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. 2010 May;6(2):91–97. doi: 10.2174/157340310791162703

Table 3.

Non-Syndromic CHD Resulting from Single Gene Defects

Cardiac Anomalies Gene
ASD, atrioventricular conduction delay, TOF, tricuspid valve abnormalities NKX2.5
ASD, VSD GATA4
ASD, hypertrophic cardiomyopathy MYH6
Cardiac septation defects associated with PHTN BMPR2
Endocardial cushion defects CRELD1, ALK2
BAV, early valve calcification NOTCH1
d-TGA PROSIT-240

ASD, atrial septal defect; TOF, tetralogy of Fallot; VSD, ventricular septal defect; TGA, transposition of the great arteries; BAV, bicuspid aortic valve; PHTN, pulmonary hypertension