Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23767
Gene Symbol: FLRT3
FLRT3
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
0.300 GermlineCausalMutation ORPHANET Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism. 23643382

2013