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: C2931788
Disease: Atypical Hemolytic Uremic Syndrome
Atypical Hemolytic Uremic Syndrome 		56 42 20 0.20 3 6.4E-02
CUI: C0034155
Disease: Purpura, Thrombotic Thrombocytopenic
Purpura, Thrombotic Thrombocytopenic 		80 0 22 0.18 0 0
CUI: C0019061
Disease: Hemolytic-Uremic Syndrome
Hemolytic-Uremic Syndrome 		110 7 24 0.16 1 7.1E-02
CUI: C0040053
Disease: Thrombosis
Thrombosis 		98 0 21 0.15 0 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia 		31 0 12 0.15 0 0
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy 		16 0 10 0.15 0 0
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		41 30 13 0.14 3 8.6E-02
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		36 0 12 0.14 0 0
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		86 46 18 0.14 3 5.9E-02
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
Disseminated Intravascular Coagulation 		117 3 21 0.13 2 0.22
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		161 43 26 0.13 3 6.2E-02
CUI: C0003460
Disease: Anuria
Anuria 		18 0 9 0.13 0 0
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		66 14 14 0.12 3 0.16
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 8 0.12 0 0
CUI: C0155765
Disease: Disease of capillaries
Disease of capillaries 		61 0 13 0.12 0 0
CUI: C2584778
Disease: Thrombotic thrombocytopenic purpura, acquired
Thrombotic thrombocytopenic purpura, acquired 		16 0 8 0.11 0 0
CUI: C1268935
Disease: Congenital Thrombotic Thrombocytopenic Purpura
Congenital Thrombotic Thrombocytopenic Purpura 		36 0 10 0.11 0 0
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		17 0 8 0.11 0 0
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease 		37 15 10 0.11 3 0.15
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome 		99 17 16 0.11 2 8.7E-02
CUI: C0155773
Disease: Portal Vein Thrombosis
Portal Vein Thrombosis 		59 8 12 0.11 3 0.23
CUI: C0025306
Disease: Meningococcemia
Meningococcemia 		20 0 8 0.11 0 0
CUI: C0036982
Disease: Shock, Hemorrhagic
Shock, Hemorrhagic 		41 0 10 0.11 0 0
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		42 0 10 0.11 0 0
CUI: C1306889
Disease: Peripheral arterial occlusive disease
Peripheral arterial occlusive disease 		35 3 9 0.10 2 0.22