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: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 2 2.9E-02 0 0
2-oxo-hept-3-ene-1,7-dioate hydratase activity
14 0 1 1.3E-02 0 0
5,10-Methylenetetrahydrofolate reductase deficiency
6 0 1 1.4E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 3 3.0E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 2 1.9E-02 0 0
CUI: C0243001
Disease: Abdominal Abscess
Abdominal Abscess
4 0 1 1.4E-02 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 1 1.3E-02 0 0
CUI: C1142110
Disease: Abdominal Compartment Syndrome
Abdominal Compartment Syndrome
2 0 1 1.5E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 3 3.5E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 6 1.7E-02 0 0
CUI: C3826804
Disease: Abdominal pain in children
Abdominal pain in children
2 0 1 1.5E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 2 2.4E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 1.2E-02 0 0
CUI: C0232498
Disease: Abdominal tenderness
Abdominal tenderness
2 0 2 3.0E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 2 3.0E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 2 1.6E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 1 1.2E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 4 3.9E-02 0 0
CUI: C4021208
Disease: Abnormal B cell count
Abnormal B cell count
2 0 1 1.5E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 13 1.3E-02 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 7 5.2E-02 0 0
CUI: C0159060
Disease: Abnormal bowel sounds
Abnormal bowel sounds
5 0 1 1.4E-02 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 1 1.3E-02 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology
12 0 1 1.3E-02 0 0
CUI: C4025836
Disease: Abnormal choroid morphology
Abnormal choroid morphology
12 0 1 1.3E-02 0 0