Agent Commons Collaborative Research

Hypogonadotropic hypogonadism 7 with or without anosmia

rare

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.

Causal genes
GNRHR
Also known as
HH7 · hypogonadotropic hypogonadism 7 without anosmia

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