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: C4324548
Disease: Non-compaction cardiomyopathy
Non-compaction cardiomyopathy 		9 0 4 0.27 0 0
CUI: C0344622
Disease: Double inlet left ventricle
Double inlet left ventricle 		4 0 2 0.17 0 0
CUI: C2910126
Disease: Patent or persistent ostium secundum defect (type II)
Patent or persistent ostium secundum defect (type II) 		4 0 2 0.17 0 0
CUI: C2910127
Disease: Patent or persistent sinus venosus defect
Patent or persistent sinus venosus defect 		4 0 2 0.17 0 0
CUI: C0521533
Disease: Atrial septal aneurysm
Atrial septal aneurysm 		5 0 2 0.15 0 0
CUI: C1409792
Disease: Coronary sinus defect
Coronary sinus defect 		5 0 2 0.15 0 0
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 2 0.13 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 2 0.13 0 0
CUI: C2677504
Disease: AUTISM, SUSCEPTIBILITY TO, 15
AUTISM, SUSCEPTIBILITY TO, 15 		9 0 2 0.12 0 0
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		39 0 5 0.11 0 0
CUI: C4732796
Disease: Apical hypertrophic cardiomyopathy
Apical hypertrophic cardiomyopathy 		10 0 2 0.11 0 0
CUI: C0242855
Disease: Congenital atresia of pulmonary valve
Congenital atresia of pulmonary valve 		11 0 2 0.11 0 0
CUI: C0392482
Disease: Common atrium
Common atrium 		11 1 2 0.11 1 0.33
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 1.0E-01 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 1.0E-01 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 1.0E-01 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 1.0E-01 0 0
CUI: C0392470
Disease: Anomalous atrioventricular excitation
Anomalous atrioventricular excitation 		1 0 1 1.0E-01 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 1.0E-01 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 1.0E-01 0 0
CUI: C0795939
Disease: AMINOPTERIN SYNDROME SINE AMINOPTERIN
AMINOPTERIN SYNDROME SINE AMINOPTERIN 		1 0 1 1.0E-01 0 0
CUI: C0869081
Disease: Congenital malformations of palate, not elsewhere classified in ICD10CM
Congenital malformations of palate, not elsewhere classified in ICD10CM 		1 0 1 1.0E-01 0 0
CUI: C0878515
Disease: Internal hydrocephalus
Internal hydrocephalus 		1 0 1 1.0E-01 0 0
CUI: C1842778
Disease: Atrial septal defect 2
Atrial septal defect 2 		1 0 1 1.0E-01 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 0 1 1.0E-01 0 0