|
OMIM |
Link |
Information gain |
01 |
|
scott syndrome
|
[NCBI]
|
0.00401727
|
|
|
bleeding disorder, east texas type
|
[NCBI]
|
0.00226391
|
|
|
thrombasthenia-thrombocytopenia, hereditary
|
[NCBI]
|
0.00174151
|
|
|
ASD1
|
[NCBI]
|
0.00174151
|
|
|
F3
|
[NCBI]
|
0.00173016
|
|
|
xm system
|
[NCBI]
|
0.00154489
|
|
|
SLE
|
[NCBI]
|
0.00147834
|
|
|
QPD
|
[NCBI]
|
0.00124792
|
|
|
PF4
|
[NCBI]
|
0.00110397
|
|
|
storage pool platelet disease
|
[NCBI]
|
0.00100792
|
|
|
PROCR
|
[NCBI]
|
0.000845632
|
|
|
GPS
|
[NCBI]
|
0.000730847
|
|
|
TFPI
|
[NCBI]
|
0.000604848
|
|
|
factor xii deficiency
|
[NCBI]
|
0.000467659
|
|
|
pseudo-von willebrand disease
|
[NCBI]
|
0.000308993
|
|
|
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency
|
[NCBI]
|
0.000286067
|
|
|
glanzmann thrombasthenia, autosomal dominant
|
[NCBI]
|
0.000286067
|
|
|
von willebrand disease
|
[NCBI]
|
0.000252179
|
|
|
RA
|
[NCBI]
|
0.000235821
|
|
|
vitamin k-dependent clotting factors, combined deficiency of, 2
|
[NCBI]
|
0.00022297
|
|
|
giant platelet syndrome
|
[NCBI]
|
0.000189879
|
|
|
prekallikrein deficiency
|
[NCBI]
|
0.00018196
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
0.000170592
|
|
|
coumarin resistance
|
[NCBI]
|
0.000149288
|
|
|
factor v and factor viii, combined deficiency of, with normal protein c and protein c inhibitor
|
[NCBI]
|
0.000142938
|
|
|
TTP
|
[NCBI]
|
0.000130127
|
|
|
PLG
|
[NCBI]
|
0.000127334
|
|
|
factors viii, ix and xi, combined deficiency of
|
[NCBI]
|
0.00011139
|
|
|
passovoy factor
|
[NCBI]
|
0.00011139
|
|
|
HPS
|
[NCBI]
|
0.000109518
|
|
|
flaujeac factor deficiency
|
[NCBI]
|
9.98101e-05
|
|
|
factor x deficiency
|
[NCBI]
|
8.9147e-05
|
|
|
F12
|
[NCBI]
|
8.38884e-05
|
|
|
PCI
|
[NCBI]
|
8.05846e-05
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
7.67958e-05
|
|
|
antiphospholipid syndrome
|
[NCBI]
|
6.92433e-05
|
|
|
THC2
|
[NCBI]
|
6.70036e-05
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
6.70036e-05
|
|
|
afibrinogenemia, congenital
|
[NCBI]
|
6.49719e-05
|
|
|
plasminogen deficiency, type i
|
[NCBI]
|
6.49719e-05
|
|
|
GGCX
|
[NCBI]
|
6.31514e-05
|
|
|
vitamin k-dependent clotting factors, combined deficiency of, 1
|
[NCBI]
|
6.31136e-05
|
|
|
COH1
|
[NCBI]
|
6.14018e-05
|
|
|
PPH1
|
[NCBI]
|
5.69558e-05
|
|
|
complement factor h deficiency
|
[NCBI]
|
5.56575e-05
|
|
|
PROS1
|
[NCBI]
|
4.82825e-05
|
|
|
