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: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 1.1E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 1.9E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 2.0E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 2 6.5E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 3 4.3E-02 0 0
CUI: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology
3 0 2 0.22 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 1 1.1E-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: C4531154
Disease: Abnormal CD4:CD8 ratio
Abnormal CD4:CD8 ratio
5 0 1 8.3E-02 0 0
CUI: C4023026
Disease: Abnormal megakaryocyte morphology
Abnormal megakaryocyte morphology
10 0 1 5.9E-02 0 0
CUI: C0855742
Disease: Abnormal platelet morphology
Abnormal platelet morphology
10 0 1 5.9E-02 0 0
CUI: C4025731
Disease: Abnormal thrombosis
Abnormal thrombosis
13 0 1 5.0E-02 0 0
Abnormality of blood and blood-forming tissues
23 0 1 3.3E-02 0 0
CUI: C4025692
Disease: Abnormality of calvarial morphology
Abnormality of calvarial morphology
8 0 1 6.7E-02 0 0
CUI: C4021808
Disease: Abnormality of earlobe
Abnormality of earlobe
9 0 1 6.2E-02 0 0
Abnormality of metabolism/homeostasis
171 0 1 5.6E-03 0 0
CUI: C4023165
Disease: Abnormality of skeletal morphology
Abnormality of skeletal morphology
1 0 1 0.12 0 0
CUI: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system
34 0 1 2.4E-02 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver
75 0 1 1.2E-02 0 0
CUI: C4025698
Disease: Abnormality of the peritoneum
Abnormality of the peritoneum
9 0 1 6.2E-02 0 0
Abnormality of the respiratory system
16 0 1 4.3E-02 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal
109 0 1 8.6E-03 0 0
CUI: C1844554
Disease: Absent fingernail
Absent fingernail
19 0 1 3.8E-02 0 0
Absent pigmentation of the ventral chest
2 0 1 0.11 0 0
CUI: C1844555
Disease: Absent toenail
Absent toenail
11 0 1 5.6E-02 0 0