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: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
50 116 23 0.27 30 7.7E-02
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
27 53 6 7.6E-02 2 5.6E-03
CUI: C2316832
Disease: Arachidonic acid measurement
Arachidonic acid measurement
4 4 4 6.9E-02 1 3.2E-03
CUI: C0523829
Disease: Phosphatidylcholine measurement
Phosphatidylcholine measurement
9 19 4 6.3E-02 4 1.2E-02
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
89 111 8 5.8E-02 7 1.7E-02
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
89 111 8 5.8E-02 7 1.7E-02
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
65 113 6 5.1E-02 5 1.2E-02
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
51 205 5 4.8E-02 4 7.9E-03
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
433 3282 22 4.7E-02 91 2.6E-02
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
96 212 6 4.1E-02 6 1.2E-02
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
48 67 4 3.9E-02 1 2.7E-03
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
80 134 5 3.8E-02 3 6.9E-03
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
138 216 7 3.7E-02 4 7.7E-03
CUI: C0036400
Disease: Scimitar Syndrome
Scimitar Syndrome
2 0 2 3.4E-02 0 0
CUI: C1735886
Disease: Bland White Garland Syndrome
Bland White Garland Syndrome
2 0 2 3.4E-02 0 0
CUI: C4748946
Disease: CARDIAC-UROGENITAL SYNDROME
CARDIAC-UROGENITAL SYNDROME
2 0 2 3.4E-02 0 0
Total Anomalous Pulmonary Venous Return 1
3 0 2 3.4E-02 0 0
CUI: C0202171
Disease: Phosphatidylinositol measurement
Phosphatidylinositol measurement
4 0 2 3.3E-02 0 0
CUI: C0018810
Disease: heart rate
heart rate
36 0 3 3.3E-02 0 0
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
39 568 3 3.2E-02 4 4.6E-03
CUI: C0344760
Disease: Congenital atresia of mitral valve
Congenital atresia of mitral valve
8 0 2 3.1E-02 0 0
CUI: C0685707
Disease: Muscular ventricular septum defect
Muscular ventricular septum defect
9 0 2 3.1E-02 0 0
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
9 0 2 3.1E-02 0 0
CUI: C0221182
Disease: Chordee
Chordee
11 0 2 3.0E-02 0 0
CUI: C0085679
Disease: Hyperchloremia
Hyperchloremia
12 0 2 2.9E-02 0 0