Hypogonadotropic hypogonadism 12 with or without anosmia

A hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21.

Also known as: eunuchoidism, familial hypogonadotropic, hypogonadotropic hypogonadism 12 with or without anosmia, FIGD, HH12, eunuchoidism familial hypogonadotropic, familial hypogonadotropic eunuchoidism, gonadotropin deficiency familial idiopathic, gonadotropin deficiency, familial idiopathic

0 clinical trials for this condition and its sub-types, 0 tagged with Hypogonadotropic hypogonadism 12 with or without anosmia itself.