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: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 1.00 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 1.00 0 0
CUI: C2673630
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder) 		1 3 1 1.00 1 3.0E-02
CUI: C3280785
Disease: VENTRICULAR SEPTAL DEFECT 3
VENTRICULAR SEPTAL DEFECT 3 		1 0 1 1.00 0 0
CUI: C3502353
Disease: Atrial Septal Defect with Atrioventricular Conduction Defects
Atrial Septal Defect with Atrioventricular Conduction Defects 		1 0 1 1.00 0 0
CUI: C2931574
Disease: Chromosome 5, monosomy 5q35
Chromosome 5, monosomy 5q35 		2 0 1 0.50 0 0
CUI: C0265881
Disease: Congenital hypoplasia of aortic arch
Congenital hypoplasia of aortic arch 		4 0 1 0.25 0 0
CUI: C1969292
Disease: Thoracic aorta calcification
Thoracic aorta calcification 		4 0 1 0.25 0 0
CUI: C2910126
Disease: Patent or persistent ostium secundum defect (type II)
Patent or persistent ostium secundum defect (type II) 		4 0 1 0.25 0 0
CUI: C2910127
Disease: Patent or persistent sinus venosus defect
Patent or persistent sinus venosus defect 		4 0 1 0.25 0 0
CUI: C0521533
Disease: Atrial septal aneurysm
Atrial septal aneurysm 		5 0 1 0.20 0 0
CUI: C0600125
Disease: Prolonged PR interval
Prolonged PR interval 		5 0 1 0.20 0 0
CUI: C1409792
Disease: Coronary sinus defect
Coronary sinus defect 		5 0 1 0.20 0 0
CUI: C4025670
Disease: Abnormality of chromosome segregation
Abnormality of chromosome segregation 		5 0 1 0.20 0 0
CUI: C3887892
Disease: Aortic Valve Disease 1
Aortic Valve Disease 1 		6 0 1 0.17 0 0
CUI: C0744669
Disease: Complex congenital heart disease
Complex congenital heart disease 		7 0 1 0.14 0 0
CUI: C1879286
Disease: Hereditary bundle branch system defect
Hereditary bundle branch system defect 		7 0 1 0.14 0 0
CUI: C0266283
Disease: Ectopic thyroid tissue (disorder)
Ectopic thyroid tissue (disorder) 		8 0 1 0.12 0 0
CUI: C0344760
Disease: Congenital atresia of mitral valve
Congenital atresia of mitral valve 		8 0 1 0.12 0 0
CUI: C3280795
Disease: HYPOPLASTIC LEFT HEART SYNDROME 2
HYPOPLASTIC LEFT HEART SYNDROME 2 		8 11 1 0.12 1 2.4E-02
CUI: C0410226
Disease: Congenital Myotonic Dystrophy
Congenital Myotonic Dystrophy 		9 0 1 0.11 0 0
CUI: C0685707
Disease: Muscular ventricular septum defect
Muscular ventricular septum defect 		9 0 1 0.11 0 0
CUI: C4324548
Disease: Non-compaction cardiomyopathy
Non-compaction cardiomyopathy 		9 0 1 0.11 0 0
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly 		10 0 1 1.0E-01 0 0
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis 		11 0 1 9.1E-02 0 0