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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory