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: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 9 7.8E-02 0 0
CUI: C0239882
Disease: Head tremor
Head tremor 		21 0 7 7.8E-02 0 0
CUI: C1836479
Disease: Saccadic smooth pursuit
Saccadic smooth pursuit 		22 0 7 7.7E-02 0 0
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		122 79 14 7.6E-02 1 1.2E-02
CUI: C2931845
Disease: Neurodegeneration with brain iron accumulation (NBIA)
Neurodegeneration with brain iron accumulation (NBIA) 		40 0 8 7.4E-02 0 0
CUI: C4024900
Disease: Atrophy/Degeneration affecting the brainstem
Atrophy/Degeneration affecting the brainstem 		27 0 7 7.3E-02 0 0
CUI: C1843921
Disease: Postural instability
Postural instability 		60 0 9 7.1E-02 0 0
CUI: C0018790
Disease: Cardiac Arrest
Cardiac Arrest 		411 0 32 7.0E-02 0 0
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy 		64 0 9 6.9E-02 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 14 6.8E-02 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 6 6.8E-02 0 0
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		373 0 28 6.7E-02 0 0
CUI: C0022595
Disease: Keratosis Follicularis
Keratosis Follicularis 		57 0 8 6.4E-02 0 0
CUI: C0012569
Disease: Diplopia
Diplopia 		75 0 9 6.3E-02 0 0
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 0 5 6.2E-02 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 14 6.2E-02 0 0
CUI: C1839780
Disease: FRAGILE X TREMOR/ATAXIA SYNDROME
FRAGILE X TREMOR/ATAXIA SYNDROME 		62 0 8 6.2E-02 0 0
CUI: C1846707
Disease: SPINOCEREBELLAR ATAXIA 17
SPINOCEREBELLAR ATAXIA 17 		28 0 6 6.1E-02 0 0
CUI: C1851920
Disease: Dopa-Responsive Dystonia
Dopa-Responsive Dystonia 		28 0 6 6.1E-02 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders 		167 0 14 6.1E-02 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 0 7 6.1E-02 0 0
CUI: C0393576
Disease: Chorea Acanthocytosis Syndrome
Chorea Acanthocytosis Syndrome 		29 0 6 6.1E-02 0 0
CUI: C1321329
Disease: Slowed saccades
Slowed saccades 		29 0 6 6.1E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 0 32 6.0E-02 0 0
CUI: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure 		12 0 5 6.0E-02 0 0