Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		35 0 11 0.15 0 0
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		29 0 10 0.15 0 0
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		44 0 10 0.12 0 0
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 13 0.11 3 2.9E-02
CUI: C0040053
Disease: Thrombosis
Thrombosis 		98 0 14 0.11 0 0
CUI: C0154841
Disease: Central retinal vein occlusion
Central retinal vein occlusion 		38 7 8 0.10 1 1.5E-02
CUI: C1868251
Disease: Neonatal alloimmune thrombocytopenia (NAIT)
Neonatal alloimmune thrombocytopenia (NAIT) 		6 0 5 0.10 0 0
CUI: C0025323
Disease: Menorrhagia
Menorrhagia 		34 0 7 9.3E-02 0 0
CUI: C2751260
Disease: Macrothrombocytopenia
Macrothrombocytopenia 		34 31 7 9.3E-02 1 1.1E-02
CUI: C0005129
Disease: Bernard-Soulier Syndrome
Bernard-Soulier Syndrome 		46 0 8 9.3E-02 0 0
CUI: C4021646
Disease: Prolonged bleeding after surgery
Prolonged bleeding after surgery 		11 0 5 9.3E-02 0 0
CUI: C3854603
Disease: FNAITP
FNAITP 		12 0 5 9.1E-02 0 0
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 7 9.0E-02 2 2.7E-02
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease 		62 78 9 8.9E-02 2 1.5E-02
CUI: C0221028
Disease: Neonatal thrombocytopenia (disorder)
Neonatal thrombocytopenia (disorder) 		15 0 5 8.6E-02 0 0
CUI: C0333209
Disease: Platelet thrombus
Platelet thrombus 		17 0 5 8.3E-02 0 0
CUI: C0007722
Disease: Cephalhematoma due to birth trauma
Cephalhematoma due to birth trauma 		7 0 4 7.8E-02 0 0
CUI: C2237512
Disease: cephalohematoma
cephalohematoma 		7 0 4 7.8E-02 0 0
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		7 0 4 7.8E-02 0 0
CUI: C1840061
Disease: SMALL PATELLA SYNDROME
SMALL PATELLA SYNDROME 		21 15 5 7.8E-02 1 1.3E-02
CUI: C1280798
Disease: Von Willebrand disease, platelet type
Von Willebrand disease, platelet type 		8 0 4 7.7E-02 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 5 7.6E-02 2 3.1E-02
CUI: C4304021
Disease: Autosomal dominant macrothrombocytopenia
Autosomal dominant macrothrombocytopenia 		9 0 4 7.5E-02 0 0
CUI: C0242231
Disease: Coronary Stenosis
Coronary Stenosis 		111 0 11 7.4E-02 0 0
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time 		39 0 6 7.4E-02 0 0