hypogonadotropic hypogonadism 12 with or without anosmia

Summary

DOID:0090072 - hypogonadotropic hypogonadism 12 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the GNRH1 gene on chromosome 8p21.

Synonyms: familial hypogonadotrophic eunuchoidism, familial idiopathic gonadotrpin deficiency

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gnrh1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013914 - hypogonadotropic hypogonadism 12 with or without anosmia

MONDO:0013914 - hypogonadotropic hypogonadism 12 with or without anosmia

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), hypogonadotropic hypogonadism (is_a)