Source: BEFREE ×
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 0 11 0.13 0 0
CUI: C0684275
Disease: Hemophilia, NOS
Hemophilia, NOS 		81 6 16 0.13 1 4.2E-02
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		40 0 11 0.13 0 0
CUI: C0019069
Disease: Hemophilia A
Hemophilia A 		142 36 21 0.12 1 1.9E-02
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		26 3 6 7.7E-02 1 4.8E-02
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		41 0 7 7.6E-02 0 0
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia 		29 0 6 7.4E-02 0 0
CUI: C0033626
Disease: Protein Deficiency
Protein Deficiency 		120 0 12 7.2E-02 0 0
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		61 0 8 7.2E-02 0 0
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		94 0 10 7.0E-02 0 0
CUI: C0332853
Disease: Anastomosis
Anastomosis 		155 0 14 7.0E-02 0 0
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		19 0 5 6.9E-02 0 0
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		20 0 5 6.8E-02 0 0
CUI: C0242342
Disease: Sheehan Syndrome
Sheehan Syndrome 		5 0 4 6.8E-02 0 0
CUI: C1279945
Disease: Acute interstitial pneumonia
Acute interstitial pneumonia 		88 0 9 6.6E-02 0 0
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia 		7 0 4 6.6E-02 0 0
CUI: C4049005
Disease: Cataract, total congenital with posterior sutural opacities in Heterozygotes
Cataract, total congenital with posterior sutural opacities in Heterozygotes 		7 0 4 6.6E-02 0 0
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		56 0 7 6.5E-02 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		41 0 6 6.5E-02 0 0
CUI: C3494187
Disease: Factor VIII Deficiency
Factor VIII Deficiency 		8 0 4 6.5E-02 0 0
CUI: C0036472
Disease: Scrub Typhus
Scrub Typhus 		58 0 7 6.4E-02 0 0
CUI: C2721734
Disease: Methylenetetrahydrofolate reductase polymorphism
Methylenetetrahydrofolate reductase polymorphism 		9 0 4 6.3E-02 0 0
CUI: C0349632
Disease: Splenic Marginal Zone B-Cell Lymphoma
Splenic Marginal Zone B-Cell Lymphoma 		93 0 9 6.3E-02 0 0
CUI: C4316812
Disease: Fibrinogen Deficiency
Fibrinogen Deficiency 		26 0 5 6.3E-02 0 0
CUI: C0015503
Disease: Factor VII Deficiency
Factor VII Deficiency 		10 0 4 6.2E-02 0 0