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: C0270749
Disease: Marie Cerebellar Ataxia
Marie Cerebellar Ataxia 		6 0 2 0.15 0 0
CUI: C1837454
Disease: SPINOCEREBELLAR ATAXIA 8
SPINOCEREBELLAR ATAXIA 8 		21 0 4 0.15 0 0
CUI: C4552213
Disease: Broad autism phenotype
Broad autism phenotype 		6 0 2 0.15 0 0
CUI: C0476217
Disease: Head movements abnormal
Head movements abnormal 		8 0 2 0.13 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 3 0.12 0 0
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 0 2 0.12 0 0
CUI: C4021765
Disease: Morphological abnormality of the central nervous system
Morphological abnormality of the central nervous system 		10 0 2 0.12 0 0
CUI: C4551520
Disease: Intention tremor
Intention tremor 		20 0 3 0.12 0 0
CUI: C0033132
Disease: Cerebellar Degenerations, Primary
Cerebellar Degenerations, Primary 		1 0 1 0.11 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 0.11 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 0.11 0 0
CUI: C0270755
Disease: Corticostriatal-Spinal Degeneration
Corticostriatal-Spinal Degeneration 		1 0 1 0.11 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 0.11 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 0.11 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 0.11 0 0
CUI: C0747149
Disease: Uncontrolled pain
Uncontrolled pain 		1 0 1 0.11 0 0
CUI: C0851121
Disease: digestive problem
digestive problem 		1 0 1 0.11 0 0
CUI: C1536114
Disease: Central pain syndrome
Central pain syndrome 		1 0 1 0.11 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 0.11 0 0
CUI: C1836050
Disease: Filaminopathy, autosomal dominant
Filaminopathy, autosomal dominant 		1 0 1 0.11 0 0
CUI: C1839785
Disease: Folate-dependent fragile site at Xq28
Folate-dependent fragile site at Xq28 		1 0 1 0.11 0 0
CUI: C1862133
Disease: Decreased finger mobility
Decreased finger mobility 		1 0 1 0.11 0 0
CUI: C2732311
Disease: Multiple system atrophy, cerebellar variant
Multiple system atrophy, cerebellar variant 		1 0 1 0.11 0 0
CUI: C2751807
Disease: Emery-Dreifuss Muscular Dystrophy 4
Emery-Dreifuss Muscular Dystrophy 4 		1 0 1 0.11 0 0
CUI: C3264595
Disease: Agoraphobia without panic disorder
Agoraphobia without panic disorder 		1 0 1 0.11 0 0