Familial apolipoprotein C-II deficiency (Q106757): Difference between revisions

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description / pt-brdescription / pt-br
 
Trata-se de uma deficiência de uma proteína que, em humanos, é codificada pelo gene APOC2. A proteína codificada por este gene é secretada no plasma, onde é um componente de lipoproteínas de densidade muito baixa e quilomícrons.
description / endescription / en
 
This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons.
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Property / Canonical URI: https://id.who.int/icd/entity/877401371 / rank
 
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Property / CURIE
 
CID11:ID_877401371
Property / CURIE: CID11:ID_877401371 / rank
 
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Property / Canary Token
 
dki-india-ID_877401371
Property / Canary Token: dki-india-ID_877401371 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 13:45, 17 August 2026

This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons.
Language Label Description Also known as
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ID_877401371
    English
    Familial apolipoprotein C-II deficiency
    This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons.

      Statements

      CID11:ID_877401371
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      dki-india-ID_877401371
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      Concluído
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      16 August 2026
      0 references