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: C0427437
Disease: MCH - low
MCH - low 		5 0 4 0.31 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria 		8 0 4 0.25 0 0
CUI: C1850534
Disease: Edema, generalized
Edema, generalized 		12 0 4 0.20 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 3 0.20 0 0
CUI: C4554651
Disease: Generalized Edema, CTCAE
Generalized Edema, CTCAE 		12 0 4 0.20 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 3 0.19 0 0
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia 		8 0 3 0.18 0 0
CUI: C1610621
Disease: Factor II mutation
Factor II mutation 		2 0 2 0.17 0 0
CUI: C0232493
Disease: Epigastric pain
Epigastric pain 		17 0 4 0.16 0 0
CUI: C0003460
Disease: Anuria
Anuria 		18 0 4 0.15 0 0
CUI: C0037011
Disease: Shoulder Pain
Shoulder Pain 		18 0 4 0.15 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 2 0.15 0 0
CUI: C3665816
Disease: Perinatal stroke
Perinatal stroke 		3 0 2 0.15 0 0
CUI: C4024948
Disease: Anterior encephalocele
Anterior encephalocele 		3 0 2 0.15 0 0
CUI: C4302342
Disease: Familial hemolytic uremic syndrome
Familial hemolytic uremic syndrome 		3 0 2 0.15 0 0
CUI: C0034063
Disease: Pulmonary Edema
Pulmonary Edema 		26 0 5 0.15 0 0
CUI: C1851789
Disease: Poor wound healing
Poor wound healing 		19 0 4 0.15 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 3 0.14 0 0
CUI: C0238457
Disease: Thrombosis of renal vein
Thrombosis of renal vein 		4 0 2 0.14 0 0
CUI: C1527411
Disease: Thrombosis of retinal vein
Thrombosis of retinal vein 		4 0 2 0.14 0 0
CUI: C1969222
Disease: Decreased serum complement factor H
Decreased serum complement factor H 		4 0 2 0.14 0 0
CUI: C0151872
Disease: Prothrombin time increased
Prothrombin time increased 		30 0 5 0.14 0 0
CUI: C0398777
Disease: Complement Factor H Deficiency
Complement Factor H Deficiency 		5 0 2 0.13 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		5 0 2 0.13 0 0
CUI: C4021636
Disease: Decreased serum complement factor B
Decreased serum complement factor B 		5 0 2 0.13 0 0