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: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 3 9.1E-02 0 0
CUI: C0042880
Disease: Vitamin K Deficiency
Vitamin K Deficiency 		19 0 4 8.9E-02 0 0
CUI: C1851789
Disease: Poor wound healing
Poor wound healing 		19 0 4 8.9E-02 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 3 8.8E-02 0 0
CUI: C3810018
Disease: Bilateral coxa valga
Bilateral coxa valga 		7 0 3 8.8E-02 0 0
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 0 3 8.6E-02 0 0
CUI: C0015503
Disease: Factor VII Deficiency
Factor VII Deficiency 		10 0 3 8.1E-02 0 0
CUI: C0034063
Disease: Pulmonary Edema
Pulmonary Edema 		26 0 4 7.7E-02 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 3 7.7E-02 0 0
CUI: C0151699
Disease: Intracranial Hemorrhage
Intracranial Hemorrhage 		40 0 5 7.7E-02 0 0
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		27 0 4 7.5E-02 0 0
CUI: C0272315
Disease: Coagulation factor deficiency syndrome
Coagulation factor deficiency syndrome 		13 0 3 7.5E-02 0 0
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		13 0 3 7.5E-02 0 0
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		43 0 5 7.4E-02 0 0
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement 		14 0 3 7.3E-02 0 0
CUI: C0409980
Disease: Primary antiphospholipid syndrome
Primary antiphospholipid syndrome 		29 0 4 7.3E-02 0 0
CUI: C1142132
Disease: Carnitine deficiency
Carnitine deficiency 		15 0 3 7.1E-02 0 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia 		31 0 4 7.0E-02 0 0
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy 		16 0 3 7.0E-02 0 0
CUI: C0432355
Disease: Hypoplasia of nipple
Hypoplasia of nipple 		33 0 4 6.8E-02 0 0
CUI: C0003460
Disease: Anuria
Anuria 		18 0 3 6.7E-02 0 0
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency 		2 0 2 6.7E-02 0 0
CUI: C0025323
Disease: Menorrhagia
Menorrhagia 		34 0 4 6.7E-02 0 0
CUI: C0272317
Disease: Hereditary factor II deficiency disease
Hereditary factor II deficiency disease 		2 0 2 6.7E-02 0 0
CUI: C0426433
Disease: Pinched nasal tip
Pinched nasal tip 		2 0 2 6.7E-02 0 0