ORPHA:99872
OBSOLETE: Hashimoto-Pritzker syndrome
inactive · referred to ORPHA:389Langerhans cell histiocytosis
Synonyms: OBSOLETE: Congenital Langerhans cell histiocytosis
- 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 Langerhans cell histiocytosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Hashimoto-Pritzker syndrome | OBSOLETE: Congenital Langerhans cell histiocytosis |
| fr | OBSOLETE : Syndrome de Hashimoto-Pritzker | OBSOLETE : Histiocytose langerhansienne congénitale |
| de | OBSOLET: Hashimoto-Pritzker-Syndrom | OBSOLET: Langerhans-Zell-Histiozytose, kongenitale |
| es | OBSOLETO: Síndrome de Hashimoto-Pritzker | OBSOLETO: Histiocitosis congénita de células de Langerhans |
| it | OBSOLETO: Sindrom di Hashimoto-Pritzker | OBSOLETO: Istiocitosi congenita a cellule di Langerhans |
| nl | OBSOLEET: Syndroom van Hashimoto-Pritzker | OBSOLEET: Congenitale Langerhanscelhistiocytose |
| pt | OBSOLETO: Síndrome Hashimoto-Pritzker | |
| pl | NIEAKTUALNE: Zespól Hashimoto i Pritzkera | NIEAKTUALNE: Wrodzona histiocytoza z komórek Langerhansa |
| cs | NEAKTUÁLNÍ: Hashimotova-Pritzkerova choroba | NEAKTUÁLNÍ: Vrozená Langerhansova histiocytóza X · NEAKTUÁLNÍ: Hashimoto-Pritzkerova choroba |
| uk | ЗАСТАРІЛО: Синдром Хашимото-Пріцкера | ЗАСТАРІЛО: Вроджений гістіоцитоз клітин Лангерганса |
| zh | 弃用:Hashimoto-Pritzker综合征 | 先天性朗格汉斯细胞组织细胞增生症 |
| tr | Eski adı: Hashimoto-Pritzker sendromu | Doğumsal Langerhans hücreli histiyositoz |
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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/99872
- This record as JSON: /data/d/99872.json