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: C0278007
Disease: Normal bowel habits
Normal bowel habits 		1 0 1 0.20 0 0
CUI: C0340957
Disease: Congenital deficiency of intrinsic factor
Congenital deficiency of intrinsic factor 		1 0 1 0.20 0 0
CUI: C0342700
Disease: Transcobalamin I Deficiency
Transcobalamin I Deficiency 		1 0 1 0.20 0 0
CUI: C0400823
Disease: Neutropenic colitis
Neutropenic colitis 		1 0 1 0.20 0 0
CUI: C1263739
Disease: Disorder of organic acid metabolism
Disorder of organic acid metabolism 		1 0 1 0.20 0 0
CUI: C1855115
Disease: Methylmalonic Aciduria, mut(0) Type
Methylmalonic Aciduria, mut(0) Type 		1 0 1 0.20 0 0
CUI: C1855116
Disease: Methylmalonic Aciduria, mut(-) Type
Methylmalonic Aciduria, mut(-) Type 		1 0 1 0.20 0 0
CUI: C2931536
Disease: Methylmalonyl-Coenzyme A mutase deficiency
Methylmalonyl-Coenzyme A mutase deficiency 		1 0 1 0.20 0 0
CUI: C4021641
Disease: Absence of intrinsic factor
Absence of intrinsic factor 		1 0 1 0.20 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 4 0.15 0 0
CUI: C0348484
Disease: Other disorders of branched-chain amino-acid metabolism
Other disorders of branched-chain amino-acid metabolism 		3 0 1 0.14 0 0
CUI: C0543641
Disease: Megaloblastic anemia, secondary
Megaloblastic anemia, secondary 		3 0 1 0.14 0 0
CUI: C0750292
Disease: Malabsorption of Vitamin B12
Malabsorption of Vitamin B12 		3 0 1 0.14 0 0
CUI: C1306856
Disease: Megaloblastic anemia due to inborn errors of metabolism
Megaloblastic anemia due to inborn errors of metabolism 		3 0 1 0.14 0 0
CUI: C1334688
Disease: Megaloblastic erythroid hyperplasia
Megaloblastic erythroid hyperplasia 		3 0 1 0.14 0 0
CUI: C1852146
Disease: DERMODISTORTIVE URTICARIA
DERMODISTORTIVE URTICARIA 		3 0 1 0.14 0 0
CUI: C1854704
Disease: Metabolic Ketosis
Metabolic Ketosis 		3 0 1 0.14 0 0
CUI: C1855114
Disease: Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency
Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency 		3 0 1 0.14 0 0
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 0 4 0.13 0 0
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		13 0 2 0.12 0 0
CUI: C0238801
Disease: Bone marrow megaloblastic (finding)
Bone marrow megaloblastic (finding) 		4 0 1 0.12 0 0
CUI: C0267537
Disease: Typhlitis
Typhlitis 		4 0 1 0.12 0 0
CUI: C0854441
Disease: Gastric mucosal lesion
Gastric mucosal lesion 		4 0 1 0.12 0 0
CUI: C0041782
Disease: Deficiency anemias
Deficiency anemias 		5 0 1 0.11 0 0
CUI: C0700216
Disease: Structural Clinical Interview for DSM-III
Structural Clinical Interview for DSM-III 		5 0 1 0.11 0 0