Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency (Q89851): Difference between revisions

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Refere-se a qualquer uma das várias doenças autossômicas recessivas resultantes de mutações de genes para enzimas que medeiam as etapas bioquímicas de produção de cortisol a partir do colesterol pelas glândulas adrenais (esteroidogênese). Este diagnóstico é devido à deficiência da citocromo P450 oxidoredutase.
description / endescription / en
 
This refers to any of several autosomal recessive diseases resulting from mutations of genes for enzymes mediating the biochemical steps of production of cortisol from cholesterol by the adrenal glands (steroidogenesis). This diagnosis is due to cytochrome P450 oxidoreductase deficiency.
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Property / Canonical URI: https://id.who.int/icd/entity/497412536 / rank
 
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CID11:ID_497412536
Property / CURIE: CID11:ID_497412536 / rank
 
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dki-india-ID_497412536
Property / Canary Token: dki-india-ID_497412536 / 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
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 16:43, 15 August 2026

This refers to any of several autosomal recessive diseases resulting from mutations of genes for enzymes mediating the biochemical steps of production of cortisol from cholesterol by the adrenal glands (steroidogenesis). This diagnosis is due to cytochrome P450 oxidoreductase deficiency.
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ID_497412536
    English
    Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
    This refers to any of several autosomal recessive diseases resulting from mutations of genes for enzymes mediating the biochemical steps of production of cortisol from cholesterol by the adrenal glands (steroidogenesis). This diagnosis is due to cytochrome P450 oxidoreductase deficiency.

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      CID11:ID_497412536
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      dki-india-ID_497412536
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      Concluído
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      13 August 2026
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