Symptom Information: Sort according to HPO 

1
(HPO:0011902) Abnormal hemoglobin Very frequent [Orphanet] 18 / 7739
2
(HPO:0001971) Hypersplenism Occasional [Orphanet] 8 / 7739
3
(HPO:0001878) Hemolytic anemia Occasional [Orphanet] 83 / 7739
4
(HPO:0002863) Myelodysplasia Occasional [Orphanet] 30 / 7739
5
(HPO:0001903) Anemia Occasional [Orphanet] 289 / 7739
6
(HPO:0001744) Splenomegaly Occasional [Orphanet] 337 / 7739
7
(HPO:0001789) Hydrops fetalis Occasional [Orphanet] 63 / 7739
8
(HPO:0001396) Cholestasis Occasional [Orphanet] 136 / 7739
9
(HPO:0001935) Microcytic anemia Very frequent [Orphanet] 32 / 7739
10
(HPO:0004840) Hypochromic microcytic anemia 15 / 7739
11
(HPO:0010978) Abnormality of immune system physiology Occasional [Orphanet] 148 / 7739
12
(HPO:0011907) Reduced alpha/beta synthesis ratio 6 / 7739
13
(HPO:0012758) Neurodevelopmental delay Occasional [Orphanet] 949 / 7739
14
(HPO:0012437) Abnormal gallbladder morphology Occasional [Orphanet] 17 / 7739