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: C0403397
Disease: Steroid-resistant nephrotic syndrome
Steroid-resistant nephrotic syndrome 		73 25 21 0.25 9 0.13
CUI: C3266102
Disease: Steroid resistant nephrotic syndrome of childhood
Steroid resistant nephrotic syndrome of childhood 		73 19 21 0.25 8 0.12
CUI: C0086432
Disease: Hyalinosis, Segmental Glomerular
Hyalinosis, Segmental Glomerular 		28 0 11 0.23 0 0
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 9 0.20 0 0
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital 		31 0 10 0.19 0 0
CUI: C1305904
Disease: Familial hematuria
Familial hematuria 		23 7 8 0.17 1 1.7E-02
CUI: C1709661
Disease: Primary Focal Segmental Glomerulosclerosis
Primary Focal Segmental Glomerulosclerosis 		18 0 7 0.17 0 0
CUI: C4049702
Disease: Focal Segmental Glomerulosclerosis, Not Otherwise Specified
Focal Segmental Glomerulosclerosis, Not Otherwise Specified 		42 6 10 0.16 1 1.7E-02
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 7 5 0.15 2 3.4E-02
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change 		7 0 4 0.12 0 0
CUI: C1858395
Disease: Tubular atrophy
Tubular atrophy 		17 0 4 9.1E-02 0 0
CUI: C2919166
Disease: Autosomal dominant focal segmental glomerulosclerosis
Autosomal dominant focal segmental glomerulosclerosis 		5 0 3 9.1E-02 0 0
CUI: C4521759
Disease: Tubular Atrophy Assessment
Tubular Atrophy Assessment 		17 0 4 9.1E-02 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 3 8.6E-02 0 0
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment 		84 0 9 8.5E-02 0 0
CUI: C0033687
Disease: Proteinuria
Proteinuria 		239 20 21 8.4E-02 2 2.8E-02
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis 		281 50 24 8.3E-02 4 4.0E-02
CUI: C0239981
Disease: Hypoalbuminemia
Hypoalbuminemia 		107 9 10 7.8E-02 2 3.3E-02
CUI: C0403399
Disease: Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome 		11 178 3 7.7E-02 1 4.3E-03
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 0 3 7.3E-02 0 0
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 3 7.3E-02 0 0
CUI: C0795949
Disease: Galloway Mowat syndrome
Galloway Mowat syndrome 		15 0 3 7.0E-02 0 0
CUI: C0027721
Disease: Lipoid nephrosis
Lipoid nephrosis 		50 0 5 6.6E-02 0 0
CUI: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis 		34 0 4 6.6E-02 0 0
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome 		51 314 5 6.5E-02 1 2.7E-03