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: C0033923
Disease: Psychomotor Performance
Psychomotor Performance
0 1 0 0 1 1.4E-02
CUI: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test
0 3 0 0 1 1.4E-02
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0 111 0 0 1 5.5E-03
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0 111 0 0 1 5.5E-03
CUI: C0236656
Disease: Dementia associated with alcoholism
Dementia associated with alcoholism
1 0 1 2.5E-02 0 0
CUI: C0262565
Disease: Anteroseptal Myocardial Infarction
Anteroseptal Myocardial Infarction
1 0 1 2.5E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta
1 0 1 2.5E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula
1 0 1 2.5E-02 0 0
CUI: C0277941
Disease: Blanching of skin
Blanching of skin
1 0 1 2.5E-02 0 0
Tetralogy of Fallot with pulmonary atresia
1 0 1 2.5E-02 0 0
Imbalance of constituents of food intake
1 0 1 2.5E-02 0 0
CUI: C0349086
Disease: Delirium co-occurrent with dementia
Delirium co-occurrent with dementia
1 0 1 2.5E-02 0 0
CUI: C0393664
Disease: Multiple Sclerosis, Acute Relapsing
Multiple Sclerosis, Acute Relapsing
1 0 1 2.5E-02 0 0
CUI: C0398641
Disease: Epstein syndrome (disorder)
Epstein syndrome (disorder)
1 0 1 2.5E-02 0 0
CUI: C0403445
Disease: Fechtner syndrome (disorder)
Fechtner syndrome (disorder)
1 0 1 2.5E-02 0 0
CUI: C0477597
Disease: Necrotising vasculopathy
Necrotising vasculopathy
1 0 1 2.5E-02 0 0
CUI: C0521161
Disease: Vasculitic rash
Vasculitic rash
1 0 1 2.5E-02 0 0
Apolipoproteins E measurement (procedure)
1 1 1 2.5E-02 1 1.4E-02
CUI: C0581386
Disease: Chronic anxiety
Chronic anxiety
1 0 1 2.5E-02 0 0
Mycobacterium tuberculosis meningitis
1 0 1 2.5E-02 0 0
CUI: C0860628
Disease: Loss of memory ability
Loss of memory ability
1 0 1 2.5E-02 0 0
CUI: C1388177
Disease: Arteriosclerosis of aorta
Arteriosclerosis of aorta
1 0 1 2.5E-02 0 0
Atrophia Maculosa Varioliformis Cutis, Familial
1 0 1 2.5E-02 0 0
MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS
1 0 1 2.5E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux
1 0 1 2.5E-02 0 0