Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Behavioral variant of frontotemporal dementia
35 0 9 0.14 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia
20 0 7 0.14 0 0
CUI: C0234144
Disease: Dysgraphia
Dysgraphia
43 0 9 0.13 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies
44 0 9 0.12 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia
18 0 6 0.12 0 0
CUI: C0424296
Disease: Social disinhibition
Social disinhibition
56 0 10 0.12 0 0
CUI: C0026884
Disease: Mutism
Mutism
47 0 9 0.12 0 0
CUI: C1836940
Disease: Thickened nuchal skin fold
Thickened nuchal skin fold
58 0 9 0.10 0 0
Neuronal loss in central nervous system
37 0 7 0.10 0 0
CUI: C0003635
Disease: Apraxias
Apraxias
71 0 10 0.10 0 0
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis
72 0 10 0.10 0 0
CUI: C0085632
Disease: Apathy
Apathy
83 0 11 0.10 0 0
Primary Progressive Aphasia (disorder)
51 0 8 1.0E-01 0 0
CUI: C0973461
Disease: Dysphasia
Dysphasia
63 0 9 9.9E-02 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 5 9.8E-02 0 0
CUI: C1847651
Disease: Rapidly progressive dementia
Rapidly progressive dementia
9 0 4 9.5E-02 0 0
Neurofibrillary degeneration (morphologic abnormality)
21 0 5 9.4E-02 0 0
CUI: C2750915
Disease: Basal ganglia gliosis
Basal ganglia gliosis
10 0 4 9.3E-02 0 0
Amyotrophic Lateral Sclerosis, Guam Form
36 0 6 9.0E-02 0 0
CUI: C0003537
Disease: Aphasia
Aphasia
86 0 10 8.8E-02 0 0
CUI: C3811918
Disease: GRN-related frontotemporal dementia
GRN-related frontotemporal dementia
112 0 12 8.8E-02 0 0
CUI: C1838681
Disease: Rapidly progressive
Rapidly progressive
38 0 6 8.7E-02 0 0
Frontotemporal Dementia With Motor Neuron Disease
13 0 4 8.7E-02 0 0
CUI: C4024946
Disease: Focal white matter lesions
Focal white matter lesions
14 0 4 8.5E-02 0 0
CUI: C0270790
Disease: Quadriparesis
Quadriparesis
42 0 6 8.2E-02 0 0