|
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,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:614841 - hypogonadotropic hypogonadism 12 with or without anosmia; hh12 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypogonadotropic hypogonadism (is_a)