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: C4024722
Disease: Reduced factor VII activity
Reduced factor VII activity 		4 0 2 0.40 0 0
CUI: C0019065
Disease: Hemoperitoneum
Hemoperitoneum 		1 0 1 0.33 0 0
CUI: C0269608
Disease: Antepartum hemorrhage
Antepartum hemorrhage 		1 0 1 0.33 0 0
CUI: C0270027
Disease: Antepartum hemorrhage affecting fetus or newborn
Antepartum hemorrhage affecting fetus or newborn 		1 0 1 0.33 0 0
CUI: C0272327
Disease: Hereditary factor X deficiency disease
Hereditary factor X deficiency disease 		1 0 1 0.33 0 0
CUI: C0339815
Disease: Anterior epistaxis
Anterior epistaxis 		1 0 1 0.33 0 0
CUI: C1835813
Disease: Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency 		1 0 1 0.33 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 0.33 0 0
CUI: C2718087
Disease: Vitamin K Deficiency Bleeding
Vitamin K Deficiency Bleeding 		1 0 1 0.33 0 0
CUI: C2873787
Disease: Deficiency of factor X [Stuart-Prower]
Deficiency of factor X [Stuart-Prower] 		1 0 1 0.33 0 0
CUI: C4023159
Disease: Reduced factor IX activity
Reduced factor IX activity 		5 0 2 0.33 0 0
CUI: C1848534
Disease: VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1 		6 0 2 0.29 0 0
CUI: C0019195
Disease: Hepatitis, Viral, Human
Hepatitis, Viral, Human 		2 0 1 0.25 0 0
CUI: C0272317
Disease: Hereditary factor II deficiency disease
Hereditary factor II deficiency disease 		2 0 1 0.25 0 0
CUI: C0549289
Disease: Thrombosis of inferior vena cava
Thrombosis of inferior vena cava 		2 0 1 0.25 0 0
CUI: C2675747
Disease: Coumarin Sensitivity
Coumarin Sensitivity 		2 0 1 0.25 0 0
CUI: C4280698
Disease: Reduced prothrombin antigen
Reduced prothrombin antigen 		2 0 1 0.25 0 0
CUI: C0272315
Disease: Coagulation factor deficiency syndrome
Coagulation factor deficiency syndrome 		13 0 3 0.23 0 0
CUI: C0342143
Disease: Hyperthyroidism secondary to amiodarone
Hyperthyroidism secondary to amiodarone 		3 0 1 0.20 0 0
CUI: C0472802
Disease: Hereditary factor VIII deficiency disease with inhibitor
Hereditary factor VIII deficiency disease with inhibitor 		3 0 1 0.20 0 0
CUI: C0587044
Disease: Left ventricular thrombus
Left ventricular thrombus 		3 0 1 0.20 0 0
CUI: C2873786
Disease: Deficiency of factor VII [stable]
Deficiency of factor VII [stable] 		3 0 1 0.20 0 0
CUI: C3658294
Disease: Hereditary Antithrombin Deficiency
Hereditary Antithrombin Deficiency 		3 0 1 0.20 0 0
CUI: C3888513
Disease: CYP2C9 polymorphism
CYP2C9 polymorphism 		3 0 1 0.20 0 0
CUI: C4024853
Disease: Increased number of skin folds
Increased number of skin folds 		3 0 1 0.20 0 0