|
OMIM |
Link |
Information gain |
01 |
|
scott syndrome
|
[NCBI]
|
0.00539188
|
|
|
FGA
|
[NCBI]
|
0.00148615
|
|
|
thrombasthenia-thrombocytopenia, hereditary
|
[NCBI]
|
0.00078076
|
|
|
FGG
|
[NCBI]
|
0.000710277
|
|
|
prekallikrein deficiency
|
[NCBI]
|
0.000677273
|
|
|
storage pool platelet disease
|
[NCBI]
|
0.000555363
|
|
|
F3
|
[NCBI]
|
0.000489025
|
|
|
F2
|
[NCBI]
|
0.000422113
|
|
|
GPS
|
[NCBI]
|
0.000395833
|
|
|
giant platelet syndrome
|
[NCBI]
|
0.000378648
|
|
|
PEE1
|
[NCBI]
|
0.00035536
|
|
|
F13A1
|
[NCBI]
|
0.000333636
|
|
|
flaujeac factor deficiency
|
[NCBI]
|
0.000305365
|
|
|
factor xii deficiency
|
[NCBI]
|
0.000298871
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
0.000275353
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
0.000245441
|
|
|
factor v deficiency
|
[NCBI]
|
0.000233172
|
|
|
factor x deficiency
|
[NCBI]
|
0.000225084
|
|
|
vitamin k-dependent clotting factors, combined deficiency of, 1
|
[NCBI]
|
0.00022187
|
|
|
antithrombin iii deficiency
|
[NCBI]
|
0.000215929
|
|
|
TFPI
|
[NCBI]
|
0.000205401
|
|
|
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency
|
[NCBI]
|
0.00019528
|
|
|
GGCX
|
[NCBI]
|
0.000194082
|
|
|
thrombophilia due to deficiency of activated protein c cofactor
|
[NCBI]
|
0.000171715
|
|
|
PLG
|
[NCBI]
|
0.000152174
|
|
|
F5F8D
|
[NCBI]
|
0.000133324
|
|
|
plasminogen deficiency, type i
|
[NCBI]
|
0.000133324
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
0.000127691
|
|
|
factor vii deficiency
|
[NCBI]
|
0.00012768
|
|
|
NS1
|
[NCBI]
|
0.000123601
|
|
|
car factor deficiency
|
[NCBI]
|
0.000113012
|
|
|
pechet factor deficiency
|
[NCBI]
|
0.000113012
|
|
|
factor ix and factor xi, combined deficiency of
|
[NCBI]
|
0.000113012
|
|
|
globulin anomaly involving beta (2a)-globulin
|
[NCBI]
|
0.000113012
|
|
|
factor v excess with spontaneous thrombosis
|
[NCBI]
|
0.000113012
|
|
|
glycogen storage disease ib
|
[NCBI]
|
0.000107525
|
|
|
PF4
|
[NCBI]
|
0.000101065
|
|
|
TBXA2R
|
[NCBI]
|
9.11581e-05
|
|
|
F8FD9
|
[NCBI]
|
9.05549e-05
|
|
|
factors viii, ix and xi, combined deficiency of
|
[NCBI]
|
9.05549e-05
|
|
|
factor vii and factor viii, combined deficiency of
|
[NCBI]
|
8.20878e-05
|
|
|
passovoy factor
|
[NCBI]
|
8.20878e-05
|
|
|
athrombia, essential
|
[NCBI]
|
8.20878e-05
|
|
|
bleeding disorder due to p2ry12 defect
|
[NCBI]
|
7.65946e-05
|
|
|
PLAT
|
[NCBI]
|
7.58001e-05
|
|
|
coumarin resistance
|
[NCBI]
|
7.25138e-05
|
|
|
FHL2
|
[NCBI]
|
6.65655e-05
|
|
|
complement component c1q, fibroblast type
|
[NCBI]
|
6.6336e-05
|
|
|
complement factor i deficiency
|
[NCBI]
|
6.42569e-05
|
|
|
PAI1
|
[NCBI]
|
6.14286e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
5.8462e-05
|
|
|
TMAU
|
[NCBI]
|
5.60441e-05
|
|
|
HPS
|
[NCBI]
|
5.54521e-05
|
|
|
CF
|
[NCBI]
|
5.46281e-05
|
|
|
complement factor h deficiency
|
[NCBI]
|
5.26008e-05
|
|
|
afibrinogenemia, congenital
|
[NCBI]
|
5.16022e-05
|
|
|
THC2
|
[NCBI]
|
5.06632e-05
|
|
|
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|
[NCBI]
|
4.8143e-05
|
|
|
P2RX1
|
[NCBI]
|
4.73789e-05
|
|
|
MADA
|
[NCBI]
|
4.46801e-05
|
|
|
CPB2
|
[NCBI]
|
4.41411e-05
|
|
|
P2RY12
|
[NCBI]
|
4.15144e-05
|
|
|
F7R
|
[NCBI]
|
3.95253e-05
|
|
|
COH1
|
[NCBI]
|
3.66559e-05
|
|
|
CMD1A
|
[NCBI]
|
3.6294e-05
|
|
|
CDG1A
|
[NCBI]
|
3.46058e-05
|
|
|
CLN3
|
[NCBI]
|
3.36783e-05
|
|
|
PTGS1
|
[NCBI]
|
3.31502e-05
|
|
|
FGB
|
[NCBI]
|
3.22578e-05
|
|
|
FCMD
|
[NCBI]
|
3.22518e-05
|
|
|
aHUS
|
[NCBI]
|
3.22518e-05
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
3.12035e-05
|
|
|
F12
|
[NCBI]
|
2.999e-05
|
|
|
CFI
|
[NCBI]
|
2.93393e-05
|
|
|
GP1BA
|
[NCBI]
|
2.81576e-05
|
|
|
LPI
|
[NCBI]
|
2.76419e-05
|
|
|
WRN
|
[NCBI]
|
2.72538e-05
|
|
|
JMML
|
[NCBI]
|
2.49664e-05
|
|
|
PTH
|
[NCBI]
|
2.32874e-05
|
|
|
C3
|
[NCBI]
|
2.16225e-05
|
|
|
PROCR
|
[NCBI]
|
2.1351e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
2.08312e-05
|
|
|
SLE
|
[NCBI]
|
1.94455e-05
|
|
|
PCI
|
[NCBI]
|
1.86067e-05
|
|
|
EGFR
|
[NCBI]
|
1.8347e-05
|
|
|
FMF
|
[NCBI]
|
1.67991e-05
|
|
|
TNF
|
[NCBI]
|
1.62898e-05
|
|
|
PXE
|
[NCBI]
|
1.21508e-05
|
|
|
CFH
|
[NCBI]
|
1.20854e-05
|
|
|
homocystinuria
|
[NCBI]
|
1.12403e-05
|
|
|
IFNA1
|
[NCBI]
|
9.73013e-06
|
|
|
WAS
|
[NCBI]
|
8.66676e-06
|
|
|
hemophilia a
|
[NCBI]
|
7.77499e-06
|
|
|
APOE
|
[NCBI]
|
5.71771e-06
|
|
|
PI
|
[NCBI]
|
4.23695e-06
|
|
|
HGF
|
[NCBI]
|
2.76407e-06
|
|
|
XDH
|
[NCBI]
|
1.75148e-06
|
|
|
CD
|
[NCBI]
|
1.46633e-06
|
|