Symptom Information: Sort according to HPO 

1
(HPO:0001669) Transposition of the great arteries Very frequent [Orphanet] 36 / 7739
2
(HPO:0001643) Patent ductus arteriosus Frequent [Orphanet] 228 / 7739
3
(HPO:0001636) Tetralogy of Fallot Very frequent [Orphanet] 104 / 7739
4
(HPO:0001660) Truncus arteriosus 21 / 7739
5
(HPO:0001719) Double outlet right ventricle 12 / 7739
6
(HPO:0001939) Abnormality of metabolism/homeostasis 328 / 7739
7
(HPO:0004414) Abnormality of the pulmonary artery Frequent [Orphanet] 50 / 7739
8
(OMIM) Conotruncal malformations 3 / 7739
9
(OMIM) Frequent microdeletions of 22q11.2 3 / 7739
10
(HPO:0012303) Abnormality of the aortic arch Frequent [Orphanet] 57 / 7739
11
(HPO:0003220) Abnormality of chromosome stability Frequent [Orphanet] 98 / 7739
12
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
13
(HPO:0000316) Hypertelorism rare [HPO:skoehler] 644 / 7739
14
(HPO:0001674) Complete atrioventricular canal defect 11 / 7739
15
(HPO:0001680) Coarctation of aorta 57 / 7739
16
(HPO:0010055) Broad hallux 56 / 7739
17
(HPO:0100259) Postaxial polydactyly 85 / 7739