Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Autosomal dominant late onset Parkinson disease
9 5 1 0.11 1 0.20
CUI: C4531121
Disease: Monotonic speech
Monotonic speech
9 0 1 0.11 0 0
CUI: C1836904
Disease: Spastic/hyperactive bladder
Spastic/hyperactive bladder
10 0 1 1.0E-01 0 0
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease
11 0 1 9.1E-02 0 0
CUI: C0548883
Disease: Low frustration tolerance
Low frustration tolerance
14 0 1 7.1E-02 0 0
Orthostatic hypotension due to autonomic dysfunction
16 0 1 6.2E-02 0 0
Parkinsonism with favorable response to dopaminergic medication
21 0 1 4.8E-02 0 0
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling
28 0 1 3.6E-02 0 0
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism
30 0 1 3.3E-02 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face
31 0 1 3.2E-02 0 0
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual
39 0 1 2.6E-02 0 0
CUI: C0085623
Disease: Akinesia
Akinesia
43 0 1 2.3E-02 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1
46 27 1 2.2E-02 1 3.7E-02
CUI: C0401149
Disease: Chronic constipation
Chronic constipation
47 0 1 2.1E-02 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor
57 0 1 1.8E-02 0 0
CUI: C1843921
Disease: Postural instability
Postural instability
60 0 1 1.7E-02 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired
60 0 1 1.7E-02 0 0
CUI: C0012569
Disease: Diplopia
Diplopia
75 0 1 1.3E-02 0 0
CUI: C0085632
Disease: Apathy
Apathy
83 0 1 1.2E-02 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0
87 0 1 1.1E-02 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0
87 0 1 1.1E-02 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls
94 0 1 1.1E-02 0 0
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome
95 34 1 1.1E-02 1 2.9E-02
CUI: C0233401
Disease: Psychiatric symptom
Psychiatric symptom
95 0 1 1.1E-02 0 0
CUI: C0017639
Disease: Gliosis
Gliosis
102 0 1 9.8E-03 0 0