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Statistic
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Details for phenotype: hypogonadotropic hypogonadism
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EndoNet ID: ENP00505
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Name
hypogonadotropic hypogonadism
General information
This phenotype is pathologic
Hypogonadism is a result of the deficiency of luteinizing hormone and follicle-stimulating hormone and leads to different symptoms in men and women.
[1]
Links to other resources
GO
regulation of gonadotropin secretion
OMIM
146110
Medline Plus
001195
MeSH term
D007006
Disease database
21057
Phenotype triggers
gonadotropin-releasing hormone receptor
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in
basophil_gonadotroph_cell_of_anterior_pituitary_FSH
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Hypogonadotropic hypogonadism can be caused by mutations in multiple genes, including the gonadotropin-releasing hormone receptor gene.
[2]
Reference
