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: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial 		18 0 8 0.20 0 0
CUI: C0342883
Disease: Cholesteryl Ester Transfer Protein Deficiency
Cholesteryl Ester Transfer Protein Deficiency 		22 0 8 0.18 0 0
CUI: C0023195
Disease: Lecithin Acyltransferase Deficiency
Lecithin Acyltransferase Deficiency 		9 0 6 0.18 0 0
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		9 0 6 0.18 0 0
CUI: C2931838
Disease: Familial HDL deficiency
Familial HDL deficiency 		10 1 6 0.17 1 3.6E-02
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		20 7 7 0.16 1 2.9E-02
CUI: C0003742
Disease: Arcus Senilis
Arcus Senilis 		13 0 6 0.16 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		28 0 8 0.16 0 0
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		8 0 5 0.15 0 0
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
Hyperlipoproteinemia Type IIb 		25 0 7 0.14 0 0
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia 		17 0 6 0.14 0 0
CUI: C3888506
Disease: LDLR mutation
LDLR mutation 		10 0 5 0.14 0 0
CUI: C0342895
Disease: Fish-Eye Disease
Fish-Eye Disease 		19 0 6 0.14 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma 		29 0 7 0.13 0 0
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial 		24 0 6 0.12 0 0
CUI: C0155210
Disease: Eyelid Xanthoma
Eyelid Xanthoma 		19 0 5 0.11 0 0
CUI: C1843366
Disease: NIEMANN-PICK DISEASE, TYPE C2
NIEMANN-PICK DISEASE, TYPE C2 		9 0 4 0.11 0 0
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias 		20 0 5 0.11 0 0
CUI: C0151691
Disease: Decreased HDL cholesterol concentration
Decreased HDL cholesterol concentration 		12 0 4 0.10 0 0
CUI: C0342881
Disease: Familial hypercholesterolemia - homozygous
Familial hypercholesterolemia - homozygous 		23 0 5 0.10 0 0
CUI: C0036489
Disease: Sea-Blue Histiocyte Syndrome
Sea-Blue Histiocyte Syndrome 		5 0 3 9.1E-02 0 0
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
Hyperkeratosis lenticularis perstans 		18 0 4 8.9E-02 0 0
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency 		6 0 3 8.8E-02 0 0
CUI: C0268406
Disease: Age-related amyloidosis
Age-related amyloidosis 		7 0 3 8.6E-02 0 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis 		20 0 4 8.5E-02 0 0