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: C4510744
Disease: 46,XY partial gonadal dysgenesis
46,XY partial gonadal dysgenesis
11 0 1 4.3E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 1.8E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology
29 0 1 2.4E-02 0 0
Abnormal atrioventricular conduction
7 0 1 5.3E-02 0 0
Abnormal cardiac exercise stress test
16 0 1 3.6E-02 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 6.2E-02 0 0
Abnormal electrophysiology of sinoatrial node origin
1 0 1 7.7E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 2.4E-02 0 0
CUI: C4021803
Disease: Abnormal eyelid morphology
Abnormal eyelid morphology
10 3 2 9.5E-02 2 0.67
CUI: C3280303
Disease: Abnormal hair whorl
Abnormal hair whorl
5 0 1 5.9E-02 0 0
CUI: C0241654
Disease: Abnormal heart valve morphology
Abnormal heart valve morphology
42 0 1 1.9E-02 0 0
CUI: C4531142
Disease: Abnormal lymphocyte physiology
Abnormal lymphocyte physiology
1 0 1 7.7E-02 0 0
CUI: C4025252
Disease: Abnormal nasal morphology
Abnormal nasal morphology
34 0 2 4.4E-02 0 0
CUI: C4022996
Disease: Abnormal sex determination
Abnormal sex determination
15 0 1 3.7E-02 0 0
CUI: C1839341
Disease: Abnormal T-wave
Abnormal T-wave
20 0 1 3.1E-02 0 0
CUI: C4020957
Disease: Abnormal trabecular bone morphology
Abnormal trabecular bone morphology
6 0 1 5.6E-02 0 0
CUI: C4025753
Disease: Abnormal tricuspid valve morphology
Abnormal tricuspid valve morphology
11 0 4 0.20 0 0
Abnormality of cardiovascular system morphology
198 0 3 1.4E-02 0 0
Abnormality of circulating leptin level
1 0 1 7.7E-02 0 0
CUI: C4025213
Disease: Abnormality of complement system
Abnormality of complement system
2 0 1 7.1E-02 0 0
Abnormality of metabolism/homeostasis
171 0 1 5.5E-03 0 0
Abnormality of prenatal development or birth
23 0 1 2.9E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.4E-03 0 0
Abnormality of skeletal muscle fiber size
8 0 1 5.0E-02 0 0