Symptom Information: Sort according to HPO 

1
(HPO:0000952) Jaundice 105 / 7739
2
(HPO:0001744) Splenomegaly 337 / 7739
3
(HPO:0001923) Reticulocytosis 28 / 7739
4
(HPO:0002240) Hepatomegaly rare [HPO:skoehler] 467 / 7739
5
(HPO:0002904) Hyperbilirubinemia 32 / 7739
6
(HPO:0010972) Anemia of inadequate production 10 / 7739
7
(OMIM) Increased iron deposition seen on liver biopsy 2 / 7739
8
(OMIM) Anemia, mild 6 / 7739
9
(OMIM) Hypercellular bone marrow with erythroid hyperplasia 1 / 7739
10
(OMIM) Normal peripheral red blood cell survival time 1 / 7739
11
(HPO:0008282) Unconjugated hyperbilirubinemia 9 / 7739
12
(OMIM) Increased excretion of urobilinogen 1 / 7739
13
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
14
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739