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: C4015619
Disease: EPILEPSY, PROGRESSIVE MYOCLONIC, 8
EPILEPSY, PROGRESSIVE MYOCLONIC, 8 		2 0 2 1.00 0 0
CUI: C0338464
Disease: Epilepsy co-occurrent and due to dementia
Epilepsy co-occurrent and due to dementia 		1 0 1 0.50 0 0
CUI: C4531036
Disease: Abdominal situs ambiguus
Abdominal situs ambiguus 		1 0 1 0.50 0 0
CUI: C0694453
Disease: Neurotic, stress-related and somatoform disorders
Neurotic, stress-related and somatoform disorders 		5 0 2 0.40 0 0
CUI: C1956410
Disease: Double Outlet Right Ventricle, Noncommitted VSD
Double Outlet Right Ventricle, Noncommitted VSD 		3 0 1 0.25 0 0
CUI: C1956411
Disease: Double Outlet Right Ventricle, Subaortic VSD
Double Outlet Right Ventricle, Subaortic VSD 		3 0 1 0.25 0 0
CUI: C1956412
Disease: Double Outlet Right Ventricle, Subpulmonary VSD
Double Outlet Right Ventricle, Subpulmonary VSD 		3 0 1 0.25 0 0
CUI: C1970501
Disease: Hypoplastic pulmonary veins
Hypoplastic pulmonary veins 		3 0 1 0.25 0 0
CUI: C0035615
Disease: Right aortic arch (disorder)
Right aortic arch (disorder) 		4 0 1 0.20 0 0
CUI: C1956413
Disease: Taussig-Bing Anomaly
Taussig-Bing Anomaly 		4 0 1 0.20 0 0
CUI: C1282979
Disease: Transient hypoparathyroidism
Transient hypoparathyroidism 		5 0 1 0.17 0 0
CUI: C0175707
Disease: Asplenia Syndrome
Asplenia Syndrome 		13 0 2 0.15 0 0
CUI: C3178807
Disease: Left Atrial Isomerism
Left Atrial Isomerism 		6 0 1 0.14 0 0
CUI: C0265357
Disease: Polysplenia Syndrome
Polysplenia Syndrome 		7 0 1 0.12 0 0
CUI: C4684942
Disease: Refractory Thyroid Gland Carcinoma
Refractory Thyroid Gland Carcinoma 		10 0 1 9.1E-02 0 0
CUI: C0242855
Disease: Congenital atresia of pulmonary valve
Congenital atresia of pulmonary valve 		11 0 1 8.3E-02 0 0
CUI: C0392482
Disease: Common atrium
Common atrium 		11 0 1 8.3E-02 0 0
CUI: C0022738
Disease: Klippel-Feil Syndrome
Klippel-Feil Syndrome 		12 0 1 7.7E-02 0 0
CUI: C0344917
Disease: Left ventricular outflow tract obstruction
Left ventricular outflow tract obstruction 		13 0 1 7.1E-02 0 0
CUI: C1857586
Disease: CONOTRUNCAL HEART MALFORMATIONS (disorder)
CONOTRUNCAL HEART MALFORMATIONS (disorder) 		13 0 1 7.1E-02 0 0
CUI: C3178806
Disease: Right Atrial Isomerism
Right Atrial Isomerism 		14 0 1 6.7E-02 0 0
CUI: C1856659
Disease: Polysplenia
Polysplenia 		15 0 1 6.2E-02 0 0
CUI: C4551903
Disease: Total anomalous pulmonary venous return
Total anomalous pulmonary venous return 		16 0 1 5.9E-02 0 0
CUI: C0751776
Disease: Atypical Inclusion-Body Disease
Atypical Inclusion-Body Disease 		17 0 1 5.6E-02 0 0
CUI: C0751777
Disease: Familial Progressive Myoclonic Epilepsy
Familial Progressive Myoclonic Epilepsy 		17 0 1 5.6E-02 0 0