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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 2.4E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 3.0E-02
Visually threatening diabetic retinopathy
0 4 0 0 1 2.8E-02
CUI: C0947912
Disease: Myasthenias
Myasthenias
0 3 0 0 1 2.9E-02
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess
0 3 0 0 2 5.9E-02
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
0 1 0 0 1 3.0E-02
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
0 1 0 0 1 3.0E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 3.0E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 3.0E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 2.9E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 2.4E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 2.9E-02
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute
2 0 1 9.7E-03 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 8.8E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 6.0E-03 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual
7 0 1 9.3E-03 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 9.4E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 1 8.3E-03 0 0
Acute and subacute liver necrosis (disorder)
6 0 1 9.3E-03 0 0
Acute vascular insufficiency of intestine (disorder)
8 0 1 9.2E-03 0 0
CUI: C0001416
Disease: Adenitis
Adenitis
9 0 1 9.1E-03 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma
8 0 1 9.2E-03 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil
2 0 1 9.7E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma
9 0 1 9.1E-03 0 0
CUI: C0001510
Disease: Postoperative adhesion
Postoperative adhesion
9 0 1 9.1E-03 0 0