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: C0202251
Disease: Vitamin B6 measurement
Vitamin B6 measurement 		5 11 2 0.12 2 6.5E-02
CUI: C0342701
Disease: Transcobalamin II deficiency
Transcobalamin II deficiency 		5 0 2 0.12 0 0
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 11 4 0.11 1 3.1E-02
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		23 33 3 9.1E-02 4 7.8E-02
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 3 8.3E-02 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 7.7E-02 0 0
CUI: C0162677
Disease: Caliciviridae Infections
Caliciviridae Infections 		1 0 1 7.7E-02 0 0
CUI: C0220743
Disease: Childhood hypophosphatasia (disorder)
Childhood hypophosphatasia (disorder) 		1 0 1 7.7E-02 0 0
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction 		1 0 1 7.7E-02 0 0
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis 		1 0 1 7.7E-02 0 0
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction 		1 0 1 7.7E-02 0 0
CUI: C0342700
Disease: Transcobalamin I Deficiency
Transcobalamin I Deficiency 		1 0 1 7.7E-02 0 0
CUI: C0343379
Disease: Enterotoxigenic Escherichia coli gastrointestinal tract infection
Enterotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 7.7E-02 0 0
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia 		1 0 1 7.7E-02 0 0
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion 		1 0 1 7.7E-02 0 0
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma 		1 0 1 7.7E-02 0 0
CUI: C1263739
Disease: Disorder of organic acid metabolism
Disorder of organic acid metabolism 		1 0 1 7.7E-02 0 0
CUI: C1739111
Disease: Fetus affected by placental transfer of anticonvulsant
Fetus affected by placental transfer of anticonvulsant 		1 0 1 7.7E-02 0 0
CUI: C1840322
Disease: ODONTOHYPOPHOSPHATASIA (disorder)
ODONTOHYPOPHOSPHATASIA (disorder) 		1 0 1 7.7E-02 0 0
CUI: C1855115
Disease: Methylmalonic Aciduria, mut(0) Type
Methylmalonic Aciduria, mut(0) Type 		1 0 1 7.7E-02 0 0
CUI: C1855116
Disease: Methylmalonic Aciduria, mut(-) Type
Methylmalonic Aciduria, mut(-) Type 		1 0 1 7.7E-02 0 0
CUI: C1855815
Disease: Skin dimple over apex of long bone angulation
Skin dimple over apex of long bone angulation 		1 0 1 7.7E-02 0 0
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type 		1 0 1 7.7E-02 0 0
CUI: C2217040
Disease: malignant neoplasm of large intestine stage IV
malignant neoplasm of large intestine stage IV 		1 0 1 7.7E-02 0 0
CUI: C2673477
Disease: Hypophosphatasia, Perinatal Lethal
Hypophosphatasia, Perinatal Lethal 		1 0 1 7.7E-02 0 0