ORPHA:3417
OBSOLETE: Van den Bosch syndrome
inactive · referred to ORPHA:79373Ectodermal dysplasia syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Ectodermal dysplasia syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Van den Bosch syndrome | |
| fr | OBSOLETE : Syndrome de Van der Bosch | |
| de | OBSOLET: Van den Bosch-Syndrom | |
| es | OBSOLETO: Síndrome de Van der Bosch | |
| it | OBSOLETO: Sindrome Van den Bosch | |
| nl | OBSOLEET: Syndroom van Van den Bosch | |
| pt | OBSOLETO: Síndrome Van den Bosch | |
| pl | NIEAKTUALNE: Zespół van den Boscha | |
| cs | NEAKTUÁLNÍ: Van den Boschův syndrom | |
| uk | Синдром Ван ден Боша | |
| zh | Van den Bosch综合征 | |
| tr | Van den Bosch sendromu |
Definition in:
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/3417
- This record as JSON: /data/d/3417.json