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: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs
20 0 1 1.5E-02 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome
15 0 1 1.6E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 6.7E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 4 1.2E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 1.6E-02 0 0
Abnormal atrioventricular conduction
7 0 1 1.9E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 8 8.4E-03 0 0
Abnormal brain FDG positron emission tomography
18 0 1 1.5E-02 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology
12 0 1 1.7E-02 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 2.0E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 3 2.9E-02 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology
70 0 1 8.5E-03 0 0
CUI: C1856019
Disease: Abnormal cortical gyration
Abnormal cortical gyration
17 0 1 1.6E-02 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery
32 0 1 1.3E-02 0 0
Abnormal electrophysiology of sinoatrial node origin
1 0 1 2.1E-02 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 1.3E-02 0 0
Abnormal form of the vertebral bodies
89 0 1 7.4E-03 0 0
CUI: C0232769
Disease: Abnormal gallbladder function
Abnormal gallbladder function
3 0 2 4.1E-02 0 0
CUI: C3280303
Disease: Abnormal hair whorl
Abnormal hair whorl
5 0 1 1.9E-02 0 0
CUI: C4531142
Disease: Abnormal lymphocyte physiology
Abnormal lymphocyte physiology
1 0 1 2.1E-02 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function
12 0 1 1.7E-02 0 0
Abnormal mitochondria in muscle tissue
39 0 1 1.2E-02 0 0
CUI: C4022687
Disease: Abnormal motor evoked potentials
Abnormal motor evoked potentials
4 0 1 2.0E-02 0 0
Abnormal motor nerve conduction velocity
3 0 1 2.0E-02 0 0
CUI: C1857704
Disease: Abnormal myelination
Abnormal myelination
49 0 1 1.0E-02 0 0