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: C0152424
Disease: Common ventricle
Common ventricle
0 5 0 0 1 1.7E-02
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia
0 2 0 0 1 1.8E-02
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma
0 1 0 0 1 1.9E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
0 1 0 0 1 1.9E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 1.6E-02
METABOLIC SYNDROME, SUSCEPTIBILITY TO
0 2 0 0 1 1.8E-02
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia
0 4 0 0 1 1.8E-02
CUI: C3274516
Disease: Single Ventricle Defect
Single Ventricle Defect
0 5 0 0 1 1.7E-02
CUI: C4016925
Disease: OBESITY, AGE AT ONSET OF
OBESITY, AGE AT ONSET OF
0 1 0 0 1 1.9E-02
Frequent episodic tension-type headache
0 1 0 0 1 1.9E-02
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase
212 0 1 2.3E-03 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture
210 0 1 2.3E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 2.4E-03 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
194 0 1 2.4E-03 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders
183 0 1 2.5E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 2.5E-03 0 0
Malignant neoplasm of large intestine
173 0 1 2.6E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 0 1 2.6E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement
169 0 1 2.6E-03 0 0
CUI: C0235874
Disease: Disease Exacerbation
Disease Exacerbation
166 0 1 2.6E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
166 0 1 2.6E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
166 0 1 2.6E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
166 0 1 2.6E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
165 0 1 2.6E-03 0 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
151 0 1 2.7E-03 0 0