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: C1859040
Disease: Medullary Cystic Kidney Disease Type 2
Medullary Cystic Kidney Disease Type 2 		5 0 5 0.45 0 0
CUI: C4551496
Disease: Hyperuricemic Nephropathy, Familial Juvenile 1
Hyperuricemic Nephropathy, Familial Juvenile 1 		6 18 5 0.42 1 5.3E-02
CUI: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1 		5 0 3 0.23 0 0
CUI: C0238157
Disease: Benign hematuria
Benign hematuria 		2 0 2 0.18 0 0
CUI: C2931253
Disease: Alport syndrome, dominant type
Alport syndrome, dominant type 		2 0 2 0.18 0 0
CUI: C3280216
Disease: HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3 		2 0 2 0.18 0 0
CUI: C2939174
Disease: Medullary cystic disease
Medullary cystic disease 		9 0 3 0.18 0 0
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 2 0.17 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 2 0.17 0 0
CUI: C1881236
Disease: Interstitial Disease
Interstitial Disease 		3 0 2 0.17 0 0
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type 		3 0 2 0.17 0 0
CUI: C3276821
Disease: Thin glomerular basement membrane
Thin glomerular basement membrane 		3 0 2 0.17 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 2 0.17 0 0
CUI: C4746547
Disease: ALPORT SYNDROME 3, AUTOSOMAL DOMINANT
ALPORT SYNDROME 3, AUTOSOMAL DOMINANT 		3 0 2 0.17 0 0
CUI: C4746745
Disease: ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE
ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE 		4 0 2 0.15 0 0
CUI: C0271858
Disease: Tertiary hyperparathyroidism
Tertiary hyperparathyroidism 		5 0 2 0.14 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 2 0.14 0 0
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 3 0.14 0 0
CUI: C3665382
Disease: 2,8-Dihydroxyadenine Urolithiasis
2,8-Dihydroxyadenine Urolithiasis 		6 0 2 0.13 0 0
CUI: C0268104
Disease: Disorder of purine metabolism
Disorder of purine metabolism 		7 0 2 0.12 0 0
CUI: C0445347
Disease: Thickening of glomerular basement membrane
Thickening of glomerular basement membrane 		7 0 2 0.12 0 0
CUI: C1567744
Disease: Alport Syndrome, Autosomal Recessive
Alport Syndrome, Autosomal Recessive 		8 0 2 0.12 0 0
CUI: C1968619
Disease: Renal corticomedullary cysts
Renal corticomedullary cysts 		8 0 2 0.12 0 0
CUI: C0027706
Disease: Hereditary nephritis
Hereditary nephritis 		9 0 2 0.11 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial 		11 0 2 1.0E-01 0 0