Hypogonadotropic hypogonadism 1 with or without anosmia

The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3.

Also known as: ANOS1 hypogonadotropic hypogonadism, hypogonadotropic hypogonadism 1 with or without anosmia, hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive, hypogonadotropic hypogonadism caused by mutation in ANOS1, HH1, KAL1, KMS, Kallmann syndrome 1

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