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: C0001889
Disease: Akinetic Mutism
Akinetic Mutism 		1 0 1 7.9E-03 0 0
CUI: C0022802
Disease: Kuru
Kuru 		1 0 1 7.9E-03 0 0
CUI: C0036659
Disease: Sensation Disorders
Sensation Disorders 		1 0 1 7.9E-03 0 0
CUI: C0155143
Disease: Acute follicular conjunctivitis
Acute follicular conjunctivitis 		1 0 1 7.9E-03 0 0
CUI: C0155379
Disease: Nystagmus associated with disorder of the vestibular system
Nystagmus associated with disorder of the vestibular system 		1 0 1 7.9E-03 0 0
CUI: C0231691
Disease: Cerebellar Gait Ataxia
Cerebellar Gait Ataxia 		1 0 1 7.9E-03 0 0
CUI: C0234174
Disease: Sucking reflex
Sucking reflex 		1 0 1 7.9E-03 0 0
CUI: C0234505
Disease: Tactile Agnosia
Tactile Agnosia 		1 0 1 7.9E-03 0 0
CUI: C0234966
Disease: Astasia
Astasia 		1 0 1 7.9E-03 0 0
CUI: C0239957
Disease: Hip stiff
Hip stiff 		1 0 1 7.9E-03 0 0
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis 		1 0 1 7.9E-03 0 0
CUI: C0270149
Disease: Perinatal respiratory distress
Perinatal respiratory distress 		1 0 1 7.9E-03 0 0
CUI: C0270712
Disease: Late cortical cerebellar atrophy
Late cortical cerebellar atrophy 		1 0 1 7.9E-03 0 0
CUI: C0271616
Disease: Precocious female puberty
Precocious female puberty 		1 0 1 7.9E-03 0 0
CUI: C0274295
Disease: Brisket disease
Brisket disease 		1 0 1 7.9E-03 0 0
CUI: C0333157
Disease: Colloid Cysts
Colloid Cysts 		1 0 1 7.9E-03 0 0
CUI: C0339666
Disease: Nystagmus and other irregular eye movements
Nystagmus and other irregular eye movements 		1 0 1 7.9E-03 0 0
CUI: C0342892
Disease: Hypolipidemia
Hypolipidemia 		1 0 1 7.9E-03 0 0
CUI: C0394004
Disease: Congenital non-progressive ataxia
Congenital non-progressive ataxia 		1 0 1 7.9E-03 0 0
CUI: C0422879
Disease: CNS symptom
CNS symptom 		1 0 1 7.9E-03 0 0
CUI: C0423729
Disease: Chest pain on breathing
Chest pain on breathing 		1 0 1 7.9E-03 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 7.9E-03 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 7.9E-03 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 7.9E-03 0 0
CUI: C0730309
Disease: Inherited optic neuropathy
Inherited optic neuropathy 		1 0 1 7.9E-03 0 0