Kallmann syndrome
MONDO:0018800Kallmann 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
3 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Hypogonadotropic hypogonadism 11 with or without anosmia
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Hypogonadotropic hypogonadism 14 with or without anosmia
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Hypogonadotropic hypogonadism 15 with or without anosmia
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Hypogonadotropic hypogonadism 16 with or without anosmia
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Hypogonadotropic hypogonadism 17 with or without anosmia
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Hypogonadotropic hypogonadism 18 with or without anosmia
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Hypogonadotropic hypogonadism 19 with or without anosmia
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Hypogonadotropic hypogonadism 1 with or without anosmia
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Hypogonadotropic hypogonadism 20 with or without anosmia
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Hypogonadotropic hypogonadism 21 with or without anosmia
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Hypogonadotropic hypogonadism 22 with or without anosmia
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Hypogonadotropic hypogonadism 2 with or without anosmia
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Hypogonadotropic hypogonadism 3 with or without anosmia
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Hypogonadotropic hypogonadism 4 with or without anosmia
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Hypogonadotropic hypogonadism 5 with or without anosmia
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Hypogonadotropic hypogonadism 6 with or without anosmia
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Hypogonadotropic hypogonadism 8 with or without anosmia
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Hypogonadotropic hypogonadism 9 with or without anosmia
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