Source: ALL
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: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 1 9.7E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 1 3.3E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 1 9.1E-04 0 0
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation 		88 0 1 1.1E-02 0 0
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency 		377 0 1 2.7E-03 0 0
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		234 0 1 4.3E-03 0 0
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		2006 0 1 5.0E-04 0 0
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		2044 0 1 4.9E-04 0 0
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block 		63 0 1 1.6E-02 0 0
CUI: C0006384
Disease: Bundle-Branch Block
Bundle-Branch Block 		12 0 1 8.3E-02 0 0
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		512 0 1 2.0E-03 0 0
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		1756 0 1 5.7E-04 0 0
CUI: C0009806
Disease: Constipation
Constipation 		424 0 1 2.4E-03 0 0
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		94 0 1 1.1E-02 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		725 0 1 1.4E-03 0 0
CUI: C0011644
Disease: Scleroderma
Scleroderma 		316 0 1 3.2E-03 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		48 0 1 2.1E-02 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		1261 0 1 7.9E-04 0 0
CUI: C0013404
Disease: Dyspnea
Dyspnea 		222 0 1 4.5E-03 0 0
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly 		10 0 1 1.0E-01 0 0
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 0 1 1.5E-02 0 0
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		225 0 1 4.4E-03 0 0
CUI: C0015672
Disease: Fatigue
Fatigue 		760 0 1 1.3E-03 0 0
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation 		1037 0 1 9.6E-04 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 0 1 1.4E-02 0 0