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: C0340957
Disease: Congenital deficiency of intrinsic factor
Congenital deficiency of intrinsic factor 		1 0 1 1.00 0 0
CUI: C4021641
Disease: Absence of intrinsic factor
Absence of intrinsic factor 		1 0 1 1.00 0 0
CUI: C0543641
Disease: Megaloblastic anemia, secondary
Megaloblastic anemia, secondary 		3 0 1 0.33 0 0
CUI: C0750292
Disease: Malabsorption of Vitamin B12
Malabsorption of Vitamin B12 		3 0 1 0.33 0 0
CUI: C1306856
Disease: Megaloblastic anemia due to inborn errors of metabolism
Megaloblastic anemia due to inborn errors of metabolism 		3 0 1 0.33 0 0
CUI: C1334688
Disease: Megaloblastic erythroid hyperplasia
Megaloblastic erythroid hyperplasia 		3 0 1 0.33 0 0
CUI: C0854441
Disease: Gastric mucosal lesion
Gastric mucosal lesion 		4 0 1 0.25 0 0
CUI: C0342701
Disease: Transcobalamin II deficiency
Transcobalamin II deficiency 		5 0 1 0.20 0 0
CUI: C0277302
Disease: Infection by Strongyloides stercoralis
Infection by Strongyloides stercoralis 		7 0 1 0.14 0 0
CUI: C4551825
Disease: Megaloblastic Anemia 1
Megaloblastic Anemia 1 		9 0 1 0.11 0 0
CUI: C3272399
Disease: Gastric Neuroendocrine Tumor
Gastric Neuroendocrine Tumor 		11 0 1 9.1E-02 0 0
CUI: C3812396
Disease: Chronic idiopathic pulmonary fibrosis
Chronic idiopathic pulmonary fibrosis 		11 0 1 9.1E-02 0 0
CUI: C0302845
Disease: MCV - raised
MCV - raised 		12 0 1 8.3E-02 0 0
CUI: C0340782
Disease: Hyperplastic lymph node
Hyperplastic lymph node 		12 0 1 8.3E-02 0 0
CUI: C0267454
Disease: Necrotic enteritis
Necrotic enteritis 		13 0 1 7.7E-02 0 0
CUI: C0158458
Disease: Acquired hallux valgus
Acquired hallux valgus 		14 0 1 7.1E-02 0 0
CUI: C0265656
Disease: Congenital hallux valgus
Congenital hallux valgus 		14 0 1 7.1E-02 0 0
CUI: C4523989
Disease: Occult hepatitis B
Occult hepatitis B 		14 0 1 7.1E-02 0 0
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		16 0 1 6.2E-02 0 0
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction 		16 0 1 6.2E-02 0 0
CUI: C2004461
Disease: Bowel dysfunction
Bowel dysfunction 		16 0 1 6.2E-02 0 0
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia 		18 0 1 5.6E-02 0 0
CUI: C0740985
Disease: Acute anaemia
Acute anaemia 		18 0 1 5.6E-02 0 0
CUI: C0848771
Disease: neurological disability
neurological disability 		18 0 1 5.6E-02 0 0
CUI: C1394891
Disease: Intrinsic Factor Deficiency
Intrinsic Factor Deficiency 		18 0 1 5.6E-02 0 0