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: C0393947
Disease: Cholinergic crisis
Cholinergic crisis 		2 0 1 0.20 0 0
CUI: C0454582
Disease: Semantic impairment
Semantic impairment 		2 0 1 0.20 0 0
CUI: C0520789
Disease: Progressive subcortical gliosis
Progressive subcortical gliosis 		2 0 1 0.20 0 0
CUI: C0728821
Disease: Parasympathomimetic Disorders
Parasympathomimetic Disorders 		2 0 1 0.20 0 0
CUI: C1142436
Disease: Sundowning
Sundowning 		2 0 1 0.20 0 0
CUI: C1845248
Disease: Outbursts
Outbursts 		2 0 1 0.20 0 0
CUI: C1855353
Disease: Fixed facial expression
Fixed facial expression 		2 0 1 0.20 0 0
CUI: C4072928
Disease: Spoken Word Recognition Deficit
Spoken Word Recognition Deficit 		8 0 2 0.20 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 2 0.18 0 0
CUI: C0919974
Disease: Abulia
Abulia 		9 0 2 0.18 0 0
CUI: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy 		9 0 2 0.18 0 0
CUI: C0001825
Disease: Agraphia
Agraphia 		3 0 1 0.17 0 0
CUI: C0007815
Disease: Cerebrospinal Fluid Rhinorrhea
Cerebrospinal Fluid Rhinorrhea 		3 0 1 0.17 0 0
CUI: C0043102
Disease: Weil Disease
Weil Disease 		3 0 1 0.17 0 0
CUI: C0392185
Disease: Verbal repetition
Verbal repetition 		3 0 1 0.17 0 0
CUI: C0406778
Disease: Dermatopathia pigmentosa reticularis
Dermatopathia pigmentosa reticularis 		3 0 1 0.17 0 0
CUI: C0474420
Disease: Inappropriate sexual behavior
Inappropriate sexual behavior 		3 0 1 0.17 0 0
CUI: C0751398
Disease: Familial Olivopontocerebellar Atrophy
Familial Olivopontocerebellar Atrophy 		3 0 1 0.17 0 0
CUI: C0751950
Disease: Neuromuscular Junction Diseases
Neuromuscular Junction Diseases 		3 0 1 0.17 0 0
CUI: C1112261
Disease: Gaze palsy
Gaze palsy 		3 0 1 0.17 0 0
CUI: C1761613
Disease: Conjunctival hyperemia
Conjunctival hyperemia 		3 0 1 0.17 0 0
CUI: C1838320
Disease: Hyperorality
Hyperorality 		10 0 2 0.17 0 0
CUI: C1839736
Disease: WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME
WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME 		3 0 1 0.17 0 0
CUI: C1849722
Disease: Polyglucosan Body Disease, Adult Form
Polyglucosan Body Disease, Adult Form 		3 0 1 0.17 0 0
CUI: C1853723
Disease: MYOPATHY, DISTAL 2
MYOPATHY, DISTAL 2 		3 0 1 0.17 0 0