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: C1855109
Disease: Methylmalonic aciduria cblA type
Methylmalonic aciduria cblA type 		1 0 1 0.50 0 0
CUI: C4531053
Disease: Elevated propionylcarnitine level
Elevated propionylcarnitine level 		1 0 1 0.50 0 0
CUI: C1848579
Disease: Decreased methylmalonyl-CoA mutase activity
Decreased methylmalonyl-CoA mutase activity 		5 0 2 0.40 0 0
CUI: C0342720
Disease: Adenosylcobalamin synthesis defect
Adenosylcobalamin synthesis defect 		2 0 1 0.33 0 0
CUI: C1848561
Disease: Methylmalonic acidemia with homocystinuria
Methylmalonic acidemia with homocystinuria 		2 0 1 0.33 0 0
CUI: C4693974
Disease: METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC 		2 0 1 0.33 0 0
CUI: C1848556
Disease: Decreased adenosylcobalamin
Decreased adenosylcobalamin 		7 0 2 0.29 0 0
CUI: C1855114
Disease: Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency
Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency 		3 0 1 0.25 0 0
CUI: C0238801
Disease: Bone marrow megaloblastic (finding)
Bone marrow megaloblastic (finding) 		4 0 1 0.20 0 0
CUI: C0268618
Disease: Cystathioninemia
Cystathioninemia 		4 0 1 0.20 0 0
CUI: C0268616
Disease: Gamma-cystathionase deficiency
Gamma-cystathionase deficiency 		5 0 1 0.17 0 0
CUI: C1848555
Disease: Hypomethioninemia
Hypomethioninemia 		5 0 1 0.17 0 0
CUI: C1848580
Disease: Decreased methionine synthase activity
Decreased methionine synthase activity 		6 0 1 0.14 0 0
CUI: C4021736
Disease: Decreased methylcobalamin
Decreased methylcobalamin 		7 0 1 0.12 0 0
CUI: C0276096
Disease: Mastitis-metritis-agalactia syndrome
Mastitis-metritis-agalactia syndrome 		23 0 2 8.7E-02 0 0
CUI: C3806347
Disease: Hyperhomocystinemia
Hyperhomocystinemia 		11 0 1 8.3E-02 0 0
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia 		14 0 1 6.7E-02 0 0
CUI: C0017925
Disease: Glycogen Storage Disease Type VI
Glycogen Storage Disease Type VI 		15 0 1 6.2E-02 0 0
CUI: C1855119
Disease: Methylmalonic aciduria
Methylmalonic aciduria 		33 0 2 6.1E-02 0 0
CUI: C0268583
Disease: Methylmalonic acidemia
Methylmalonic acidemia 		44 0 2 4.5E-02 0 0
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		23 0 1 4.2E-02 0 0
CUI: C0040038
Disease: Thromboembolism
Thromboembolism 		25 0 1 3.8E-02 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 1 3.7E-02 0 0
CUI: C0162275
Disease: Ketonuria
Ketonuria 		26 0 1 3.7E-02 0 0
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 0 1 3.3E-02 0 0