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: C0026837
Disease: Muscle Rigidity
Muscle Rigidity 		320 25 125 0.17 7 1.0E-01
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		373 95 119 0.15 8 5.8E-02
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease 		255 41 42 5.7E-02 5 5.7E-02
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility 		45 6 19 3.4E-02 3 5.5E-02
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		607 47 82 7.8E-02 5 5.3E-02
CUI: C0042798
Disease: Low Vision
Low Vision 		157 51 24 3.6E-02 5 5.1E-02
CUI: C0087169
Disease: Withdrawal Symptoms
Withdrawal Symptoms 		126 10 12 1.9E-02 3 5.1E-02
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
PARKINSON DISEASE, LATE-ONSET 		247 76 58 8.1E-02 6 4.9E-02
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 16 76 0.13 3 4.6E-02
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders 		1515 85 174 9.3E-02 6 4.6E-02
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		122 79 49 8.2E-02 5 4.0E-02
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 27 12 2.1E-02 3 3.9E-02
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 54 28 4.0E-02 4 3.9E-02
CUI: C0031154
Disease: Peritonitis
Peritonitis 		15 2 3 5.6E-03 2 3.8E-02
CUI: C0221163
Disease: Motor Disorders
Motor Disorders 		25 2 6 1.1E-02 2 3.8E-02
CUI: C0264172
Disease: Barrel chest
Barrel chest 		18 2 1 1.8E-03 2 3.8E-02
CUI: C3554055
Disease: PEROXISOME BIOGENESIS DISORDER 14B
PEROXISOME BIOGENESIS DISORDER 14B 		2 2 1 1.9E-03 2 3.8E-02
CUI: C0085623
Disease: Akinesia
Akinesia 		43 3 21 3.8E-02 2 3.8E-02
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		34 3 18 3.3E-02 2 3.8E-02
CUI: C1860121
Disease: Decreased testosterone in males
Decreased testosterone in males 		2 3 1 1.9E-03 2 3.8E-02
CUI: C4024790
Disease: Adult-onset night blindness
Adult-onset night blindness 		5 3 1 1.9E-03 2 3.8E-02
CUI: C4025708
Disease: Cerebellar malformation
Cerebellar malformation 		2 3 1 1.9E-03 2 3.8E-02
CUI: C0241688
Disease: Peripheral visual field loss
Peripheral visual field loss 		19 4 1 1.8E-03 2 3.7E-02
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual 		39 5 14 2.5E-02 2 3.6E-02
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 6 10 1.7E-02 2 3.6E-02