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: C0266632
Disease: Ectopic spleen
Ectopic spleen
1 0 1 0.25 0 0
CUI: C3164429
Disease: Indeterminate atrial arrangement
Indeterminate atrial arrangement
1 1 1 0.25 1 1.00
CUI: C3178807
Disease: Left Atrial Isomerism
Left Atrial Isomerism
6 0 2 0.25 0 0
Unbalanced atrioventricular canal defect
1 1 1 0.25 1 1.00
Congenitally corrected transposition of the great arteries with ventricular septal defect
1 0 1 0.25 0 0
CUI: C4310668
Disease: HETEROTAXY, VISCERAL, 8, AUTOSOMAL
HETEROTAXY, VISCERAL, 8, AUTOSOMAL
1 2 1 0.25 1 0.50
CUI: C4531036
Disease: Abdominal situs ambiguus
Abdominal situs ambiguus
1 0 1 0.25 0 0
CUI: C4539783
Disease: SPERMATOGENIC FAILURE 18
SPERMATOGENIC FAILURE 18
1 0 1 0.25 0 0
CUI: C4539798
Disease: CILIARY DYSKINESIA, PRIMARY, 37
CILIARY DYSKINESIA, PRIMARY, 37
1 0 1 0.25 0 0
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome
7 0 2 0.22 0 0
CUI: C1866091
Disease: Left-Right Axis Malformations
Left-Right Axis Malformations
2 0 1 0.20 0 0
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6
2 0 1 0.20 0 0
CUI: C4015619
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC, 8
EPILEPSY, PROGRESSIVE MYOCLONIC, 8
2 0 1 0.20 0 0
CUI: C1167664
Disease: Situs ambiguous
Situs ambiguous
9 0 2 0.18 0 0
CUI: C0344692
Disease: Isomerism of atrial appendages
Isomerism of atrial appendages
3 0 1 0.17 0 0
CUI: C1876171
Disease: Polyasplenia
Polyasplenia
3 0 1 0.17 0 0
CUI: C1876172
Disease: VAH, AUTOSOMAL RECESSIVE
VAH, AUTOSOMAL RECESSIVE
3 0 1 0.17 0 0
Heterotaxy, Visceroatrial, Autosomal Recessive
3 0 1 0.17 0 0
Double Outlet Right Ventricle, Noncommitted VSD
3 0 1 0.17 0 0
Double Outlet Right Ventricle, Subaortic VSD
3 0 1 0.17 0 0
Double Outlet Right Ventricle, Subpulmonary VSD
3 0 1 0.17 0 0
CUI: C1970501
Disease: Hypoplastic pulmonary veins
Hypoplastic pulmonary veins
3 0 1 0.17 0 0
Isomerism of atrial appendages with asplenia or polysplenia
3 0 1 0.17 0 0
CUI: C1956413
Disease: Taussig-Bing Anomaly
Taussig-Bing Anomaly
4 0 1 0.14 0 0
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome
13 0 2 0.13 0 0