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: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 1 1.1E-02 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 1 1.3E-02 0 0
3 beta-Hydroxysteroid dehydrogenase deficiency
9 0 1 1.4E-02 0 0
CUI: C2936403
Disease: 46, XX Disorders of Sex Development
46, XX Disorders of Sex Development
6 0 1 1.4E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 6.0E-03 0 0
CUI: C1291077
Disease: Abdominal bloating
Abdominal bloating
10 0 1 1.4E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 2.7E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 4 4.1E-03 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 1 1.3E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 1 8.1E-03 0 0
CUI: C4021982
Disease: Abnormal eating behavior
Abnormal eating behavior
8 0 1 1.4E-02 0 0
Abnormal liver function tests during pregnancy
3 0 1 1.5E-02 0 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation
32 0 1 1.0E-02 0 0
Abnormal mitochondria in muscle tissue
39 0 1 9.7E-03 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance
15 0 1 1.3E-02 0 0
CUI: C0151746
Disease: Abnormal renal function
Abnormal renal function
12 0 1 1.3E-02 0 0
CUI: C3163801
Disease: Abnormality of aortic arch
Abnormality of aortic arch
13 0 1 1.3E-02 0 0
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve
50 0 1 8.8E-03 0 0
Abnormality of blood and blood-forming tissues
23 0 1 1.1E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel
96 0 1 6.3E-03 0 0
CUI: C4293672
Disease: Abnormality of mesentery morphology
Abnormality of mesentery morphology
3 0 1 1.5E-02 0 0
Abnormality of pelvic girdle bone morphology
55 0 1 8.4E-03 0 0
CUI: C3164374
Disease: Abnormality of pulmonary valve
Abnormality of pulmonary valve
40 0 1 9.6E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 3.6E-03 0 0
Abnormality of the autonomic nervous system
3 0 1 1.5E-02 0 0