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: C1395088
Disease: Nervous system--Degeneration
Nervous system--Degeneration
4 0 3 0.30 0 0
CUI: C1866751
Disease: Spinocerebellar tract degeneration
Spinocerebellar tract degeneration
15 0 5 0.26 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2
18 0 5 0.23 0 0
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10
2 0 2 0.22 0 0
Sporadic adult-onset ataxia of unknown etiology
3 0 2 0.20 0 0
CUI: C1408507
Disease: Supranuclear ophthalmoplegia
Supranuclear ophthalmoplegia
5 0 2 0.17 0 0
CUI: C0270749
Disease: Marie Cerebellar Ataxia
Marie Cerebellar Ataxia
6 0 2 0.15 0 0
CUI: C3711380
Disease: Huntington Disease-Like Syndrome
Huntington Disease-Like Syndrome
6 0 2 0.15 0 0
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration
14 0 3 0.15 0 0
CUI: C1866753
Disease: Impaired horizontal smooth pursuit
Impaired horizontal smooth pursuit
7 0 2 0.14 0 0
CUI: C1997740
Disease: Segmental dystonia
Segmental dystonia
15 0 3 0.14 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position
26 0 4 0.13 0 0
CUI: C1836392
Disease: Dysmetric saccades
Dysmetric saccades
18 0 3 0.12 0 0
CUI: C4551520
Disease: Intention tremor
Intention tremor
20 0 3 0.12 0 0
CUI: C0159104
Disease: Electrooculogram abnormal
Electrooculogram abnormal
1 0 1 0.11 0 0
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis
1 0 1 0.11 0 0
CUI: C0751668
Disease: Machado-Joseph Disease Type I
Machado-Joseph Disease Type I
1 0 1 0.11 0 0
CUI: C0751669
Disease: Machado-Joseph Disease Type II
Machado-Joseph Disease Type II
1 0 1 0.11 0 0
CUI: C0751670
Disease: Machado-Joseph Disease Type III
Machado-Joseph Disease Type III
1 0 1 0.11 0 0
CUI: C0751671
Disease: Machado-Joseph Disease Type IV
Machado-Joseph Disease Type IV
1 0 1 0.11 0 0
CUI: C1837454
Disease: SPINOCEREBELLAR ATAXIA 8
SPINOCEREBELLAR ATAXIA 8
21 0 3 0.11 0 0
CUI: C1856697
Disease: Mitochondrial malic enzyme reduced
Mitochondrial malic enzyme reduced
1 0 1 0.11 0 0
CUI: C1862359
Disease: Facial-lingual fasciculations
Facial-lingual fasciculations
1 0 1 0.11 0 0
MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)
1 0 1 0.11 0 0
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
1 0 1 0.11 0 0