ORPHA:3460
Torg-Winchester syndrome
inactive · moved to ORPHA:371428Multicentric osteolysis-nodulosis-arthropathy spectrum
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Multicentric osteolysis-nodulosis-arthropathy spectrum
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Torg-Winchester syndrome | |
| fr | Syndrome de Torg-Winchester | |
| de | Torg-Winchester-Syndrom | |
| es | Síndrome de Torg-Winchester | |
| it | Sindrome Torg-Winchester | |
| nl | Syndroom van Torg-Winchester | |
| pt | Síndrome Torg-Winchester | |
| pl | Zespół Torga i Winchestera | Zespół Winchestera |
| cs | Winchesterův-Torgův syndrom | Winchesterův syndrom · Winchester-Torgův syndrom |
| uk | Синдром Торга-Вінчестера | Синдром Вінчестера |
| zh | Torg-Winchester综合征 | Winchester综合征 |
| tr | Torg-Winchester sendromu | Winchester sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C1850155 | E | validated | |
| MedDRA | 10078901 | 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/3460
- This record as JSON: /data/d/3460.json