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: C4521759
Disease: Tubular Atrophy Assessment
Tubular Atrophy Assessment
17 0 17 1.00 0 0
CUI: C1968619
Disease: Renal corticomedullary cysts
Renal corticomedullary cysts
8 0 7 0.39 0 0
Tubular basement membrane disintegration
4 0 4 0.24 0 0
CUI: C2939174
Disease: Medullary cystic disease
Medullary cystic disease
9 0 4 0.18 0 0
CUI: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1
5 0 3 0.16 0 0
Autosomal dominant tubulointerstitial kidney disease
13 0 4 0.15 0 0
Multiple small medullary renal cysts
6 0 3 0.15 0 0
CUI: C1865872
Disease: NEPHRONOPHTHISIS 2
NEPHRONOPHTHISIS 2
14 0 4 0.15 0 0
CUI: C1855681
Disease: Nephronophthisis, familial juvenile
Nephronophthisis, familial juvenile
17 0 4 0.13 0 0
CUI: C4551979
Disease: Nephronophthisis 1
Nephronophthisis 1
18 0 4 0.13 0 0
Renal dysplasia and retinal aplasia (disorder)
20 0 4 0.12 0 0
Hyperuricemic Nephropathy, Familial Juvenile 2
2 0 2 0.12 0 0
CUI: C1881236
Disease: Interstitial Disease
Interstitial Disease
3 0 2 0.11 0 0
CUI: C0020258
Disease: Hydrocephalus, Normal Pressure
Hydrocephalus, Normal Pressure
44 0 6 0.11 0 0
Renal hepatic pancreatic dysplasia Dandy Walker cyst
4 0 2 0.11 0 0
Thickened superior cerebellar peduncle
4 0 2 0.11 0 0
CUI: C1408258
Disease: Kidney damage
Kidney damage
5 6 2 1.0E-01 1 0.17
Medullary Cystic Kidney Disease Type 2
5 0 2 1.0E-01 0 0
CUI: C1691228
Disease: Cystic Kidney Diseases
Cystic Kidney Diseases
50 0 6 9.8E-02 0 0
CUI: C1858392
Disease: NEPHRONOPHTHISIS 3
NEPHRONOPHTHISIS 3
6 0 2 9.5E-02 0 0
Hyperuricemic Nephropathy, Familial Juvenile 1
6 18 2 9.5E-02 1 5.6E-02
CUI: C0175692
Disease: Johanson-Blizzard syndrome
Johanson-Blizzard syndrome
7 0 2 9.1E-02 0 0
CUI: C0311245
Disease: Congenital cystic kidney disease
Congenital cystic kidney disease
31 0 4 9.1E-02 0 0
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change
7 0 2 9.1E-02 0 0
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
31 0 4 9.1E-02 0 0