diabetes insipidus, nephrogenic, x-linked
|
[NCBI]
|
4.74197e-05
|
|
|
factor vii deficiency
|
[NCBI]
|
4.64046e-05
|
|
|
VKORC1
|
[NCBI]
|
4.62529e-05
|
|
|
PROZ
|
[NCBI]
|
4.48217e-05
|
|
|
F13A1
|
[NCBI]
|
4.21143e-05
|
|
|
homocysteinemia
|
[NCBI]
|
4.15441e-05
|
|
|
CJD
|
[NCBI]
|
3.93473e-05
|
|
|
aHUS
|
[NCBI]
|
3.85883e-05
|
|
|
THBD
|
[NCBI]
|
3.81221e-05
|
|
|
FGA
|
[NCBI]
|
3.62199e-05
|
|
|
PLAT
|
[NCBI]
|
3.31514e-05
|
|
|
CPB2
|
[NCBI]
|
3.2287e-05
|
|
|
hemophilia a
|
[NCBI]
|
2.58574e-05
|
|
|
ews/fli1-activated transcript 2
|
[NCBI]
|
2.49315e-05
|
|
|
STATH
|
[NCBI]
|
2.49315e-05
|
|
|
AD
|
[NCBI]
|
2.45519e-05
|
|
|
SPINT2
|
[NCBI]
|
2.31195e-05
|
|
|
F2R
|
[NCBI]
|
2.08036e-05
|
|
|
factor v deficiency
|
[NCBI]
|
2.05509e-05
|
|
|
RPL29
|
[NCBI]
|
1.98142e-05
|
|
|
MMRN1
|
[NCBI]
|
1.90541e-05
|
|
|
HTN3
|
[NCBI]
|
1.78019e-05
|
|
|
F13B
|
[NCBI]
|
1.59492e-05
|
|
|
PXE
|
[NCBI]
|
1.56753e-05
|
|
|
pta deficiency
|
[NCBI]
|
1.3281e-05
|
|
|
EPO
|
[NCBI]
|
1.2991e-05
|
|
|
HEMB
|
[NCBI]
|
1.234e-05
|
|
|
PAI1
|
[NCBI]
|
1.06586e-05
|
|
|
VEGF
|
[NCBI]
|
1.03301e-05
|
|
|
EGF
|
[NCBI]
|
9.83177e-06
|
|
|
MST1
|
[NCBI]
|
9.79503e-06
|
|
|
HLA-DRA
|
[NCBI]
|
9.79503e-06
|
|
|
MPO
|
[NCBI]
|
9.7616e-06
|
|
|
AVP
|
[NCBI]
|
9.52325e-06
|
|
|
AFP
|
[NCBI]
|
8.47589e-06
|
|
|
MMP9
|
[NCBI]
|
8.1121e-06
|
|
|
ALB
|
[NCBI]
|
7.97745e-06
|
|
|
HGF
|
[NCBI]
|
7.49828e-06
|
|
|
STAT6
|
[NCBI]
|
6.39339e-06
|
|
|
GFAP
|
[NCBI]
|
6.34249e-06
|
|
|
HRG
|
[NCBI]
|
6.14009e-06
|
|
|
GH1
|
[NCBI]
|
5.46459e-06
|
|
|
CFH
|
[NCBI]
|
4.82032e-06
|
|
|
antithrombin iii deficiency
|
[NCBI]
|
4.78572e-06
|
|
|
HMBS
|
[NCBI]
|
3.70111e-06
|
|
|
AGER
|
[NCBI]
|
3.43769e-06
|
|
|
IL6
|
[NCBI]
|
3.21658e-06
|
|
|
temporal arteritis
|
[NCBI]
|
2.86556e-06
|
|
|
GRP
|
[NCBI]
|
2.48974e-06
|
|
|
MBP
|
[NCBI]
|
2.30506e-06
|
|
|
APOE
|
[NCBI]
|
2.29825e-06
|
|
|
TNF
|
[NCBI]
|
1.8002e-06
|
|
|
SERPINA6
|
[NCBI]
|
1.51366e-06
|
|
|
SDC2
|
[NCBI]
|
1.49316e-06
|
|
|
LRP1
|
[NCBI]
|
1.04223e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
8.00522e-07
|
|
|
APOB
|
[NCBI]
|
5.08588e-07
|
|
|
SHBG
|
[NCBI]
|
4.15389e-07
|
|
|
RNASE3
|
[NCBI]
|
2.97376e-07
|
|
|
TNFRSF11B
|
[NCBI]
|
1.35583e-07
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
1.33519e-07
|
|
|
XDH
|
[NCBI]
|
1.14169e-07
|
|
|
CTGF
|
[NCBI]
|
1.12761e-07
|
|
|
TLR4
|
[NCBI]
|
5.4684e-08
|
|