Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.320 Biomarker CTD_human [Genetic origin of non-syndromic cleft lip and palate. TWIST, a candidate gene? Research protocol]. 18082115

2007
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.320 Biomarker CTD_human Syndromic craniosynostosis with elbow joint contracture. 16465081

2006
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.320 Biomarker CTD_human An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis. 10631169

2000