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: C1567744
Disease: Alport Syndrome, Autosomal Recessive
Alport Syndrome, Autosomal Recessive 		8 0 6 0.24 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 5 0.22 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease 		12 9 6 0.21 3 0.23
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 8 6 0.20 1 7.1E-02
CUI: C0086432
Disease: Hyalinosis, Segmental Glomerular
Hyalinosis, Segmental Glomerular 		28 0 8 0.19 0 0
CUI: C1868672
Disease: NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE 		31 53 8 0.17 1 1.7E-02
CUI: C1709661
Disease: Primary Focal Segmental Glomerulosclerosis
Primary Focal Segmental Glomerulosclerosis 		18 0 6 0.17 0 0
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 6 0.15 0 0
CUI: C0027706
Disease: Hereditary nephritis
Hereditary nephritis 		9 0 4 0.14 0 0
CUI: C4049702
Disease: Focal Segmental Glomerulosclerosis, Not Otherwise Specified
Focal Segmental Glomerulosclerosis, Not Otherwise Specified 		42 0 8 0.14 0 0
CUI: C2749515
Disease: Collapsing glomerulopathy
Collapsing glomerulopathy 		10 0 4 0.14 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial 		11 22 4 0.13 1 3.6E-02
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 3 0.13 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 3 0.13 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 3 0.13 0 0
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment 		84 0 12 0.13 0 0
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital 		31 0 6 0.12 0 0
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome 		51 314 8 0.12 2 6.3E-03
CUI: C2919166
Disease: Autosomal dominant focal segmental glomerulosclerosis
Autosomal dominant focal segmental glomerulosclerosis 		5 0 3 0.12 0 0
CUI: C0239937
Disease: Microscopic hematuria
Microscopic hematuria 		15 0 4 0.12 0 0
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 0 3 0.11 0 0
CUI: C0445347
Disease: Thickening of glomerular basement membrane
Thickening of glomerular basement membrane 		7 0 3 0.11 0 0
CUI: C0854078
Disease: Diabetic end stage renal disease
Diabetic end stage renal disease 		7 0 3 0.11 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 3 0.11 0 0
CUI: C0333497
Disease: Segmental glomerulosclerosis
Segmental glomerulosclerosis 		9 0 3 0.10 0 0