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 0.17 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome
1 0 1 0.17 0 0
CUI: C0268160
Disease: Deficiency of fructokinase
Deficiency of fructokinase
1 0 1 0.17 0 0
CUI: C0405584
Disease: Sucrose intolerance
Sucrose intolerance
1 0 1 0.17 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia
1 0 1 0.17 0 0
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease
1 0 1 0.17 0 0
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)
1 49 1 0.17 1 1.1E-02
CUI: C3495361
Disease: Gigantiform Cementoma, Familial
Gigantiform Cementoma, Familial
1 0 1 0.17 0 0
CUI: C4022857
Disease: Reduced aldolase level
Reduced aldolase level
1 0 1 0.17 0 0
CUI: C4024713
Disease: Transient aminoaciduria
Transient aminoaciduria
1 0 1 0.17 0 0
CUI: C0341934
Disease: Transient hypertension of pregnancy
Transient hypertension of pregnancy
2 0 1 0.14 0 0
CUI: C0586738
Disease: Calf muscle weakness
Calf muscle weakness
2 0 1 0.14 0 0
CUI: C1408247
Disease: Renal disease (acute) NOS
Renal disease (acute) NOS
2 0 1 0.14 0 0
CUI: C1833739
Disease: Diaphyseal cortical sclerosis
Diaphyseal cortical sclerosis
2 0 1 0.14 0 0
CUI: C1839865
Disease: Bicarbonaturia
Bicarbonaturia
2 0 1 0.14 0 0
CUI: C2750076
Disease: Miyoshi Muscular Dystrophy 3
Miyoshi Muscular Dystrophy 3
2 8 1 0.14 1 1.9E-02
CUI: C4022392
Disease: Early onset of sexual maturation
Early onset of sexual maturation
2 0 1 0.14 0 0
CUI: C4025182
Disease: Exercise-induced hemolysis
Exercise-induced hemolysis
2 0 1 0.14 0 0
CUI: C0036474
Disease: Scurvy
Scurvy
3 0 1 0.12 0 0
CUI: C0085397
Disease: Pasteurellaceae Infections
Pasteurellaceae Infections
3 0 1 0.12 0 0
CUI: C0221152
Disease: Obstipation
Obstipation
3 0 1 0.12 0 0
CUI: C0234972
Disease: Convulsive disorder
Convulsive disorder
3 0 1 0.12 0 0
CUI: C0266335
Disease: Congenital anomaly of the bladder
Congenital anomaly of the bladder
3 0 1 0.12 0 0
CUI: C0268419
Disease: Acatalasia
Acatalasia
3 0 1 0.12 0 0
CUI: C0948643
Disease: Hyperuricosuria
Hyperuricosuria
3 0 1 0.12 0 0