FGF3, fibroblast growth factor 3, 2248

N. diseases: 200; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1833693
Disease: Otodental Dysplasia
Otodental Dysplasia
0.320 GeneticVariation disease BEFREE In addition, gene FGF3 haploinsufficiency was likely to be the cause of otodental syndrome. 28151902 2017
CUI: C1833693
Disease: Otodental Dysplasia
Otodental Dysplasia
0.320 Biomarker disease BEFREE These data suggest that FGF3 haploinsufficiency is likely to be the cause of otodental syndrome. 17656375 2007
CUI: C1833693
Disease: Otodental Dysplasia
Otodental Dysplasia
0.320 ChromosomalRearrangement disease ORPHANET These data suggest that FGF3 haploinsufficiency is likely to be the cause of otodental syndrome. 17656375 2007