Anosmic congenital hypogonadotropic hypogonadism (Q106515): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 13:30, 17 August 2026
Anosmic congenital hypogonadotropic hypogonadism (Kallmann syndrome) is a congenital genetic disorder characterised by the association of hypogonadotropic hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1053735191 |
||
| English | Anosmic congenital hypogonadotropic hypogonadism |
Anosmic congenital hypogonadotropic hypogonadism (Kallmann syndrome) is a congenital genetic disorder characterised by the association of hypogonadotropic hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs). |
Statements
CID11:ID_1053735191
0 references
dki-india-ID_1053735191
0 references
Concluído
0 references
