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Up to: Congenital hypogonadotropic hypogonadism
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.
This condition has no sub-types.