|
OMIM |
Link |
Information gain |
01 |
|
DHS
|
[NCBI]
|
0.0026029
|
|
|
hematocrit/hemoglobin quantitative trait locus on chromosome 6
|
[NCBI]
|
0.00135014
|
|
|
pseudohyperkalemia, familial, 1, due to red cell leak
|
[NCBI]
|
0.000801832
|
|
|
stomatocytosis i
|
[NCBI]
|
0.000624978
|
|
|
restless legs syndrome, susceptibility to, 1
|
[NCBI]
|
0.000543053
|
|
|
EPO
|
[NCBI]
|
0.000339604
|
|
|
sickle cell anemia
|
[NCBI]
|
0.000169875
|
|
|
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema
|
[NCBI]
|
0.000129669
|
|
|
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type
|
[NCBI]
|
0.000122866
|
|
|
G6PD
|
[NCBI]
|
0.00011929
|
|
|
erythrocytosis, familial, 1
|
[NCBI]
|
9.73394e-05
|
|
|
HBFQTL1
|
[NCBI]
|
8.23432e-05
|
|
|
HBB
|
[NCBI]
|
5.12703e-05
|
|
|
thrombocytosis, familial x-linked
|
[NCBI]
|
5.03151e-05
|
|
|
SPTA1
|
[NCBI]
|
4.76877e-05
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
4.69748e-05
|
|
|
EPB72
|
[NCBI]
|
3.23914e-05
|
|
|
GPX1
|
[NCBI]
|
2.44711e-05
|
|
|
ALDH2
|
[NCBI]
|
2.26942e-05
|
|
|
HBD
|
[NCBI]
|
2.00326e-05
|
|
|
TF
|
[NCBI]
|
1.87037e-05
|
|
|
PAEP
|
[NCBI]
|
1.70055e-05
|
|
|
TPMT
|
[NCBI]
|
1.58659e-05
|
|
|
MG
|
[NCBI]
|
1.31522e-05
|
|
|
EPOR
|
[NCBI]
|
1.30794e-05
|
|
|
ACHE
|
[NCBI]
|
1.14955e-05
|
|
|
HBA1
|
[NCBI]
|
1.13031e-05
|
|
|
RA
|
[NCBI]
|
9.31273e-06
|
|
|
SLE
|
[NCBI]
|
9.07506e-06
|
|
|
ALB
|
[NCBI]
|
7.56674e-06
|
|
|
XDH
|
[NCBI]
|
6.17765e-06
|
|
|
ADA
|
[NCBI]
|
4.5479e-06
|
|
|
TYMS
|
[NCBI]
|
4.40423e-06
|
|
|
CF
|
[NCBI]
|
3.22026e-06
|
|
|
TNF
|
[NCBI]
|
1.83896e-06
|
|
|
PTH
|
[NCBI]
|
3.70451e-10
|
|