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: C1852146
Disease: DERMODISTORTIVE URTICARIA
DERMODISTORTIVE URTICARIA 		3 0 1 0.33 0 0
CUI: C0238801
Disease: Bone marrow megaloblastic (finding)
Bone marrow megaloblastic (finding) 		4 0 1 0.25 0 0
CUI: C0267537
Disease: Typhlitis
Typhlitis 		4 0 1 0.25 0 0
CUI: C0041782
Disease: Deficiency anemias
Deficiency anemias 		5 0 1 0.20 0 0
CUI: C0342701
Disease: Transcobalamin II deficiency
Transcobalamin II deficiency 		5 0 1 0.20 0 0
CUI: C0700216
Disease: Structural Clinical Interview for DSM-III
Structural Clinical Interview for DSM-III 		5 0 1 0.20 0 0
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		16 0 1 6.2E-02 0 0
CUI: C0858867
Disease: Reticulocytopenia
Reticulocytopenia 		17 0 1 5.9E-02 0 0
CUI: C0002888
Disease: Anemia, Megaloblastic
Anemia, Megaloblastic 		26 0 1 3.8E-02 0 0
CUI: C0026633
Disease: Mouth Abnormalities
Mouth Abnormalities 		26 0 1 3.8E-02 0 0
CUI: C3887639
Disease: Autoimmune gastritis
Autoimmune gastritis 		28 0 1 3.6E-02 0 0
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 0 1 3.4E-02 0 0
CUI: C1855119
Disease: Methylmalonic aciduria
Methylmalonic aciduria 		33 0 1 3.0E-02 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability 		34 0 1 2.9E-02 0 0
CUI: C0205649
Disease: Adenoma, Monomorphic
Adenoma, Monomorphic 		36 0 1 2.8E-02 0 0
CUI: C0205651
Disease: Adenoma, Trabecular
Adenoma, Trabecular 		37 0 1 2.7E-02 0 0
CUI: C0205650
Disease: Papillary adenoma
Papillary adenoma 		39 0 1 2.6E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 2.3E-02 0 0
CUI: C0205648
Disease: Adenoma, Microcystic
Adenoma, Microcystic 		45 0 1 2.2E-02 0 0
CUI: C0205646
Disease: Adenoma, Basal Cell
Adenoma, Basal Cell 		49 0 1 2.0E-02 0 0
CUI: C0002886
Disease: Anemia, Macrocytic
Anemia, Macrocytic 		51 0 1 2.0E-02 0 0
CUI: C1853238
Disease: Conotruncal defect
Conotruncal defect 		51 0 1 2.0E-02 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis 		55 0 1 1.8E-02 0 0
CUI: C1858991
Disease: Childhood Ataxia with Central Nervous System Hypomyelinization
Childhood Ataxia with Central Nervous System Hypomyelinization 		59 0 1 1.7E-02 0 0
CUI: C0917996
Disease: Cerebral Aneurysm
Cerebral Aneurysm 		65 0 1 1.5E-02 0 0