hypogonadotropic hypogonadism 17 with or without anosmia Disease Ontology Browser

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Disease Ontology Browser

hypogonadotropic hypogonadism 17 with or without anosmia (DOID:0090079)
Alliance: disease page
Alt IDs: OMIM:615266, ICD10CM:E23.0
Definition: A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the SPRY4 gene on chromosome 5q31, sometimes in association with mutations 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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