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: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 1 2.6E-02 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome
12 0 1 5.3E-02 0 0
5,10-Methylenetetrahydrofolate reductase deficiency
6 0 1 7.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation
32 0 1 2.6E-02 0 0
CUI: C4023026
Disease: Abnormal megakaryocyte morphology
Abnormal megakaryocyte morphology
10 0 3 0.20 0 0
CUI: C4023145
Disease: Abnormal umbilical stump bleeding
Abnormal umbilical stump bleeding
5 0 4 0.44 0 0
CUI: C3163801
Disease: Abnormality of aortic arch
Abnormality of aortic arch
13 0 1 5.0E-02 0 0
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve
50 0 1 1.8E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel
96 0 1 9.7E-03 0 0
CUI: C3164374
Disease: Abnormality of pulmonary valve
Abnormality of pulmonary valve
40 0 1 2.1E-02 0 0
CUI: C4021745
Disease: Abnormality of the musculature
Abnormality of the musculature
24 0 1 3.2E-02 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx
23 0 1 3.3E-02 0 0
CUI: C4021797
Disease: Abnormality of the thorax
Abnormality of the thorax
40 0 1 2.1E-02 0 0
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils
12 0 1 5.3E-02 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual
7 0 1 7.1E-02 0 0
CUI: C1456418
Disease: Absence of muscle
Absence of muscle
12 0 1 5.3E-02 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation
111 0 1 8.5E-03 0 0
CUI: C1405984
Disease: Absent radius
Absent radius
24 0 1 3.2E-02 0 0
CUI: C0702166
Disease: Acne
Acne
167 0 1 5.7E-03 0 0
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia
7 0 1 7.1E-02 0 0
CUI: C2363755
Disease: Acquired Protein S Deficiency
Acquired Protein S Deficiency
4 0 1 9.1E-02 0 0
CUI: C2585317
Disease: Acquired thrombophilia
Acquired thrombophilia
8 0 1 6.7E-02 0 0
CUI: C0030044
Disease: Acrocephaly
Acrocephaly
35 0 1 2.4E-02 0 0
Activated Partial Thromboplastin Time measurement
17 0 1 4.2E-02 0 0