46,XY disorder of sex development due to isolated 17, 20 lyase deficiency (Q91110): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_513865687 | |||
| Property / CURIE: CID11:ID_513865687 / rank | |||
Normal rank | |||
Revision as of 18:06, 15 August 2026
This refers to disorder of sex development due to a rare endocrine and autosomal recessive genetic disorder which is characterised by a complete or partial loss of 17,20-lyase activity and, in turn, impaired production of the androgen and estrogen sex steroids.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_513865687 |
||
| English | 46,XY disorder of sex development due to isolated 17, 20 lyase deficiency |
This refers to disorder of sex development due to a rare endocrine and autosomal recessive genetic disorder which is characterised by a complete or partial loss of 17,20-lyase activity and, in turn, impaired production of the androgen and estrogen sex steroids. |
Statements
CID11:ID_513865687
0 references
