Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, classic form, salt wasting (Q107753): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Isso se refere 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 supra-renais (esteroidogênese). Este diagnóstico é devido à deficiência da 21 -hidroxilase, forma clássica, perdedora de sal
@@ 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 21-hydroxylase deficiency, classic form, salt wasting.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1057771841
@@ Property / Canonical URI: https://id.who.int/icd/entity/1057771841 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1057771841
@@ Property / CURIE: CID11:ID_1057771841 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1057771841
@@ Property / Canary Token: dki-india-ID_1057771841 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-16T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-16T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 16 August 2026 / rank @@
+Normal rank

Latest revision as of 14:47, 17 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 21-hydroxylase deficiency, classic form, salt wasting.

Language	Label	Description	Also known as
default for all languages	ID_1057771841
English	Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, classic form, salt wasting	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 21-hydroxylase deficiency, classic form, salt wasting.