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: C0154089
Disease: Carcinoma in situ of penis
Carcinoma in situ of penis 		1 0 1 8.3E-02 0 0
CUI: C0234458
Disease: Dream disorder
Dream disorder 		1 0 1 8.3E-02 0 0
CUI: C0272080
Disease: Hemoglobin D disease
Hemoglobin D disease 		1 0 1 8.3E-02 0 0
CUI: C0278007
Disease: Normal bowel habits
Normal bowel habits 		1 0 1 8.3E-02 0 0
CUI: C0340957
Disease: Congenital deficiency of intrinsic factor
Congenital deficiency of intrinsic factor 		1 0 1 8.3E-02 0 0
CUI: C0427483
Disease: Finding of bite cells
Finding of bite cells 		1 0 1 8.3E-02 0 0
CUI: C0458118
Disease: Total body pain syndrome
Total body pain syndrome 		1 0 1 8.3E-02 0 0
CUI: C0580550
Disease: Lymphocyte count abnormal
Lymphocyte count abnormal 		1 1 1 8.3E-02 1 1.00
CUI: C0862953
Disease: Cholangiocarcinoma non-resectable
Cholangiocarcinoma non-resectable 		1 0 1 8.3E-02 0 0
CUI: C1264000
Disease: Sickle cell-Hemoglobin O Arab disease
Sickle cell-Hemoglobin O Arab disease 		1 0 1 8.3E-02 0 0
CUI: C1274408
Disease: Chronic plaque-like oral candidiasis
Chronic plaque-like oral candidiasis 		1 0 1 8.3E-02 0 0
CUI: C1306229
Disease: Dyschromatosis universalis
Dyschromatosis universalis 		1 0 1 8.3E-02 0 0
CUI: C1836705
Disease: Pseudohyperkalemia, Familial, 2, due to Red Cell Leak
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak 		1 0 1 8.3E-02 0 0
CUI: C1848552
Disease: Methylmalonic Aciduria and Homocystinuria, CblD Type
Methylmalonic Aciduria and Homocystinuria, CblD Type 		1 0 1 8.3E-02 0 0
CUI: C1848553
Disease: Homocystinuria, CblD Type, Variant 1
Homocystinuria, CblD Type, Variant 1 		1 0 1 8.3E-02 0 0
CUI: C1848554
Disease: Methylmalonic Aciduria, CblD Type, Variant 2
Methylmalonic Aciduria, CblD Type, Variant 2 		1 0 1 8.3E-02 0 0
CUI: C1857719
Disease: Anemia, Diamond-Blackfan, 3
Anemia, Diamond-Blackfan, 3 		1 0 1 8.3E-02 0 0
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		1 0 1 8.3E-02 0 0
CUI: C1861395
Disease: Small hypothenar eminence
Small hypothenar eminence 		1 0 1 8.3E-02 0 0
CUI: C2675511
Disease: Diamond-Blackfan Anemia 8
Diamond-Blackfan Anemia 8 		1 0 1 8.3E-02 0 0
CUI: C2675512
Disease: Diamond-Blackfan Anemia 7
Diamond-Blackfan Anemia 7 		1 0 1 8.3E-02 0 0
CUI: C2698518
Disease: Bite Cell Count (procedure)
Bite Cell Count (procedure) 		1 0 1 8.3E-02 0 0
CUI: C3161373
Disease: Dominant thalassemia
Dominant thalassemia 		1 0 1 8.3E-02 0 0
CUI: C3274463
Disease: Sickle Beta 0 Thalassemia
Sickle Beta 0 Thalassemia 		1 0 1 8.3E-02 0 0
CUI: C3806688
Disease: Solute carrier family 35 member A2 congenital disorder of glycosylation
Solute carrier family 35 member A2 congenital disorder of glycosylation 		1 12 1 8.3E-02 1 8.3E-02