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: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria
7 0 2 0.29 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant
5 0 1 0.17 0 0
Steroid-dependent nephrotic syndrome
6 0 1 0.14 0 0
CUI: C3825926
Disease: Nephrotic syndrome in children
Nephrotic syndrome in children
6 0 1 0.14 0 0
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change
7 0 1 0.12 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome
7 0 1 0.12 0 0
CUI: C0268732
Disease: Nephritic syndrome
Nephritic syndrome
8 0 1 0.11 0 0
Alport Syndrome, Autosomal Recessive
8 0 1 0.11 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial
11 0 1 8.3E-02 0 0
Finnish congenital nephrotic syndrome
11 0 1 8.3E-02 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease
12 9 1 7.7E-02 1 1.0E-01
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked
13 0 1 7.1E-02 0 0
Autosomal dominant tubulointerstitial kidney disease
13 0 1 7.1E-02 0 0
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
31 53 2 6.5E-02 2 3.8E-02
CUI: C4054325
Disease: Obesity Related Glomerulopathy
Obesity Related Glomerulopathy
16 0 1 5.9E-02 0 0
Primary Focal Segmental Glomerulosclerosis
18 0 1 5.3E-02 0 0
Mesangioproliferative glomerulonephritis
21 0 1 4.5E-02 0 0
Diffuse mesangial sclerosis (disorder)
22 0 1 4.3E-02 0 0
CUI: C1305904
Disease: Familial hematuria
Familial hematuria
23 7 1 4.2E-02 1 0.12
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
51 72 2 3.9E-02 2 2.8E-02
CUI: C0086432
Disease: Hyalinosis, Segmental Glomerular
Hyalinosis, Segmental Glomerular
28 0 1 3.4E-02 0 0
CUI: C2721603
Disease: Henoch-Schonlein purpura nephritis
Henoch-Schonlein purpura nephritis
29 0 1 3.3E-02 0 0
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital
31 0 1 3.1E-02 0 0
Steroid-sensitive nephrotic syndrome
36 11 1 2.7E-02 1 8.3E-02
CUI: C1838681
Disease: Rapidly progressive
Rapidly progressive
38 0 1 2.6E-02 0 0