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: C0020480
Disease: Hyperlipoproteinemia Type IV
Hyperlipoproteinemia Type IV 		11 0 9 0.30 0 0
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
Hyperkeratosis lenticularis perstans 		18 11 9 0.24 7 0.25
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial 		24 9 10 0.24 1 3.1E-02
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
Hyperlipoproteinemia Type IIb 		25 16 10 0.23 1 2.6E-02
CUI: C0342883
Disease: Cholesteryl Ester Transfer Protein Deficiency
Cholesteryl Ester Transfer Protein Deficiency 		22 0 9 0.22 0 0
CUI: C0020476
Disease: Hyperlipoproteinemias
Hyperlipoproteinemias 		49 7 13 0.20 5 0.19
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		20 0 8 0.20 0 0
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		9 0 6 0.19 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma 		29 0 9 0.19 0 0
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia 		17 0 7 0.18 0 0
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial 		18 0 7 0.18 0 0
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias 		20 11 7 0.17 1 2.9E-02
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type I 		36 64 9 0.16 1 1.1E-02
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		8 0 5 0.16 0 0
CUI: C0039292
Disease: Tangier Disease
Tangier Disease 		31 0 8 0.16 0 0
CUI: C3888506
Disease: LDLR mutation
LDLR mutation 		10 21 5 0.15 1 2.3E-02
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
Familial hypercholesterolemia - heterozygous 		42 34 9 0.15 1 1.8E-02
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		27 53 7 0.15 1 1.3E-02
CUI: C4524040
Disease: Atherogenic dyslipidaemia
Atherogenic dyslipidaemia 		36 9 8 0.14 1 3.1E-02
CUI: C0155733
Disease: Atherosclerosis of aorta
Atherosclerosis of aorta 		37 0 8 0.14 0 0
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		91 28 14 0.13 3 6.1E-02
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency 		6 0 4 0.13 0 0
CUI: C0342881
Disease: Familial hypercholesterolemia - homozygous
Familial hypercholesterolemia - homozygous 		23 72 6 0.13 1 1.1E-02
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
Premature coronary artery atherosclerosis 		87 43 13 0.13 1 1.5E-02
CUI: C1706412
Disease: Lipidemias
Lipidemias 		18 0 5 0.12 0 0