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: C0016479
Disease: Food Poisoning
Food Poisoning 		1 0 1 0.12 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome 		1 0 1 0.12 0 0
CUI: C0268916
Disease: Atrophy of vas deferens
Atrophy of vas deferens 		1 0 1 0.12 0 0
CUI: C0400875
Disease: Hollow visceral neuropathy
Hollow visceral neuropathy 		1 0 1 0.12 0 0
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease 		1 0 1 0.12 0 0
CUI: C1864172
Disease: Peroxisome Biogenesis Disorder, Complementation Group G
Peroxisome Biogenesis Disorder, Complementation Group G 		10 0 2 0.12 0 0
CUI: C2931840
Disease: Aspartylglucosamidase (AGA) deficiency
Aspartylglucosamidase (AGA) deficiency 		1 0 1 0.12 0 0
CUI: C4017301
Disease: ASPARTYLGLUCOSAMINURIA, FINNISH TYPE
ASPARTYLGLUCOSAMINURIA, FINNISH TYPE 		1 0 1 0.12 0 0
CUI: C4552078
Disease: PSEUDO-TORCH SYNDROME 1
PSEUDO-TORCH SYNDROME 1 		1 0 1 0.12 0 0
CUI: C0341934
Disease: Transient hypertension of pregnancy
Transient hypertension of pregnancy 		2 0 1 0.11 0 0
CUI: C0580413
Disease: Prothrombin time low
Prothrombin time low 		2 0 1 0.11 0 0
CUI: C2931662
Disease: Baraitser Brett Piesowicz syndrome
Baraitser Brett Piesowicz syndrome 		2 0 1 0.11 0 0
CUI: C4021591
Disease: Reduced number of intrahepatic bile ducts
Reduced number of intrahepatic bile ducts 		2 0 1 0.11 0 0
CUI: C4025182
Disease: Exercise-induced hemolysis
Exercise-induced hemolysis 		2 0 1 0.11 0 0
CUI: C2939175
Disease: Meconium ileus
Meconium ileus 		24 0 3 0.10 0 0
CUI: C0003950
Disease: Ascariasis
Ascariasis 		3 0 1 1.0E-01 0 0
CUI: C0030424
Disease: Paragonimiasis
Paragonimiasis 		3 0 1 1.0E-01 0 0
CUI: C0036474
Disease: Scurvy
Scurvy 		3 0 1 1.0E-01 0 0
CUI: C0085397
Disease: Pasteurellaceae Infections
Pasteurellaceae Infections 		3 0 1 1.0E-01 0 0
CUI: C0221152
Disease: Obstipation
Obstipation 		3 0 1 1.0E-01 0 0
CUI: C0234221
Disease: Acroparesthesia
Acroparesthesia 		3 0 1 1.0E-01 0 0
CUI: C0234972
Disease: Convulsive disorder
Convulsive disorder 		3 0 1 1.0E-01 0 0
CUI: C0268419
Disease: Acatalasia
Acatalasia 		3 0 1 1.0E-01 0 0
CUI: C0687713
Disease: Gastrointestinal Pain
Gastrointestinal Pain 		3 0 1 1.0E-01 0 0
CUI: C2931868
Disease: Catalase deficiency
Catalase deficiency 		3 0 1 1.0E-01 0 0