About   Help   FAQ
Disease Ontology Browser
hypogonadotropic hypogonadism 12 with or without anosmia (DOID:0090072)
Alliance: disease page
Synonyms: familial hypogonadotrophic eunuchoidism; familial idiopathic gonadotrpin deficiency
Alt IDs: OMIM:614841, ICD10CM:E23.0
Definition: A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the GNRH1 gene on chromosome 8p21.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/15/2019
MGI 6.14
The Jackson Laboratory