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hypogonadotropic hypogonadism 1 with or without anosmia (DOID:0090094)
Alliance: disease page
Synonyms: dysplasia olfactogenitalis of de morsier
Alt IDs: OMIM:308700, ICD10CM:E23.0
Definition: A hypogonadotropic hypogonadism that has_material_basis_in mutation in the KAL1 gene on chromosome Xp22.3, 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
03/19/2024
MGI 6.23
The Jackson Laboratory