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: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency
0 11 0 0 1 9.1E-02
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0 80 0 0 1 1.3E-02
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome
0 163 0 0 1 6.1E-03
CUI: C1843367
Disease: Poor school performance
Poor school performance
0 411 0 0 1 2.4E-03
CUI: C1859846
Disease: Childhood-onset truncal obesity
Childhood-onset truncal obesity
0 4 0 0 1 0.25
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder)
0 65 0 0 1 1.5E-02
CUI: C3808410
Disease: Gastrointestinal malrotation
Gastrointestinal malrotation
0 2 0 0 1 0.50
CUI: C4021330
Disease: Curved toe phalanx
Curved toe phalanx
0 1 0 0 1 1.00
CUI: C4022906
Disease: Delayed social development
Delayed social development
0 1 0 0 1 1.00
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 8.3E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 3.7E-03 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
188 0 1 4.9E-03 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
64 0 1 1.2E-02 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
243 0 1 3.8E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly
138 0 1 6.4E-03 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease
111 0 1 7.8E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders
9 0 1 3.7E-02 0 0
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms
23 0 1 2.4E-02 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 3.7E-02 0 0
CUI: C0001818
Disease: Agoraphobia
Agoraphobia
29 0 1 2.1E-02 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 1.6E-02 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria
76 0 1 1.1E-02 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia
86 0 1 9.6E-03 0 0
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta
61 0 1 1.3E-02 0 0
CUI: C0002792
Disease: anaphylaxis
anaphylaxis
180 0 1 5.1E-03 0 0