|
OMIM |
Link |
Information
gain |
01 |
|
|
stomatocytosis ii
|
[NCBI]
|
0.00202368
|
|
|
|
splenic hypoplasia
|
[NCBI]
|
0.00202368
|
|
|
|
CDAN3
|
[NCBI]
|
0.00160371
|
|
|
|
stomatocytosis i
|
[NCBI]
|
0.0011173
|
|
|
|
CDAN2
|
[NCBI]
|
0.0011173
|
|
|
|
THC2
|
[NCBI]
|
0.000426283
|
|
|
|
HBB
|
[NCBI]
|
0.00015519
|
|
|
|
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to
|
[NCBI]
|
0.000120837
|
|
|
|
complement factor i deficiency
|
[NCBI]
|
0.000117986
|
|
|
|
WAS
|
[NCBI]
|
0.00011421
|
|
|
|
crigler-najjar syndrome, type ii
|
[NCBI]
|
0.000111108
|
|
|
|
erythrocytosis, familial, 2
|
[NCBI]
|
0.000109212
|
|
|
|
OPTB3
|
[NCBI]
|
0.000101568
|
|
|
|
OPTB1
|
[NCBI]
|
0.000101568
|
|
|
|
gilbert syndrome
|
[NCBI]
|
9.91127e-05
|
|
|
|
glycogen storage disease vii
|
[NCBI]
|
8.43063e-05
|
|
|
|
pyruvate kinase deficiency of red cells
|
[NCBI]
|
7.85038e-05
|
|
|
|
LNS
|
[NCBI]
|
7.58782e-05
|
|
|
|
G6PD
|
[NCBI]
|
7.58294e-05
|
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
6.24339e-05
|
|
|
|
diphosphoglycerate mutase deficiency of erythrocyte
|
[NCBI]
|
3.05451e-05
|
|
|
|
THY1
|
[NCBI]
|
2.88596e-05
|
|
|
|
CA2
|
[NCBI]
|
2.78131e-05
|
|
|
|
GZMA
|
[NCBI]
|
2.69387e-05
|
|
|
|
GZMB
|
[NCBI]
|
2.67408e-05
|
|
|
|
AK1
|
[NCBI]
|
2.52289e-05
|
|
|
|
anemia, sideroblastic, x-linked
|
[NCBI]
|
2.50846e-05
|
|
|
|
HS
|
[NCBI]
|
2.33924e-05
|
|
|
|
HBD
|
[NCBI]
|
2.15709e-05
|
|
|
|
HPRT1
|
[NCBI]
|
1.86158e-05
|
|
|
|
HBA2
|
[NCBI]
|
1.78034e-05
|
|
|
|
HBA1
|
[NCBI]
|
1.30624e-05
|
|
|
|
TNFSF6
|
[NCBI]
|
6.23481e-06
|
|
