Symptom Information: Sort according to HPO 

1
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
2
(HPO:0001629) Ventricular septal defect 316 / 7739
3
(HPO:0001631) Atria septal defect rare [HPO:skoehler] 274 / 7739
4
(HPO:0001642) Pulmonic stenosis rare [HPO:skoehler] 89 / 7739