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 1.4E-02 0 0
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 6.9E-03 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 8.7E-03 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 3 3.4E-02 0 0
CUI: C0796137
Disease: 3C syndrome
3C syndrome
4 0 1 1.6E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 1.2E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome
1 0 1 1.6E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 9.5E-03 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 4 4.2E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 9.8E-03 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 1 1.4E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 3 8.3E-03 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 2 2.9E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 8.0E-03 0 0
Abnormal atrioventricular conduction
7 0 1 1.5E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 16 1.7E-02 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 7.4E-03 0 0
Abnormal brain FDG positron emission tomography
18 0 1 1.3E-02 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 1.6E-02 0 0
Abnormal electrophysiology of sinoatrial node origin
1 0 1 1.6E-02 0 0
CUI: C4021662
Disease: Abnormal endocardium morphology
Abnormal endocardium morphology
23 0 1 1.2E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 1.1E-02 0 0
CUI: C4021803
Disease: Abnormal eyelid morphology
Abnormal eyelid morphology
10 0 1 1.4E-02 0 0
Abnormal form of the vertebral bodies
89 0 2 1.4E-02 0 0
CUI: C3280303
Disease: Abnormal hair whorl
Abnormal hair whorl
5 0 1 1.5E-02 0 0