Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Amyotrophic Lateral Sclerosis With Dementia
30 0 29 0.78 0 0
Frontotemporal Dementia With Motor Neuron Disease
13 0 8 0.20 0 0
Fatigable weakness of swallowing muscles
39 0 12 0.19 0 0
Primary Progressive Nonfluent Aphasia
21 0 9 0.19 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm
48 0 12 0.17 0 0
Behavioral variant of frontotemporal dementia
35 0 10 0.16 0 0
Abnormal lower motor neuron morphology
23 0 8 0.16 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia
56 0 12 0.15 0 0
CUI: C0522224
Disease: Paralysed
Paralysed
68 0 13 0.14 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
44 0 10 0.14 0 0
Fatigable weakness of respiratory muscles
60 0 12 0.14 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0
87 0 14 0.13 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0
87 0 14 0.13 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis
19 0 6 0.12 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia
20 0 6 0.12 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia
20 0 6 0.12 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 6 0.11 0 0
CUI: C0085631
Disease: Agitation
Agitation
109 0 14 0.11 0 0
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease
186 0 21 0.10 0 0
Abnormal brain FDG positron emission tomography
18 0 5 0.10 0 0
CUI: C0085632
Disease: Apathy
Apathy
83 0 11 0.10 0 0
Primary Progressive Aphasia (disorder)
51 0 8 0.10 0 0
CUI: C0003113
Disease: Anomia
Anomia
8 0 4 1.0E-01 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 5 1.0E-01 0 0
Neuronal loss in the cerebral cortex
8 0 4 1.0E-01 0 0