|
OMIM |
Link |
Information gain |
01 |
|
F3
|
[NCBI]
|
0.0023711
|
|
|
TFPI
|
[NCBI]
|
0.00121111
|
|
|
myeloproliferative syndrome, transient
|
[NCBI]
|
0.000892148
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
0.000342594
|
|
|
SLE
|
[NCBI]
|
0.000200327
|
|
|
PCI
|
[NCBI]
|
0.000142572
|
|
|
PLG
|
[NCBI]
|
0.000134022
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000131947
|
|
|
PF4
|
[NCBI]
|
9.1232e-05
|
|
|
respiratory distress syndrome in premature infants
|
[NCBI]
|
8.88018e-05
|
|
|
CPB2
|
[NCBI]
|
8.79648e-05
|
|
|
ALMS
|
[NCBI]
|
6.0147e-05
|
|
|
VTN
|
[NCBI]
|
5.58766e-05
|
|
|
CORT
|
[NCBI]
|
5.06841e-05
|
|
|
sickle cell anemia
|
[NCBI]
|
4.80374e-05
|
|
|
TNF
|
[NCBI]
|
4.71677e-05
|
|
|
IFNA2
|
[NCBI]
|
4.28199e-05
|
|
|
PAI1
|
[NCBI]
|
2.70052e-05
|
|
|
VEGF
|
[NCBI]
|
2.56362e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
2.40116e-05
|
|
|
GIST
|
[NCBI]
|
2.15747e-05
|
|
|
RA
|
[NCBI]
|
2.03048e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
1.88628e-05
|
|
|
FGA
|
[NCBI]
|
1.84378e-05
|
|
|
factor v deficiency
|
[NCBI]
|
1.72744e-05
|
|
|
antithrombin iii deficiency
|
[NCBI]
|
1.50518e-05
|
|
|
SPINK1
|
[NCBI]
|
1.09326e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
9.31249e-06
|
|
|
KLK3
|
[NCBI]
|
4.89501e-06
|
|
|
GNRH1
|
[NCBI]
|
4.82519e-06
|
|
|
AVP
|
[NCBI]
|
1.27229e-06
|
|
|
HGF
|
[NCBI]
|
1.19037e-06
|
|