ORPHA:1271
Bowen syndrome
inactive · moved to ORPHA:912Zellweger 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 Zellweger syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Bowen syndrome | |
| fr | Syndrome de Bowen | |
| de | Bowen-Syndrom | |
| es | Síndrome de Bowen | |
| it | Sindrome di Bowen | |
| nl | Syndroom van Bowen | |
| pt | Síndrome Bowen | |
| pl | Zespół Bowena | |
| cs | Bowenův syndrom | |
| uk | Синдром Боуена | |
| zh | Bowen综合征 | |
| tr | Bowen sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 211200 | E | validated | |
| UMLS | C1859404 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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/1271
- This record as JSON: /data/d/1271.json