Symptom Information: Sort according to HPO 

1
 (HPO:0002024) Malabsorption Very frequent [Orphanet] 142 / 7739
2
 (HPO:0002570) Steatorrhea 31 / 7739
3
 (HPO:0002240) Hepatomegaly Very frequent [Orphanet] 467 / 7739
4
 (HPO:0001410) Decreased liver function Very frequent [Orphanet] 59 / 7739
5
 (HPO:0001394) Cirrhosis Frequent [Orphanet] 102 / 7739
6
 (HPO:0000952) Jaundice 105 / 7739
7
 (HPO:0001396) Cholestasis Very frequent [Orphanet] 136 / 7739
8
 (HPO:0100626) Chronic hepatic failure Frequent [Orphanet] 7 / 7739
9
 (HPO:0003010) Prolonged bleeding time Frequent [Orphanet] 88 / 7739
10
 (HPO:0001744) Splenomegaly Very frequent [Orphanet] 337 / 7739
11
 (HPO:0001399) Hepatic failure 80 / 7739
12
 (HPO:0001406) Intrahepatic cholestasis 16 / 7739
13
 (HPO:0001508) Failure to thrive 454 / 7739
14
 (HPO:0002014) Diarrhea 225 / 7739
15
 (HPO:0002904) Hyperbilirubinemia 32 / 7739
16
 (HPO:0002910) Elevated hepatic transaminases Very frequent [Orphanet] 158 / 7739
17
 (HPO:0003155) Elevated alkaline phosphatase 52 / 7739
18
 (HPO:0003256) Abnormality of the coagulation cascade 19 / 7739
19
 (HPO:0004349) Reduced bone mineral density Occasional [Orphanet] 165 / 7739
20
 (OMIM) Giant cell transformation on biopsy 1 / 7739
21
 (OMIM) Canalicular cholestasis 1 / 7739
22
 (OMIM) Hepatocyte necrosis 1 / 7739
23
 (OMIM) Liver failure before adulthood 1 / 7739
24
 (OMIM) Septal fibrosis 2 / 7739
25
 (OMIM) Malabsorption of fat and fat-soluble vitamins 7 / 7739
26
 (OMIM) Coagulopathy secondary to liver disease 4 / 7739
27
 (OMIM) Normal serum levels of gamma-GGT (231950) 2 / 7739
28
 (OMIM) Decreased or absent serum and urinary chenodeoxycholic acid and cholic acid 1 / 7739
29
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739
30
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739
31
 (HPO:0003623) Neonatal onset 22 / 7739