Isolated oxidative phosphorylation defects with variable phenotype, not elsewhere classified (Q102280): Difference between revisions

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description / pt-brdescription / pt-br
 
Refere-se à via metabólica isolada na qual as mitocôndrias nas células usam sua estrutura, enzimas e energia liberada pela oxidação de nutrientes para reformar o ATP. Este diagnóstico é com fenótipo variável, não classificado em outra parte.
description / endescription / en
 
This refers to isolated metabolic pathway in which the mitochondria in cells use their structure, enzymes, and energy released by the oxidation of nutrients to reform ATP. This diagnosis is with variable phenotype, not elsewhere classified.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/901344409 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_901344409
Property / CURIE: CID11:ID_901344409 / rank
 
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Property / Canary Token
 
dki-india-ID_901344409
Property / Canary Token: dki-india-ID_901344409 / rank
 
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Property / Verification Status
 
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
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 19:13, 16 August 2026

This refers to isolated metabolic pathway in which the mitochondria in cells use their structure, enzymes, and energy released by the oxidation of nutrients to reform ATP. This diagnosis is with variable phenotype, not elsewhere classified.
Language Label Description Also known as
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ID_901344409
    English
    Isolated oxidative phosphorylation defects with variable phenotype, not elsewhere classified
    This refers to isolated metabolic pathway in which the mitochondria in cells use their structure, enzymes, and energy released by the oxidation of nutrients to reform ATP. This diagnosis is with variable phenotype, not elsewhere classified.

      Statements

      CID11:ID_901344409
      0 references
      dki-india-ID_901344409
      0 references
      Concluído
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      15 August 2026
      0 references