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: C1836392
Disease: Dysmetric saccades
Dysmetric saccades
18 0 8 0.23 0 0
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus
10 0 6 0.21 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular
86 0 15 0.16 0 0
Abnormality of ocular smooth pursuit
5 0 4 0.15 0 0
CUI: C1837454
Disease: SPINOCEREBELLAR ATAXIA 8
SPINOCEREBELLAR ATAXIA 8
21 0 5 0.12 0 0
Autosomal dominant cerebellar ataxia
31 0 6 0.12 0 0
Loss of Purkinje cells in the cerebellar vermis
5 0 3 0.11 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position
26 0 5 0.11 0 0
CUI: C0427190
Disease: Ataxia, Truncal
Ataxia, Truncal
68 0 9 0.11 0 0
EEG with generalized epileptiform discharges
6 4 3 0.11 1 0.25
Lymphedema, microcephaly and chorioretinopathy syndrome
7 0 3 0.10 0 0
Morphological abnormality of the pyramidal tract
18 0 4 0.10 0 0
CUI: C1321329
Disease: Slowed saccades
Slowed saccades
29 0 5 0.10 0 0
CUI: C0742028
Disease: Cerebellar vermis atrophy
Cerebellar vermis atrophy
32 0 5 9.6E-02 0 0
CUI: C0239882
Disease: Head tremor
Head tremor
21 0 4 9.5E-02 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia
136 0 14 9.5E-02 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia
21 0 4 9.5E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense
33 0 5 9.4E-02 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary
35 0 5 9.1E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 7 9.1E-02 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 0 16 8.8E-02 0 0
CUI: C0234979
Disease: Dysdiadochokinesis
Dysdiadochokinesis
49 0 6 8.8E-02 0 0
CUI: C0278184
Disease: Scanning speech
Scanning speech
13 0 3 8.6E-02 0 0
SPINOCEREBELLAR ATAXIA 31 (disorder)
13 0 3 8.6E-02 0 0
CUI: C0234366
Disease: Ataxic
Ataxic
15 0 3 8.1E-02 0 0