Term Name: hypogonadotropic hypogonadism 12 with or without anosmia
Synonyms: familial hypogonadotrophic eunuchoidism, familial idiopathic gonadotrpin deficiency
Definition: A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the GNRH1 gene on chromosome 8p21.
Ontology: Human Disease [DOID:0090072]   ( DOID:0090072 )

Relationships
is a type of: autosomal recessive disease hypogonadotropic hypogonadism