Familial partial lipodystrophy associated with PLIN1 mutations (Q97021): 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 | ||
Refere-se a uma condição de pele autossômica dominante caracterizada pela perda de gordura subcutânea. Este diagnóstico é devido às mutações PLIN1. | |||
| description / en | description / en | ||
This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is associated with PLIN1 mutations. | |||
Revision as of 13:03, 16 August 2026
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 |
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| 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. |
