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: C0021845
Disease: Intestinal Perforation
Intestinal Perforation
0 3 0 0 1 1.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.2E-02
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer
0 2 0 0 1 1.2E-02
CUI: C0342153
Disease: Congenital thyroid hypoplasia
Congenital thyroid hypoplasia
0 5 0 0 2 2.3E-02
Severe nonproliferative diabetic retinopathy
0 3 0 0 1 1.2E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
0 13 0 0 1 1.1E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE
0 26 0 0 1 9.3E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.2E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.2E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 1.2E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 1.1E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 1.2E-02
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 1 3.6E-03 0 0
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis
22 0 1 3.4E-03 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 3.5E-03 0 0
CUI: C0001079
Disease: Achondrogenesis
Achondrogenesis
4 0 1 3.6E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 3.5E-03 0 0
Acute and subacute liver necrosis (disorder)
6 0 1 3.6E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis
9 0 1 3.5E-03 0 0
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction
24 0 1 3.4E-03 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma
21 0 1 3.4E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma
9 0 1 3.5E-03 0 0
CUI: C0001510
Disease: Postoperative adhesion
Postoperative adhesion
9 0 1 3.5E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders
9 0 1 3.5E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
43 0 1 3.2E-03 0 0