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: C0333497
Disease: Segmental glomerulosclerosis
Segmental glomerulosclerosis 		9 0 3 0.23 0 0
CUI: C2749515
Disease: Collapsing glomerulopathy
Collapsing glomerulopathy 		10 0 3 0.21 0 0
CUI: C3536572
Disease: End stage renal disease due to hypertension
End stage renal disease due to hypertension 		5 0 2 0.20 0 0
CUI: C0848765
Disease: Hearing disability
Hearing disability 		6 0 2 0.18 0 0
CUI: C0026244
Disease: Mitochondrial Swelling
Mitochondrial Swelling 		1 0 1 0.14 0 0
CUI: C0040559
Disease: Toxoplasmosis, Animal
Toxoplasmosis, Animal 		1 0 1 0.14 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 0.14 0 0
CUI: C0268796
Disease: Arteriolar nephrosclerosis
Arteriolar nephrosclerosis 		1 0 1 0.14 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 0.14 0 0
CUI: C0345218
Disease: Low anorectal malformation
Low anorectal malformation 		1 0 1 0.14 0 0
CUI: C0398641
Disease: Epstein syndrome (disorder)
Epstein syndrome (disorder) 		1 0 1 0.14 0 0
CUI: C0403445
Disease: Fechtner syndrome (disorder)
Fechtner syndrome (disorder) 		1 0 1 0.14 0 0
CUI: C0858925
Disease: Deafness labyrinthine
Deafness labyrinthine 		1 0 1 0.14 0 0
CUI: C1834478
Disease: MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS
MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS 		1 0 1 0.14 0 0
CUI: C1842035
Disease: Giant Platelet Syndrome with Thrombocytopenia
Giant Platelet Syndrome with Thrombocytopenia 		1 0 1 0.14 0 0
CUI: C1859728
Disease: Coronary Sclerosis, Medial, of Infancy
Coronary Sclerosis, Medial, of Infancy 		1 0 1 0.14 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 0.14 0 0
CUI: C1863659
Disease: DEAFNESS, AUTOSOMAL DOMINANT 17
DEAFNESS, AUTOSOMAL DOMINANT 17 		1 0 1 0.14 0 0
CUI: C2675525
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO 		1 0 1 0.14 0 0
CUI: C2931297
Disease: Yusho Disease
Yusho Disease 		1 0 1 0.14 0 0
CUI: C2931716
Disease: Deafness, autosomal dominant nonsyndromic sensorineural 17
Deafness, autosomal dominant nonsyndromic sensorineural 17 		1 0 1 0.14 0 0
CUI: C3280556
Disease: PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS 		1 0 1 0.14 0 0
CUI: C3495555
Disease: Carnosinemia
Carnosinemia 		1 0 1 0.14 0 0
CUI: C3809781
Disease: Cole disease
Cole disease 		1 0 1 0.14 0 0
CUI: C4021547
Disease: Neutrophil inclusion bodies
Neutrophil inclusion bodies 		1 0 1 0.14 0 0