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: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 2.4E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 3 9.2E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 2 2.1E-03 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 1 2.5E-02 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology
12 0 1 2.6E-02 0 0
CUI: C1856019
Disease: Abnormal cortical gyration
Abnormal cortical gyration
17 0 1 2.3E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 1.8E-02 0 0
CUI: C2675111
Disease: Abnormal eyelash morphology
Abnormal eyelash morphology
39 0 1 1.5E-02 0 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology
12 0 1 2.6E-02 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance
15 0 1 2.4E-02 0 0
CUI: C0855742
Disease: Abnormal platelet morphology
Abnormal platelet morphology
10 0 1 2.8E-02 0 0
CUI: C0151854
Disease: Abnormal platelets
Abnormal platelets
11 0 1 2.7E-02 0 0
CUI: C4021087
Disease: Abnormal social behavior
Abnormal social behavior
19 0 1 2.2E-02 0 0
Abnormal upper motor neuron morphology
20 0 1 2.2E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 7.1E-03 0 0
Abnormality of blood and blood-forming tissues
23 0 1 2.0E-02 0 0
CUI: C4520981
Disease: Abnormality of the basal ganglia
Abnormality of the basal ganglia
17 0 1 2.3E-02 0 0
Abnormality of the hypothalamus-pituitary axis
70 0 1 1.0E-02 0 0
CUI: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system
34 0 2 3.4E-02 0 0
CUI: C4025726
Disease: Abnormality of the pleura
Abnormality of the pleura
10 0 1 2.8E-02 0 0
Abnormality of the respiratory system
16 0 1 2.4E-02 0 0
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
148 0 2 1.2E-02 0 0
Abnormality of the spinocerebellar tracts
3 0 1 3.4E-02 0 0
CUI: C4022403
Disease: Abnormality of the substantia nigra
Abnormality of the substantia nigra
3 0 1 3.4E-02 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
127 0 1 6.5E-03 0 0