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: C0751781
Disease: Dentatorubral-Pallidoluysian Atrophy
Dentatorubral-Pallidoluysian Atrophy 		95 0 27 0.13 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 32 0.12 0 0
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked 		126 0 26 0.11 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		64 0 18 9.9E-02 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 15 9.9E-02 0 0
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		176 0 27 9.5E-02 0 0
CUI: C0949664
Disease: Tauopathies
Tauopathies 		245 0 32 9.2E-02 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 22 8.8E-02 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 17 8.8E-02 0 0
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain 		213 0 28 8.7E-02 0 0
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7 		78 0 17 8.7E-02 0 0
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
Amyotrophic Lateral Sclerosis, Familial 		130 0 21 8.6E-02 0 0
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		373 0 40 8.5E-02 0 0
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1 		102 4 18 8.2E-02 1 6.7E-02
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy 		64 20 15 8.2E-02 1 3.2E-02
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 0 43 8.1E-02 0 0
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		66 0 15 8.1E-02 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 0 24 7.8E-02 0 0
CUI: C0426980
Disease: Motor symptoms
Motor symptoms 		100 0 17 7.8E-02 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 11 7.7E-02 0 0
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		186 0 23 7.7E-02 0 0
CUI: C1839780
Disease: FRAGILE X TREMOR/ATAXIA SYNDROME
FRAGILE X TREMOR/ATAXIA SYNDROME 		62 0 14 7.7E-02 0 0
CUI: C0235031
Disease: Neurologic Symptoms
Neurologic Symptoms 		233 0 26 7.6E-02 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		35 0 12 7.6E-02 0 0
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		320 0 32 7.6E-02 0 0