Apolipoprotein A-I deficiency (Q97100): Difference between revisions
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Refere-se à deficiência de uma proteína que em humanos é codificada pelo gene APOA1. Tem papel específico no metabolismo lipídico. | |||
| description / en | description / en | ||
This refers to the deficiency in a protein that in humans is encoded by the APOA1 gene. It has a specific role in lipid metabolism. | |||
Revision as of 13:08, 16 August 2026
This refers to the deficiency in a protein that in humans is encoded by the APOA1 gene. It has a specific role in lipid metabolism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_104825191 |
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| English | Apolipoprotein A-I deficiency |
This refers to the deficiency in a protein that in humans is encoded by the APOA1 gene. It has a specific role in lipid metabolism. |
