ORPHA:98307
Acquired 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired lipodystrophy | |
| fr | Lipodystrophie acquise | |
| de | Lipodystrophie, erworbene | |
| es | Lipodistrofia adquirida | |
| it | Lipodistrofia acquisita | |
| nl | Verworven lipodystrofie | |
| pt | Lipodistrofia adquirida | |
| pl | Lipodystrofia nabyta | |
| cs | Získané lipodystrofie | |
| uk | Набута ліподистрофія | |
| zh | 获得性脂肪营养不良 | |
| tr | Edinsel lipodistrofi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020089 | E | validated | |
| UMLS | C0877192 | E | validated | |
| MedDRA | 10049287 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:90970Primary lipodystrophy
rare skin diseases; rare endocrine diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/98307
- This record as JSON: /data/d/98307.json