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: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.5E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 4 4.4E-03 0 0
Abnormal cardiac exercise stress test
16 0 1 3.6E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 4 5.9E-02 0 0
CUI: C4021741
Disease: Abnormal cortical bone morphology
Abnormal cortical bone morphology
41 0 1 1.9E-02 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery
32 0 1 2.3E-02 0 0
CUI: C4025706
Disease: Abnormal globus pallidus morphology
Abnormal globus pallidus morphology
10 0 1 4.5E-02 0 0
CUI: C0241654
Disease: Abnormal heart valve morphology
Abnormal heart valve morphology
42 0 1 1.9E-02 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility
45 0 1 1.8E-02 0 0
CUI: C0151854
Disease: Abnormal platelets
Abnormal platelets
11 0 3 0.14 0 0
CUI: C1839341
Disease: Abnormal T-wave
Abnormal T-wave
20 0 1 3.1E-02 0 0
CUI: C1850601
Disease: Abnormality of brainstem morphology
Abnormality of brainstem morphology
21 0 1 3.0E-02 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology
86 0 1 1.0E-02 0 0
Abnormality of metabolism/homeostasis
171 0 1 5.5E-03 0 0
CUI: C4023408
Disease: Abnormality of mouth size
Abnormality of mouth size
3 0 2 0.14 0 0
CUI: C4023691
Disease: Abnormality of pain sensation
Abnormality of pain sensation
6 0 2 0.12 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
CUI: C4023528
Disease: Abnormality of skin morphology
Abnormality of skin morphology
16 0 1 3.6E-02 0 0
CUI: C4025660
Disease: Abnormality of the ankles
Abnormality of the ankles
17 0 1 3.4E-02 0 0
CUI: C4520981
Disease: Abnormality of the basal ganglia
Abnormality of the basal ganglia
17 0 1 3.4E-02 0 0
CUI: C4021735
Disease: Abnormality of the hip bone
Abnormality of the hip bone
40 0 1 1.9E-02 0 0
CUI: C4025676
Disease: Abnormality of the knee
Abnormality of the knee
10 0 1 4.5E-02 0 0
CUI: C4021745
Disease: Abnormality of the musculature
Abnormality of the musculature
24 0 1 2.8E-02 0 0