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 0.20 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria 		8 0 4 0.17 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 4 0.15 0 0
CUI: C1850534
Disease: Edema, generalized
Edema, generalized 		12 0 4 0.15 0 0
CUI: C4554651
Disease: Generalized Edema, CTCAE
Generalized Edema, CTCAE 		12 0 4 0.15 0 0
CUI: C4021816
Disease: Abnormality of the gingiva
Abnormality of the gingiva 		13 0 4 0.14 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 3 0.14 0 0
CUI: C0302810
Disease: Uremia syndrome
Uremia syndrome 		7 0 3 0.13 0 0
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		17 0 4 0.12 0 0
CUI: C0232493
Disease: Epigastric pain
Epigastric pain 		17 0 4 0.12 0 0
CUI: C4477095
Disease: Increased lactate dehydrogenase activity
Increased lactate dehydrogenase activity 		27 0 5 0.12 0 0
CUI: C0037011
Disease: Shoulder Pain
Shoulder Pain 		18 0 4 0.12 0 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia 		31 0 5 0.11 0 0
CUI: C0151539
Disease: Blood urea increased
Blood urea increased 		12 0 3 0.11 0 0
CUI: C1837512
Disease: Decreased serum complement C3
Decreased serum complement C3 		12 0 3 0.11 0 0
CUI: C0023510
Disease: Leukocyte Disorders
Leukocyte Disorders 		2 0 2 0.11 0 0
CUI: C0162154
Disease: Atrophic scar
Atrophic scar 		23 0 4 0.11 0 0
CUI: C0269855
Disease: Hematoma of cord
Hematoma of cord 		2 0 2 0.11 0 0
CUI: C4024916
Disease: Decreased number of small peripheral myelinated nerve fibers
Decreased number of small peripheral myelinated nerve fibers 		2 0 2 0.11 0 0
CUI: C4280712
Disease: Delayed onset bleeding
Delayed onset bleeding 		2 0 2 0.11 0 0
CUI: C0220679
Disease: Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified 		3 0 2 1.0E-01 0 0
CUI: C1852021
Disease: Drusen, Radial, Autosomal Dominant
Drusen, Radial, Autosomal Dominant 		3 0 2 1.0E-01 0 0
CUI: C4021962
Disease: Genital hernia
Genital hernia 		3 0 2 1.0E-01 0 0
CUI: C4023143
Disease: Bleeding with minor or no trauma
Bleeding with minor or no trauma 		3 0 2 1.0E-01 0 0
CUI: C4025789
Disease: Psychotic mentation
Psychotic mentation 		3 0 2 1.0E-01 0 0