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 8.3E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 6.2E-03 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
14 0 2 1.7E-02 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 1 7.4E-03 0 0
5,10-Methylenetetrahydrofolate reductase deficiency
6 6 1 8.8E-03 1 8.3E-02
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 2 1.3E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 2 1.4E-02 0 0
CUI: C0549357
Disease: Abdominal adhesions
Abdominal adhesions
6 0 2 1.8E-02 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 1 8.5E-03 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 7.7E-03 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 3 2.5E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
82 0 6 3.3E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 3 2.4E-02 0 0
CUI: C0232498
Disease: Abdominal tenderness
Abdominal tenderness
2 0 1 9.2E-03 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 9.2E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
61 0 2 1.2E-02 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
19 0 1 7.9E-03 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 3 2.1E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
820 101 24 2.7E-02 2 1.9E-02
CUI: C0231557
Disease: Abnormal bone formation
Abnormal bone formation
12 0 2 1.7E-02 0 0
CUI: C0263634
Disease: Abnormal granulation tissue
Abnormal granulation tissue
6 0 1 8.8E-03 0 0
CUI: C0266782
Disease: Abnormal yolk sac
Abnormal yolk sac
1 0 1 9.3E-03 0 0
Abnormality of cardiovascular system morphology
30 0 2 1.5E-02 0 0
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
120 0 7 3.2E-02 0 0
CUI: C4021821
Disease: Abnormality of the urinary system
Abnormality of the urinary system
15 0 1 8.2E-03 0 0