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: C0750292
Disease: Malabsorption of Vitamin B12
Malabsorption of Vitamin B12 		3 0 3 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 3 0.33 0 0
CUI: C0854441
Disease: Gastric mucosal lesion
Gastric mucosal lesion 		4 0 3 0.30 0 0
CUI: C1394891
Disease: Intrinsic Factor Deficiency
Intrinsic Factor Deficiency 		18 0 6 0.29 0 0
CUI: C0543641
Disease: Megaloblastic anemia, secondary
Megaloblastic anemia, secondary 		3 0 2 0.20 0 0
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		16 0 4 0.19 0 0
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction 		16 0 4 0.19 0 0
CUI: C2004461
Disease: Bowel dysfunction
Bowel dysfunction 		16 0 3 0.14 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 4 0.13 0 0
CUI: C0740985
Disease: Acute anaemia
Acute anaemia 		18 0 3 0.12 0 0
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 0 4 0.12 0 0
CUI: C0016479
Disease: Food Poisoning
Food Poisoning 		1 0 1 0.11 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome 		1 0 1 0.11 0 0
CUI: C0278007
Disease: Normal bowel habits
Normal bowel habits 		1 0 1 0.11 0 0
CUI: C0340957
Disease: Congenital deficiency of intrinsic factor
Congenital deficiency of intrinsic factor 		1 0 1 0.11 0 0
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease 		1 0 1 0.11 0 0
CUI: C4016819
Disease: MEGALOBLASTIC ANEMIA 1, FINNISH TYPE
MEGALOBLASTIC ANEMIA 1, FINNISH TYPE 		1 2 1 0.11 1 1.4E-02
CUI: C4016948
Disease: MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE 		1 2 1 0.11 2 2.9E-02
CUI: C4021641
Disease: Absence of intrinsic factor
Absence of intrinsic factor 		1 0 1 0.11 0 0
CUI: C4302250
Disease: Dengue with warning signs
Dengue with warning signs 		1 0 1 0.11 0 0
CUI: C4302370
Disease: Benign lymphoepithelial lesion of lacrimal gland
Benign lymphoepithelial lesion of lacrimal gland 		1 0 1 0.11 0 0
CUI: C4748806
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25 		1 0 1 0.11 0 0
CUI: C0008690
Disease: Chronic anterior uveitis
Chronic anterior uveitis 		2 0 1 1.0E-01 0 0
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2 		2 0 1 1.0E-01 0 0
CUI: C0341934
Disease: Transient hypertension of pregnancy
Transient hypertension of pregnancy 		2 0 1 1.0E-01 0 0