Hypogonadotropic hypogonadism 7 with or without anosmia

A hypogonadotropic hypogonadism that has material basis in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported.

Also known as: hypogonadotropic hypogonadism 7 with or without anosmia, hypogonadotropic hypogonadism 7 without anosmia, HH7, hypogonadism, isolated hypogonadotropic, idiopathic hypogonadotropic hypogonadism

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