ORPHA:2346
OBSOLETE: Angioosteohypertrophic syndrome
inactive · referred to ORPHA:68419Rare vascular anomaly
Synonyms: OBSOLETE: Klippel-Trénaunay-Weber syndrome
- Type
- Clinical group
- 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 Rare vascular anomaly
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Angioosteohypertrophic syndrome | OBSOLETE: Klippel-Trénaunay-Weber syndrome |
| fr | OBSOLETE : Syndrome angio-ostéo-hypertrophique | OBSOLETE : Syndrome de Klippel-Trénaunay-Weber |
| de | OBSOLET: Angio-osteo-hypertrophisches Syndrom | OBSOLET: Klippel-Trénaunay-Weber-Syndrom |
| es | OBSOLETO: Síndrome angio-osteo-hipertrófico | OBSOLETO: Síndrome de Klippel-Trénaunay-Weber |
| it | OBSOLETO: Sindrome angio-osteoipertrofica | OBSOLETO: Sindrome di Klippel-Trénaunay-Weber |
| nl | OBSOLEET: Angio-osteohypertrofisch syndroom | NIET ZELDZAME ZIEKTE IN EUROPA: Syndroom van Klippel-Trénaunay-Weber |
| pt | OBSOLETO: Síndrome angio-osteohipertrófica | OBSOLETO: Síndrome Klippel-Trénaunay-Weber |
| pl | NIEAKTUALNE: Zespół przerostu naczyń i kości | = en |
| cs | NEAKTUÁLNÍ: Angioosteohypertrofický syndrom | NEAKTUÁLNÍ: Klippelův-Trénaunayův-Weberův syndrom · NEAKTUÁLNÍ: Klippel-Trénaunay-Weberův syndrom |
| uk | Ангіоостеогіпертрофічний синдром | Синдром Кліппеля-Треноне-Вебера |
| zh | 先天性静脉畸形骨肥大综合征 | Klippel-Trénaunay-Weber综合征 |
| tr | Anjiyoosteohipertrofik sendrom | Klippel-Trénaunay-Weber sendromu |
Definition in:
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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/2346
- This record as JSON: /data/d/2346.json