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: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		580 48 57 8.5E-02 1 7.1E-03
CUI: C4553976
Disease: Urinary Urgency, CTCAE 5
Urinary Urgency, CTCAE 5 		34 0 14 8.5E-02 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 19 8.3E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 54 48 8.2E-02 4 2.8E-02
CUI: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE 		299 0 33 8.0E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 0 13 7.9E-02 0 0
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 12 7.8E-02 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 67 33 7.6E-02 1 6.3E-03
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 21 7.6E-02 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 0 37 7.5E-02 0 0
CUI: C1849156
Disease: Spastic Ataxia
Spastic Ataxia 		28 3 12 7.5E-02 1 1.1E-02
CUI: C2673431
Disease: Abnormality of the periventricular white matter
Abnormality of the periventricular white matter 		45 0 13 7.4E-02 0 0
CUI: C0393556
Disease: Complicated hereditary spastic paraplegia
Complicated hereditary spastic paraplegia 		16 0 11 7.4E-02 0 0
CUI: C0009024
Disease: Clonus
Clonus 		60 4 14 7.4E-02 1 1.0E-02
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 120 39 7.1E-02 1 4.7E-03
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 27 22 7.1E-02 2 1.7E-02
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		116 0 17 7.0E-02 0 0
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy 		156 32 19 6.8E-02 1 8.1E-03
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 21 15 6.8E-02 1 8.8E-03
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease 		30 0 11 6.7E-02 0 0
CUI: C2673700
Disease: Brisk reflexes
Brisk reflexes 		31 0 11 6.7E-02 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 14 18 6.7E-02 1 9.4E-03
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 12 6.7E-02 0 0
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder) 		16 13 10 6.7E-02 2 1.9E-02
CUI: C1843175
Disease: Hyperreflexia in upper limbs
Hyperreflexia in upper limbs 		16 0 10 6.7E-02 0 0