ORPHA:3419
OBSOLETE: Van Regemorter-Pierquin-Vamos syndrome
inactive · referred to ORPHA:459787Lethal multiple congenital anomalies/dysmorphic syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Lethal multiple congenital anomalies/dysmorphic syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Van Regemorter-Pierquin-Vamos syndrome | |
| fr | OBSOLETE : Syndrome de Van Regemorter-Pierquin-Vamos | |
| de | OBSOLET: Van-Regemorte-Pierquin-Vamos-Syndrom | |
| es | OBSOLETO: Síndrome de Van Regemorter-Pierquin-Vamos | |
| it | OBSOLETO: Sindrome di Van Regemorter-Pierquin-Vamos | |
| nl | OBSOLEET: Syndroom van Van Regemorter-Pierquin-Vamos | |
| pt | OBSOLETO: Síndrome Van Regemorter-Pierquin-Vamos | |
| pl | NIEAKTUALNE: Zespól Van Regemortera, Pierquina i Vamosa | |
| cs | NEAKTUÁLNÍ: Van Regemorterův-Pierquinův-Vamosův syndrom | NEAKTUÁLNÍ: Van Regemorter-Pierquin-Vamosův syndrom |
| uk | ЗАСТАРІЛО: Синдром Ван Регемортера-Пєркіна-Вамоса | |
| zh | 弃用：Van Regemorter-Pierquin-Vamos综合征 | |
| tr | Eski adı: Van Regemorter-Pierquin-Vamos sendromu |
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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/3419
- This record as JSON: /data/d/3419.json