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: C1305904
Disease: Familial hematuria
Familial hematuria 		23 7 16 7.0E-02 2 0.17
CUI: C0238304
Disease: Chronic interstitial nephritis
Chronic interstitial nephritis 		18 1 9 3.9E-02 1 0.14
CUI: C0268749
Disease: Fibrillary glomerulonephritis
Fibrillary glomerulonephritis 		2 1 1 4.5E-03 1 0.14
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease 		12 9 8 3.6E-02 2 0.14
CUI: C4022832
Disease: Mild proteinuria
Mild proteinuria 		1 1 1 4.5E-03 1 0.14
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth 		4 2 2 9.0E-03 1 0.12
CUI: C4016901
Disease: NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO
NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO 		2 2 1 4.5E-03 1 0.12
CUI: C1281440
Disease: Familial obesity
Familial obesity 		0 3 0 0 1 0.11
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity 		6 3 1 4.4E-03 1 0.11
CUI: C3888044
Disease: Nephrogenic Systemic Fibrosis
Nephrogenic Systemic Fibrosis 		12 3 6 2.6E-02 1 0.11
CUI: C0032273
Disease: Pneumoconiosis
Pneumoconiosis 		33 4 2 7.9E-03 1 1.0E-01
CUI: C0271638
Disease: Type 2 diabetes mellitus in obese
Type 2 diabetes mellitus in obese 		7 4 1 4.4E-03 1 1.0E-01
CUI: C0746556
Disease: metabolic disturbance
metabolic disturbance 		29 4 4 1.6E-02 1 1.0E-01
CUI: C0027707
Disease: Nephritis, Interstitial
Nephritis, Interstitial 		79 5 23 8.3E-02 1 9.1E-02
CUI: C0041349
Disease: Nephritis, Tubulointerstitial
Nephritis, Tubulointerstitial 		92 6 27 9.4E-02 1 8.3E-02
CUI: C1332166
Disease: Adenocarcinoma of the gastroesophageal junction
Adenocarcinoma of the gastroesophageal junction 		32 6 2 8.0E-03 1 8.3E-02
CUI: C3874381
Disease: Childhood nephrotic syndrome
Childhood nephrotic syndrome 		23 6 4 1.7E-02 1 8.3E-02
CUI: C0017979
Disease: Glycosuria
Glycosuria 		53 7 8 3.0E-02 1 7.7E-02
CUI: C0259749
Disease: Autonomic neuropathy
Autonomic neuropathy 		29 7 6 2.5E-02 1 7.7E-02
CUI: C3280845
Disease: CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E 		1 7 1 4.5E-03 1 7.7E-02
CUI: C0271055
Disease: Rhegmatogenous retinal detachment
Rhegmatogenous retinal detachment 		47 8 10 3.9E-02 1 7.1E-02
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 8 10 4.5E-02 1 7.1E-02
CUI: C0917805
Disease: Transient Cerebral Ischemia
Transient Cerebral Ischemia 		98 9 12 3.9E-02 1 6.7E-02
CUI: C1135196
Disease: Heart Failure, Diastolic
Heart Failure, Diastolic 		55 9 4 1.5E-02 1 6.7E-02
CUI: C1851347
Disease: Familial Mediterranean Fever, Autosomal Dominant
Familial Mediterranean Fever, Autosomal Dominant 		1 9 1 4.5E-03 1 6.7E-02