|OBO ID: DOID:0090078|
|Term Name:||hypogonadotropic hypogonadism 7 with or without anosmia||Search Ontology:|
|Definition:||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. (2)|
|Ontology:||Human Disease (DOID:0090078)|
|is a type of:||
OTHER hypogonadotropic hypogonadism 7 with or without anosmia PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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