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: C4518339
Disease: Sporadic adult-onset ataxia of unknown etiology
Sporadic adult-onset ataxia of unknown etiology 		3 0 2 0.67 0 0
CUI: C0036659
Disease: Sensation Disorders
Sensation Disorders 		1 0 1 0.50 0 0
CUI: C0270712
Disease: Late cortical cerebellar atrophy
Late cortical cerebellar atrophy 		1 0 1 0.50 0 0
CUI: C0751497
Disease: Special Senses Disorders
Special Senses Disorders 		1 0 1 0.50 0 0
CUI: C1856697
Disease: Mitochondrial malic enzyme reduced
Mitochondrial malic enzyme reduced 		1 0 1 0.50 0 0
CUI: C4021047
Disease: Impaired visually enhanced vestibulo-ocular reflex
Impaired visually enhanced vestibulo-ocular reflex 		1 0 1 0.50 0 0
CUI: C4025641
Disease: Decreased pyruvate carboxylase activity
Decreased pyruvate carboxylase activity 		1 0 1 0.50 0 0
CUI: C0742191
Disease: Cervical spinal cord atrophy
Cervical spinal cord atrophy 		2 0 1 0.33 0 0
CUI: C1853250
Disease: SPINOCEREBELLAR ATAXIA 23
SPINOCEREBELLAR ATAXIA 23 		2 0 1 0.33 0 0
CUI: C4237239
Disease: Opioid use disorder, severe
Opioid use disorder, severe 		2 0 1 0.33 0 0
CUI: C4310780
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23 		2 0 1 0.33 0 0
CUI: C0393578
Disease: Pallidoluysian degeneration
Pallidoluysian degeneration 		3 0 1 0.25 0 0
CUI: C0476369
Disease: Echocardiogram abnormal
Echocardiogram abnormal 		3 0 1 0.25 0 0
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia 		3 0 1 0.25 0 0
CUI: C3807295
Disease: CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT
CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT 		3 0 1 0.25 0 0
CUI: C4024943
Disease: Decreased amplitude of sensory action potentials
Decreased amplitude of sensory action potentials 		3 0 1 0.25 0 0
CUI: C1395088
Disease: Nervous system--Degeneration
Nervous system--Degeneration 		4 0 1 0.20 0 0
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		5 0 1 0.17 0 0
CUI: C3711370
Disease: Spastic Paraplegia Type 7
Spastic Paraplegia Type 7 		5 0 1 0.17 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 1 0.17 0 0
CUI: C0030200
Disease: Pain, Intractable
Pain, Intractable 		6 0 1 0.14 0 0
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration 		14 0 2 0.14 0 0
CUI: C0042875
Disease: Vitamin E Deficiency
Vitamin E Deficiency 		6 0 1 0.14 0 0
CUI: C0152027
Disease: Sensory Disorders
Sensory Disorders 		6 0 1 0.14 0 0
CUI: C3273225
Disease: Hereditary Neurodegenerative Disorder
Hereditary Neurodegenerative Disorder 		6 0 1 0.14 0 0