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Summary Literature (0)
DOID:3614 - Kallmann syndrome

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

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

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

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018800 - Kallmann syndrome


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

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