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: C3665365
Disease: Arteriosclerotic cardiovascular disease, NOS
Arteriosclerotic cardiovascular disease, NOS 		58 0 8 9.3E-02 0 0
CUI: C0598784
Disease: Dyslipoproteinemias
Dyslipoproteinemias 		24 0 5 9.1E-02 0 0
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		27 0 5 8.6E-02 0 0
CUI: C0020481
Disease: Hyperlipoproteinemia Type V
Hyperlipoproteinemia Type V 		3 0 3 8.3E-02 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma 		29 0 5 8.3E-02 0 0
CUI: C4521075
Disease: Childhood Overweight
Childhood Overweight 		4 0 3 8.1E-02 0 0
CUI: C4704955
Disease: Infant Overweight
Infant Overweight 		4 0 3 8.1E-02 0 0
CUI: C4704956
Disease: Adolescent Overweight
Adolescent Overweight 		4 0 3 8.1E-02 0 0
CUI: C1706412
Disease: Lipidemias
Lipidemias 		18 0 4 8.0E-02 0 0
CUI: C4700045
Disease: Non-ST-segment elevation myocardial infarction (NSTEMI)
Non-ST-segment elevation myocardial infarction (NSTEMI) 		18 0 4 8.0E-02 0 0
CUI: C4021729
Disease: Increased VLDL cholesterol concentration
Increased VLDL cholesterol concentration 		5 0 3 7.9E-02 0 0
CUI: C4553478
Disease: Infantile Obesity
Infantile Obesity 		5 0 3 7.9E-02 0 0
CUI: C0264683
Disease: Coronary artery atheroma
Coronary artery atheroma 		6 0 3 7.7E-02 0 0
CUI: C0342335
Disease: insulin resistance in diabetes
insulin resistance in diabetes 		21 0 4 7.5E-02 0 0
CUI: C0302507
Disease: Parainfluenza Virus Infections
Parainfluenza Virus Infections 		7 0 3 7.5E-02 0 0
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		8 0 3 7.3E-02 0 0
CUI: C0342881
Disease: Familial hypercholesterolemia - homozygous
Familial hypercholesterolemia - homozygous 		23 0 4 7.3E-02 0 0
CUI: C0549399
Disease: Low density lipoprotein increased
Low density lipoprotein increased 		23 0 4 7.3E-02 0 0
CUI: C2609253
Disease: Macrovascular disease
Macrovascular disease 		23 0 4 7.3E-02 0 0
CUI: C0023195
Disease: Lecithin Acyltransferase Deficiency
Lecithin Acyltransferase Deficiency 		9 0 3 7.1E-02 0 0
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		9 0 3 7.1E-02 0 0
CUI: C0024759
Disease: Mansonelliasis
Mansonelliasis 		10 0 3 7.0E-02 0 0
CUI: C0342880
Disease: Polygenic hypercholesterolemia
Polygenic hypercholesterolemia 		10 0 3 7.0E-02 0 0
CUI: C0342907
Disease: Sitosterolemia
Sitosterolemia 		11 0 3 6.8E-02 0 0
CUI: C1563937
Disease: Atherogenesis
Atherogenesis 		59 0 6 6.7E-02 0 0