Symptom Information: Sort according to HPO 

1
(HPO:0000964) Eczema Occasional [Orphanet] 81 / 7739
2
(HPO:0000969) Edema Occasional [Orphanet] 117 / 7739
3
(HPO:0000992) Cutaneous photosensitivity Very frequent [Orphanet] 75 / 7739
4
(HPO:0001025) Urticaria Very frequent [Orphanet] 73 / 7739
5
(HPO:0001394) Cirrhosis Occasional [Orphanet] 102 / 7739
6
(HPO:0001935) Microcytic anemia Occasional [Orphanet] 32 / 7739
7
(HPO:0010783) Erythema Very frequent [Orphanet] 138 / 7739
8
(HPO:0012437) Abnormal gallbladder morphology Occasional [Orphanet] 17 / 7739
9
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
10
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
11
(HPO:0000989) Pruritus 111 / 7739
12
(HPO:0001081) Cholelithiasis 36 / 7739
13
(HPO:0001399) Hepatic failure 80 / 7739
14
(HPO:0001878) Hemolytic anemia 83 / 7739
15
(HPO:0002155) Hypertriglyceridemia 67 / 7739
16
(HPO:0011463) Childhood onset 65 / 7739