FGF9, fibroblast growth factor 9, 2254

N. diseases: 153; N. variants: 2
Disease: Congenital abnormal Synostosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039093
Disease: Congenital abnormal Synostosis
Congenital abnormal Synostosis 		0.010 GeneticVariation disease BEFREE We have demonstrated for the first time that mutations in FGF9 cause craniosynostosis in humans and confirm that FGF9 mutations cause multiple synostoses. 28730625 2017