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: C1704321
Disease: Nephrotic Syndrome, Minimal Change
Nephrotic Syndrome, Minimal Change 		85 10 50 0.58 10 0.14
CUI: C1533172
Disease: Infantile nystagmus syndrome
Infantile nystagmus syndrome 		54 8 25 0.31 7 9.6E-02
CUI: C0868908
Disease: Pancolitis
Pancolitis 		29 11 9 0.13 2 2.5E-02
CUI: C0027721
Disease: Lipoid nephrosis
Lipoid nephrosis 		50 3 11 0.12 2 2.7E-02
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss 		72 38 13 0.12 1 9.2E-03
CUI: C0403397
Disease: Steroid-resistant nephrotic syndrome
Steroid-resistant nephrotic syndrome 		73 25 13 0.12 8 9.0E-02
CUI: C3266102
Disease: Steroid resistant nephrotic syndrome of childhood
Steroid resistant nephrotic syndrome of childhood 		73 19 13 0.12 8 9.6E-02
CUI: C3887641
Disease: Recurrent hepatitis
Recurrent hepatitis 		35 5 9 0.12 1 1.3E-02
CUI: C0403396
Disease: Steroid-sensitive nephrotic syndrome
Steroid-sensitive nephrotic syndrome 		36 11 9 0.12 3 3.7E-02
CUI: C2717865
Disease: Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis 		86 0 14 0.11 0 0
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis 		197 33 25 0.11 1 9.6E-03
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases 		69 0 12 0.11 0 0
CUI: C0086445
Disease: Idiopathic Membranous Glomerulonephritis
Idiopathic Membranous Glomerulonephritis 		79 13 13 0.11 1 1.2E-02
CUI: C0399447
Disease: Early onset periodontitis
Early onset periodontitis 		21 0 7 0.11 0 0
CUI: C3874381
Disease: Childhood nephrotic syndrome
Childhood nephrotic syndrome 		23 6 7 0.10 4 5.4E-02
CUI: C2895206
Disease: Autoimmune disease (systemic) NOS
Autoimmune disease (systemic) NOS 		37 0 8 1.0E-01 0 0
CUI: C2733158
Disease: Cerebral Small Vessel Diseases
Cerebral Small Vessel Diseases 		62 6 10 9.7E-02 1 1.3E-02
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction 		17 0 6 9.7E-02 0 0
CUI: C2584620
Disease: Thrombophilia, hereditary
Thrombophilia, hereditary 		17 9 6 9.7E-02 1 1.3E-02
CUI: C0403398
Disease: Steroid-dependent nephrotic syndrome
Steroid-dependent nephrotic syndrome 		6 0 5 9.6E-02 0 0
CUI: C3825926
Disease: Nephrotic syndrome in children
Nephrotic syndrome in children 		6 1 5 9.6E-02 1 1.4E-02
CUI: C2721603
Disease: Henoch-Schonlein purpura nephritis
Henoch-Schonlein purpura nephritis 		29 0 7 9.6E-02 0 0
CUI: C1277187
Disease: Left ventricular systolic dysfunction
Left ventricular systolic dysfunction 		41 0 8 9.5E-02 0 0
CUI: C1709661
Disease: Primary Focal Segmental Glomerulosclerosis
Primary Focal Segmental Glomerulosclerosis 		18 0 6 9.5E-02 0 0
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		76 15 11 9.5E-02 1 1.2E-02