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: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
36 0 3 7.1E-02 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology
70 0 1 1.3E-02 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery
32 0 1 2.5E-02 0 0
Abnormal form of the vertebral bodies
89 0 2 2.1E-02 0 0
CUI: C4025252
Disease: Abnormal nasal morphology
Abnormal nasal morphology
34 0 1 2.4E-02 0 0
Abnormal pigmentation of the oral mucosa
1 0 1 0.11 0 0
CUI: C0234649
Disease: Abnormal saccadic eye movement
Abnormal saccadic eye movement
17 0 1 4.0E-02 0 0
CUI: C1834129
Disease: Abnormal vertebral morphology
Abnormal vertebral morphology
28 0 1 2.8E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 8.1E-03 0 0
CUI: C4020869
Disease: Abnormality of abdomen morphology
Abnormality of abdomen morphology
17 0 3 0.13 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 1 8.9E-03 0 0
Abnormality of cardiovascular system morphology
198 0 2 9.8E-03 0 0
Abnormality of endocrine pancreas physiology
4 0 1 8.3E-02 0 0
CUI: C4023583
Disease: Abnormality of iron homeostasis
Abnormality of iron homeostasis
5 0 1 7.7E-02 0 0
Abnormality of metabolism/homeostasis
171 0 1 5.6E-03 0 0
Abnormality of ocular smooth pursuit
5 0 1 7.7E-02 0 0
Abnormality of the hypothalamus-pituitary axis
70 0 4 5.3E-02 0 0
CUI: C1842083
Disease: Abnormality of the ribs
Abnormality of the ribs
69 0 1 1.3E-02 0 0
CUI: C1840382
Disease: Abnormality of the ureter
Abnormality of the ureter
19 0 1 3.7E-02 0 0
CUI: C4021821
Disease: Abnormality of the urinary system
Abnormality of the urinary system
50 0 1 1.7E-02 0 0
CUI: C4021862
Disease: Absent epiphyses
Absent epiphyses
2 0 1 1.0E-01 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 4.8E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 4.2E-03 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen
41 0 3 6.4E-02 0 0