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 3 0.25 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 2 0.20 0 0
CUI: C3825926
Disease: Nephrotic syndrome in children
Nephrotic syndrome in children 		6 0 2 0.18 0 0
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 0 3 0.18 0 0
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 3 0.18 0 0
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 0 2 0.17 0 0
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change 		7 0 2 0.17 0 0
CUI: C1836890
Disease: Hypoplasia of the ciliary body
Hypoplasia of the ciliary body 		1 0 1 0.14 0 0
CUI: C1842898
Disease: Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		1 0 1 0.14 0 0
CUI: C3280113
Disease: NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES
NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES 		1 10 1 0.14 6 0.35
CUI: C3489732
Disease: Familial mesangial sclerosis
Familial mesangial sclerosis 		1 0 1 0.14 0 0
CUI: C3501249
Disease: Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome
Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome 		1 0 1 0.14 0 0
CUI: C4021055
Disease: Absent muscle fiber merosin
Absent muscle fiber merosin 		1 0 1 0.14 0 0
CUI: C4476808
Disease: Microcoria
Microcoria 		1 0 1 0.14 0 0
CUI: C4748327
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23
MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 		1 0 1 0.14 0 0
CUI: C0238157
Disease: Benign hematuria
Benign hematuria 		2 0 1 0.12 0 0
CUI: C0240017
Disease: Intercostal muscle weakness
Intercostal muscle weakness 		2 0 1 0.12 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial 		11 0 2 0.12 0 0
CUI: C0403399
Disease: Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome 		11 0 2 0.12 0 0
CUI: C2931253
Disease: Alport syndrome, dominant type
Alport syndrome, dominant type 		2 0 1 0.12 0 0
CUI: C2931861
Disease: Hemorrhagic hereditary nephritis
Hemorrhagic hereditary nephritis 		2 0 1 0.12 0 0
CUI: C4016901
Disease: NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO
NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO 		2 0 1 0.12 0 0
CUI: C4020790
Disease: Medullary sponge kidney disease
Medullary sponge kidney disease 		2 0 1 0.12 0 0
CUI: C4022580
Disease: Unfavorable response of muscle weakness to acetylcholine esterase inhibitors
Unfavorable response of muscle weakness to acetylcholine esterase inhibitors 		2 0 1 0.12 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease 		12 0 2 0.12 0 0