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: C1857662
Disease: COACH syndrome
COACH syndrome 		4 0 3 0.43 0 0
CUI: C1855284
Disease: Intrahepatic biliary atresia
Intrahepatic biliary atresia 		9 0 4 0.36 0 0
CUI: C0175692
Disease: Johanson-Blizzard syndrome
Johanson-Blizzard syndrome 		7 0 3 0.30 0 0
CUI: C1408258
Disease: Kidney damage
Kidney damage 		5 0 2 0.22 0 0
CUI: C0035091
Disease: Renal Tubular Transport, Inborn Errors
Renal Tubular Transport, Inborn Errors 		1 0 1 0.17 0 0
CUI: C1306162
Disease: Kidney replacement disorder
Kidney replacement disorder 		1 0 1 0.17 0 0
CUI: C1835934
Disease: Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria 		1 0 1 0.17 0 0
CUI: C1839874
Disease: Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis 		1 0 1 0.17 0 0
CUI: C1853153
Disease: JOUBERT SYNDROME 6
JOUBERT SYNDROME 6 		1 0 1 0.17 0 0
CUI: C1861627
Disease: Butterfly vertebral arch
Butterfly vertebral arch 		1 0 1 0.17 0 0
CUI: C1866053
Disease: Deafness, Congenital Heart Defects, and Posterior Embryotoxon
Deafness, Congenital Heart Defects, and Posterior Embryotoxon 		1 0 1 0.17 0 0
CUI: C1968619
Disease: Renal corticomedullary cysts
Renal corticomedullary cysts 		8 0 2 0.17 0 0
CUI: C1969052
Disease: MECKEL SYNDROME, TYPE 5
MECKEL SYNDROME, TYPE 5 		1 0 1 0.17 0 0
CUI: C1969053
Disease: JOUBERT SYNDROME 7
JOUBERT SYNDROME 7 		1 0 1 0.17 0 0
CUI: C2676788
Disease: JOUBERT SYNDROME 9 (disorder)
JOUBERT SYNDROME 9 (disorder) 		1 0 1 0.17 0 0
CUI: C2676790
Disease: MECKEL SYNDROME, TYPE 6 (disorder)
MECKEL SYNDROME, TYPE 6 (disorder) 		1 0 1 0.17 0 0
CUI: C3150796
Disease: NEPHRONOPHTHISIS 11
NEPHRONOPHTHISIS 11 		1 0 1 0.17 0 0
CUI: C4016445
Disease: NEPHROLITHIASIS, X-LINKED RECESSIVE
NEPHROLITHIASIS, X-LINKED RECESSIVE 		1 0 1 0.17 0 0
CUI: C4017203
Disease: BARDET-BIEDL SYNDROME 14, MODIFIER OF
BARDET-BIEDL SYNDROME 14, MODIFIER OF 		1 0 1 0.17 0 0
CUI: C1858395
Disease: Tubular atrophy
Tubular atrophy 		17 0 3 0.15 0 0
CUI: C4020869
Disease: Abnormality of abdomen morphology
Abnormality of abdomen morphology 		17 0 3 0.15 0 0
CUI: C4521759
Disease: Tubular Atrophy Assessment
Tubular Atrophy Assessment 		17 0 3 0.15 0 0
CUI: C0344975
Disease: Pulmonary Atresia with Intact Ventricular Septum
Pulmonary Atresia with Intact Ventricular Septum 		2 0 1 0.14 0 0
CUI: C0403443
Disease: Renal Failure, Progressive, with Hypertension
Renal Failure, Progressive, with Hypertension 		2 0 1 0.14 0 0
CUI: C1845168
Disease: Hypophosphatemic Rickets, X-Linked Recessive
Hypophosphatemic Rickets, X-Linked Recessive 		2 0 1 0.14 0 0