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: C4024912
Disease: Occipital myelomeningocele
Occipital myelomeningocele 		9 0 9 0.53 0 0
CUI: C3266101
Disease: 22q11 partial monosomy syndrome
22q11 partial monosomy syndrome 		12 0 9 0.45 0 0
CUI: C4021161
Disease: Multiple suture craniosynostosis
Multiple suture craniosynostosis 		12 0 9 0.45 0 0
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils 		12 0 9 0.45 0 0
CUI: C3163801
Disease: Abnormality of aortic arch
Abnormality of aortic arch 		13 0 9 0.43 0 0
CUI: C0032209
Disease: Platybasia
Platybasia 		18 0 9 0.35 0 0
CUI: C0243002
Disease: Tricuspid Atresia
Tricuspid Atresia 		18 0 9 0.35 0 0
CUI: C0795907
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME 		18 0 9 0.35 0 0
CUI: C1860127
Disease: Impaired T cell function
Impaired T cell function 		18 0 9 0.35 0 0
CUI: C0020546
Disease: Hypertensive crisis
Hypertensive crisis 		19 0 9 0.33 0 0
CUI: C1843517
Disease: Retinal arteriolar tortuosity
Retinal arteriolar tortuosity 		23 0 9 0.29 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx 		23 0 9 0.29 0 0
CUI: C0039621
Disease: Tetany
Tetany 		24 0 9 0.28 0 0
CUI: C0431406
Disease: Asymmetric crying face association
Asymmetric crying face association 		25 0 9 0.27 0 0
CUI: C0078982
Disease: Arhinencephaly
Arhinencephaly 		35 0 10 0.24 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		31 0 9 0.23 0 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation 		32 0 9 0.23 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus 		34 0 9 0.21 0 0
CUI: C4021797
Disease: Abnormality of the thorax
Abnormality of the thorax 		40 0 10 0.21 0 0
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		35 0 9 0.21 0 0
CUI: C0266383
Disease: Uterine Anomalies
Uterine Anomalies 		35 0 9 0.21 0 0
CUI: C0036508
Disease: Seborrheic dermatitis
Seborrheic dermatitis 		39 0 9 0.19 0 0
CUI: C3164374
Disease: Abnormality of pulmonary valve
Abnormality of pulmonary valve 		40 0 9 0.19 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 9 0.17 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		46 0 9 0.17 0 0