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: C3266843
Disease: 47, XYY syndrome
47, XYY syndrome
9 0 1 8.5E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome
1 0 1 9.1E-03 0 0
CUI: C1861360
Disease: 6 metacarpals
6 metacarpals
3 0 2 1.8E-02 0 0
7-Dehydrocholesterol Reductase Deficiency
1 0 1 9.1E-03 0 0
CUI: C0265425
Disease: 9p partial monosomy syndrome
9p partial monosomy syndrome
1 0 1 9.1E-03 0 0
CUI: C3711390
Disease: 9q22.3 Microdeletion
9q22.3 Microdeletion
1 0 1 9.1E-03 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 6.6E-03 0 0
CUI: C2931850
Disease: Aase Smith syndrome 2
Aase Smith syndrome 2
16 0 1 8.0E-03 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 3 1.4E-02 0 0
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism
8 0 2 1.7E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 8.2E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 5 1.2E-02 0 0
CUI: C4087490
Disease: Abdominal tuberculosis
Abdominal tuberculosis
2 0 1 9.0E-03 0 0
CUI: C0266574
Disease: Ablepharon
Ablepharon
20 0 2 1.6E-02 0 0
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology
29 0 5 3.7E-02 0 0
Abnormal basal ganglia MRI signal intensity
7 0 1 8.6E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 8 7.9E-03 0 0
CUI: C4023161
Disease: Abnormal bone ossification
Abnormal bone ossification
3 0 1 8.9E-03 0 0
Abnormal brain FDG positron emission tomography
18 0 1 7.9E-03 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 1 8.1E-03 0 0
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology
32 0 5 3.6E-02 0 0
CUI: C4025680
Disease: Abnormal cartilage morphology
Abnormal cartilage morphology
2 0 1 9.0E-03 0 0
CUI: C4025711
Disease: Abnormal caudate nucleus morphology
Abnormal caudate nucleus morphology
9 0 5 4.4E-02 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology
12 0 1 8.3E-03 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 3 2.1E-02 0 0