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: C0403398
Disease: Steroid-dependent nephrotic syndrome
Steroid-dependent nephrotic syndrome 		6 0 2 0.20 0 0
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		7 7 2 0.18 1 0.14
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change 		7 0 2 0.18 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 2 0.18 0 0
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		1 0 1 0.17 0 0
CUI: C4022677
Disease: Female anorgasmia
Female anorgasmia 		1 0 1 0.17 0 0
CUI: C4302250
Disease: Dengue with warning signs
Dengue with warning signs 		1 0 1 0.17 0 0
CUI: C4302370
Disease: Benign lymphoepithelial lesion of lacrimal gland
Benign lymphoepithelial lesion of lacrimal gland 		1 0 1 0.17 0 0
CUI: C0008690
Disease: Chronic anterior uveitis
Chronic anterior uveitis 		2 0 1 0.14 0 0
CUI: C0541938
Disease: Epigastric burning
Epigastric burning 		2 0 1 0.14 0 0
CUI: C0749201
Disease: Orthostatic syncope
Orthostatic syncope 		2 0 1 0.14 0 0
CUI: C1274377
Disease: Vibrio vulnificus infection
Vibrio vulnificus infection 		2 0 1 0.14 0 0
CUI: C1838877
Disease: Myoglobinuria, Recurrent
Myoglobinuria, Recurrent 		2 0 1 0.14 0 0
CUI: C1868524
Disease: Autonomic erectile dysfunction
Autonomic erectile dysfunction 		2 0 1 0.14 0 0
CUI: C4016901
Disease: NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO
NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO 		2 0 1 0.14 0 0
CUI: C4022830
Disease: Heavy proteinuria
Heavy proteinuria 		2 0 1 0.14 0 0
CUI: C4746986
Disease: ALPORT SYNDROME 1, X-LINKED
ALPORT SYNDROME 1, X-LINKED 		2 0 1 0.14 0 0
CUI: C0403399
Disease: Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome 		11 0 2 0.13 0 0
CUI: C0232865
Disease: Functional proteinuria
Functional proteinuria 		3 0 1 0.12 0 0
CUI: C0585544
Disease: Downbeat nystagmus
Downbeat nystagmus 		3 0 1 0.12 0 0
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		3 0 1 0.12 0 0
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 2 0.12 0 0
CUI: C0854441
Disease: Gastric mucosal lesion
Gastric mucosal lesion 		4 0 1 0.11 0 0
CUI: C1839860
Disease: Elevated amniotic fluid alpha-fetoprotein
Elevated amniotic fluid alpha-fetoprotein 		4 0 1 0.11 0 0
CUI: C1853124
Disease: NEPHROTIC SYNDROME, TYPE 3
NEPHROTIC SYNDROME, TYPE 3 		4 0 1 0.11 0 0