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: C1858712
Disease: Spastic paraplegia 10, autosomal dominant
Spastic paraplegia 10, autosomal dominant 		16 10 12 9.4E-02 1 2.0E-02
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 21 9.2E-02 0 0
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence 		151 0 23 9.2E-02 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		580 48 59 9.2E-02 1 1.1E-02
CUI: C1846566
Disease: Degeneration of the lateral corticospinal tracts
Degeneration of the lateral corticospinal tracts 		21 0 12 9.1E-02 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 17 8.9E-02 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 0 36 8.8E-02 0 0
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		186 0 25 8.8E-02 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 18 8.6E-02 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 22 8.6E-02 0 0
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 21 17 8.5E-02 1 1.6E-02
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease 		30 0 12 8.5E-02 0 0
CUI: C1295585
Disease: Decreased vibratory sense
Decreased vibratory sense 		33 0 12 8.3E-02 0 0
CUI: C0742038
Disease: Cerebellar signs
Cerebellar signs 		24 0 11 8.1E-02 0 0
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		66 0 14 8.0E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 54 45 8.0E-02 2 2.2E-02
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 20 7.8E-02 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 17 21 7.7E-02 2 3.6E-02
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		116 0 17 7.7E-02 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 120 39 7.4E-02 1 6.3E-03
CUI: C0393555
Disease: Pure hereditary spastic paraplegia
Pure hereditary spastic paraplegia 		9 0 9 7.3E-02 0 0
CUI: C0751604
Disease: Hereditary X-Linked Recessive Spastic Paraplegia
Hereditary X-Linked Recessive Spastic Paraplegia 		10 0 9 7.3E-02 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 101 9 7.3E-02 3 2.2E-02
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 14 7.2E-02 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		389 0 34 7.1E-02 0 0