ORPHA:99875
OBSOLETE: Ehlers-Danlos syndrome type 7A
inactive · referred to ORPHA:1899Arthrochalasia Ehlers-Danlos syndrome
Synonyms: OBSOLETE: EDS VIIA
- 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 7A | OBSOLETE: EDS VIIA |
| fr | OBSOLETE : Syndrome d'Ehlers-Danlos type 7A | OBSOLETE : EDS VIIA · OBSOLETE : SED VIIA |
| de | OBSOLET: Ehlers-Danlos-Syndrom Typ 7A | OBSOLET: EDS VIIA |
| es | OBSOLETO: Síndrome de Ehlers-Danlos tipo 7A | OBSOLETO: SED VIIA |
| it | OBSOLETO: Sindrome di Ehlers-Danlos, tipo 7A | OBSOLETO: EDS VIIA · OBSOLETO: EDS 7A |
| nl | OBSOLEET: Syndroom van Ehlers-Danlos type 7A | OBSOLEET: EDS VIIA |
| pt | OBSOLETO: Síndrome Ehlers-Danlos tipo 7A | |
| pl | NIEAKTUALNE: Zespól Ehlersa i Danlosa typu 7A | NIEAKTUALNE: EDS VIIA |
| cs | NEAKTUÁLNÍ: Ehlersův-Danlosův syndrom, typ 7A | NEAKTUÁLNÍ: EDS VIIA · NEAKTUÁLNÍ: Ehlers-Danlosův syndrom, typ 7A |
| uk | ЗАСТАРІЛО: Синдром Елерса-Данлоса, тип 7А | ЗАСТАРІЛО: EDS VIIA |
| zh | 弃用：Ehlers-Danlos综合征7A型 | EDS VIIA |
| tr | Eski adı: Ehlers-Danlos sendromu tip 7A | EDS VIIA |
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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/99875
- This record as JSON: /data/d/99875.json