ORPHA:99876
OBSOLETE: Ehlers-Danlos syndrome type 7B
inactive · referred to ORPHA:1899Arthrochalasia Ehlers-Danlos syndrome
Synonyms: OBSOLETE: EDS VIIB
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Arthrochalasia Ehlers-Danlos syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Ehlers-Danlos syndrome type 7B | OBSOLETE: EDS VIIB |
| fr | OBSOLETE : Syndrome d'Ehlers-Danlos type 7B | OBSOLETE : EDS VIIB · OBSOLETE : SED VIIB |
| de | OBSOLET: Ehlers-Danlos-Syndrom Typ 7B | OBSOLET: EDS VIIB |
| es | OBSOLETO: Síndrome de Ehlers-Danlos tipo 7B | OBSOLETO: SED VIIB |
| it | OBSOLETO: Sindrome di Ehlers-Danlos, tipo 7B | OBSOLETO: EDS VIIB · OBSOLETO: EDS 7B |
| nl | OBSOLEET: Syndroom van Ehlers-Danlos type 7B | OBSOLEET: EDS VIIB |
| pt | OBSOLETO: Síndrome Ehlers-Danlos tipo 7B | |
| pl | NIEAKTUALNE: Zespól Ehlersa i Danlosa typu 7B | NIEAKTUALNE: EDS VIIB |
| cs | NEAKTUÁLNÍ: Ehlersův-Danlosův syndrom, typ 7B | NEAKTUÁLNÍ: EDS VIIB · NEAKTUÁLNÍ: Ehlers-Danlosův syndrom, typ 7B |
| uk | ЗАСТАРІЛО: Синдром Елерса-Данлоса, тип 7B | ЗАСТАРІЛО: EDS VIIB |
| zh | 弃用：Ehlers-Danlos综合征7B型 | EDS VIIB |
| tr | Eski adı: Ehlers-Danlos sendromu tip 7B | EDS VIIB |
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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/99876
- This record as JSON: /data/d/99876.json