Symptom Information: Sort according to HPO 

1
(HPO:0001321) Cerebellar hypoplasia 114 / 7739
2
(HPO:0001631) Atria septal defect 274 / 7739
3
(HPO:0001636) Tetralogy of Fallot 104 / 7739
4
(HPO:0001696) Situs inversus totalis 44 / 7739
5
(HPO:0002132) Porencephaly 18 / 7739
6
(HPO:0002335) Agenesis of cerebellar vermis 25 / 7739
7
(OMIM) Bilateral porencephaly 1 / 7739
8
(OMIM) Absent vermis 1 / 7739
9
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739