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: C0004134
Disease: Ataxia
Ataxia 		868 0 1 1.2E-03 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		384 0 1 2.6E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 0 1 2.3E-03 0 0
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		66 0 1 1.5E-02 0 0
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		5473 0 1 1.8E-04 0 0
CUI: C0012569
Disease: Diplopia
Diplopia 		75 0 1 1.3E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 0 1 2.1E-03 0 0
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
Toxic Epidermal Necrolysis 		143 0 1 7.0E-03 0 0
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest 		411 0 1 2.4E-03 0 0
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		978 0 1 1.0E-03 0 0
CUI: C0024408
Disease: Machado-Joseph Disease
Machado-Joseph Disease 		135 0 1 7.4E-03 0 0
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		340 0 1 2.9E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 0 1 1.0E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		580 0 1 1.7E-03 0 0
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		2872 0 1 3.5E-04 0 0
CUI: C0036391
Disease: Schwartz-Jampel Syndrome
Schwartz-Jampel Syndrome 		77 0 1 1.3E-02 0 0
CUI: C0037769
Disease: West Syndrome
West Syndrome 		149 0 1 6.7E-03 0 0
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration 		14 0 1 7.1E-02 0 0
CUI: C0038379
Disease: Strabismus
Strabismus 		716 0 1 1.4E-03 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 1 6.4E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia 		539 0 1 1.9E-03 0 0
CUI: C0206669
Disease: Hepatocellular Adenoma
Hepatocellular Adenoma 		114 0 1 8.8E-03 0 0
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		877 0 1 1.1E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 1 1.1E-03 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 1 6.5E-03 0 0