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: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
389 0 46 9.0E-02 0 0
CUI: C1834570
Disease: Myoclonic dystonia
Myoclonic dystonia
19 0 15 8.8E-02 0 0
Neurodegeneration with brain iron accumulation (NBIA)
40 0 16 8.4E-02 0 0
CUI: C0752207
Disease: Familial Dystonia
Familial Dystonia
15 0 14 8.3E-02 0 0
CUI: C1997740
Disease: Segmental dystonia
Segmental dystonia
15 9 14 8.3E-02 4 9.5E-02
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 37 8.2E-02 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
218 0 29 8.1E-02 0 0
CUI: C1843921
Disease: Postural instability
Postural instability
60 0 17 8.1E-02 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
580 0 55 7.9E-02 0 0
CUI: C3887506
Disease: Hyperkinesia
Hyperkinesia
80 0 18 7.9E-02 0 0
CUI: C0752105
Disease: Parkinsonism, Juvenile
Parkinsonism, Juvenile
40 0 15 7.8E-02 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 68 73 7.6E-02 2 1.9E-02
CUI: C0235031
Disease: Neurologic Symptoms
Neurologic Symptoms
233 0 28 7.5E-02 0 0
CUI: C0234378
Disease: Static Tremor
Static Tremor
62 0 16 7.5E-02 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia
136 0 21 7.4E-02 0 0
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration
165 0 23 7.4E-02 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE
477 0 44 7.3E-02 0 0
CUI: C0234133
Disease: Extrapyramidal sign
Extrapyramidal sign
116 0 19 7.2E-02 0 0
CUI: C1851920
Disease: Dopa-Responsive Dystonia
Dopa-Responsive Dystonia
28 33 13 7.1E-02 1 1.4E-02
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign
155 0 21 7.0E-02 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 46 7.0E-02 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism
34 0 13 6.9E-02 0 0
CUI: C0085584
Disease: Encephalopathies
Encephalopathies
457 0 40 6.8E-02 0 0
CUI: C0018524
Disease: Hallucinations
Hallucinations
178 0 22 6.8E-02 0 0
CUI: C0575081
Disease: Gait abnormality
Gait abnormality
312 0 30 6.7E-02 0 0