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: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 11 0.13 1 7.2E-03
CUI: C0684275
Disease: Hemophilia, NOS
Hemophilia, NOS 		82 8 16 0.13 2 1.5E-02
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 0 11 0.12 0 0
CUI: C0019069
Disease: Hemophilia A
Hemophilia A 		143 295 22 0.12 29 7.4E-02
CUI: C0003838
Disease: Arterial Occlusive Diseases
Arterial Occlusive Diseases 		35 0 7 8.0E-02 0 0
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		117 0 13 8.0E-02 0 0
CUI: C3494187
Disease: Factor VIII Deficiency
Factor VIII Deficiency 		9 0 5 7.9E-02 0 0
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		66 0 9 7.8E-02 0 0
CUI: C0272324
Disease: Mild hereditary factor VIII deficiency disease
Mild hereditary factor VIII deficiency disease 		11 6 5 7.7E-02 1 7.7E-03
CUI: C0332853
Disease: Anastomosis
Anastomosis 		155 0 15 7.5E-02 0 0
CUI: C0272315
Disease: Coagulation factor deficiency syndrome
Coagulation factor deficiency syndrome 		13 0 5 7.5E-02 0 0
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 0 7 7.4E-02 0 0
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		30 3 6 7.2E-02 1 7.9E-03
CUI: C0033626
Disease: Protein Deficiency
Protein Deficiency 		125 0 12 7.0E-02 0 0
CUI: C0240671
Disease: Partial thromboplastin time increased (finding)
Partial thromboplastin time increased (finding) 		18 0 5 6.9E-02 0 0
CUI: C0042880
Disease: Vitamin K Deficiency
Vitamin K Deficiency 		19 0 5 6.8E-02 0 0
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 0 5 6.8E-02 0 0
CUI: C4321502
Disease: Factor XI Deficiency
Factor XI Deficiency 		6 0 4 6.6E-02 0 0
CUI: C1279945
Disease: Acute interstitial pneumonia
Acute interstitial pneumonia 		88 0 9 6.5E-02 0 0
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
Hereditary Factor XI Deficiency 		7 0 4 6.5E-02 0 0
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia 		7 0 4 6.5E-02 0 0
CUI: C0036472
Disease: Scrub Typhus
Scrub Typhus 		58 0 7 6.4E-02 0 0
CUI: C4049005
Disease: Cataract, total congenital with posterior sutural opacities in Heterozygotes
Cataract, total congenital with posterior sutural opacities in Heterozygotes 		8 0 4 6.3E-02 0 0
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		59 0 7 6.3E-02 0 0
CUI: C0003855
Disease: Arteriovenous fistula
Arteriovenous fistula 		93 0 9 6.3E-02 0 0