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: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs
20 3 3 1.3E-02 1 2.4E-03
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 16 13 4.6E-02 1 2.3E-03
CUI: C4021622
Disease: 2-4 toe cutaneous syndactyly
2-4 toe cutaneous syndactyly
1 0 1 4.7E-03 0 0
CUI: C4023736
Disease: 2-5 finger syndactyly
2-5 finger syndactyly
1 0 1 4.7E-03 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
1 9 1 4.7E-03 2 4.8E-03
CUI: C1834062
Disease: 3-4 toe syndactyly
3-4 toe syndactyly
4 0 1 4.7E-03 0 0
CUI: C4023731
Disease: 4-5 finger syndactyly
4-5 finger syndactyly
3 2 3 1.4E-02 1 2.4E-03
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 3.2E-03 0 0
ABDOMINAL OBESITY-METABOLIC SYNDROME 3
2 0 1 4.7E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
231 11 8 1.8E-02 2 4.8E-03
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
6 0 1 4.6E-03 0 0
CUI: C4021527
Disease: Abdominal wall muscle weakness
Abdominal wall muscle weakness
9 0 1 4.6E-03 0 0
Abnormal aggressive, impulsive or violent behavior
2 3 1 4.7E-03 1 2.4E-03
CUI: C4022916
Disease: Abnormal aldolase level
Abnormal aldolase level
16 0 1 4.4E-03 0 0
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology
29 1 1 4.2E-03 1 2.4E-03
CUI: C0522216
Disease: Abnormal auditory evoked potential
Abnormal auditory evoked potential
11 2 1 4.5E-03 1 2.4E-03
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
97 20 15 5.1E-02 4 9.4E-03
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 3.5E-03 0 0
CUI: C4023161
Disease: Abnormal bone ossification
Abnormal bone ossification
3 0 1 4.7E-03 0 0
CUI: C4025680
Disease: Abnormal cartilage morphology
Abnormal cartilage morphology
2 0 1 4.7E-03 0 0
CUI: C4021520
Disease: Abnormal cerebral artery morphology
Abnormal cerebral artery morphology
3 1 1 4.7E-03 1 2.4E-03
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 1 4.1E-03 0 0
CUI: C4021152
Disease: Abnormal CNS myelination
Abnormal CNS myelination
9 4 2 9.2E-03 1 2.4E-03
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology
16 0 1 4.4E-03 0 0
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement
0 5 0 0 1 2.4E-03