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 / en | description / 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. | |||
Revision as of 16:42, 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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_497412536 |
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| 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. |
