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: C2931850
Disease: Aase Smith syndrome 2
Aase Smith syndrome 2
16 0 1 4.3E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 9.1E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.4E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 2 2.2E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 1.2E-02 0 0
CUI: C1855670
Disease: Abnormal cornea morphology
Abnormal cornea morphology
9 0 1 6.2E-02 0 0
CUI: C0349705
Disease: Abnormal hemoglobin finding
Abnormal hemoglobin finding
9 0 1 6.2E-02 0 0
Abnormal lactate dehydrogenase activity
19 0 1 3.8E-02 0 0
CUI: C4477036
Disease: Abnormal location of the eyebrow
Abnormal location of the eyebrow
1 0 1 0.12 0 0
CUI: C4023026
Disease: Abnormal megakaryocyte morphology
Abnormal megakaryocyte morphology
10 0 1 5.9E-02 0 0
CUI: C1290508
Disease: Abnormal number of teeth
Abnormal number of teeth
3 0 1 1.0E-01 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 1 1.5E-02 0 0
CUI: C0855740
Disease: Abnormal platelet function
Abnormal platelet function
21 0 1 3.6E-02 0 0
Abnormality of multiple cell lineages in the bone marrow
2 0 1 0.11 0 0
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray
34 0 1 2.4E-02 0 0
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
28 0 1 2.9E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.5E-03 0 0
CUI: C1852464
Disease: Abnormality of the cervical spine
Abnormality of the cervical spine
12 0 1 5.3E-02 0 0
CUI: C0744356
Disease: Abnormality of the genital system
Abnormality of the genital system
36 0 1 2.3E-02 0 0
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna
85 0 1 1.1E-02 0 0
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
148 0 1 6.5E-03 0 0
CUI: C4021821
Disease: Abnormality of the urinary system
Abnormality of the urinary system
50 0 1 1.8E-02 0 0
CUI: C2931753
Disease: Achromatopsia incomplete, X-linked
Achromatopsia incomplete, X-linked
2 0 1 0.11 0 0
CUI: C0027859
Disease: Acoustic Neuroma
Acoustic Neuroma
131 0 2 1.5E-02 0 0