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: C0010403
Disease: Cryoglobulinemia
Cryoglobulinemia
0 7 0 0 1 8.7E-04
CUI: C0033923
Disease: Psychomotor Performance
Psychomotor Performance
0 1 0 0 1 8.8E-04
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency
0 1 0 0 1 8.8E-04
Heparin-induced thrombocytopenia with thrombosis
0 1 0 0 1 8.8E-04
CUI: C0523550
Disease: Catalase measurement
Catalase measurement
0 2 0 0 1 8.7E-04
CUI: C0678189
Disease: Hyperlipidemia, group A
Hyperlipidemia, group A
0 1 0 0 1 8.8E-04
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait
0 2 0 0 1 8.7E-04
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 1 8.7E-04
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 1 8.7E-04
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
0 1 0 0 1 8.8E-04
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement
0 8 0 0 1 8.7E-04
CUI: C3890352
Disease: P-Selectin Measurement
P-Selectin Measurement
0 2 0 0 1 8.7E-04
CUI: C3899405
Disease: Decreased Attention
Decreased Attention
0 3 0 0 1 8.7E-04
CUI: C4050627
Disease: Soluble P-Selectin Measurement
Soluble P-Selectin Measurement
0 3 0 0 1 8.7E-04
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 2.0E-03 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 2.0E-03 0 0
Acute vascular insufficiency of intestine (disorder)
8 0 1 2.0E-03 0 0
CUI: C0001364
Disease: Massive Hepatic Necrosis
Massive Hepatic Necrosis
2 0 1 2.1E-03 0 0
CUI: C0001442
Disease: Adenosarcoma
Adenosarcoma
9 0 1 2.0E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders
9 4 1 2.0E-03 1 8.7E-04
CUI: C0001630
Disease: Adrenal Rest Tumor
Adrenal Rest Tumor
2 0 1 2.1E-03 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic
17 0 1 2.0E-03 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 2.0E-03 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
43 0 1 1.9E-03 0 0
CUI: C0001816
Disease: Agnosia
Agnosia
17 0 1 2.0E-03 0 0