Localized lipodystrophy
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Unknown
- Age of onset
- All ages
- Status
- active
A rare group of acquired lipodystrophies that are characterized by loss of subcutaneous tissue from generally small regions of the body, either single or multiple areas, and are not typically associated with metabolic complications. Some cases may involve lipohypertrophy (insulin). This group includes pressure-induced localized lipoatrophy, drug-induced localized lipodystrophy, panniculitis- induced localized lipodystrophy, centrifugal lipodystrophy, and idiopathic localized lipodystrophy.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Localized lipodystrophy | |
| fr | Lipodystrophie localisée | |
| de | Lipodystrophie, lokale | |
| es | Lipodistrofias localizadas | |
| it | Lipodistrofia localizzata | |
| nl | Gelokaliseerde lipodystrofie | |
| pt | Lipodistrofia localizada | |
| pl | Lipodystrofia zlokalizowana | |
| cs | Lokalizovaná forma lipodystrofie | |
| uk | Локалізована ліподистрофія | |
| zh | 局限性脂质营养不良 | |
| tr | Lokalize lipodistrofi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019194 | E | validated | |
| MONDO | 19194 | E | validated | |
| UMLS | C4329999 | E | validated | |
| GARD | 5867 | E | validated | |
| MedDRA | 10088837 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98307Acquired lipodystrophy
rare skin diseases; rare endocrine diseases
Genes
0 directOrphanet records no gene directly on this code.
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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79088
- This record as JSON: /data/d/79088.json