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: C0426396
Disease: Urine looks dark
Urine looks dark 		6 0 1 1.0E-01 0 0
CUI: C1720821
Disease: Membranoproliferative Glomerulonephritis, Type III
Membranoproliferative Glomerulonephritis, Type III 		6 0 1 1.0E-01 0 0
CUI: C3666017
Disease: Cholangiopathy
Cholangiopathy 		6 0 1 1.0E-01 0 0
CUI: C4024644
Disease: Multiple small medullary renal cysts
Multiple small medullary renal cysts 		6 0 1 1.0E-01 0 0
CUI: C0155120
Disease: Corneal Dystrophy, Band-Shaped
Corneal Dystrophy, Band-Shaped 		7 0 1 9.1E-02 0 0
CUI: C0266548
Disease: Axenfeld anomaly (disorder)
Axenfeld anomaly (disorder) 		7 0 1 9.1E-02 0 0
CUI: C0268742
Disease: Membranoproliferative Glomerulonephritis, Type I
Membranoproliferative Glomerulonephritis, Type I 		7 0 1 9.1E-02 0 0
CUI: C1837549
Disease: SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2
SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2 		7 0 1 9.1E-02 0 0
CUI: C0332886
Disease: Coarctation
Coarctation 		8 0 1 8.3E-02 0 0
CUI: C0917715
Disease: Hajdu-Cheney Syndrome
Hajdu-Cheney Syndrome 		8 0 1 8.3E-02 0 0
CUI: C1855284
Disease: Intrahepatic biliary atresia
Intrahepatic biliary atresia 		9 0 1 7.7E-02 0 0
CUI: C3805247
Disease: Late onset neutropenia
Late onset neutropenia 		9 0 1 7.7E-02 0 0
CUI: C4025573
Disease: Increased muscle fatiguability
Increased muscle fatiguability 		9 0 1 7.7E-02 0 0
CUI: C4527152
Disease: Tricuspid Valve Regurgitation Velocity
Tricuspid Valve Regurgitation Velocity 		9 0 1 7.7E-02 0 0
CUI: C0020951
Disease: Immune Complex Diseases
Immune Complex Diseases 		10 0 1 7.1E-02 0 0
CUI: C0268743
Disease: Membranoproliferative Glomerulonephritis, Type II
Membranoproliferative Glomerulonephritis, Type II 		10 0 1 7.1E-02 0 0
CUI: C0282631
Disease: Facies
Facies 		10 0 1 7.1E-02 0 0
CUI: C0948368
Disease: Kaufman-McKusick syndrome
Kaufman-McKusick syndrome 		10 0 1 7.1E-02 0 0
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		42 0 3 6.8E-02 0 0
CUI: C1839454
Disease: PROPERDIN DEFICIENCY, X-LINKED
PROPERDIN DEFICIENCY, X-LINKED 		11 0 1 6.7E-02 0 0
CUI: C2364016
Disease: Systemic sclerosis [scleroderma]
Systemic sclerosis [scleroderma] 		11 0 1 6.7E-02 0 0
CUI: C1837512
Disease: Decreased serum complement C3
Decreased serum complement C3 		12 0 1 6.2E-02 0 0
CUI: C0029810
Disease: Other specified iron deficiency anemias
Other specified iron deficiency anemias 		13 0 1 5.9E-02 0 0
CUI: C0085581
Disease: Restrictive lung disease
Restrictive lung disease 		13 0 1 5.9E-02 0 0
CUI: C0277942
Disease: Butterfly rash
Butterfly rash 		13 0 1 5.9E-02 0 0