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: C3178807
Disease: Left Atrial Isomerism
Left Atrial Isomerism 		6 0 6 0.86 0 0
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		13 0 7 0.54 0 0
CUI: C3178806
Disease: Right Atrial Isomerism
Right Atrial Isomerism 		14 0 7 0.50 0 0
CUI: C0344692
Disease: Isomerism of atrial appendages
Isomerism of atrial appendages 		3 0 3 0.43 0 0
CUI: C1876171
Disease: Polyasplenia
Polyasplenia 		3 0 3 0.43 0 0
CUI: C1876172
Disease: VAH, AUTOSOMAL RECESSIVE
VAH, AUTOSOMAL RECESSIVE 		3 0 3 0.43 0 0
CUI: C1876173
Disease: Heterotaxy, Visceroatrial, Autosomal Recessive
Heterotaxy, Visceroatrial, Autosomal Recessive 		3 0 3 0.43 0 0
CUI: C2910124
Disease: Isomerism of atrial appendages with asplenia or polysplenia
Isomerism of atrial appendages with asplenia or polysplenia 		3 0 3 0.43 0 0
CUI: C1167664
Disease: Situs ambiguous
Situs ambiguous 		9 0 4 0.33 0 0
CUI: C1956410
Disease: Double Outlet Right Ventricle, Noncommitted VSD
Double Outlet Right Ventricle, Noncommitted VSD 		3 0 2 0.25 0 0
CUI: C1956411
Disease: Double Outlet Right Ventricle, Subaortic VSD
Double Outlet Right Ventricle, Subaortic VSD 		3 0 2 0.25 0 0
CUI: C1956412
Disease: Double Outlet Right Ventricle, Subpulmonary VSD
Double Outlet Right Ventricle, Subpulmonary VSD 		3 0 2 0.25 0 0
CUI: C0035615
Disease: Right aortic arch (disorder)
Right aortic arch (disorder) 		4 0 2 0.22 0 0
CUI: C1956413
Disease: Taussig-Bing Anomaly
Taussig-Bing Anomaly 		4 0 2 0.22 0 0
CUI: C3257801
Disease: Dextrotransposition of aorta
Dextrotransposition of aorta 		4 0 2 0.22 0 0
CUI: C1837341
Disease: Transposition of the Great Arteries, Dextro-Looped 1
Transposition of the Great Arteries, Dextro-Looped 1 		6 0 2 0.18 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 7 0.18 0 0
CUI: C1856659
Disease: Polysplenia
Polysplenia 		15 0 3 0.16 0 0
CUI: C0266632
Disease: Ectopic spleen
Ectopic spleen 		1 0 1 0.14 0 0
CUI: C4225217
Disease: HETEROTAXY, VISCERAL, 7, AUTOSOMAL
HETEROTAXY, VISCERAL, 7, AUTOSOMAL 		1 0 1 0.14 0 0
CUI: C4274029
Disease: Biliary atresia with splenic malformation syndrome
Biliary atresia with splenic malformation syndrome 		1 0 1 0.14 0 0
CUI: C4531036
Disease: Abdominal situs ambiguus
Abdominal situs ambiguus 		1 0 1 0.14 0 0
CUI: C3536741
Disease: Discordant ventriculoarterial connection
Discordant ventriculoarterial connection 		10 0 2 0.13 0 0
CUI: C0265865
Disease: Mesocardia
Mesocardia 		2 0 1 0.12 0 0
CUI: C0392482
Disease: Common atrium
Common atrium 		11 0 2 0.12 0 0