Kallmann syndrome

MONDO:0018800

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).

Also known as: Olfacto-genital pathological sequence, congenital hypogonadotropic hypogonadism with anosmia, hypogonadotropic hypogonadism with anosmia

9 clinical trials for this condition and its sub-types.

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