FOXC2, forkhead box C2, 2303

N. diseases: 168; N. variants: 18
Disease: Tetralogy of Fallot ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.400 Biomarker disease CTD_human Functionally significant, rare transcription factor variants in tetralogy of Fallot. 25093829 2014
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.400 Biomarker disease HPO