Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6870
Gene Symbol: TACR3
TACR3
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.500 GermlineCausalMutation ORPHANET Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism. 23643382

2013
Entrez Id: 6870
Gene Symbol: TACR3
TACR3
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.500 GermlineCausalMutation ORPHANET TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction. 19079066

2009