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: C1848580
Disease: Decreased methionine synthase activity
Decreased methionine synthase activity 		6 0 3 0.43 0 0
CUI: C1848556
Disease: Decreased adenosylcobalamin
Decreased adenosylcobalamin 		7 0 3 0.38 0 0
CUI: C4021736
Disease: Decreased methylcobalamin
Decreased methylcobalamin 		7 0 3 0.38 0 0
CUI: C0268618
Disease: Cystathioninemia
Cystathioninemia 		4 0 2 0.33 0 0
CUI: C0268616
Disease: Gamma-cystathionase deficiency
Gamma-cystathionase deficiency 		5 0 2 0.29 0 0
CUI: C1848555
Disease: Hypomethioninemia
Hypomethioninemia 		5 0 2 0.29 0 0
CUI: C1848579
Disease: Decreased methylmalonyl-CoA mutase activity
Decreased methylmalonyl-CoA mutase activity 		5 0 2 0.29 0 0
CUI: C0400823
Disease: Neutropenic colitis
Neutropenic colitis 		1 0 1 0.25 0 0
CUI: C1848552
Disease: Methylmalonic Aciduria and Homocystinuria, CblD Type
Methylmalonic Aciduria and Homocystinuria, CblD Type 		1 0 1 0.25 0 0
CUI: C1848553
Disease: Homocystinuria, CblD Type, Variant 1
Homocystinuria, CblD Type, Variant 1 		1 0 1 0.25 0 0
CUI: C1848554
Disease: Methylmalonic Aciduria, CblD Type, Variant 2
Methylmalonic Aciduria, CblD Type, Variant 2 		1 0 1 0.25 0 0
CUI: C1848578
Disease: METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE (disorder)
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE (disorder) 		1 0 1 0.25 0 0
CUI: C3806347
Disease: Hyperhomocystinemia
Hyperhomocystinemia 		11 0 3 0.25 0 0
CUI: C1272348
Disease: Disorder of vitamin B12
Disorder of vitamin B12 		2 0 1 0.20 0 0
CUI: C1848561
Disease: Methylmalonic acidemia with homocystinuria
Methylmalonic acidemia with homocystinuria 		2 0 1 0.20 0 0
CUI: C4693974
Disease: METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC 		2 0 1 0.20 0 0
CUI: C1852146
Disease: DERMODISTORTIVE URTICARIA
DERMODISTORTIVE URTICARIA 		3 0 1 0.17 0 0
CUI: C1855114
Disease: Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency
Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency 		3 0 1 0.17 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 4 0.15 0 0
CUI: C0267537
Disease: Typhlitis
Typhlitis 		4 0 1 0.14 0 0
CUI: C0041782
Disease: Deficiency anemias
Deficiency anemias 		5 0 1 0.12 0 0
CUI: C0342701
Disease: Transcobalamin II deficiency
Transcobalamin II deficiency 		5 0 1 0.12 0 0
CUI: C0700216
Disease: Structural Clinical Interview for DSM-III
Structural Clinical Interview for DSM-III 		5 0 1 0.12 0 0
CUI: C1855119
Disease: Methylmalonic aciduria
Methylmalonic aciduria 		33 0 4 0.12 0 0
CUI: C0017675
Disease: Glossitis
Glossitis 		7 0 1 1.0E-01 0 0