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 2.7E-02 0 0
CUI: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 2 7.1E-02 0 0
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
7 0 2 6.9E-02 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 2 1.9E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 2 2.6E-02 0 0
6-pyruvoyl-tetrahydropterin synthase deficiency
5 0 1 3.6E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 3 5.1E-02 0 0
CUI: C0243001
Disease: Abdominal Abscess
Abdominal Abscess
4 0 1 3.7E-02 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 1 3.0E-02 0 0
CUI: C1142110
Disease: Abdominal Compartment Syndrome
Abdominal Compartment Syndrome
2 0 1 4.0E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 2 4.4E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 6 1.9E-02 0 0
CUI: C3826804
Disease: Abdominal pain in children
Abdominal pain in children
2 0 1 4.0E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 1 2.4E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 2.5E-02 0 0
CUI: C0232498
Disease: Abdominal tenderness
Abdominal tenderness
2 0 2 8.3E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 4.0E-02 0 0
CUI: C0919934
Disease: Abdominal wall infection
Abdominal wall infection
1 0 1 4.2E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.1E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 3 4.8E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 12 1.3E-02 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 2 2.1E-02 0 0
CUI: C0231557
Disease: Abnormal bone formation
Abnormal bone formation
12 0 1 2.9E-02 0 0
CUI: C0159060
Disease: Abnormal bowel sounds
Abnormal bowel sounds
5 0 1 3.6E-02 0 0
Abnormal cardiac ventricular function
6 0 1 3.4E-02 0 0