Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2253
Gene Symbol: FGF8
FGF8
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.560 GermlineCausalMutation ORPHANET Nonsense mutations in FGF8 gene causing different degrees of human gonadotropin-releasing deficiency. 20463092

2010
Entrez Id: 2253
Gene Symbol: FGF8
FGF8
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.560 GermlineCausalMutation ORPHANET Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice. 18596921

2008