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: C0431709
Disease: Adult type polycystic kidney disease type 1
Adult type polycystic kidney disease type 1 		1 0 1 0.50 0 0
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		1 0 1 0.50 0 0
CUI: C4022677
Disease: Female anorgasmia
Female anorgasmia 		1 0 1 0.50 0 0
CUI: C4022832
Disease: Mild proteinuria
Mild proteinuria 		1 1 1 0.50 1 2.2E-03
CUI: C0477728
Disease: Hereditary nephropathy
Hereditary nephropathy 		2 0 1 0.33 0 0
CUI: C0746984
Disease: Obstructive ventilatory defect
Obstructive ventilatory defect 		2 0 1 0.33 0 0
CUI: C0749201
Disease: Orthostatic syncope
Orthostatic syncope 		2 0 1 0.33 0 0
CUI: C1838877
Disease: Myoglobinuria, Recurrent
Myoglobinuria, Recurrent 		2 0 1 0.33 0 0
CUI: C1839884
Disease: Leiomyomatosis, esophageal and vulval, with nephropathy
Leiomyomatosis, esophageal and vulval, with nephropathy 		2 0 1 0.33 0 0
CUI: C1865276
Disease: Global glomerulosclerosis
Global glomerulosclerosis 		2 0 1 0.33 0 0
CUI: C1868524
Disease: Autonomic erectile dysfunction
Autonomic erectile dysfunction 		2 0 1 0.33 0 0
CUI: C4022830
Disease: Heavy proteinuria
Heavy proteinuria 		2 0 1 0.33 0 0
CUI: C4024984
Disease: Diffuse leiomyomatosis
Diffuse leiomyomatosis 		2 0 1 0.33 0 0
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 1 0.25 0 0
CUI: C0585544
Disease: Downbeat nystagmus
Downbeat nystagmus 		3 0 1 0.25 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 1 0.25 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 1 0.25 0 0
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		3 0 1 0.25 0 0
CUI: C0038604
Disease: Subungual exostoses
Subungual exostoses 		4 0 1 0.20 0 0
CUI: C0086533
Disease: Leiomyoma, Epithelioid
Leiomyoma, Epithelioid 		4 0 1 0.20 0 0
CUI: C2931857
Disease: Double cortex
Double cortex 		4 0 1 0.20 0 0
CUI: C4021775
Disease: High-frequency sensorineural hearing impairment
High-frequency sensorineural hearing impairment 		4 0 1 0.20 0 0
CUI: C4023481
Disease: EEG with focal spikes
EEG with focal spikes 		4 0 1 0.20 0 0
CUI: C1408258
Disease: Kidney damage
Kidney damage 		5 0 1 0.17 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 1 0.17 0 0