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Disease Ontology Browser
hypogonadotropic hypogonadism 18 with or without anosmia (DOID:0090076)
Alliance: disease page
Alt IDs: OMIM:615267, ICD10CM:E23.0
Definition: A hypogonadotropic hypogonadism that has_material_basis_in heterozygous or homozygous mutation in the IL17RD gene on chromosome 3p14, sometimes in association with mutation in other genes.


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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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory