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: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 9 0.30 0 0
CUI: C0393524
Disease: Cerebellar Ataxia, Late Onset
Cerebellar Ataxia, Late Onset 		9 0 4 0.15 0 0
CUI: C1861736
Disease: SPINOCEREBELLAR ATAXIA 31 (disorder)
SPINOCEREBELLAR ATAXIA 31 (disorder) 		13 0 4 0.13 0 0
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration 		14 0 4 0.13 0 0
CUI: C0270749
Disease: Marie Cerebellar Ataxia
Marie Cerebellar Ataxia 		6 0 3 0.12 0 0
CUI: C1837458
Disease: Impaired smooth pursuit
Impaired smooth pursuit 		25 0 5 0.12 0 0
CUI: C1963674
Disease: Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 10 		9 0 3 0.11 0 0
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 0 3 0.11 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 5 0.11 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		64 0 8 0.10 0 0
CUI: C0238045
Disease: Carotid-Cavernous Sinus Fistula
Carotid-Cavernous Sinus Fistula 		2 0 2 9.5E-02 0 0
CUI: C1265768
Disease: Calcified aneurysm
Calcified aneurysm 		2 0 2 9.5E-02 0 0
CUI: C1868737
Disease: Vertebral artery hypoplasia
Vertebral artery hypoplasia 		2 0 2 9.5E-02 0 0
CUI: C3898139
Disease: New or Worsening Symptom
New or Worsening Symptom 		2 0 2 9.5E-02 0 0
CUI: C4703564
Disease: Aortopulmonary collateral arteries
Aortopulmonary collateral arteries 		2 0 2 9.5E-02 0 0
CUI: C0158623
Disease: Congenital anomaly of coronary artery
Congenital anomaly of coronary artery 		3 0 2 9.1E-02 0 0
CUI: C0234366
Disease: Ataxic
Ataxic 		15 0 3 9.1E-02 0 0
CUI: C1866751
Disease: Spinocerebellar tract degeneration
Spinocerebellar tract degeneration 		15 0 3 9.1E-02 0 0
CUI: C3472711
Disease: Spinocerebellar ataxia 36
Spinocerebellar ataxia 36 		4 0 2 8.7E-02 0 0
CUI: C0751781
Disease: Dentatorubral-Pallidoluysian Atrophy
Dentatorubral-Pallidoluysian Atrophy 		95 0 9 8.4E-02 0 0
CUI: C0340896
Disease: Vascular graft infection
Vascular graft infection 		5 0 2 8.3E-02 0 0
CUI: C1836392
Disease: Dysmetric saccades
Dysmetric saccades 		18 0 3 8.3E-02 0 0
CUI: C4021761
Disease: Morphological abnormality of the pyramidal tract
Morphological abnormality of the pyramidal tract 		18 0 3 8.3E-02 0 0
CUI: C0027125
Disease: Myotonia
Myotonia 		19 0 3 8.1E-02 0 0
CUI: C0340517
Disease: Atrial thrombosis
Atrial thrombosis 		6 0 2 8.0E-02 0 0