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: C0003119
Disease: Anophthalmos
Anophthalmos 		89 0 17 0.12 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 12 0.12 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome 		12 0 9 0.12 0 0
CUI: C4021161
Disease: Multiple suture craniosynostosis
Multiple suture craniosynostosis 		12 0 9 0.12 0 0
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils 		12 0 9 0.12 0 0
CUI: C0345354
Disease: Radial polydactyly
Radial polydactyly 		51 0 13 0.12 0 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation 		32 0 11 0.11 0 0
CUI: C3163801
Disease: Abnormality of aortic arch
Abnormality of aortic arch 		13 0 9 0.11 0 0
CUI: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE 		299 0 38 0.11 0 0
CUI: C0266383
Disease: Uterine Anomalies
Uterine Anomalies 		35 0 11 0.11 0 0
CUI: C0431406
Disease: Asymmetric crying face association
Asymmetric crying face association 		25 0 10 0.11 0 0
CUI: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine 		77 0 15 0.11 0 0
CUI: C0264303
Disease: Laryngomalacia
Laryngomalacia 		67 0 14 0.11 0 0
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		312 0 38 0.11 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		27 0 10 0.11 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly 		59 0 13 0.11 0 0
CUI: C0032209
Disease: Platybasia
Platybasia 		18 0 9 0.11 0 0
CUI: C0243002
Disease: Tricuspid Atresia
Tricuspid Atresia 		18 0 9 0.11 0 0
CUI: C0431565
Disease: Hamartoma of tongue
Hamartoma of tongue 		18 0 9 0.11 0 0
CUI: C0795907
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME 		18 0 9 0.11 0 0
CUI: C1860127
Disease: Impaired T cell function
Impaired T cell function 		18 0 9 0.11 0 0
CUI: C1851853
Disease: Midline notch of upper alveolar ridge
Midline notch of upper alveolar ridge 		8 0 8 0.11 0 0
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve 		50 0 12 0.11 0 0
CUI: C0020546
Disease: Hypertensive crisis
Hypertensive crisis 		19 0 9 0.11 0 0
CUI: C1848595
Disease: Mesoaxial polydactyly
Mesoaxial polydactyly 		9 0 8 0.11 0 0