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 1.00 0 0
CUI: C0022802
Disease: Kuru
Kuru 		1 0 1 1.00 0 0
CUI: C0155379
Disease: Nystagmus associated with disorder of the vestibular system
Nystagmus associated with disorder of the vestibular system 		1 0 1 1.00 0 0
CUI: C0333157
Disease: Colloid Cysts
Colloid Cysts 		1 0 1 1.00 0 0
CUI: C0917967
Disease: Pupillary Functions, Abnormal
Pupillary Functions, Abnormal 		1 0 1 1.00 0 0
CUI: C1847650
Disease: SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES
SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES 		1 0 1 1.00 0 0
CUI: C1864112
Disease: HUNTINGTON DISEASE-LIKE 1
HUNTINGTON DISEASE-LIKE 1 		1 0 1 1.00 0 0
CUI: C1969957
Disease: Creutzfeldt-Jakob Disease, Heidenhain Variant
Creutzfeldt-Jakob Disease, Heidenhain Variant 		1 0 1 1.00 0 0
CUI: C2316460
Disease: Pseudobulbar affect
Pseudobulbar affect 		1 0 1 1.00 0 0
CUI: C2931022
Disease: Amyloidosis, Cerebral, with Spongiform Encephalopathy
Amyloidosis, Cerebral, with Spongiform Encephalopathy 		1 0 1 1.00 0 0
CUI: C2931859
Disease: Acquired CJD
Acquired CJD 		1 0 1 1.00 0 0
CUI: C4022162
Disease: Amyloidosis of peripheral nerves
Amyloidosis of peripheral nerves 		1 0 1 1.00 0 0
CUI: C4073149
Disease: Simultanapraxia
Simultanapraxia 		1 0 1 1.00 0 0
CUI: C4275003
Disease: Familial Creutzfeldt-Jakob
Familial Creutzfeldt-Jakob 		1 0 1 1.00 0 0
CUI: C4303462
Disease: Acquired prion disease
Acquired prion disease 		1 0 1 1.00 0 0
CUI: C4303482
Disease: Familial Alzheimer-like prion disease
Familial Alzheimer-like prion disease 		1 0 1 1.00 0 0
CUI: C4303527
Disease: Variably protease sensitive prionopathy
Variably protease sensitive prionopathy 		1 0 1 1.00 0 0
CUI: C4698645
Disease: Nor98
Nor98 		1 0 1 1.00 0 0
CUI: C0520789
Disease: Progressive subcortical gliosis
Progressive subcortical gliosis 		2 0 1 0.50 0 0
CUI: C0751645
Disease: Human Transmissible Spongiform Encephalopathies, Inherited
Human Transmissible Spongiform Encephalopathies, Inherited 		2 0 1 0.50 0 0
CUI: C1135993
Disease: Wasting Disease, Chronic
Wasting Disease, Chronic 		2 0 1 0.50 0 0
CUI: C1852476
Disease: Loss of facial expression
Loss of facial expression 		2 0 1 0.50 0 0
CUI: C4021216
Disease: EEG with persistent abnormal rhythmic activity
EEG with persistent abnormal rhythmic activity 		2 0 1 0.50 0 0
CUI: C4476619
Disease: Poor visual behavior for age
Poor visual behavior for age 		2 0 1 0.50 0 0
CUI: C4698644
Disease: Atypical scrapie
Atypical scrapie 		2 0 1 0.50 0 0