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 3 4.9E-02 0 0
CUI: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis
6 0 1 1.8E-02 0 0
11-Beta-Hydroxysteroid Dehydrogenase Type 1 Deficiency
1 0 1 2.0E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 2 1.9E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 2 1 1.3E-02 1 6.2E-02
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 1 1.6E-02 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 1.6E-02 0 0
5,10-Methylenetetrahydrofolate reductase deficiency
6 6 2 3.7E-02 1 5.0E-02
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 1 1.1E-02 0 0
CUI: C1142214
Disease: Abdominal cocoon
Abdominal cocoon
1 0 1 2.0E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 1.4E-02 0 0
CUI: C0270858
Disease: Abdominal Migraine
Abdominal Migraine
9 0 1 1.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 2 5.7E-03 0 0
CUI: C3826804
Disease: Abdominal pain in children
Abdominal pain in children
2 0 1 2.0E-02 0 0
CUI: C0232498
Disease: Abdominal tenderness
Abdominal tenderness
2 0 1 2.0E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 2.0E-02 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 1.7E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 8.8E-03 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 1 1 1.4E-02 1 6.7E-02
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 1.1E-02 0 0
CUI: C4021524
Disease: Abnormal adipose tissue morphology
Abnormal adipose tissue morphology
6 0 1 1.8E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 121 28 3.0E-02 6 4.6E-02
Abnormal brain FDG positron emission tomography
18 0 4 6.2E-02 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology
12 0 1 1.6E-02 0 0
CUI: C4025836
Disease: Abnormal choroid morphology
Abnormal choroid morphology
12 0 1 1.6E-02 0 0