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: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency
8 0 5 0.23 0 0
CUI: C0023195
Disease: Lecithin Acyltransferase Deficiency
Lecithin Acyltransferase Deficiency
9 22 5 0.22 3 7.3E-02
CUI: C0271288
Disease: Corneal guttata
Corneal guttata
6 0 4 0.19 0 0
Cholesteryl Ester Transfer Protein Deficiency
22 0 6 0.17 0 0
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1
9 0 4 0.17 0 0
CUI: C4699184
Disease: Fuchs
Fuchs
10 5 4 0.16 1 3.8E-02
CUI: C0039292
Disease: Tangier Disease
Tangier Disease
31 0 6 0.14 0 0
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2
6 1 3 0.14 1 4.5E-02
CUI: C0268406
Disease: Age-related amyloidosis
Age-related amyloidosis
7 0 3 0.13 0 0
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia
17 0 4 0.12 0 0
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
18 0 4 0.12 0 0
Corneal dystrophy, Fuchs' endothelial, 1
9 0 3 0.12 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
28 0 5 0.12 0 0
CUI: C3888506
Disease: LDLR mutation
LDLR mutation
10 0 3 0.12 0 0
CUI: C0474444
Disease: Corneal stromal edema
Corneal stromal edema
2 0 2 0.11 0 0
CUI: C0003742
Disease: Arcus Senilis
Arcus Senilis
13 0 3 0.10 0 0
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial
24 0 4 0.10 0 0
CUI: C0024439
Disease: Macular corneal dystrophy
Macular corneal dystrophy
5 0 2 9.1E-02 0 0
CUI: C0544008
Disease: Chandler syndrome
Chandler syndrome
6 0 2 8.7E-02 0 0
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias
20 0 3 8.3E-02 0 0
Schnyder crystalline corneal dystrophy
7 0 2 8.3E-02 0 0
CUI: C0018179
Disease: Granular Dystrophy, Corneal
Granular Dystrophy, Corneal
8 0 2 8.0E-02 0 0
CUI: C1857569
Disease: CORNEAL ENDOTHELIAL DYSTROPHY 2
CORNEAL ENDOTHELIAL DYSTROPHY 2
9 0 2 7.7E-02 0 0
CUI: C0795956
Disease: Chylomicron retention disease
Chylomicron retention disease
10 0 2 7.4E-02 0 0
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
Hyperlipoproteinemia Type IIb
25 0 3 7.3E-02 0 0