Symptom Information: Sort according to HPO 

1
 (HPO:0000072) Hydroureter Frequent [Orphanet] 146 / 7739
2
 (HPO:0000126) Hydronephrosis 119 / 7739
3
 (HPO:0001539) Omphalocele Occasional [Orphanet] 102 / 7739
4
 (HPO:0100806) Sepsis Occasional [Orphanet] 48 / 7739
5
 (HPO:0001561) Polyhydramnios Frequent [Orphanet] 191 / 7739
6
 (HPO:0004298) Abnormality of the abdominal wall Very frequent [Orphanet] 20 / 7739
7
 (HPO:0001537) Umbilical hernia Occasional [Orphanet] 206 / 7739
8
 (HPO:0100544) Neoplasm of the heart Occasional [Orphanet] 7 / 7739
9
 (HPO:0000110) Renal dysplasia 44 / 7739
10
 (HPO:0002017) Nausea and vomiting Very frequent [Orphanet] 134 / 7739
11
 (HPO:0002250) Abnormality of the large intestine Frequent [Orphanet] 32 / 7739
12
 (HPO:0100771) Hypoperistalsis 5 / 7739
13
 (HPO:0030680) Abnormality of cardiovascular system morphology Occasional [Orphanet] 355 / 7739
14
 (HPO:0002566) Intestinal malrotation Frequent [Orphanet] 89 / 7739
15
 (HPO:0004388) Microcolon 5 / 7739
16
 (HPO:0000021) Megacystis 7 / 7739
17
 (HPO:0001518) Small for gestational age 107 / 7739
18
 (HPO:0001562) Oligohydramnios 75 / 7739
19
 (HPO:0001791) Fetal ascites 4 / 7739
20
 (HPO:0002579) Gastrointestinal dysmotility Very frequent [Orphanet] 11 / 7739
21
 (HPO:0003270) Abdominal distention 46 / 7739
22
 (HPO:0009023) Abdominal wall muscle weakness 12 / 7739
23
 (HPO:0010956) Fetal megacystis 5 / 7739
24
 (OMIM) Microileum 1 / 7739
25
 (OMIM) Malrotation of the gut 2 / 7739
26
 (MedDRA:10049416) Short-bowel syndrome 2 / 7739
27
 (OMIM) Abundant intestinal ganglion cells 1 / 7739
28
 (HPO:0000035) Abnormality of the testis Occasional [Orphanet] 296 / 7739
29
 (HPO:0000107) Renal cyst Frequent [Orphanet] 126 / 7739
30
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739
31
 (HPO:0000079) Abnormality of the urinary system Very frequent [Orphanet] 88 / 7739
32
 (HPO:0012851) Colonic stenosis Very frequent [Orphanet] 3 / 7739
33
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739