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Up to: Syndromic disease · Hypogonadotropic hypogonadism

Kallmann syndrome

Kallmann syndrome (KS) is a developmental genetic disorder characterized by the association of congenital hypogonadotropic hypogonadism (CHH) due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs).

3 trials tagged with this condition →

Hypogonadotropic hypogonadism 1 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 11 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 14 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 15 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 16 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 17 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 18 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 19 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 2 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 20 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 21 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 22 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 3 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 4 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 5 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 6 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 8 with or without anosmia 0 trials
Hypogonadotropic hypogonadism 9 with or without anosmia 0 trials