Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Focal Segmental Glomerulosclerosis, Not Otherwise Specified
42 0 11 0.14 0 0
Primary Focal Segmental Glomerulosclerosis
18 0 7 0.12 0 0
CUI: C0848548
Disease: hypertensive nephropathy
hypertensive nephropathy
55 0 10 0.11 0 0
CUI: C2733158
Disease: Cerebral Small Vessel Diseases
Cerebral Small Vessel Diseases
62 0 10 0.10 0 0
CUI: C0027719
Disease: Nephrosclerosis
Nephrosclerosis
41 0 8 0.10 0 0
Non-obstructive reflux-associated chronic pyelonephritis (disorder)
13 0 5 9.4E-02 0 0
CUI: C3495566
Disease: Reflux nephropathy (disorder)
Reflux nephropathy (disorder)
13 0 5 9.4E-02 0 0
CUI: C0008476
Disease: Chondromatosis, Synovial
Chondromatosis, Synovial
18 0 5 8.6E-02 0 0
CUI: C0029427
Disease: Synovial osteochondromatosis
Synovial osteochondromatosis
18 0 5 8.6E-02 0 0
CUI: C0334331
Disease: Juxtaglomerular tumor
Juxtaglomerular tumor
6 0 4 8.5E-02 0 0
CUI: C0268790
Disease: Renal vascular disorder
Renal vascular disorder
22 0 5 8.1E-02 0 0
CUI: C0342199
Disease: Iodine deficiency syndrome
Iodine deficiency syndrome
22 0 5 8.1E-02 0 0
CUI: C0020455
Disease: Hypergammaglobulinemia
Hypergammaglobulinemia
36 0 6 8.0E-02 0 0
CUI: C0155668
Disease: Old myocardial infarction
Old myocardial infarction
9 0 4 8.0E-02 0 0
CUI: C0240225
Disease: Liver mass
Liver mass
36 0 6 8.0E-02 0 0
CUI: C0242528
Disease: Azotemia
Azotemia
9 0 4 8.0E-02 0 0
CUI: C0333497
Disease: Segmental glomerulosclerosis
Segmental glomerulosclerosis
9 0 4 8.0E-02 0 0
CUI: C2749515
Disease: Collapsing glomerulopathy
Collapsing glomerulopathy
10 0 4 7.8E-02 0 0
CUI: C0221271
Disease: Elastosis perforans serpiginosa
Elastosis perforans serpiginosa
66 0 8 7.8E-02 0 0
CUI: C0025205
Disease: Melanoma, Experimental
Melanoma, Experimental
25 0 5 7.7E-02 0 0
CUI: C0152451
Disease: Chronic glomerulonephritis
Chronic glomerulonephritis
41 0 6 7.5E-02 0 0
CUI: C0036330
Disease: Schistosomiasis mansoni
Schistosomiasis mansoni
27 0 5 7.5E-02 0 0
Neuropathy due to human immunodeficiency virus
13 0 4 7.4E-02 0 0
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked
13 0 4 7.4E-02 0 0
CUI: C3805043
Disease: Vascular cognitive impairment
Vascular cognitive impairment
42 0 6 7.4E-02 0 0