Peroxisomal D-bifunctional enzyme deficiency (Q88702): Difference between revisions

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Refere ao distúrbio de oxidação de ácidos graxos peroxissomais autossômicos recessivos. Os distúrbios peroxissomais são geralmente causados ​​por uma combinação de defeitos de montagem peroxissomal ou por deficiências de enzimas peroxissômicas específicas.
description / endescription / en
 
This refers to the autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific peroxisomal enzymes.
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Property / Canonical URI: https://id.who.int/icd/entity/996981847 / rank
 
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CID11:ID_996981847
Property / CURIE: CID11:ID_996981847 / rank
 
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dki-india-ID_996981847
Property / Canary Token: dki-india-ID_996981847 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 15:05, 15 August 2026

This refers to the autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific peroxisomal enzymes.
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ID_996981847
    English
    Peroxisomal D-bifunctional enzyme deficiency
    This refers to the autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific peroxisomal enzymes.

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      CID11:ID_996981847
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      dki-india-ID_996981847
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      Concluído
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      13 August 2026
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