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: C0013421
Disease: Dystonia
Dystonia
0 97 0 0 1 9.3E-03
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0 87 0 0 1 1.0E-02
Xeroderma Pigmentosum, Complementation Group D
0 111 0 0 1 8.3E-03
Erythrocytosis due to low atmospheric pressure
0 13 0 0 1 4.3E-02
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 9.1E-02
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders
0 37 0 0 1 2.1E-02
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations
0 3 0 0 1 7.7E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 9.1E-02
CUI: C0852711
Disease: Sickle Cell Dactylitis
Sickle Cell Dactylitis
0 7 0 0 1 5.9E-02
CORONARY ARTERY DISEASE, MODIFIER OF
0 1 0 0 1 9.1E-02
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0 1 0 0 1 9.1E-02
CUI: C2242595
Disease: Mucosal atrophy
Mucosal atrophy
0 5 0 0 1 6.7E-02
CUI: C3890602
Disease: Bodily Pain
Bodily Pain
0 4 0 0 1 7.1E-02
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0 1 0 0 1 9.1E-02
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.1E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.2E-02 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 1 4.0E-02 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
188 0 1 4.8E-03 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae
12 0 1 3.1E-02 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans
64 0 1 1.2E-02 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 4.0E-02 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 4.8E-02 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis
11 3 1 3.2E-02 1 7.7E-02
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis
130 49 1 6.7E-03 2 3.4E-02
CUI: C0001403
Disease: Addison Disease
Addison Disease
111 0 1 7.6E-03 0 0