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: C0159104
Disease: Electrooculogram abnormal
Electrooculogram abnormal 		1 0 1 1.00 0 0
CUI: C0751668
Disease: Machado-Joseph Disease Type I
Machado-Joseph Disease Type I 		1 0 1 1.00 0 0
CUI: C0751669
Disease: Machado-Joseph Disease Type II
Machado-Joseph Disease Type II 		1 0 1 1.00 0 0
CUI: C0751670
Disease: Machado-Joseph Disease Type III
Machado-Joseph Disease Type III 		1 0 1 1.00 0 0
CUI: C0751671
Disease: Machado-Joseph Disease Type IV
Machado-Joseph Disease Type IV 		1 0 1 1.00 0 0
CUI: C4285818
Disease: Reduced facial expression
Reduced facial expression 		2 0 1 0.50 0 0
CUI: C2586031
Disease: Hereditary antithrombin III deficiency
Hereditary antithrombin III deficiency 		3 0 1 0.33 0 0
CUI: C2363915
Disease: Cerebellar ischaemia
Cerebellar ischaemia 		4 0 1 0.25 0 0
CUI: C1408507
Disease: Supranuclear ophthalmoplegia
Supranuclear ophthalmoplegia 		5 0 1 0.20 0 0
CUI: C0268384
Disease: Familial Amyloid Neuropathy, Portuguese Type
Familial Amyloid Neuropathy, Portuguese Type 		6 0 1 0.17 0 0
CUI: C0030508
Disease: Parasomnia
Parasomnia 		7 0 1 0.14 0 0
CUI: C1866753
Disease: Impaired horizontal smooth pursuit
Impaired horizontal smooth pursuit 		7 0 1 0.14 0 0
CUI: C0271386
Disease: Vertical Nystagmus
Vertical Nystagmus 		9 0 1 0.11 0 0
CUI: C1963674
Disease: Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 10 		9 0 1 0.11 0 0
CUI: C4022417
Disease: Degeneration of the striatum
Degeneration of the striatum 		9 0 1 0.11 0 0
CUI: C0265218
Disease: Neu-Laxova syndrome
Neu-Laxova syndrome 		10 0 1 1.0E-01 0 0
CUI: C3805092
Disease: Methylenetetrahydrofolate reductase gene mutation
Methylenetetrahydrofolate reductase gene mutation 		11 0 1 9.1E-02 0 0
CUI: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure 		12 0 1 8.3E-02 0 0
CUI: C1863843
Disease: Neuronal intranuclear inclusion disease
Neuronal intranuclear inclusion disease 		12 0 1 8.3E-02 0 0
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		13 0 1 7.7E-02 0 0
CUI: C1847117
Disease: Dilated fourth ventricle
Dilated fourth ventricle 		13 0 1 7.7E-02 0 0
CUI: C0034341
Disease: Pyruvate Carboxylase Deficiency Disease
Pyruvate Carboxylase Deficiency Disease 		14 0 1 7.1E-02 0 0
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 1 7.1E-02 0 0
CUI: C0234366
Disease: Ataxic
Ataxic 		15 0 1 6.7E-02 0 0
CUI: C0684219
Disease: Myokymia
Myokymia 		15 0 1 6.7E-02 0 0