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Summary Literature (2)
DOID:3614 - Kallmann syndrome


Disease Ontology Definition:A hypogonadotropic hypogonadism with a defective sense of smell (anosmia or hyposmia).

Synonyms: Hypogonadism with anosmia, Hypogonadism with anosmia (disorder), Kallman syndrome, Kallman's syndrome, familial hypogonadism with anosmia


In Mondo Disease Ontology:
MONDO:0018800 - Kallmann syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : sox10, spry4, fgf8, il17rd, hesx1, anos1, prokr2, flrt3, prok2, dcc, chd7, hs6st1, sema3a, dusp6, tacr3, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hypogonadotropic hypogonadism (is_a)