Familial partial lipodystrophy associated with PLIN1 mutations (Q97021)
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This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is associated with PLIN1 mutations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_98904071 |
||
| English | Familial partial lipodystrophy associated with PLIN1 mutations |
This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is associated with PLIN1 mutations. |
