTUALNE: Dzieciecy zespól Sjögrena | |
| cs | NEAKTUÁLNÍ: Pediatrický Sjögrenův syndrom | |
| uk | ЗАСТАРІЛО: Синдром Шегрена у дітей | |
| zh | 弃用：小儿Sj÷gren综合征 | |
| tr | Eski adı: Pediatrik Sjögren sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
4
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/93566
- This record as JSON: /data/d/93566.json