ORPHA:263558
OBSOLETE: Peeling skin syndrome type C
inactive · referred to ORPHA:263543Generalized peeling skin syndrome
Synonyms: OBSOLETE: Generalized deciduous skin type C · OBSOLETE: Generalized peeling skin syndrome type C
- 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 Generalized peeling skin syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Peeling skin syndrome type C | OBSOLETE: Generalized deciduous skin type C · OBSOLETE: Generalized peeling skin syndrome type C |
| fr | OBSOLETE : Peeling skin syndrome généralisé type C | OBSOLETE : Peau déciduale généralisée type C |
| de | OBSOLET: Peeling-Skin-Syndrom Typ C | OBSOLET: Peeling-Skin-Syndrom, generalisiertes, Typ C |
| es | OBSOLETO: Síndrome de descamación de la piel tipo C | OBSOLETO: Piel decidual generalizada tipo C · OBSOLETO: Síndrome generalizado de descamación de la piel tipo C |
| it | OBSOLETO: Sindrome 'peeling skin' tipo C | OBSOLETO: Sindrome ''peeling skin'' generalizzata, tipo C · OBSOLETO: Pelle deciduale generalizzata, tipo C |
| nl | OBSOLEET: 'Peeling skin'-syndroom type C | OBSOLEET: Gegeneraliseerde 'peeling skin'-syndroom type C · OBSOLEET: Gegeneraliseerde afschilferende huid type C |
| pt | OBSOLETO: Síndrome de pele descamativa generalizado, tipo C | |
| pl | NIEAKTUALNE: Uogólniony zespół złuszczania skóry typu C | = en |
| cs | NEAKTUÁLNÍ: Generalizovaný syndrom loupající se kůže, typ C | NEAKTUÁLNÍ: Generalizovaná opadavá kůže, typ C |
| uk | ЗАСТАРІЛО: Синдром лущення шкіри, тип С | ЗАСТАРІЛО: Генералізована листяна шкіра типу С · ЗАСТАРІЛО: Синдром генералізованого лущення шкіри типу С |
| zh | 皮肤剥脱综合征C型 | 广泛性皮肤剥脱综合征C型 |
| tr | Peeling cilt sendromu tip C | Jeneralize deri dökülmesi tip C · Jeneralize cilt soyulması sendromu tip C |
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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/263558
- This record as JSON: /data/d/263558.json