ORPHA:137871
OBSOLETE: Laminopathy type Decaudain-Vigouroux
inactive · referred to ORPHA:2348Familial partial lipodystrophy, Dunnigan type
Synonyms: OBSOLETE: Laminopathy with severe metabolic syndrome and myopathy
- 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 Familial partial lipodystrophy, Dunnigan type
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Laminopathy type Decaudain-Vigouroux | OBSOLETE: Laminopathy with severe metabolic syndrome and myopathy |
| fr | OBSOLETE : Laminopathie type Decaudain-Vigouroux | OBSOLETE : Laminopathie avec syndrome métabolique sévère et myopathie |
| de | OBSOLET: Laminopathie Typ Decaudain-Vigouroux | OBSOLET: Laminopathie mit schwerem metabolischen Syndrom und Myopathie |
| es | OBSOLETO: Laminopatía tipo Decaudain-Vigouroux | OBSOLETO: Laminopatía con síndrome metabólico grave y miopatía |
| it | OBSOLETO: Laminopatia tipo Decaudain-Vigouroux | OBSOLETO: Laminopatia con sindrome metabolica grave e miopatia |
| nl | OBSOLEET: Laminopathie type Decaudain-Vigouroux | OBSOLEET: Laminopathie met ernstig metabool syndroom en myopathie |
| pt | OBSOLETO: Laminopatia, tipo Decaudain-Vigouroux | OBSOLETO: Laminopatia com síndrome metabólico grave e miopatia |
| pl | NIEAKTUALNE: Laminopatia typu Decaudaina i Vigouroux | NIEAKTUALNE: Laminopatia z ciężkim zespołem metabolicznym i miopatią |
| cs | NEAKTUÁLNÍ: Laminopatie, typ Decaudainové-Vigourouxové | NEAKTUÁLNÍ: Laminopatie s těžkým metabolickým syndromem a myopatií · NEAKTUÁLNÍ: Laminopatie, typ Decaudain-Vigourouxové |
| uk | ЗАСТАРІЛО: Ламінопатія типу Декадена-Вігуру | ЗАСТАРІЛО: Ламінопатія з тяжким метаболічним синдромом та міопатією |
| zh | 弃用：Decaudain Vigouroux型核纤层蛋白病 | 核纤层蛋白病伴有严重代谢综合征和肌病 |
| tr | Eski adı: Laminopati tipi Decaudain-Vigouroux | Ağır metabolik sendrom ve miyopatili laminopati |
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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/137871
- This record as JSON: /data/d/137871.json