Familial partial lipodystrophy due to lamin-A mutations (Q97034)
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This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is due to lamin-A mutations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_743641234 |
||
| English | Familial partial lipodystrophy due to lamin-A mutations |
This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is due to lamin-A mutations. |
Statements
CID11:ID_743641234
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dki-india-ID_743641234
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Concluído
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15 August 2026
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