Localized lipodystrophy
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 2 |
| OrphanetNr: | 79088 |
| OMIM Id: |
|
| ICD-10: |
E88.1 |
| UMLs: |
|
| MeSH: |
|
| MedDRA: |
|
| Snomed: |
|
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Unknown [Orphanet] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Acquired lipodystrophy
-Rare endocrine disease -Rare genetic disease -Rare skin disease |
Symptom Information:
|
|
(HPO:0009125) | Lipodystrophy | Very frequent [Orphanet] | 54 / 7739 | |||
|
|
(HPO:0003549) | Abnormality of connective tissue | Very frequent [Orphanet] | 22 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|