Familial partial lipodystrophy due to lamin-A mutations (Q97034): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 13:04, 16 August 2026
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
0 references
dki-india-ID_743641234
0 references
Concluído
0 references
