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: C1963674
Disease: Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 10 		9 0 4 1.0E-01 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 10 9.9E-02 0 0
CUI: C0016719
Disease: Friedreich Ataxia
Friedreich Ataxia 		88 0 11 9.8E-02 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia 		21 0 5 9.8E-02 0 0
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 0 4 9.8E-02 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 18 9.5E-02 0 0
CUI: C0393519
Disease: Cerebellar Ataxia, Early Onset
Cerebellar Ataxia, Early Onset 		12 0 4 9.3E-02 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor 		95 0 11 9.2E-02 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive 		48 0 7 9.2E-02 0 0
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		13 0 4 9.1E-02 0 0
CUI: C1837458
Disease: Impaired smooth pursuit
Impaired smooth pursuit 		25 0 5 9.1E-02 0 0
CUI: C4518339
Disease: Sporadic adult-onset ataxia of unknown etiology
Sporadic adult-onset ataxia of unknown etiology 		3 0 3 8.6E-02 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 0 10 8.5E-02 0 0
CUI: C1321329
Disease: Slowed saccades
Slowed saccades 		29 0 5 8.5E-02 0 0
CUI: C1395088
Disease: Nervous system--Degeneration
Nervous system--Degeneration 		4 0 3 8.3E-02 0 0
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		30 0 5 8.3E-02 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 4 8.2E-02 0 0
CUI: C1408507
Disease: Supranuclear ophthalmoplegia
Supranuclear ophthalmoplegia 		5 0 3 8.1E-02 0 0
CUI: C1849146
Disease: Loss of Purkinje cells in the cerebellar vermis
Loss of Purkinje cells in the cerebellar vermis 		5 0 3 8.1E-02 0 0
CUI: C3711370
Disease: Spastic Paraplegia Type 7
Spastic Paraplegia Type 7 		5 0 3 8.1E-02 0 0
CUI: C4275170
Disease: Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 		5 0 3 8.1E-02 0 0
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5 		48 0 6 7.8E-02 0 0
CUI: C0423083
Disease: Hypermetric saccades
Hypermetric saccades 		7 0 3 7.7E-02 0 0
CUI: C1837454
Disease: SPINOCEREBELLAR ATAXIA 8
SPINOCEREBELLAR ATAXIA 8 		21 0 4 7.7E-02 0 0
CUI: C1853761
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 		21 0 4 7.7E-02 0 0