ORPHA:3160
OBSOLETE: Vascular disruption sequence
inactive · referred to ORPHA:93890Rare developmental defect during embryogenesis
- 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 Rare developmental defect during embryogenesis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Vascular disruption sequence | |
| fr | OBSOLETE : Séquence de disruption vasculaire | |
| de | OBSOLET: Vaskuläre Gefäßunterbrechung | |
| es | OBSOLETO: Secuencia de disrupción vascular | |
| it | OBSOLETO: Sequenza da amputazione vascolare | |
| nl | OBSOLEET: Vasculaire disruptiesequentie | |
| pt | OBSOLETO: Sequência de disrupção vascular | |
| pl | NIEAKTUALNE: Sekwencja dysrupcji naczyniowej | |
| cs | NEAKTUÁLNÍ: Sekvence přerušení cév | |
| uk | ЗАСТАРІЛО: Послідовність судинних порушень | |
| zh | 弃用：血管破坏序列征 | |
| tr | Eski adı: Vasküler bozulma dizisi |
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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/3160
- This record as JSON: /data/d/3160.json