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: C0268583
Disease: Methylmalonic acidemia
Methylmalonic acidemia 		44 35 32 0.71 4 0.11
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 0 11 0.22 0 0
CUI: C1848556
Disease: Decreased adenosylcobalamin
Decreased adenosylcobalamin 		7 0 7 0.21 0 0
CUI: C3806347
Disease: Hyperhomocystinemia
Hyperhomocystinemia 		11 0 7 0.19 0 0
CUI: C1848579
Disease: Decreased methylmalonyl-CoA mutase activity
Decreased methylmalonyl-CoA mutase activity 		5 0 5 0.15 0 0
CUI: C1848580
Disease: Decreased methionine synthase activity
Decreased methionine synthase activity 		6 0 5 0.15 0 0
CUI: C0276096
Disease: Mastitis-metritis-agalactia syndrome
Mastitis-metritis-agalactia syndrome 		23 3 7 0.14 2 0.40
CUI: C4021736
Disease: Decreased methylcobalamin
Decreased methylcobalamin 		7 0 5 0.14 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 7 0.13 0 0
CUI: C0019880
Disease: Homocystinuria
Homocystinuria 		39 0 8 0.12 0 0
CUI: C0238801
Disease: Bone marrow megaloblastic (finding)
Bone marrow megaloblastic (finding) 		4 0 4 0.12 0 0
CUI: C1848555
Disease: Hypomethioninemia
Hypomethioninemia 		5 0 4 0.12 0 0
CUI: C0796208
Disease: MENTAL RETARDATION, X-LINKED 3
MENTAL RETARDATION, X-LINKED 3 		3 7 3 9.1E-02 1 1.0E-01
CUI: C0268618
Disease: Cystathioninemia
Cystathioninemia 		4 0 3 8.8E-02 0 0
CUI: C0268616
Disease: Gamma-cystathionase deficiency
Gamma-cystathionase deficiency 		5 0 3 8.6E-02 0 0
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		23 0 4 7.7E-02 0 0
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia 		14 0 3 6.8E-02 0 0
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2 		2 0 2 6.1E-02 0 0
CUI: C0342720
Disease: Adenosylcobalamin synthesis defect
Adenosylcobalamin synthesis defect 		2 0 2 6.1E-02 0 0
CUI: C1272348
Disease: Disorder of vitamin B12
Disorder of vitamin B12 		2 0 2 6.1E-02 0 0
CUI: C1848561
Disease: Methylmalonic acidemia with homocystinuria
Methylmalonic acidemia with homocystinuria 		2 0 2 6.1E-02 0 0
CUI: C1855102
Disease: Methylmalonic aciduria cblB type
Methylmalonic aciduria cblB type 		2 0 2 6.1E-02 0 0
CUI: C1855128
Disease: Methylcobalamin Deficiency, CblG Type
Methylcobalamin Deficiency, CblG Type 		2 0 2 6.1E-02 0 0
CUI: C3711369
Disease: Succinate-Coa Ligase Deficiency
Succinate-Coa Ligase Deficiency 		2 0 2 6.1E-02 0 0
CUI: C4693974
Disease: METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC 		2 0 2 6.1E-02 0 0