Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2248
Gene Symbol: FGF3
FGF3
CUI: C0000846
Disease: Agenesis
Agenesis 		0.020 GeneticVariation BEFREE Homozygous mutations in the fibroblast growth factor 3 (FGF3) gene have recently been discovered in an autosomal recessive form of syndromic deafness characterized by complete labyrinthine aplasia (Michel aplasia), microtia, and microdontia (OMIM 610706 - LAMM). 18435799

2008
Entrez Id: 2248
Gene Symbol: FGF3
FGF3
CUI: C0000846
Disease: Agenesis
Agenesis 		0.020 GeneticVariation BEFREE Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia. 17236138

2007