FGFR4, fibroblast growth factor receptor 4, 2264

N. diseases: 220; N. variants: 19
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0.010 GeneticVariation disease BEFREE Mutations in this domain of FGFR4 are unlikely to contribute significantly to craniosynostosis in humans. 9682222 1998