Symptom Information: Sort according to HPO 

1
(HPO:0001530) Mild postnatal growth retardation 7 / 7739
2
(HPO:0001789) Hydrops fetalis 63 / 7739
3
(HPO:0003352) Endopolyploidy on chromosome studies of bone marrow 2 / 7739
4
(HPO:0003655) Reduced activity of N-acetylglucosaminyltransferase II 2 / 7739
5
(HPO:0005532) Macrocytic dyserythropoietic anemia 1 / 7739
6
(HPO:0006579) Prolonged neonatal jaundice 25 / 7739
7
(OMIM) Moderate growth retardation 1 / 7739
8
(OMIM) Megaloblastoid erythroblasts with nuclear chromatin bridges 1 / 7739
9
(HPO:0010972) Anemia of inadequate production 10 / 7739
10
(OMIM) Gaucher-like bone marrow histiocytes 1 / 7739
11
(OMIM) Mild hemochromatosis 1 / 7739
12
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
13
(HPO:0001159) Syndactyly rare [HPO:skoehler] 140 / 7739
14
(HPO:0001744) Splenomegaly 337 / 7739
15
(HPO:0001923) Reticulocytosis 28 / 7739
16
(HPO:0004447) Poikilocytosis 16 / 7739
17
(HPO:0011273) Anisocytosis 8 / 7739
18
(HPO:0012132) Erythroid hyperplasia 4 / 7739