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Summary Literature (0)
DOID:0090080 - hypogonadotropic hypogonadism 16 with or without anosmia

Disease Ontology Definition:A hypogonadotropic hypogonadism that has_material_basis_in mutation in the SEMA3A gene on chromosome 7, sometimes in association with mutations in other genes.

Synonyms:

Xenbase Genes : sema3a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013961 - hypogonadotropic hypogonadism 16 with or without anosmia


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), hypogonadotropic hypogonadism (is_a)