Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
(Idiopathic) normal pressure hydrocephalus
14 0 1 2.4E-02 0 0
CUI: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 1 2.9E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 1.4E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 6 9.8E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 2 1.5E-02 0 0
CUI: C0243001
Disease: Abdominal Abscess
Abdominal Abscess
4 0 1 3.1E-02 0 0
CUI: C1142214
Disease: Abdominal cocoon
Abdominal cocoon
1 0 1 3.4E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 2 4.0E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 5 1.5E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 3 6.8E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 2.2E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 3.3E-02 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 2.7E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 2 2.2E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 4 6.1E-02 0 0
CUI: C4021524
Disease: Abnormal adipose tissue morphology
Abnormal adipose tissue morphology
6 0 1 2.9E-02 0 0
CUI: C4022916
Disease: Abnormal aldolase level
Abnormal aldolase level
16 0 1 2.3E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 11 1.2E-02 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 2 2.0E-02 0 0
Abnormal form of the vertebral bodies
89 0 2 1.7E-02 0 0
CUI: C0263634
Disease: Abnormal granulation tissue
Abnormal granulation tissue
6 0 2 6.1E-02 0 0
Abnormal lactate dehydrogenase activity
19 0 1 2.1E-02 0 0
CUI: C4025758
Disease: Abnormal myocardium morphology
Abnormal myocardium morphology
19 0 1 2.1E-02 0 0
CUI: C4022739
Disease: Abnormal neuron morphology
Abnormal neuron morphology
8 0 1 2.8E-02 0 0
CUI: C4023573
Disease: Abnormal number of permanent teeth
Abnormal number of permanent teeth
9 0 1 2.7E-02 0 0