Anosmic congenital hypogonadotropic hypogonadism (Q106515): Difference between revisions
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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).
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| 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). |
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CID11:ID_1053735191
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dki-india-ID_1053735191
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