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: C1969292
Disease: Thoracic aorta calcification
Thoracic aorta calcification 		4 0 4 0.67 0 0
CUI: C0856748
Disease: Aneurysm of aortic arch
Aneurysm of aortic arch 		20 0 4 0.18 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 0.17 0 0
CUI: C0232308
Disease: P pulmonale by EKG (finding)
P pulmonale by EKG (finding) 		1 0 1 0.17 0 0
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 0.17 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 0.17 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 0.17 0 0
CUI: C0748427
Disease: Right atrial enlargement
Right atrial enlargement 		1 0 1 0.17 0 0
CUI: C0858925
Disease: Deafness labyrinthine
Deafness labyrinthine 		1 0 1 0.17 0 0
CUI: C1859728
Disease: Coronary Sclerosis, Medial, of Infancy
Coronary Sclerosis, Medial, of Infancy 		1 0 1 0.17 0 0
CUI: C2673630
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder) 		1 0 1 0.17 0 0
CUI: C3276096
Disease: ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS 		1 0 1 0.17 0 0
CUI: C3280785
Disease: VENTRICULAR SEPTAL DEFECT 3
VENTRICULAR SEPTAL DEFECT 3 		1 0 1 0.17 0 0
CUI: C3502353
Disease: Atrial Septal Defect with Atrioventricular Conduction Defects
Atrial Septal Defect with Atrioventricular Conduction Defects 		1 0 1 0.17 0 0
CUI: C3809781
Disease: Cole disease
Cole disease 		1 0 1 0.17 0 0
CUI: C4014970
Disease: ADAMS-OLIVER SYNDROME 5
ADAMS-OLIVER SYNDROME 5 		1 0 1 0.17 0 0
CUI: C4025269
Disease: Generalized arterial calcification
Generalized arterial calcification 		1 0 1 0.17 0 0
CUI: C4479496
Disease: CRANIOSYNOSTOSIS 7
CRANIOSYNOSTOSIS 7 		1 0 1 0.17 0 0
CUI: C4479677
Disease: CRANIOSYNOSTOSIS 7, SUSCEPTIBILITY TO
CRANIOSYNOSTOSIS 7, SUSCEPTIBILITY TO 		1 0 1 0.17 0 0
CUI: C4551985
Disease: ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1 		1 0 1 0.17 0 0
CUI: C4693563
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5 		1 0 1 0.17 0 0
CUI: C1836653
Disease: Ascending aortic dissection
Ascending aortic dissection 		25 0 4 0.15 0 0
CUI: C0020441
Disease: Hypercementosis
Hypercementosis 		2 0 1 0.14 0 0
CUI: C0278769
Disease: Chronic lymphocytic leukaemia stage 3
Chronic lymphocytic leukaemia stage 3 		2 0 1 0.14 0 0
CUI: C0344963
Disease: Right hypoplastic heart syndrome
Right hypoplastic heart syndrome 		2 0 1 0.14 0 0