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: C0403399
Disease: Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome 		11 178 7 0.20 3 1.6E-02
CUI: C1868672
Disease: NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE 		31 0 10 0.19 0 0
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 8 0.18 0 0
CUI: C4049702
Disease: Focal Segmental Glomerulosclerosis, Not Otherwise Specified
Focal Segmental Glomerulosclerosis, Not Otherwise Specified 		42 0 10 0.16 0 0
CUI: C0403397
Disease: Steroid-resistant nephrotic syndrome
Steroid-resistant nephrotic syndrome 		73 25 13 0.14 1 3.0E-02
CUI: C3266102
Disease: Steroid resistant nephrotic syndrome of childhood
Steroid resistant nephrotic syndrome of childhood 		73 0 13 0.14 0 0
CUI: C0086432
Disease: Hyalinosis, Segmental Glomerular
Hyalinosis, Segmental Glomerular 		28 0 7 0.13 0 0
CUI: C1305904
Disease: Familial hematuria
Familial hematuria 		23 0 6 0.12 0 0
CUI: C1709661
Disease: Primary Focal Segmental Glomerulosclerosis
Primary Focal Segmental Glomerulosclerosis 		18 0 5 0.11 0 0
CUI: C0950121
Disease: Denys-Drash Syndrome
Denys-Drash Syndrome 		15 0 4 9.5E-02 0 0
CUI: C0027721
Disease: Lipoid nephrosis
Lipoid nephrosis 		50 0 7 9.5E-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: C0242597
Disease: Leukocyte-Adhesion Deficiency Syndrome
Leukocyte-Adhesion Deficiency Syndrome 		6 0 3 8.8E-02 0 0
CUI: C0027720
Disease: Nephrosis
Nephrosis 		68 0 8 8.8E-02 0 0
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 7 3 8.6E-02 1 6.7E-02
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 13 3 8.6E-02 1 4.8E-02
CUI: C1737225
Disease: Mesangioproliferative glomerulonephritis
Mesangioproliferative glomerulonephritis 		21 0 4 8.3E-02 0 0
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome 		51 0 6 7.9E-02 0 0
CUI: C4743661
Disease: Leukocyte Adhesion Deficiency Type 3
Leukocyte Adhesion Deficiency Type 3 		11 0 3 7.7E-02 0 0
CUI: C0848548
Disease: hypertensive nephropathy
hypertensive nephropathy 		55 0 6 7.5E-02 0 0
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment 		84 0 8 7.5E-02 0 0
CUI: C1306571
Disease: Hepatic Insufficiency
Hepatic Insufficiency 		13 0 3 7.3E-02 0 0
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: C0020258
Disease: Hydrocephalus, Normal Pressure
Hydrocephalus, Normal Pressure 		44 0 5 7.1E-02 0 0