ORPHA:1155
OBSOLETE: Arthrogryposis due to muscular dystrophy
inactive · referred to ORPHA:1037Arthrogryposis multiplex congenita
- 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 Arthrogryposis multiplex congenita
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Arthrogryposis due to muscular dystrophy | |
| fr | OBSOLETE : Arthrogrypose par dystrophie musculaire | |
| de | OBSOLET: Arthrogrypose infolge Muskeldystrophie | |
| es | OBSOLETO: Artrogriposis por distrofia muscular | |
| it | OBSOLETO: Artrogriposi da distrofia muscolare | |
| nl | OBSOLEET: Artrogrypose als gevolg van spierdystrofie | |
| pt | OBSOLETO: Artrogripose por distrofia muscular | |
| pl | NIEAKTUALNE: Artogrypoza spowodowana dystrofia miesni | |
| cs | NEAKTUÁLNÍ: Artrogrypóza způsobená svalovou dystrofií | |
| uk | ЗАСТАРІЛО: Артрогрипоз внаслідок мязової дистрофії | |
| zh | 弃用：肌营养不良症所致关节挛缩 | |
| tr | Eski adı: Kas distrofisine bağlı artrogripozis |
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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/1155
- This record as JSON: /data/d/1155.json