Source: ALL
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: C2700617
Disease: Irritation - emotion
Irritation - emotion 		147 14 22 7.8E-02 3 8.3E-02
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 27 28 0.11 4 8.3E-02
CUI: C0038018
Disease: Spondylolysis
Spondylolysis 		9 2 1 6.1E-03 2 8.0E-02
CUI: C0575803
Disease: Radial deviation of hand
Radial deviation of hand 		4 2 1 6.3E-03 2 8.0E-02
CUI: C1829460
Disease: Tongue thrusting
Tongue thrusting 		5 2 3 1.9E-02 2 8.0E-02
CUI: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge 		11 2 2 1.2E-02 2 8.0E-02
CUI: C1851313
Disease: Limited shoulder movement
Limited shoulder movement 		5 2 1 6.3E-03 2 8.0E-02
CUI: C1851542
Disease: Limited hip movement
Limited hip movement 		10 2 2 1.2E-02 2 8.0E-02
CUI: C1859347
Disease: Abnormal subcutaneous fat tissue distribution
Abnormal subcutaneous fat tissue distribution 		9 2 3 1.9E-02 2 8.0E-02
CUI: C4021227
Disease: Underdeveloped nasolabial fold
Underdeveloped nasolabial fold 		3 2 2 1.3E-02 2 8.0E-02
CUI: C4021251
Disease: Dysplasia of the femoral head
Dysplasia of the femoral head 		3 2 1 6.3E-03 2 8.0E-02
CUI: C4021742
Disease: Abnormality of the humerus
Abnormality of the humerus 		10 2 1 6.1E-03 2 8.0E-02
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		140 16 7 2.4E-02 3 7.9E-02
CUI: C1854882
Disease: Absent speech
Absent speech 		232 72 47 0.14 7 7.8E-02
CUI: C3275799
Disease: Spondylolisthesis at L5-S1
Spondylolisthesis at L5-S1 		2 3 1 6.4E-03 2 7.7E-02
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption 		139 4 7 2.4E-02 2 7.4E-02
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin 		11 4 2 1.2E-02 2 7.4E-02
CUI: C4021152
Disease: Abnormal CNS myelination
Abnormal CNS myelination 		9 4 4 2.5E-02 2 7.4E-02
CUI: C4025741
Disease: Clinodactyly of the 5th toe
Clinodactyly of the 5th toe 		13 4 4 2.4E-02 2 7.4E-02
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 49 68 0.14 5 7.2E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		389 50 28 5.4E-02 5 7.1E-02
CUI: C1836479
Disease: Saccadic smooth pursuit
Saccadic smooth pursuit 		22 5 3 1.7E-02 2 7.1E-02
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement 		7 5 2 1.2E-02 2 7.1E-02
CUI: C1847524
Disease: Hyperopic astigmatism
Hyperopic astigmatism 		9 5 3 1.9E-02 2 7.1E-02
CUI: C4025724
Disease: Abnormality of the cerebral ventricles
Abnormality of the cerebral ventricles 		4 5 2 1.3E-02 2 7.1E-02