FGFR2, fibroblast growth factor receptor 2, 2263

N. diseases: 93; N. variants: 98
Disease: Multiple congenital anomalies ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		0.400 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