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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)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory