ORPHA:1256
OBSOLETE: Blepharophimosis-radioulnar synostosis syndrome
inactive · referred to ORPHA:93459Syndrome with synostosis or other joint formation defect
Synonyms: OBSOLETE: Jorgenson-Lenz syndrome
- 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 Syndrome with synostosis or other joint formation defect
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Blepharophimosis-radioulnar synostosis syndrome | OBSOLETE: Jorgenson-Lenz syndrome |
| fr | OBSOLETE : Syndrome de blépharophimosis-synostose radio-cubitale | OBSOLETE : Syndrome de Jorgenson-Lenz |
| de | OBSOLET: Blepharophimose-radioulnare Synostose-Syndrom | |
| es | OBSOLETO: Síndrome de blefarofimosis-sinostosis radiocubital | OBSOLETO: Síndrome de Jorgenson-Lenz |
| it | OBSOLETO: Sindrome blefarofimosi-sinostosi radioulnare | OBSOLETO: Sindrome di Jorgenson-Lenz |
| nl | OBSOLEET: Blefarofimose - radio-ulnaire synostose-syndroom | OBSOLEET: Syndroom van Jorgenson-Lenz |
| pt | OBSOLETO: Síndrome de blefarofimose-sinostose radio-cubital | |
| pl | NIEAKTUALNE: Zwezenie szpary powiekowej - synostoza promieniowo-lokciowa | NIEAKTUALNE: Zespół Jorgensona i Lenza |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující blefarofimózu a radioulnární synostózu | NEAKTUÁLNÍ: Jorgensonův-Lenzův syndrom · NEAKTUÁLNÍ: Jorgenson-Lenzův syndrom |
| uk | Синдром блефарофімозно-радіоульнарного синостозу | ЗАСТАРІЛО: Синдром Йоргенсона-Ленца |
| zh | 弃用：睑裂狭小-尺桡关节融合综合征 | Jorgenson-Lenz综合征 |
| tr | Eski adı: Blefarofimosis-radioulnar sinostozis sendromu | Jorgenson-Lenz 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/1256
- This record as JSON: /data/d/1256.json