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: C0016202
Disease: Flatfoot
Flatfoot 		285 38 1 3.5E-03 1 2.6E-02
CUI: C0028949
Disease: Oligomenorrhea
Oligomenorrhea 		37 1 1 2.5E-02 1 1.00
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		560 179 1 1.8E-03 1 5.6E-03
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 135 1 1.2E-03 1 7.4E-03
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		311 74 2 6.4E-03 1 1.4E-02
CUI: C0040147
Disease: Thyroiditis
Thyroiditis 		104 7 1 9.3E-03 1 0.14
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		153 37 1 6.4E-03 1 2.7E-02
CUI: C0086437
Disease: Joint laxity
Joint laxity 		224 15 1 4.4E-03 1 6.7E-02
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		508 121 1 2.0E-03 1 8.3E-03
CUI: C0265252
Disease: Coffin-Lowry syndrome
Coffin-Lowry syndrome 		23 25 1 3.8E-02 1 4.0E-02
CUI: C0392188
Disease: Abnormal rapid eye movement sleep
Abnormal rapid eye movement sleep 		11 1 1 7.1E-02 1 1.00
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		91 19 3 3.3E-02 1 5.3E-02
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 25 1 6.2E-03 1 4.0E-02
CUI: C1837404
Disease: High, narrow palate
High, narrow palate 		129 21 3 2.3E-02 1 4.8E-02
CUI: C1842366
Disease: Low anterior hairline
Low anterior hairline 		71 17 1 1.4E-02 1 5.9E-02
CUI: C1850601
Disease: Abnormality of brainstem morphology
Abnormality of brainstem morphology 		21 2 1 4.2E-02 1 0.50
CUI: C1854114
Disease: Short nose
Short nose 		265 23 1 3.7E-03 1 4.3E-02
CUI: C4022728
Disease: Abnormal upper to lower segment ratio
Abnormal upper to lower segment ratio 		1 1 1 0.25 1 1.00
CUI: C4023791
Disease: Abnormality of the clivus
Abnormality of the clivus 		2 1 1 0.20 1 1.00
CUI: C4083076
Disease: Increased head circumference
Increased head circumference 		11 1 1 7.1E-02 1 1.00
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 3 2.7E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 3.9E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		209 0 1 4.7E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 5.6E-03 0 0
CUI: C0002382
Disease: Alveolar Bone Loss
Alveolar Bone Loss 		101 0 1 9.6E-03 0 0