Hypogonadotropic hypogonadism 2 with or without anosmia

Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGFR1 gene.

Also known as: FGFR1 hypogonadotropic hypogonadism, hypogonadotropic hypogonadism 2 with or without anosmia, hypogonadotropic hypogonadism caused by mutation in FGFR1, HH2, KAL2, Kallmann syndrome 2

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