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: C0009806
Disease: Constipation
Constipation
424 0 1 2.4E-03 0 0
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
1282 0 1 7.8E-04 0 0
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
1576 0 1 6.3E-04 0 0
CUI: C0010598
Disease: Cyclothymic Disorder
Cyclothymic Disorder
4 0 1 0.25 0 0
CUI: C0011071
Disease: Sudden death
Sudden death
30 0 1 3.3E-02 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
389 0 1 2.6E-03 0 0
CUI: C0011570
Disease: Mental Depression
Mental Depression
1478 0 1 6.8E-04 0 0
CUI: C0011574
Disease: Involutional Depression
Involutional Depression
25 0 1 4.0E-02 0 0
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
1719 0 1 5.8E-04 0 0
Diabetes Mellitus, Non-Insulin-Dependent
3134 0 1 3.2E-04 0 0
CUI: C0011876
Disease: Cataract due to diabetes mellitus
Cataract due to diabetes mellitus
22 0 1 4.5E-02 0 0
CUI: C0013132
Disease: Drooling
Drooling
95 0 1 1.1E-02 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy
1215 0 1 8.2E-04 0 0
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
717 0 1 1.4E-03 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma
770 0 1 1.3E-03 0 0
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest
411 0 1 2.4E-03 0 0
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
406 0 1 2.5E-03 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
384 0 1 2.6E-03 0 0
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
138 0 1 7.2E-03 0 0
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis
92 0 1 1.1E-02 0 0
CUI: C0020503
Disease: Hyperparathyroidism, Secondary
Hyperparathyroidism, Secondary
68 0 1 1.5E-02 0 0
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
2322 0 1 4.3E-04 0 0
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
420 0 1 2.4E-03 0 0
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes
973 0 1 1.0E-03 0 0
CUI: C0021368
Disease: Inflammation
Inflammation
467 0 1 2.1E-03 0 0