ORPHA:300763
Laminopathy with lipodystrophy
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Laminopathy with lipodystrophy | |
| fr | Laminopathie avec lipodystrophie | |
| de | Laminopathie mit Lipodystrophie | |
| es | Laminopatía con lipodistrofia | |
| it | Laminopatia con lipodistrofia | |
| nl | Laminopathie met lipodystrofie | |
| pt | Laminopatia com lipodistrofia | |
| pl | Laminopatia z lipodystrofią | |
| cs | Laminopatie s lipodystrofií | |
| uk | Ламінопатія з ліподистрофією | |
| zh | 核纤层蛋白病伴脂肪萎缩综合征 | |
| tr | Lipodistrofi ile seyreden laminopati |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681084 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98301Laminopathy
rare genetic diseases
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/300763
- This record as JSON: /data/d/300763.json