FOXH1, forkhead box H1, 8928

N. diseases: 67; N. variants: 3
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