ORPHA:68388
OBSOLETE: Neurofibromatosis
inactive · referred to ORPHA:98196Malformation syndrome with hamartosis
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Malformation syndrome with hamartosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Neurofibromatosis | |
| fr | OBSOLETE : Neurofibromatose | |
| de | OBSOLET: Neurofibromatose | |
| es | OBSOLETO: Neurofibromatosis | |
| it | OBSOLETO: Neurofibromatosi | |
| nl | OBSOLEET: Neurofibromatose | |
| pt | OBSOLETO: Neurofibromatose | |
| pl | NIEAKTUALNE: Neurofibromatoza | |
| cs | NEAKTUÁLNÍ: Neurofibromatóza | |
| uk | ЗАСТАРІЛО: Нейрофіброматоз | |
| zh | 弃用：神经纤维瘤病 | |
| tr | Eski adı: Nörofibromatoz |
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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/68388
- This record as JSON: /data/d/68388.json