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: C0338460
Disease: Argyrophilic grain disease
Argyrophilic grain disease 		18 7 5 0.15 1 5.3E-02
CUI: C0001825
Disease: Agraphia
Agraphia 		3 1 3 0.14 1 7.7E-02
CUI: C0015644
Disease: Muscular fasciculation
Muscular fasciculation 		99 0 15 0.14 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis 		19 0 5 0.14 0 0
CUI: C4022574
Disease: Limb apraxia
Limb apraxia 		3 0 3 0.14 0 0
CUI: C4025723
Disease: Abnormal upper motor neuron morphology
Abnormal upper motor neuron morphology 		20 0 5 0.14 0 0
CUI: C4082769
Disease: Chronic Traumatic Encephalopathy
Chronic Traumatic Encephalopathy 		12 0 4 0.14 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0 		87 0 13 0.14 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0 		87 0 13 0.14 0 0
CUI: C0349390
Disease: Non-fluent aphasia
Non-fluent aphasia 		4 0 3 0.14 0 0
CUI: C0520716
Disease: Pallidopontonigral degeneration
Pallidopontonigral degeneration 		4 1 3 0.14 1 7.7E-02
CUI: C4274665
Disease: Logopenic progressive aphasia
Logopenic progressive aphasia 		4 0 3 0.14 0 0
CUI: C0393554
Disease: Amyotrophic Lateral Sclerosis With Dementia
Amyotrophic Lateral Sclerosis With Dementia 		30 0 6 0.13 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 9 0.13 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy 		48 0 8 0.13 0 0
CUI: C3811918
Disease: GRN-related frontotemporal dementia
GRN-related frontotemporal dementia 		112 20 15 0.13 1 3.1E-02
CUI: C1392786
Disease: Cognitive changes
Cognitive changes 		50 0 8 0.13 0 0
CUI: C3711380
Disease: Huntington Disease-Like Syndrome
Huntington Disease-Like Syndrome 		6 0 3 0.12 0 0
CUI: C4022587
Disease: Fatigable weakness of respiratory muscles
Fatigable weakness of respiratory muscles 		60 0 9 0.12 0 0
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis 		72 0 10 0.12 0 0
CUI: C0234509
Disease: Finger Agnosia
Finger Agnosia 		7 0 3 0.12 0 0
CUI: C0973461
Disease: Dysphasia
Dysphasia 		63 0 9 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: C0338630
Disease: Senile Paranoid Dementia
Senile Paranoid Dementia 		8 0 3 0.12 0 0
CUI: C1853934
Disease: Deposits immunoreactive to beta-amyloid protein
Deposits immunoreactive to beta-amyloid protein 		8 0 3 0.12 0 0