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: C0009439
Disease: Choledochal Cyst, Type I
Choledochal Cyst, Type I 		5 0 5 1.00 0 0
CUI: C1257796
Disease: Choledochal Cyst, Type II
Choledochal Cyst, Type II 		5 0 5 1.00 0 0
CUI: C1257798
Disease: Choledochal Cyst, Type IV
Choledochal Cyst, Type IV 		5 0 5 1.00 0 0
CUI: C1257799
Disease: Choledochal Cyst, Type V
Choledochal Cyst, Type V 		5 0 5 1.00 0 0
CUI: C0034066
Disease: Pulmonary embolism with pulmonary infarction
Pulmonary embolism with pulmonary infarction 		1 0 1 0.20 0 0
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis 		1 0 1 0.20 0 0
CUI: C0332882
Disease: congenital obstruction
congenital obstruction 		1 0 1 0.20 0 0
CUI: C0340037
Disease: Young Syndrome
Young Syndrome 		1 0 1 0.20 0 0
CUI: C0398349
Disease: Distal intestinal obstruction syndrome
Distal intestinal obstruction syndrome 		1 0 1 0.20 0 0
CUI: C0403819
Disease: Acquired obstructive azoospermia
Acquired obstructive azoospermia 		1 0 1 0.20 0 0
CUI: C0686586
Disease: Acute leukemia in remission
Acute leukemia in remission 		1 0 1 0.20 0 0
CUI: C0740266
Disease: Anal and rectal conditions
Anal and rectal conditions 		1 0 1 0.20 0 0
CUI: C0860006
Disease: Hypotonic dehydration
Hypotonic dehydration 		1 0 1 0.20 0 0
CUI: C0877664
Disease: Gastrointestinal cramps
Gastrointestinal cramps 		1 0 1 0.20 0 0
CUI: C0940747
Disease: Pancreatic Duct Stenosis
Pancreatic Duct Stenosis 		1 0 1 0.20 0 0
CUI: C0948783
Disease: Bronchopulmonary infection
Bronchopulmonary infection 		1 0 1 0.20 0 0
CUI: C1332178
Disease: Adult Acute Leukemia in Remission
Adult Acute Leukemia in Remission 		1 0 1 0.20 0 0
CUI: C1332938
Disease: Childhood Acute Leukemia in Remission
Childhood Acute Leukemia in Remission 		1 0 1 0.20 0 0
CUI: C1833541
Disease: Caroli disease isolated
Caroli disease isolated 		1 0 1 0.20 0 0
CUI: C1862554
Disease: COLTON-NULL PHENOTYPE
COLTON-NULL PHENOTYPE 		1 0 1 0.20 0 0
CUI: C1865433
Disease: VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF
VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF 		1 0 1 0.20 0 0
CUI: C1865553
Disease: HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO
HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 0.20 0 0
CUI: C4016791
Disease: SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS
SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS 		1 0 1 0.20 0 0
CUI: C4016792
Disease: PANCREATITIS, IDIOPATHIC, SUSCEPTIBILITY TO
PANCREATITIS, IDIOPATHIC, SUSCEPTIBILITY TO 		1 0 1 0.20 0 0
CUI: C4017631
Disease: BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1, MODIFIER OF
BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1, MODIFIER OF 		1 0 1 0.20 0 0