Normosmic congenital hypogonadotropic hypogonadism (Q106516): Difference between revisions
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Revision as of 13:30, 17 August 2026
This is a normosmic congenital condition which is characterised by hypogonadism due to an impaired secretion of gonadotropins, including follicle-stimulating hormone (FSH) and luteinizing hormone (LH), by the pituitary gland in the brain, and in turn decreased gonadotropin levels and a resultant lack of sex steroid production.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1675702254 |
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| English | Normosmic congenital hypogonadotropic hypogonadism |
This is a normosmic congenital condition which is characterised by hypogonadism due to an impaired secretion of gonadotropins, including follicle-stimulating hormone (FSH) and luteinizing hormone (LH), by the pituitary gland in the brain, and in turn decreased gonadotropin levels and a resultant lack of sex steroid production. |
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CID11:ID_1675702254
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