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: C3811918
Disease: GRN-related frontotemporal dementia
GRN-related frontotemporal dementia 		112 0 17 0.11 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies 		44 0 10 0.10 0 0
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities 		83 0 12 9.0E-02 0 0
CUI: C1863843
Disease: Neuronal intranuclear inclusion disease
Neuronal intranuclear inclusion disease 		12 0 6 8.8E-02 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 6 8.7E-02 0 0
CUI: C2931845
Disease: Neurodegeneration with brain iron accumulation (NBIA)
Neurodegeneration with brain iron accumulation (NBIA) 		40 0 8 8.5E-02 0 0
CUI: C0521858
Disease: Decreased drug resistance
Decreased drug resistance 		15 0 6 8.5E-02 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 0 19 8.0E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 6 7.8E-02 0 0
CUI: C1837454
Disease: SPINOCEREBELLAR ATAXIA 8
SPINOCEREBELLAR ATAXIA 8 		21 0 6 7.8E-02 0 0
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
Behavioral variant of frontotemporal dementia 		35 0 7 7.8E-02 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		64 0 9 7.7E-02 0 0
CUI: C0024408
Disease: Machado-Joseph Disease
Machado-Joseph Disease 		135 0 14 7.7E-02 0 0
CUI: C0338457
Disease: Aphasia, Progressive
Aphasia, Progressive 		10 0 5 7.5E-02 0 0
CUI: C1859807
Disease: AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder) 		25 0 6 7.4E-02 0 0
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		186 0 17 7.4E-02 0 0
CUI: C0751713
Disease: Inclusion Body Myopathy, Sporadic
Inclusion Body Myopathy, Sporadic 		84 0 10 7.4E-02 0 0
CUI: C1843477
Disease: Epidermolysis Bullosa Simplex Superficialis
Epidermolysis Bullosa Simplex Superficialis 		11 0 5 7.4E-02 0 0
CUI: C3267047
Disease: Autoimmune necrotizing myopathy
Autoimmune necrotizing myopathy 		11 0 5 7.4E-02 0 0
CUI: C0016412
Disease: Folic Acid Deficiency
Folic Acid Deficiency 		70 0 9 7.3E-02 0 0
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1 		102 0 11 7.2E-02 0 0
CUI: C0206631
Disease: Lipomatous neoplasm
Lipomatous neoplasm 		14 0 5 7.0E-02 0 0
CUI: C0333440
Disease: Hyaline body
Hyaline body 		14 0 5 7.0E-02 0 0
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		122 0 12 7.0E-02 0 0
CUI: C0272401
Disease: Virchow's node (disorder)
Virchow's node (disorder) 		30 0 6 7.0E-02 0 0