|
1
|
(HPO:0000952)
|
Jaundice |
|
|
|
|
105 / 7739
|
|
2
|
(HPO:0001081)
|
Cholelithiasis |
|
|
|
|
36 / 7739
|
|
3
|
(HPO:0001744)
|
Splenomegaly |
|
|
|
|
337 / 7739
|
|
4
|
(HPO:0001923)
|
Reticulocytosis |
|
|
|
|
28 / 7739
|
|
5
|
(HPO:0003352)
|
Endopolyploidy on chromosome studies of bone marrow |
|
|
|
|
2 / 7739
|
|
6
|
(HPO:0003655)
|
Reduced activity of N-acetylglucosaminyltransferase II |
|
|
|
|
2 / 7739
|
|
7
|
(HPO:0010972)
|
Anemia of inadequate production |
|
|
|
|
10 / 7739
|
|
8
|
(HPO:0001903)
|
Anemia |
|
|
|
|
289 / 7739
|
|
9
|
(HPO:0001878)
|
Hemolytic anemia |
|
|
|
|
83 / 7739
|
|
10
|
(OMIM)
|
Erythroblast morphologic abnormalities |
|
|
|
|
1 / 7739
|
|
11
|
(OMIM)
|
Multinucleated erythroblasts |
|
|
|
|
1 / 7739
|
|
12
|
(OMIM)
|
Osmotic fragility of red blood cells |
|
|
|
|
1 / 7739
|
|
13
|
(OMIM)
|
Hypoglycosylation of red blood cell membranes |
|
|
|
|
1 / 7739
|
|
14
|
(OMIM)
|
Increased serum unconjugated bilirubin |
|
|
|
|
1 / 7739
|
|
15
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|