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: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 67 34 9.7E-02 1 1.3E-02
CUI: C1321329
Disease: Slowed saccades
Slowed saccades 		29 0 8 9.4E-02 0 0
CUI: C0742028
Disease: Cerebellar vermis atrophy
Cerebellar vermis atrophy 		32 0 8 9.1E-02 0 0
CUI: C4551520
Disease: Intention tremor
Intention tremor 		20 6 7 9.1E-02 1 6.2E-02
CUI: C1963674
Disease: Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 10 		9 0 6 9.0E-02 0 0
CUI: C1836479
Disease: Saccadic smooth pursuit
Saccadic smooth pursuit 		22 0 7 8.9E-02 0 0
CUI: C0262404
Disease: Cerebellar degeneration
Cerebellar degeneration 		60 0 10 8.8E-02 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 9 8.7E-02 0 0
CUI: C0039496
Disease: Temporomandibular Joint Dysfunction Syndrome
Temporomandibular Joint Dysfunction Syndrome 		24 0 7 8.6E-02 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 120 40 8.6E-02 3 2.3E-02
CUI: C4024900
Disease: Atrophy/Degeneration affecting the brainstem
Atrophy/Degeneration affecting the brainstem 		27 0 7 8.3E-02 0 0
CUI: C0521858
Disease: Decreased drug resistance
Decreased drug resistance 		15 0 6 8.2E-02 0 0
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked 		126 0 14 8.0E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 0 7 7.8E-02 0 0
CUI: C3714753
Disease: RETINOSCHISIS 1, X-LINKED, JUVENILE
RETINOSCHISIS 1, X-LINKED, JUVENILE 		33 0 7 7.8E-02 0 0
CUI: C1839780
Disease: FRAGILE X TREMOR/ATAXIA SYNDROME
FRAGILE X TREMOR/ATAXIA SYNDROME 		62 0 9 7.7E-02 0 0
CUI: C0239882
Disease: Head tremor
Head tremor 		21 0 6 7.6E-02 0 0
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia 		36 9 7 7.5E-02 1 5.3E-02
CUI: C0156149
Disease: Gastrointestinal tract vascular insufficiency
Gastrointestinal tract vascular insufficiency 		68 0 9 7.3E-02 0 0
CUI: C2004435
Disease: Vascular insufficiency of intestine
Vascular insufficiency of intestine 		68 0 9 7.3E-02 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 14 7.3E-02 0 0
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 0 5 7.2E-02 0 0
CUI: C1843477
Disease: Epidermolysis Bullosa Simplex Superficialis
Epidermolysis Bullosa Simplex Superficialis 		11 0 5 7.1E-02 0 0
CUI: C3267047
Disease: Autoimmune necrotizing myopathy
Autoimmune necrotizing myopathy 		11 0 5 7.1E-02 0 0
CUI: C0016719
Disease: Friedreich Ataxia
Friedreich Ataxia 		88 0 10 7.0E-02 0 0