Hypogonadotropic hypogonadism 6 with or without anosmia

Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGF8 gene.

Also known as: FGF8 hypogonadotropic hypogonadism, hypogonadotropic hypogonadism 6 with or without anosmia, hypogonadotropic hypogonadism caused by mutation in FGF8, KAL6, HH6, Kallmann syndrome 6

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