|
OMIM |
Link |
Information
gain |
01 |
|
|
G6PD
|
[NCBI]
|
0.00275389
|
|
|
|
red cell phospholipid defect with hemolysis
|
[NCBI]
|
0.00267377
|
|
|
|
pyruvate kinase deficiency of red cells
|
[NCBI]
|
0.00183556
|
|
|
|
DHS
|
[NCBI]
|
0.00122189
|
|
|
|
adenosine triphosphatase deficiency, anemia due to
|
[NCBI]
|
0.00111789
|
|
|
|
PKLR
|
[NCBI]
|
0.000773549
|
|
|
|
hexokinase deficiency hemolytic anemia
|
[NCBI]
|
0.00064567
|
|
|
|
pseudohyperkalemia, familial, 1, due to red cell leak
|
[NCBI]
|
0.000625244
|
|
|
|
GPI
|
[NCBI]
|
0.000554341
|
|
|
|
stomatocytosis i
|
[NCBI]
|
0.0005041
|
|
|
|
glycogen storage disease vii
|
[NCBI]
|
0.000302006
|
|
|
|
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to
|
[NCBI]
|
0.000253857
|
|
|
|
TPI1
|
[NCBI]
|
0.000184495
|
|
|
|
gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to
|
[NCBI]
|
0.000182036
|
|
|
|
phosphoglycerate kinase 1 deficiency
|
[NCBI]
|
0.000156899
|
|
|
|
hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities
|
[NCBI]
|
0.000124742
|
|
|
|
diphosphoglycerate mutase deficiency of erythrocyte
|
[NCBI]
|
0.000121651
|
|
|
|
PGK1
|
[NCBI]
|
0.00010702
|
|
|
|
ALDOA
|
[NCBI]
|
9.59554e-05
|
|
|
|
ovalocytosis, hereditary hemolytic
|
[NCBI]
|
9.38016e-05
|
|
|
|
HBB
|
[NCBI]
|
9.27449e-05
|
|
|
|
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to
|
[NCBI]
|
8.42118e-05
|
|
|
|
cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly
|
[NCBI]
|
8.42118e-05
|
|
|
|
adenosine deaminase, elevated, hemolytic anemia due to
|
[NCBI]
|
7.59315e-05
|
|
|
|
AK1
|
[NCBI]
|
7.417e-05
|
|
|
|
hemoglobin--variants for which the chain carrying the mutation is unknown or uncertain
|
[NCBI]
|
7.0493e-05
|
|
|
|
HK1
|
[NCBI]
|
3.80326e-05
|
|
|
|
GPX1
|
[NCBI]
|
3.32139e-05
|
|
|
|
HBA1
|
[NCBI]
|
1.28023e-05
|
|
|
|
ADA
|
[NCBI]
|
5.94653e-07
|
|
