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: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 17 3.7E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 8 4.3E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 5.2E-03 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 5.7E-03 0 0
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect
8 0 1 5.5E-03 0 0
CUI: C0919934
Disease: Abdominal wall infection
Abdominal wall infection
1 0 1 5.7E-03 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 5.5E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 4 1.7E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 5 2.4E-02 0 0
CUI: C4021524
Disease: Abnormal adipose tissue morphology
Abnormal adipose tissue morphology
6 0 2 1.1E-02 0 0
Abnormal aggressive, impulsive or violent behavior
2 0 1 5.7E-03 0 0
Abnormal atrioventricular conduction
7 0 1 5.5E-03 0 0
Abnormal axonemal organization of respiratory motile cilia
3 0 1 5.6E-03 0 0
CUI: C4021208
Disease: Abnormal B cell count
Abnormal B cell count
2 0 2 1.1E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 39 3.7E-02 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 8 3.3E-02 0 0
CUI: C4023161
Disease: Abnormal bone ossification
Abnormal bone ossification
3 0 1 5.6E-03 0 0
Abnormal brain FDG positron emission tomography
18 0 1 5.2E-03 0 0
Abnormal cardiac ventricular function
6 0 1 5.6E-03 0 0
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology
32 0 1 4.9E-03 0 0
CUI: C4021847
Disease: Abnormal cartilage collagen
Abnormal cartilage collagen
1 0 1 5.7E-03 0 0
CUI: C4025680
Disease: Abnormal cartilage morphology
Abnormal cartilage morphology
2 0 1 5.7E-03 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 5.6E-03 0 0
Abnormal central microtubular pair morphology of respiratory motile cilia
2 0 1 5.7E-03 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 2 9.6E-03 0 0