ORPHA:254707
Faisalabad histiocytosis
inactive · moved to ORPHA:168569H syndrome
Synonyms: FHC
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to H syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Faisalabad histiocytosis | FHC |
| fr | Histiocytose de Faisalabad | = en |
| de | Faisalabad-Histiozytose | = en |
| es | Histiocitosis de Faisalabad | = en |
| it | Istiocitosi di Faisalabad | = en |
| nl | Faisalabad histiocytose | = en |
| pt | Histiocitose de Faisalabad | = en |
| pl | Histiocytoza Faisalabad | = en |
| cs | Faisalabadská histiocytóza | = en |
| uk | Фейсалабадський гістіоцитоз | = en |
| zh | 费萨拉巴德组织细胞增多症 | = en |
| tr | Faisalabad histiyositozi | = en |
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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.
5
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/254707
- This record as JSON: /data/d/254707.json