FGFR2, fibroblast growth factor receptor 2, 2263

N. diseases: 93; N. variants: 98
Disease: Craniofacial Abnormalities ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.320 Biomarker group CTD_human [Genetic origin of non-syndromic cleft lip and palate. TWIST, a candidate gene? Research protocol]. 18082115 2007
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.320 Biomarker group CTD_human Syndromic craniosynostosis with elbow joint contracture. 16465081 2006
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.320 Biomarker group 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