ORPHA:338
Familial multiple fibrofolliculoma
inactive · moved to ORPHA:122Birt-Hogg-Dubé syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Birt-Hogg-Dubé syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Familial multiple fibrofolliculoma | |
| fr | Fibrofolliculomes multiples familiaux | |
| de | Fibrofollikulom, familiäres multiples | |
| es | Fibrofoliculomas múltiples familiares | |
| it | Fibrofolliculomi multipli familiari | |
| nl | Familiaal meervoudig fibrofolliculoom | |
| pt | Fibrofoliculoma múltiplo familiar | |
| pl | Rodzinne mnogie włókniakoziarniszczaki | |
| cs | Familiární mnohočetný fibrofolikulom | |
| uk | Сімейна множинна фіброфолікулома | |
| zh | 家族性多发性纤维毛囊瘤 | |
| tr | Ailesel çoklu fibrofolikülom |
2
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.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/338
- This record as JSON: /data/d/338.json