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: C4022811
Disease: Abnormality of nervous system physiology
Abnormality of nervous system physiology 		6 0 6 1.00 0 0
CUI: C4022924
Disease: Abnormal eye physiology
Abnormal eye physiology 		6 0 6 1.00 0 0
CUI: C4024924
Disease: Cerebral artery atherosclerosis
Cerebral artery atherosclerosis 		6 0 6 1.00 0 0
CUI: C1860488
Disease: Abnormal internal carotid artery morphology
Abnormal internal carotid artery morphology 		7 0 6 0.86 0 0
CUI: C1848486
Disease: Premature arteriosclerosis
Premature arteriosclerosis 		9 0 6 0.67 0 0
CUI: C4021654
Disease: Precocious atherosclerosis
Precocious atherosclerosis 		9 0 6 0.67 0 0
CUI: C4021796
Disease: Renal steatosis
Renal steatosis 		12 0 6 0.50 0 0
CUI: C0221253
Disease: Xanthoma tendinosum
Xanthoma tendinosum 		15 0 6 0.40 0 0
CUI: C0342880
Disease: Polygenic hypercholesterolemia
Polygenic hypercholesterolemia 		10 0 4 0.33 0 0
CUI: C2749759
Disease: Macrothrombocytopenia-Stomatocytosis, Mediterranean
Macrothrombocytopenia-Stomatocytosis, Mediterranean 		2 0 2 0.33 0 0
CUI: C3888506
Disease: LDLR mutation
LDLR mutation 		10 0 4 0.33 0 0
CUI: C0342907
Disease: Sitosterolemia
Sitosterolemia 		11 0 4 0.31 0 0
CUI: C1096249
Disease: Calcification of the aorta
Calcification of the aorta 		21 0 6 0.29 0 0
CUI: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis 		23 0 6 0.26 0 0
CUI: C0342881
Disease: Familial hypercholesterolemia - homozygous
Familial hypercholesterolemia - homozygous 		23 0 6 0.26 0 0
CUI: C0549399
Disease: Low density lipoprotein increased
Low density lipoprotein increased 		23 0 6 0.26 0 0
CUI: C0302164
Disease: Tuberous xanthoma
Tuberous xanthoma 		4 0 2 0.25 0 0
CUI: C1859495
Disease: Episodic hemolytic anemia
Episodic hemolytic anemia 		4 0 2 0.25 0 0
CUI: C2919414
Disease: Low density lipoprotein receptor mutation
Low density lipoprotein receptor mutation 		4 0 2 0.25 0 0
CUI: C3151466
Disease: HEPATIC LIPASE DEFICIENCY (disorder)
HEPATIC LIPASE DEFICIENCY (disorder) 		5 0 2 0.22 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma 		29 0 6 0.21 0 0
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency 		6 0 2 0.20 0 0
CUI: C0018808
Disease: Heart murmur
Heart murmur 		31 0 6 0.19 0 0
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
Hyperlipoproteinemia Type IIb 		25 0 5 0.19 0 0
CUI: C0155210
Disease: Eyelid Xanthoma
Eyelid Xanthoma 		19 0 4 0.19 0 0