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: C1855126
Disease: 3-Methylglutaconic Aciduria Type IV
3-Methylglutaconic Aciduria Type IV
4 0 1 5.3E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 1.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C4022916
Disease: Abnormal aldolase level
Abnormal aldolase level
16 0 6 0.23 0 0
Abnormal atrioventricular conduction
7 0 1 4.5E-02 0 0
CUI: C1260922
Disease: Abnormal breathing
Abnormal breathing
5 0 1 5.0E-02 0 0
Abnormal cardiac exercise stress test
16 0 1 3.2E-02 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 5.3E-02 0 0
Abnormal electrophysiology of sinoatrial node origin
1 0 1 6.2E-02 0 0
CUI: C4021662
Disease: Abnormal endocardium morphology
Abnormal endocardium morphology
23 0 1 2.6E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 2.3E-02 0 0
CUI: C4021803
Disease: Abnormal eyelid morphology
Abnormal eyelid morphology
10 0 1 4.0E-02 0 0
CUI: C4022946
Disease: Abnormal glycosylation
Abnormal glycosylation
6 0 1 4.8E-02 0 0
CUI: C3280303
Disease: Abnormal hair whorl
Abnormal hair whorl
5 0 1 5.0E-02 0 0
CUI: C0241654
Disease: Abnormal heart valve morphology
Abnormal heart valve morphology
42 0 2 3.6E-02 0 0
Abnormal lactate dehydrogenase activity
19 0 6 0.21 0 0
CUI: C4531142
Disease: Abnormal lymphocyte physiology
Abnormal lymphocyte physiology
1 0 1 6.2E-02 0 0
Abnormal mitochondria in muscle tissue
39 0 1 1.9E-02 0 0
CUI: C1839341
Disease: Abnormal T-wave
Abnormal T-wave
20 0 1 2.9E-02 0 0
CUI: C4020957
Disease: Abnormal trabecular bone morphology
Abnormal trabecular bone morphology
6 0 1 4.8E-02 0 0
CUI: C4025845
Disease: Abnormality iris morphology
Abnormality iris morphology
27 0 3 7.5E-02 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 2 1.7E-02 0 0
Abnormality of cellular immune system
4 0 1 5.3E-02 0 0
Abnormality of circulating leptin level
1 0 1 6.2E-02 0 0
CUI: C4025213
Disease: Abnormality of complement system
Abnormality of complement system
2 0 1 5.9E-02 0 0