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: C4025774
Disease: 1-3 toe syndactyly
1-3 toe syndactyly
1 0 1 2.9E-02 0 0
CUI: C4023728
Disease: 1-5 finger syndactyly
1-5 finger syndactyly
3 0 1 2.7E-02 0 0
CUI: C4021235
Disease: 1-5 toe syndactyly
1-5 toe syndactyly
1 0 1 2.9E-02 0 0
CUI: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs
20 0 1 1.9E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 9 0.16 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 9 0.24 0 0
CUI: C4023115
Disease: 3-4 finger cutaneous syndactyly
3-4 finger cutaneous syndactyly
3 0 1 2.7E-02 0 0
CUI: C1856889
Disease: 3-4 finger syndactyly
3-4 finger syndactyly
4 0 1 2.6E-02 0 0
CUI: C0574083
Disease: 3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 2
30 0 1 1.6E-02 0 0
CUI: C0796137
Disease: 3C syndrome
3C syndrome
4 0 1 2.6E-02 0 0
CUI: C1861360
Disease: 6 metacarpals
6 metacarpals
3 0 1 2.7E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 2 2.7E-02 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 1 2.3E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.0E-03 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 1 1.9E-02 0 0
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology
29 0 1 1.6E-02 0 0
Abnormal basal ganglia MRI signal intensity
7 0 1 2.4E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 3 3.2E-03 0 0
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology
32 0 1 1.5E-02 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology
70 0 1 9.6E-03 0 0
CUI: C1856019
Disease: Abnormal cortical gyration
Abnormal cortical gyration
17 0 2 4.0E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 1.6E-02 0 0
Abnormal form of the vertebral bodies
89 0 3 2.5E-02 0 0
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement
22 0 1 1.8E-02 0 0
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney
40 0 1 1.4E-02 0 0