Symptom Information: Sort according to HPO 

1
 (HPO:0001629) Ventricular septal defect rare [HPO:skoehler] 316 / 7739
2
 (HPO:0001631) Atria septal defect 274 / 7739
3
 (HPO:0001674) Complete atrioventricular canal defect 11 / 7739
4
 (HPO:0006695) Atrioventricular canal defect rare [HPO:skoehler] 27 / 7739
5
 (OMIM) Pulmonary valve thickening or stenosis 1 / 7739
6
 (OMIM) Cardiac valve insufficiency (in some patients) 1 / 7739
7
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739