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: C0034066
Disease: Pulmonary embolism with pulmonary infarction
Pulmonary embolism with pulmonary infarction 		1 0 1 0.25 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 0.25 0 0
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis 		1 0 1 0.25 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 0.25 0 0
CUI: C0269852
Disease: Vasa Previa
Vasa Previa 		1 0 1 0.25 0 0
CUI: C0332882
Disease: congenital obstruction
congenital obstruction 		1 0 1 0.25 0 0
CUI: C0334390
Disease: Acinar cell tumor
Acinar cell tumor 		1 0 1 0.25 0 0
CUI: C0340037
Disease: Young Syndrome
Young Syndrome 		1 0 1 0.25 0 0
CUI: C0341248
Disease: Chronic duodenitis
Chronic duodenitis 		1 0 1 0.25 0 0
CUI: C0392180
Disease: Necrosis of placenta
Necrosis of placenta 		1 0 1 0.25 0 0
CUI: C0398349
Disease: Distal intestinal obstruction syndrome
Distal intestinal obstruction syndrome 		1 0 1 0.25 0 0
CUI: C0403819
Disease: Acquired obstructive azoospermia
Acquired obstructive azoospermia 		1 0 1 0.25 0 0
CUI: C0740266
Disease: Anal and rectal conditions
Anal and rectal conditions 		1 0 1 0.25 0 0
CUI: C0860006
Disease: Hypotonic dehydration
Hypotonic dehydration 		1 0 1 0.25 0 0
CUI: C0877664
Disease: Gastrointestinal cramps
Gastrointestinal cramps 		1 0 1 0.25 0 0
CUI: C0948783
Disease: Bronchopulmonary infection
Bronchopulmonary infection 		1 0 1 0.25 0 0
CUI: C1167752
Disease: Graft ischaemia
Graft ischaemia 		1 0 1 0.25 0 0
CUI: C1335461
Disease: Postsurgical Stage I Hepatoblastoma
Postsurgical Stage I Hepatoblastoma 		1 0 1 0.25 0 0
CUI: C1844663
Disease: ISLETS OF LANGERHANS, ABSENCE OF
ISLETS OF LANGERHANS, ABSENCE OF 		1 0 1 0.25 0 0
CUI: C1863080
Disease: ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF
ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF 		1 0 1 0.25 0 0
CUI: C1863081
Disease: alpha-Fetoprotein Deficiency
alpha-Fetoprotein Deficiency 		1 0 1 0.25 0 0
CUI: C1865433
Disease: VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF
VAS DEFERENS, CONGENITAL BILATERAL ABSENCE OF 		1 0 1 0.25 0 0
CUI: C1865553
Disease: HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO
HYPERTRYPSINEMIA, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 0.25 0 0
CUI: C4016791
Disease: SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS
SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS 		1 0 1 0.25 0 0
CUI: C4016792
Disease: PANCREATITIS, IDIOPATHIC, SUSCEPTIBILITY TO
PANCREATITIS, IDIOPATHIC, SUSCEPTIBILITY TO 		1 0 1 0.25 0 0