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 1.7E-02 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 1 1.9E-02 0 0
CUI: C0852698
Disease: 17,20-desmolase deficiency
17,20-desmolase deficiency
1 0 1 2.2E-02 0 0
17-Alpha-Hydroxylase/17,20 Lyase Deficiency
4 0 1 2.1E-02 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 7.8E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.0E-02 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 1 1.9E-02 0 0
CUI: C0574084
Disease: 3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 3
12 0 1 1.8E-02 0 0
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development
29 0 1 1.4E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 1.4E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 5 6.4E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 1.2E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 3 2.1E-02 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 1 1.9E-02 0 0
CUI: C0232487
Disease: Abdominal discomfort
Abdominal discomfort
3 0 1 2.1E-02 0 0
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
23 0 1 1.5E-02 0 0
CUI: C0000734
Disease: Abdominal mass
Abdominal mass
2 0 1 2.2E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 9 2.7E-02 0 0
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
18 0 1 1.6E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 1.6E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 2.2E-02 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 1.9E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 2 1.9E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 1.2E-02 0 0
CUI: C4021524
Disease: Abnormal adipose tissue morphology
Abnormal adipose tissue morphology
6 0 1 2.0E-02 0 0