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: C0005911
Disease: Body Weight Changes
Body Weight Changes
1 0 1 1.0E-01 0 0
CUI: C0016479
Disease: Food Poisoning
Food Poisoning
1 0 1 1.0E-01 0 0
Other specified diseases of pancreas
1 0 1 1.0E-01 0 0
CUI: C0158369
Disease: Swelling of limb
Swelling of limb
1 0 1 1.0E-01 0 0
CUI: C0238110
Disease: Chronic epididymitis
Chronic epididymitis
1 0 1 1.0E-01 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome
1 0 1 1.0E-01 0 0
CUI: C0267896
Disease: Mucocele of gallbladder
Mucocele of gallbladder
1 0 1 1.0E-01 0 0
Inherited disorder of bilirubin metabolism
1 0 1 1.0E-01 0 0
CUI: C0268889
Disease: Prostatic Obstruction
Prostatic Obstruction
1 0 1 1.0E-01 0 0
recurrent childhood brain stem glioma
1 0 1 1.0E-01 0 0
Physiological hyperbilirubinemia (disorder)
1 0 1 1.0E-01 0 0
CUI: C0543515
Disease: Sucrase deficiency
Sucrase deficiency
1 0 1 1.0E-01 0 0
CUI: C0600039
Disease: Urinary outflow obstruction
Urinary outflow obstruction
1 0 1 1.0E-01 0 0
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease
1 0 1 1.0E-01 0 0
CUI: C0694575
Disease: Macular fibrosis
Macular fibrosis
1 0 1 1.0E-01 0 0
CUI: C0699848
Disease: Disaccharidase deficiency
Disaccharidase deficiency
1 0 1 1.0E-01 0 0
CUI: C0948393
Disease: Oedematous pancreatitis
Oedematous pancreatitis
1 0 1 1.0E-01 0 0
CUI: C1401086
Disease: Peripheral Vascular Insufficiency
Peripheral Vascular Insufficiency
1 0 1 1.0E-01 0 0
CUI: C1531394
Disease: Perinatal jaundice
Perinatal jaundice
1 0 1 1.0E-01 0 0
CUI: C2853945
Disease: Non-follicular lymphoma
Non-follicular lymphoma
1 0 1 1.0E-01 0 0
CUI: C2931837
Disease: Familial hypertryptophanemia
Familial hypertryptophanemia
1 0 1 1.0E-01 0 0
CUI: C3249879
Disease: Combat Fatigue
Combat Fatigue
1 0 1 1.0E-01 0 0
CUI: C3266628
Disease: Persistent asthma
Persistent asthma
1 0 1 1.0E-01 0 0
CUI: C3502107
Disease: Breastfeeding Jaundice
Breastfeeding Jaundice
1 0 1 1.0E-01 0 0
CUI: C3888554
Disease: UGT1A1 gene polymorphism
UGT1A1 gene polymorphism
1 0 1 1.0E-01 0 0