|
OMIM |
Link |
Information gain |
01 |
|
thrombasthenia-thrombocytopenia, hereditary
|
[NCBI]
|
0.00116883
|
|
|
storage pool platelet disease
|
[NCBI]
|
0.000893464
|
|
|
GPS
|
[NCBI]
|
0.000807256
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
0.000690748
|
|
|
giant platelet syndrome
|
[NCBI]
|
0.000165225
|
|
|
athrombia, essential
|
[NCBI]
|
0.000151213
|
|
|
bleeding disorder due to p2ry12 defect
|
[NCBI]
|
0.000133927
|
|
|
THC2
|
[NCBI]
|
0.000108383
|
|
|
P2RY12
|
[NCBI]
|
4.32957e-05
|
|
|
PLAT
|
[NCBI]
|
3.56478e-05
|
|
|
FGG
|
[NCBI]
|
3.27139e-05
|
|
|
factor x deficiency
|
[NCBI]
|
3.13423e-05
|
|
|
CFB
|
[NCBI]
|
3.07596e-05
|
|
|
FGA
|
[NCBI]
|
2.86371e-05
|
|
|
von willebrand disease
|
[NCBI]
|
2.55171e-05
|
|
|
PLG
|
[NCBI]
|
2.20329e-05
|
|
|
FRAP1
|
[NCBI]
|
1.53811e-05
|
|
|
F3
|
[NCBI]
|
1.0972e-05
|
|