has material basis in germline mutation in GNRHR hypogonadotropic hypogonadism 7 with or without anosmia https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/hypogonadotropic_hypogonadism_7_with_or_without_anosmia UMLS:C0342384 MONDO:0007794 OMIM:146110 NANDO:1200382 HH7 MEDGEN:87440 idiopathic hypogonadotropic hypogonadism GARD:0002897 MESH:C562785 SCTID:123953004 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. DOID:0090078 hypogonadism, isolated hypogonadotropic hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 7 without anosmia ICD9:253.4 congenital hypogonadotropic hypogonadism