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: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1 		5 0 4 0.29 0 0
CUI: C2939174
Disease: Medullary cystic disease
Medullary cystic disease 		9 0 4 0.22 0 0
CUI: C1859040
Disease: Medullary Cystic Kidney Disease Type 2
Medullary Cystic Kidney Disease Type 2 		5 0 3 0.20 0 0
CUI: C4551496
Disease: Hyperuricemic Nephropathy, Familial Juvenile 1
Hyperuricemic Nephropathy, Familial Juvenile 1 		6 18 3 0.19 1 5.0E-02
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 3 0.18 0 0
CUI: C0041323
Disease: Tuberculosis, Oral
Tuberculosis, Oral 		2 0 2 0.15 0 0
CUI: C1858395
Disease: Tubular atrophy
Tubular atrophy 		17 0 4 0.15 0 0
CUI: C2751310
Disease: Hyperuricemic Nephropathy, Familial Juvenile 2
Hyperuricemic Nephropathy, Familial Juvenile 2 		2 0 2 0.15 0 0
CUI: C3280216
Disease: HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3 		2 0 2 0.15 0 0
CUI: C4521759
Disease: Tubular Atrophy Assessment
Tubular Atrophy Assessment 		17 0 4 0.15 0 0
CUI: C4551979
Disease: Nephronophthisis 1
Nephronophthisis 1 		18 0 4 0.15 0 0
CUI: C0342793
Disease: Malonic aciduria
Malonic aciduria 		3 0 2 0.14 0 0
CUI: C1881236
Disease: Interstitial Disease
Interstitial Disease 		3 0 2 0.14 0 0
CUI: C4020705
Disease: Glomerulocystic kidney disease
Glomerulocystic kidney disease 		11 0 3 0.14 0 0
CUI: C0266239
Disease: Congenital anomaly of bile ducts
Congenital anomaly of bile ducts 		4 0 2 0.13 0 0
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 0 3 0.13 0 0
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 4 0.13 0 0
CUI: C3665382
Disease: 2,8-Dihydroxyadenine Urolithiasis
2,8-Dihydroxyadenine Urolithiasis 		6 0 2 0.12 0 0
CUI: C3825926
Disease: Nephrotic syndrome in children
Nephrotic syndrome in children 		6 0 2 0.12 0 0
CUI: C0268104
Disease: Disorder of purine metabolism
Disorder of purine metabolism 		7 0 2 0.11 0 0
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 0 2 0.11 0 0
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change 		7 0 2 0.11 0 0
CUI: C1855681
Disease: Nephronophthisis, familial juvenile
Nephronophthisis, familial juvenile 		17 0 3 0.11 0 0
CUI: C0238304
Disease: Chronic interstitial nephritis
Chronic interstitial nephritis 		18 0 3 0.11 0 0
CUI: C0158687
Disease: Congenital malformation of genital organs
Congenital malformation of genital organs 		8 0 2 0.11 0 0