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: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology
29 0 1 3.3E-02 0 0
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology
32 0 1 3.0E-02 0 0
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney
40 0 1 2.4E-02 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility
45 0 1 2.2E-02 0 0
CUI: C4025881
Disease: Abnormal oral frenulum morphology
Abnormal oral frenulum morphology
19 0 1 5.0E-02 0 0
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve
50 0 1 2.0E-02 0 0
Abnormality of cardiovascular system morphology
198 0 1 5.0E-03 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability
34 0 1 2.9E-02 0 0
CUI: C4021750
Disease: Abnormality of femur morphology
Abnormality of femur morphology
33 0 1 2.9E-02 0 0
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray
34 0 1 2.9E-02 0 0
CUI: C0281842
Disease: Abnormality of the fallopian tube
Abnormality of the fallopian tube
22 0 1 4.3E-02 0 0
CUI: C4021816
Disease: Abnormality of the gingiva
Abnormality of the gingiva
13 0 1 7.1E-02 0 0
Abnormality of the hypothalamus-pituitary axis
70 0 1 1.4E-02 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver
75 0 1 1.3E-02 0 0
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear
95 0 1 1.0E-02 0 0
CUI: C4022016
Disease: Abnormality of the preputium
Abnormality of the preputium
22 0 1 4.3E-02 0 0
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue
25 0 1 3.8E-02 0 0
CUI: C4021185
Disease: Absent crus of helix
Absent crus of helix
1 0 1 0.50 0 0
CUI: C0342526
Disease: Absent testes
Absent testes
24 0 2 8.3E-02 0 0
CUI: C4021814
Disease: Accessory oral frenulum
Accessory oral frenulum
12 0 1 7.7E-02 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
120 0 1 8.3E-03 0 0
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis
149 0 1 6.7E-03 0 0
CUI: C0151860
Disease: Acquired porencephaly
Acquired porencephaly
34 0 1 2.9E-02 0 0
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia
633 0 1 1.6E-03 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease
111 0 1 8.9E-03 0 0