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Disease Ontology Browser
hypogonadotropic hypogonadism 9 with or without anosmia (DOID:0090085)
Alliance: disease page
Alt IDs: OMIM:614838, ICD10CM:E23.0
Definition: A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the NELF gene on chromosome 9q34, sometimes in association with mutation in another gene.


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
02/18/2020
MGI 6.14
The Jackson Laboratory