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: C4021736
Disease: Decreased methylcobalamin
Decreased methylcobalamin
7 0 7 0.27 0 0
CUI: C3806347
Disease: Hyperhomocystinemia
Hyperhomocystinemia
11 0 7 0.23 0 0
Decreased methionine synthase activity
6 0 6 0.23 0 0
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency
29 11 10 0.22 2 0.18
CUI: C1848555
Disease: Hypomethioninemia
Hypomethioninemia
5 0 5 0.19 0 0
Neural tube defect, folate-sensitive
8 0 5 0.17 0 0
CUI: C0238801
Disease: Bone marrow megaloblastic (finding)
Bone marrow megaloblastic (finding)
4 0 4 0.15 0 0
CUI: C0342701
Disease: Transcobalamin II deficiency
Transcobalamin II deficiency
5 0 4 0.15 0 0
CUI: C1848556
Disease: Decreased adenosylcobalamin
Decreased adenosylcobalamin
7 0 4 0.14 0 0
CUI: C1855119
Disease: Methylmalonic aciduria
Methylmalonic aciduria
33 0 7 0.13 0 0
CUI: C4551825
Disease: Megaloblastic Anemia 1
Megaloblastic Anemia 1
9 0 4 0.13 0 0
CUI: C0019880
Disease: Homocystinuria
Homocystinuria
39 0 7 0.12 0 0
CUI: C0543641
Disease: Megaloblastic anemia, secondary
Megaloblastic anemia, secondary
3 0 3 0.12 0 0
CUI: C0750292
Disease: Malabsorption of Vitamin B12
Malabsorption of Vitamin B12
3 0 3 0.12 0 0
Megaloblastic anemia due to inborn errors of metabolism
3 0 3 0.12 0 0
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement
23 0 5 0.11 0 0
CUI: C0268618
Disease: Cystathioninemia
Cystathioninemia
4 0 3 0.11 0 0
CUI: C0268616
Disease: Gamma-cystathionase deficiency
Gamma-cystathionase deficiency
5 0 3 0.11 0 0
Decreased methylmalonyl-CoA mutase activity
5 0 3 0.11 0 0
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious
16 0 4 0.11 0 0
CUI: C1394891
Disease: Intrinsic Factor Deficiency
Intrinsic Factor Deficiency
18 0 4 1.0E-01 0 0
CUI: C0268583
Disease: Methylmalonic acidemia
Methylmalonic acidemia
44 0 6 9.4E-02 0 0
Methylenetetrahydrofolate reductase polymorphism
9 7 3 9.4E-02 1 0.12
CUI: C1565321
Disease: Cholera Infantum
Cholera Infantum
12 0 3 8.6E-02 0 0
CUI: C1853238
Disease: Conotruncal defect
Conotruncal defect
51 45 6 8.5E-02 1 2.2E-02