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: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 5.6E-03 0 0
CUI: C0271383
Disease: Symptomatic Nystagmus
Symptomatic Nystagmus 		1 0 1 5.6E-03 0 0
CUI: C0271384
Disease: Spontaneous Ocular Nystagmus
Spontaneous Ocular Nystagmus 		1 0 1 5.6E-03 0 0
CUI: C0271387
Disease: Rebound Nystagmus
Rebound Nystagmus 		1 0 1 5.6E-03 0 0
CUI: C0271389
Disease: Jerk Nystagmus
Jerk Nystagmus 		1 0 1 5.6E-03 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor 		1 0 1 5.6E-03 0 0
CUI: C0333494
Disease: Phlebosclerosis
Phlebosclerosis 		1 0 1 5.6E-03 0 0
CUI: C0334454
Disease: Dermatofibrosarcoma Protuberans, Myxoid
Dermatofibrosarcoma Protuberans, Myxoid 		1 0 1 5.6E-03 0 0
CUI: C0338483
Disease: Migraine with Prolonged Aura
Migraine with Prolonged Aura 		1 0 1 5.6E-03 0 0
CUI: C0341217
Disease: Dieulafoy's vascular malformation
Dieulafoy's vascular malformation 		1 0 1 5.6E-03 0 0
CUI: C0343713
Disease: Gonococcal arthritis dermatitis syndrome
Gonococcal arthritis dermatitis syndrome 		1 0 1 5.6E-03 0 0
CUI: C0344297
Disease: Choroidal sclerosis
Choroidal sclerosis 		1 0 1 5.6E-03 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 5.6E-03 0 0
CUI: C0398641
Disease: Epstein syndrome (disorder)
Epstein syndrome (disorder) 		1 0 1 5.6E-03 0 0
CUI: C0403445
Disease: Fechtner syndrome (disorder)
Fechtner syndrome (disorder) 		1 0 1 5.6E-03 0 0
CUI: C0406726
Disease: Orofaciodigital syndrome 3
Orofaciodigital syndrome 3 		1 0 1 5.6E-03 0 0
CUI: C0406727
Disease: Orofaciodigital syndrome 4
Orofaciodigital syndrome 4 		1 0 1 5.6E-03 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 5.6E-03 0 0
CUI: C0431379
Disease: Laminar heterotopia
Laminar heterotopia 		1 0 1 5.6E-03 0 0
CUI: C0431766
Disease: Congenital malformation syndromes involving limbs
Congenital malformation syndromes involving limbs 		1 0 1 5.6E-03 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 5.6E-03 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 5.6E-03 0 0
CUI: C0454594
Disease: Surface dyslexia
Surface dyslexia 		1 0 1 5.6E-03 0 0
CUI: C0478093
Disease: Other congenital malformation syndromes with other skeletal changes
Other congenital malformation syndromes with other skeletal changes 		1 0 1 5.6E-03 0 0
CUI: C0520731
Disease: Retraction Nystagmus
Retraction Nystagmus 		1 0 1 5.6E-03 0 0