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 		0.120 GeneticVariation disease BEFREE Our data suggest that, although the UFD1L gene is mapped to 22q11 and is expressed during early murine development at both cardiac and cranial neural crests, it is not responsible for the majority of tetralogy of Fallot cases in humans. 11485030 2001
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.120 Biomarker disease BEFREE The SRO in TF patients with del22q11 was at or close to the ADU breakpoint and centromeric to the UFD1L gene. 11455393 2001
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.120 Biomarker disease HPO