ORPHA:2029
Multiple non-ossifying fibromatosis
inactive · moved to ORPHA:636Neurofibromatosis type 1
Synonyms: Jaffe-Campanacci syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Neurofibromatosis type 1
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Multiple non-ossifying fibromatosis | Jaffe-Campanacci syndrome |
| fr | Fibromatose multiple non ossifiante | Syndrome de Jaffe-Campanacci |
| de | Fibromatose, multiple nicht ossifizierende | Jaffe-Campanacci-Syndrom |
| es | Fibromatosis múltiple no osificante | Síndrome de Jaffe-Campanacci |
| it | Fibromatosi multipla non ossificante | Sindrome di Jaffe-Campanacci |
| nl | Multipele niet-ossificerende fibromatose | Syndroom van Jaffe-Campanacci |
| pt | Fibromatose múltipla não-ossificante | Síndrome Jaffe-Campanacci |
| pl | Mnoga włókniakowatość niekostniejąca | Zespół Jaffe i Campanacci |
| cs | Mnohočetná neosifikující fibromatóza | Jaffeho-Campanacciho syndrom · Jaffe-Campanacciho syndrom |
| uk | Множинний неосифікуючий фіброматоз | Синдром Яффе-Кампаначі |
| zh | 多发性非骨化性纤维瘤病 | Jaffe-Campanacci综合征 |
| tr | Çoklu kemikleşmeyen fibromatoz | Jaffe-Campanacci sendromu |
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/2029
- This record as JSON: /data/d/2029.json