TCF7L1, transcription factor 7 like 1, 83439

N. diseases: 39; N. variants: 6
Disease: Congenital Abnormality ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.010 GeneticVariation group BEFREE Defects in the cardiovascular system in Tcf7l1-null mouse were considered secondary to mesoderm malformation. 30326964 2018