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: C0854078
Disease: Diabetic end stage renal disease
Diabetic end stage renal disease 		7 0 3 0.21 0 0
CUI: C0333497
Disease: Segmental glomerulosclerosis
Segmental glomerulosclerosis 		9 0 3 0.19 0 0
CUI: C3536572
Disease: End stage renal disease due to hypertension
End stage renal disease due to hypertension 		5 0 2 0.15 0 0
CUI: C1305904
Disease: Familial hematuria
Familial hematuria 		23 0 4 0.14 0 0
CUI: C1709661
Disease: Primary Focal Segmental Glomerulosclerosis
Primary Focal Segmental Glomerulosclerosis 		18 0 3 0.12 0 0
CUI: C0020951
Disease: Immune Complex Diseases
Immune Complex Diseases 		10 0 2 0.11 0 0
CUI: C2930930
Disease: Abdominal obesity metabolic syndrome
Abdominal obesity metabolic syndrome 		10 0 2 0.11 0 0
CUI: C0155616
Disease: Secondary hypertension
Secondary hypertension 		22 0 3 0.10 0 0
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 3 0.10 0 0
CUI: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis 		1 0 1 1.0E-01 0 0
CUI: C0264878
Disease: Heart valve stenosis
Heart valve stenosis 		1 0 1 1.0E-01 0 0
CUI: C0268796
Disease: Arteriolar nephrosclerosis
Arteriolar nephrosclerosis 		1 0 1 1.0E-01 0 0
CUI: C0344688
Disease: Patent Ductus Venosus
Patent Ductus Venosus 		1 0 1 1.0E-01 0 0
CUI: C0398641
Disease: Epstein syndrome (disorder)
Epstein syndrome (disorder) 		1 0 1 1.0E-01 0 0
CUI: C0403445
Disease: Fechtner syndrome (disorder)
Fechtner syndrome (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF 		1 0 1 1.0E-01 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF 		1 0 1 1.0E-01 0 0
CUI: C1832253
Disease: INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF 		1 0 1 1.0E-01 0 0
CUI: C1834478
Disease: MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS
MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS 		1 0 1 1.0E-01 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1 		1 0 1 1.0E-01 0 0
CUI: C1842035
Disease: Giant Platelet Syndrome with Thrombocytopenia
Giant Platelet Syndrome with Thrombocytopenia 		1 0 1 1.0E-01 0 0
CUI: C1861512
Disease: Cochleosaccular degeneration of the inner ear and progressive cataracts
Cochleosaccular degeneration of the inner ear and progressive cataracts 		1 0 1 1.0E-01 0 0
CUI: C1863659
Disease: DEAFNESS, AUTOSOMAL DOMINANT 17
DEAFNESS, AUTOSOMAL DOMINANT 17 		1 0 1 1.0E-01 0 0
CUI: C2675525
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO 		1 0 1 1.0E-01 0 0
CUI: C2931716
Disease: Deafness, autosomal dominant nonsyndromic sensorineural 17
Deafness, autosomal dominant nonsyndromic sensorineural 17 		1 0 1 1.0E-01 0 0