Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, classic form, simple virilizing (Q107757): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_2008316472 | |||
| Property / CURIE: CID11:ID_2008316472 / rank | |||
Normal rank | |||
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, simply virilizing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2008316472 |
||
| English | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, classic form, simple virilizing |
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, simply virilizing. |
Statements
CID11:ID_2008316472
0 references
