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: C0340285
Disease: Triple vessel disease of the heart
Triple vessel disease of the heart 		1 0 1 1.00 0 0
CUI: C0349415
Disease: Gram-positive septic shock
Gram-positive septic shock 		1 0 1 1.00 0 0
CUI: C1863551
Disease: HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3
HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3 		1 0 1 1.00 0 0
CUI: C4707954
Disease: Low density lipoprotein receptor adaptor protein 1 mutation
Low density lipoprotein receptor adaptor protein 1 mutation 		1 0 1 1.00 0 0
CUI: C4310756
Disease: HYPERALDOSTERONISM, FAMILIAL, TYPE IV
HYPERALDOSTERONISM, FAMILIAL, TYPE IV 		3 0 1 0.33 0 0
CUI: C2919414
Disease: Low density lipoprotein receptor mutation
Low density lipoprotein receptor mutation 		4 0 1 0.25 0 0
CUI: C0152417
Disease: Congenital stenosis of aortic valve
Congenital stenosis of aortic valve 		5 0 1 0.20 0 0
CUI: C0264683
Disease: Coronary artery atheroma
Coronary artery atheroma 		6 0 1 0.17 0 0
CUI: C3549252
Disease: response to statin
response to statin 		6 0 1 0.17 0 0
CUI: C4022811
Disease: Abnormality of nervous system physiology
Abnormality of nervous system physiology 		6 0 1 0.17 0 0
CUI: C4022924
Disease: Abnormal eye physiology
Abnormal eye physiology 		6 0 1 0.17 0 0
CUI: C4024924
Disease: Cerebral artery atherosclerosis
Cerebral artery atherosclerosis 		6 0 1 0.17 0 0
CUI: C4025000
Disease: Myocardial steatosis
Myocardial steatosis 		6 0 1 0.17 0 0
CUI: C0342879
Disease: Primary hypercholesterolemia
Primary hypercholesterolemia 		7 0 1 0.14 0 0
CUI: C1860488
Disease: Abnormal internal carotid artery morphology
Abnormal internal carotid artery morphology 		7 0 1 0.14 0 0
CUI: C1854107
Disease: Hyperaldosteronism, Familial, Type II
Hyperaldosteronism, Familial, Type II 		8 0 1 0.12 0 0
CUI: C0948807
Disease: Hepatic impairment
Hepatic impairment 		9 0 1 0.11 0 0
CUI: C1848486
Disease: Premature arteriosclerosis
Premature arteriosclerosis 		9 0 1 0.11 0 0
CUI: C4021654
Disease: Precocious atherosclerosis
Precocious atherosclerosis 		9 0 1 0.11 0 0
CUI: C0342880
Disease: Polygenic hypercholesterolemia
Polygenic hypercholesterolemia 		10 0 1 1.0E-01 0 0
CUI: C3888506
Disease: LDLR mutation
LDLR mutation 		10 0 1 1.0E-01 0 0
CUI: C0342907
Disease: Sitosterolemia
Sitosterolemia 		11 0 1 9.1E-02 0 0
CUI: C3267047
Disease: Autoimmune necrotizing myopathy
Autoimmune necrotizing myopathy 		11 0 1 9.1E-02 0 0
CUI: C0751007
Disease: Intracranial Atherosclerosis
Intracranial Atherosclerosis 		12 0 1 8.3E-02 0 0
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 		12 0 1 8.3E-02 0 0