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: C1859372
Disease: Calcification of Joints and Arteries
Calcification of Joints and Arteries 		3 0 2 3.8E-02 0 0
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
Premature coronary artery atherosclerosis 		87 43 5 3.8E-02 3 1.2E-02
CUI: C3151466
Disease: HEPATIC LIPASE DEFICIENCY (disorder)
HEPATIC LIPASE DEFICIENCY (disorder) 		5 0 2 3.7E-02 0 0
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency 		6 0 2 3.6E-02 0 0
CUI: C4022811
Disease: Abnormality of nervous system physiology
Abnormality of nervous system physiology 		6 0 2 3.6E-02 0 0
CUI: C4022924
Disease: Abnormal eye physiology
Abnormal eye physiology 		6 0 2 3.6E-02 0 0
CUI: C4024924
Disease: Cerebral artery atherosclerosis
Cerebral artery atherosclerosis 		6 0 2 3.6E-02 0 0
CUI: C4025000
Disease: Myocardial steatosis
Myocardial steatosis 		6 0 2 3.6E-02 0 0
CUI: C1849618
Disease: Accelerated atherosclerosis
Accelerated atherosclerosis 		7 0 2 3.6E-02 0 0
CUI: C1860488
Disease: Abnormal internal carotid artery morphology
Abnormal internal carotid artery morphology 		7 0 2 3.6E-02 0 0
CUI: C0155733
Disease: Atherosclerosis of aorta
Atherosclerosis of aorta 		37 0 3 3.5E-02 0 0
CUI: C0473583
Disease: Nevus elasticus
Nevus elasticus 		37 0 3 3.5E-02 0 0
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		96 212 5 3.5E-02 3 7.2E-03
CUI: C1843366
Disease: NIEMANN-PICK DISEASE, TYPE C2
NIEMANN-PICK DISEASE, TYPE C2 		9 0 2 3.4E-02 0 0
CUI: C1848486
Disease: Premature arteriosclerosis
Premature arteriosclerosis 		9 0 2 3.4E-02 0 0
CUI: C2697764
Disease: Interleukin 16 Measurement
Interleukin 16 Measurement 		9 0 2 3.4E-02 0 0
CUI: C4021654
Disease: Precocious atherosclerosis
Precocious atherosclerosis 		9 0 2 3.4E-02 0 0
CUI: C0005396
Disease: Bile Duct Neoplasms
Bile Duct Neoplasms 		11 0 2 3.3E-02 0 0
CUI: C0151854
Disease: Abnormal platelets
Abnormal platelets 		11 0 2 3.3E-02 0 0
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
Familial hypercholesterolemia - heterozygous 		42 0 3 3.3E-02 0 0
CUI: C0342907
Disease: Sitosterolemia
Sitosterolemia 		11 0 2 3.3E-02 0 0
CUI: C0883409
Disease: Cardiac troponin I measurement
Cardiac troponin I measurement 		11 0 2 3.3E-02 0 0
CUI: C4021796
Disease: Renal steatosis
Renal steatosis 		12 0 2 3.3E-02 0 0
CUI: C4476910
Disease: Thin-cap fibroatheroma
Thin-cap fibroatheroma 		12 0 2 3.3E-02 0 0
CUI: C0002982
Disease: Angioid Streaks
Angioid Streaks 		13 0 2 3.2E-02 0 0