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: C0015523
Disease: Hereditary Factor XI Deficiency
Hereditary Factor XI Deficiency 		7 0 5 7.8E-02 0 0
CUI: C0344724
Disease: Ostium secundum atrial septal defect
Ostium secundum atrial septal defect 		37 10 7 7.6E-02 2 2.3E-02
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		23 5 6 7.6E-02 3 3.7E-02
CUI: C0684275
Disease: Hemophilia, NOS
Hemophilia, NOS 		82 0 10 7.5E-02 0 0
CUI: C1264041
Disease: von Willebrand Disease, Type 3
von Willebrand Disease, Type 3 		11 17 5 7.4E-02 7 8.0E-02
CUI: C0019069
Disease: Hemophilia A
Hemophilia A 		143 295 14 7.3E-02 2 5.4E-03
CUI: C0013491
Disease: Ecchymosis
Ecchymosis 		41 0 7 7.3E-02 0 0
CUI: C0018924
Disease: Hemarthrosis
Hemarthrosis 		13 0 5 7.1E-02 0 0
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		29 0 6 7.1E-02 0 0
CUI: C0277919
Disease: Postthrombotic Syndrome
Postthrombotic Syndrome 		14 0 5 7.0E-02 0 0
CUI: C0007274
Disease: Carotid Artery Thrombosis
Carotid Artery Thrombosis 		30 0 6 7.0E-02 0 0
CUI: C0019080
Disease: Hemorrhage
Hemorrhage 		47 0 7 6.9E-02 0 0
CUI: C0242342
Disease: Sheehan Syndrome
Sheehan Syndrome 		16 2 5 6.8E-02 1 1.3E-02
CUI: C2584778
Disease: Thrombotic thrombocytopenic purpura, acquired
Thrombotic thrombocytopenic purpura, acquired 		16 0 5 6.8E-02 0 0
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		161 43 14 6.7E-02 3 2.5E-02
CUI: C0948441
Disease: Venoocclusive disease
Venoocclusive disease 		34 4 6 6.7E-02 1 1.2E-02
CUI: C1306889
Disease: Peripheral arterial occlusive disease
Peripheral arterial occlusive disease 		35 3 6 6.6E-02 2 2.5E-02
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 9 5 6.5E-02 4 4.8E-02
CUI: C0272323
Disease: Moderate hereditary factor VIII deficiency disease
Moderate hereditary factor VIII deficiency disease 		4 0 4 6.5E-02 0 0
CUI: C0796004
Disease: Kabuki make-up syndrome
Kabuki make-up syndrome 		37 0 6 6.5E-02 0 0
CUI: C1282968
Disease: von Willebrand Disease, Type 2A
von Willebrand Disease, Type 2A 		4 17 4 6.5E-02 6 6.7E-02
CUI: C0019243
Disease: Angioedemas, Hereditary
Angioedemas, Hereditary 		54 0 7 6.4E-02 0 0
CUI: C0154841
Disease: Central retinal vein occlusion
Central retinal vein occlusion 		38 7 6 6.4E-02 2 2.4E-02
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		230 93 17 6.2E-02 5 3.0E-02
CUI: C0003855
Disease: Arteriovenous fistula
Arteriovenous fistula 		93 0 9 6.2E-02 0 0