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: C1848555
Disease: Hypomethioninemia
Hypomethioninemia
5 0 2 6.2E-02 0 0
CUI: C4022906
Disease: Delayed social development
Delayed social development
5 1 2 6.2E-02 1 9.1E-02
Decreased methionine synthase activity
6 0 2 6.1E-02 0 0
CUI: C0019034
Disease: Hemoglobin SC Disease
Hemoglobin SC Disease
7 0 2 5.9E-02 0 0
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis
25 5 3 5.9E-02 4 0.33
CUI: C1848556
Disease: Decreased adenosylcobalamin
Decreased adenosylcobalamin
7 0 2 5.9E-02 0 0
CUI: C4021736
Disease: Decreased methylcobalamin
Decreased methylcobalamin
7 0 2 5.9E-02 0 0
Neural tube defect, folate-sensitive
8 0 2 5.7E-02 0 0
CUI: C0588008
Disease: Severe depression
Severe depression
46 0 4 5.6E-02 0 0
CUI: C0035302
Disease: Retinal Artery Occlusion
Retinal Artery Occlusion
9 1 2 5.6E-02 1 9.1E-02
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy
29 41 3 5.5E-02 1 2.0E-02
CUI: C0340968
Disease: Deficiency of pyruvate kinase
Deficiency of pyruvate kinase
10 63 2 5.4E-02 1 1.4E-02
CUI: C1859846
Disease: Childhood-onset truncal obesity
Childhood-onset truncal obesity
11 4 2 5.3E-02 1 7.1E-02
CUI: C0038219
Disease: Status Dysraphicus
Status Dysraphicus
12 0 2 5.1E-02 0 0
CUI: C1513269
Disease: Microcysts
Microcysts
12 0 2 5.1E-02 0 0
CUI: C1565321
Disease: Cholera Infantum
Cholera Infantum
12 0 2 5.1E-02 0 0
CUI: C0020580
Disease: Hypesthesia
Hypesthesia
33 0 3 5.1E-02 0 0
CUI: C1704378
Disease: Heymann Nephritis
Heymann Nephritis
13 0 2 5.0E-02 0 0
CUI: C0079758
Disease: Lymphoma, Mixed-Cell, Follicular
Lymphoma, Mixed-Cell, Follicular
15 0 2 4.8E-02 0 0
CUI: C0266508
Disease: Rachischisis
Rachischisis
15 0 2 4.8E-02 0 0
CUI: C1956132
Disease: Lymphoma, Follicular, Grade 2
Lymphoma, Follicular, Grade 2
15 0 2 4.8E-02 0 0
CUI: C1956131
Disease: Lymphoma, Follicular, Grade 3
Lymphoma, Follicular, Grade 3
16 0 2 4.7E-02 0 0
CUI: C0376286
Disease: Avitaminosis
Avitaminosis
17 0 2 4.5E-02 0 0
CUI: C1510471
Disease: Vitamin Deficiency
Vitamin Deficiency
17 0 2 4.5E-02 0 0
Fast acetylator due to N-acetyltransferase enzyme variant
17 9 2 4.5E-02 1 5.3E-02