Familial partial lipodystrophy due to lamin-A mutations (Q97034): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Isso se refere a uma condição de pele autossômica dominante caracterizada pela perda de gordura subcutânea. Este diagnóstico é devido às mutações da lamina-A. | |||
| description / en | description / en | ||
This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is due to lamin-A mutations. | |||
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 |
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| 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. |
