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: C0749098
Disease: Hematoma, Subdural, Acute
Hematoma, Subdural, Acute 		1 0 1 1.0E-01 0 0
CUI: C0751797
Disease: Intracranial Hematoma, Traumatic
Intracranial Hematoma, Traumatic 		1 0 1 1.0E-01 0 0
CUI: C0866188
Disease: Renal thrombosis
Renal thrombosis 		1 0 1 1.0E-01 0 0
CUI: C1096494
Disease: Gastroduodenal haemorrhage
Gastroduodenal haemorrhage 		1 0 1 1.0E-01 0 0
CUI: C1142442
Disease: Intrahepatic biloma
Intrahepatic biloma 		1 0 1 1.0E-01 0 0
CUI: C1843832
Disease: VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 		1 0 1 1.0E-01 0 0
CUI: C2585960
Disease: Heterozygous protein C deficiency
Heterozygous protein C deficiency 		1 0 1 1.0E-01 0 0
CUI: C2674321
Disease: Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant
Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant 		1 0 1 1.0E-01 0 0
CUI: C2674322
Disease: Protein C Deficiency, Acquired
Protein C Deficiency, Acquired 		1 0 1 1.0E-01 0 0
CUI: C2676759
Disease: THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE 		1 0 1 1.0E-01 0 0
CUI: C2718087
Disease: Vitamin K Deficiency Bleeding
Vitamin K Deficiency Bleeding 		1 0 1 1.0E-01 0 0
CUI: C3203356
Disease: Factor II deficiency
Factor II deficiency 		1 0 1 1.0E-01 0 0
CUI: C3280672
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2 		1 0 1 1.0E-01 0 0
CUI: C3281153
Disease: EFAVIRENZ, POOR METABOLISM OF
EFAVIRENZ, POOR METABOLISM OF 		1 0 1 1.0E-01 0 0
CUI: C3805089
Disease: Hyperfibrinolysis
Hyperfibrinolysis 		12 0 2 1.0E-01 0 0
CUI: C3890031
Disease: prothrombin type 3 phenotype
prothrombin type 3 phenotype 		1 0 1 1.0E-01 0 0
CUI: C4016343
Disease: DYSPROTHROMBINEMIA PROTHROMBIN HIMI-II
DYSPROTHROMBINEMIA PROTHROMBIN HIMI-II 		1 0 1 1.0E-01 0 0
CUI: C4021097
Disease: Reduced prothrombin activity
Reduced prothrombin activity 		1 0 1 1.0E-01 0 0
CUI: C4329969
Disease: Factor VIII Inactivation
Factor VIII Inactivation 		1 0 1 1.0E-01 0 0
CUI: C4708643
Disease: Acroangiodermatitis of skin
Acroangiodermatitis of skin 		1 0 1 1.0E-01 0 0
CUI: C4722227
Disease: Hypoprothrombinemias
Hypoprothrombinemias 		1 0 1 1.0E-01 0 0
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		35 0 4 9.8E-02 0 0
CUI: C0019080
Disease: Hemorrhage
Hemorrhage 		47 0 5 9.6E-02 0 0
CUI: C0018924
Disease: Hemarthrosis
Hemarthrosis 		13 0 2 9.5E-02 0 0
CUI: C0272315
Disease: Coagulation factor deficiency syndrome
Coagulation factor deficiency syndrome 		13 0 2 9.5E-02 0 0