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: C0234979
Disease: Dysdiadochokinesis
Dysdiadochokinesis
49 0 1 2.0E-02 0 0
CUI: C3714534
Disease: dowling-degos disease
dowling-degos disease
53 0 1 1.9E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 1 1.7E-02 0 0
CUI: C0262404
Disease: Cerebellar degeneration
Cerebellar degeneration
60 0 1 1.7E-02 0 0
Spinocerebellar Ataxia Type 6 (disorder)
64 0 1 1.6E-02 0 0
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases
66 0 1 1.5E-02 0 0
CUI: C0427190
Disease: Ataxia, Truncal
Ataxia, Truncal
68 0 1 1.5E-02 0 0
CUI: C0012569
Disease: Diplopia
Diplopia
75 0 1 1.3E-02 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2
76 0 1 1.3E-02 0 0
CUI: C0036391
Disease: Schwartz-Jampel Syndrome
Schwartz-Jampel Syndrome
77 0 1 1.3E-02 0 0
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7
78 0 1 1.3E-02 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular
86 0 1 1.2E-02 0 0
Aspirin exacerbated respiratory disease
94 0 1 1.1E-02 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor
95 0 1 1.1E-02 0 0
Dentatorubral-Pallidoluysian Atrophy
95 0 1 1.1E-02 0 0
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1
102 0 1 9.8E-03 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies
104 0 1 9.6E-03 0 0
CUI: C0206669
Disease: Hepatocellular Adenoma
Hepatocellular Adenoma
114 0 1 8.8E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria
127 0 1 7.9E-03 0 0
CUI: C0024408
Disease: Machado-Joseph Disease
Machado-Joseph Disease
135 0 1 7.4E-03 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia
136 0 1 7.4E-03 0 0
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
Toxic Epidermal Necrolysis
143 0 1 7.0E-03 0 0
CUI: C0037769
Disease: West Syndrome
West Syndrome
149 0 1 6.7E-03 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign
155 0 1 6.5E-03 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar
156 0 1 6.4E-03 0 0