hypogonadotropic hypogonadism 5 with or without anosmia Disease Ontology Browser

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Disease Ontology Browser

hypogonadotropic hypogonadism 5 with or without anosmia (DOID:0090084)
Alliance: disease page
Alt IDs: OMIM:612370, ICD10CM:E23.0
Definition: A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the CHD7 gene on chromosome 8q12.

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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