Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (Q89854): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
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 de 11-beta-hidroxilase. | |||
| 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 11-beta-hydroxylase deficiency. | |||
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 11-beta-hydroxylase deficiency.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_791376680 |
||
| English | Congenital adrenal hyperplasia due to 11-beta-hydroxylase 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 11-beta-hydroxylase deficiency. |
