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: C0270736
Disease: Essential Tremor
Essential Tremor 		122 79 27 0.12 1 1.1E-02
CUI: C0012569
Disease: Diplopia
Diplopia 		75 5 22 0.12 3 0.17
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 17 0.12 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 17 0.12 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 17 0.12 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 17 0.12 0 0
CUI: C0241700
Disease: Voice Fatigue
Voice Fatigue 		20 0 16 0.12 0 0
CUI: C0234378
Disease: Static Tremor
Static Tremor 		62 3 20 0.11 2 0.12
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		148 0 28 0.11 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		60 12 19 0.11 1 3.7E-02
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 15 0.11 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 32 18 0.11 1 2.1E-02
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		176 0 30 0.11 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 54 60 0.11 2 2.9E-02
CUI: C0240735
Disease: Personality Change
Personality Change 		43 0 17 0.11 0 0
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		126 0 25 0.11 0 0
CUI: C0240341
Disease: Micrographia
Micrographia 		14 0 14 0.11 0 0
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 14 0.11 0 0
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration 		165 0 28 0.10 0 0
CUI: C3805715
Disease: Short stepped shuffling gait
Short stepped shuffling gait 		16 0 14 0.10 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 28 0.10 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0 		87 0 20 1.0E-01 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0 		87 0 20 1.0E-01 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus 		265 34 36 9.9E-02 2 4.2E-02
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 24 17 9.8E-02 1 2.6E-02