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: C0003550
Disease: Broca Aphasia
Broca Aphasia 		11 0 4 0.14 0 0
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
Behavioral variant of frontotemporal dementia 		35 0 7 0.14 0 0
CUI: C4022574
Disease: Limb apraxia
Limb apraxia 		3 0 3 0.14 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 5 0.14 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia 		20 0 5 0.14 0 0
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
Posterior cortical atrophy syndrome 		12 0 4 0.14 0 0
CUI: C0542223
Disease: Loss of speech
Loss of speech 		37 0 7 0.14 0 0
CUI: C4021799
Disease: Restrictive behavior
Restrictive behavior 		13 0 4 0.13 0 0
CUI: C4024936
Disease: Temporal cortical atrophy
Temporal cortical atrophy 		13 0 4 0.13 0 0
CUI: C0424296
Disease: Social disinhibition
Social disinhibition 		56 0 9 0.13 0 0
CUI: C0546126
Disease: Acute Confusional Senile Dementia
Acute Confusional Senile Dementia 		99 0 14 0.13 0 0
CUI: C0750900
Disease: Alzheimer's Disease, Focal Onset
Alzheimer's Disease, Focal Onset 		99 0 14 0.13 0 0
CUI: C0036489
Disease: Sea-Blue Histiocyte Syndrome
Sea-Blue Histiocyte Syndrome 		5 0 3 0.13 0 0
CUI: C0233522
Disease: Inappropriate behavior
Inappropriate behavior 		14 0 4 0.13 0 0
CUI: C0424290
Disease: Compulsive hoarding
Compulsive hoarding 		14 0 4 0.13 0 0
CUI: C0338582
Disease: Sporadic Cerebral Amyloid Angiopathy
Sporadic Cerebral Amyloid Angiopathy 		6 0 3 0.12 0 0
CUI: C1839042
Disease: Upper motor neuron dysfunction
Upper motor neuron dysfunction 		16 0 4 0.12 0 0
CUI: C1858680
Disease: Familial encephalopathy with neuroserpin inclusion bodies
Familial encephalopathy with neuroserpin inclusion bodies 		7 0 3 0.12 0 0
CUI: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation 		26 0 5 0.12 0 0
CUI: C1850496
Disease: Neuronal loss in central nervous system
Neuronal loss in central nervous system 		37 0 6 0.12 0 0
CUI: C0003537
Disease: Aphasia
Aphasia 		86 0 11 0.11 0 0
CUI: C4022798
Disease: Abnormal brain FDG positron emission tomography
Abnormal brain FDG positron emission tomography 		18 0 4 0.11 0 0
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		30 0 5 0.11 0 0
CUI: C0282513
Disease: Primary Progressive Aphasia (disorder)
Primary Progressive Aphasia (disorder) 		51 0 7 0.11 0 0
CUI: C0338457
Disease: Aphasia, Progressive
Aphasia, Progressive 		10 0 3 0.11 0 0