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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)
