Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2248
Gene Symbol: FGF3
FGF3 		0.320 GeneticVariation disease BEFREE In addition, gene FGF3 haploinsufficiency was likely to be the cause of otodental syndrome. 28151902 2017
Entrez Id: 2248
Gene Symbol: FGF3
FGF3 		0.320 Biomarker disease BEFREE These data suggest that FGF3 haploinsufficiency is likely to be the cause of otodental syndrome. 17656375 2007
Entrez Id: 2248
Gene Symbol: FGF3
FGF3 		0.320 ChromosomalRearrangement disease ORPHANET These data suggest that FGF3 haploinsufficiency is likely to be the cause of otodental syndrome. 17656375 2007