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 0.11 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome
1 0 1 0.11 0 0
CUI: C0278007
Disease: Normal bowel habits
Normal bowel habits
1 0 1 0.11 0 0
Congenital deficiency of intrinsic factor
1 0 1 0.11 0 0
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease
1 0 1 0.11 0 0
MEGALOBLASTIC ANEMIA 1, FINNISH TYPE
1 2 1 0.11 1 1.4E-02
MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
1 2 1 0.11 2 2.9E-02
CUI: C4021641
Disease: Absence of intrinsic factor
Absence of intrinsic factor
1 0 1 0.11 0 0
CUI: C4302250
Disease: Dengue with warning signs
Dengue with warning signs
1 0 1 0.11 0 0
Benign lymphoepithelial lesion of lacrimal gland
1 0 1 0.11 0 0
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25
1 0 1 0.11 0 0
CUI: C0008690
Disease: Chronic anterior uveitis
Chronic anterior uveitis
2 0 1 1.0E-01 0 0
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2
2 0 1 1.0E-01 0 0
CUI: C0341934
Disease: Transient hypertension of pregnancy
Transient hypertension of pregnancy
2 0 1 1.0E-01 0 0
3-@METHYLGLUTACONIC ACIDURIA, TYPE I
2 0 1 1.0E-01 0 0
CUI: C0541938
Disease: Epigastric burning
Epigastric burning
2 0 1 1.0E-01 0 0
CUI: C1274377
Disease: Vibrio vulnificus infection
Vibrio vulnificus infection
2 0 1 1.0E-01 0 0
Methylcobalamin Deficiency, CblG Type
2 0 1 1.0E-01 0 0
CUI: C4025182
Disease: Exercise-induced hemolysis
Exercise-induced hemolysis
2 0 1 1.0E-01 0 0
CUI: C0036474
Disease: Scurvy
Scurvy
3 0 1 9.1E-02 0 0
CUI: C0085397
Disease: Pasteurellaceae Infections
Pasteurellaceae Infections
3 0 1 9.1E-02 0 0
CUI: C0221152
Disease: Obstipation
Obstipation
3 0 1 9.1E-02 0 0
CUI: C0234972
Disease: Convulsive disorder
Convulsive disorder
3 0 1 9.1E-02 0 0
CUI: C0268419
Disease: Acatalasia
Acatalasia
3 0 1 9.1E-02 0 0
CUI: C0342704
Disease: Deficiency of Cobalamin G
Deficiency of Cobalamin G
3 0 1 9.1E-02 0 0