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: C0548883
Disease: Low frustration tolerance
Low frustration tolerance 		14 0 9 0.17 0 0
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 2 10 0.17 2 0.12
CUI: C1868528
Disease: Orthostatic hypotension due to autonomic dysfunction
Orthostatic hypotension due to autonomic dysfunction 		16 0 8 0.15 0 0
CUI: C4531121
Disease: Monotonic speech
Monotonic speech 		9 0 7 0.14 0 0
CUI: C1836904
Disease: Spastic/hyperactive bladder
Spastic/hyperactive bladder 		10 0 7 0.14 0 0
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling 		28 0 8 0.12 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 8 0.11 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		33 6 7 9.6E-02 1 4.8E-02
CUI: C1843921
Disease: Postural instability
Postural instability 		60 0 9 9.2E-02 0 0
CUI: C4317146
Disease: Acid reflux
Acid reflux 		50 58 8 9.0E-02 2 2.8E-02
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual 		39 0 7 8.9E-02 0 0
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder 		40 4 7 8.7E-02 1 5.3E-02
CUI: C0085623
Disease: Akinesia
Akinesia 		43 0 7 8.4E-02 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		57 0 8 8.3E-02 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		60 12 8 8.1E-02 1 3.7E-02
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
Autosomal dominant late onset Parkinson disease 		9 0 4 7.7E-02 0 0
CUI: C4072908
Disease: Induced vaginal delivery
Induced vaginal delivery 		10 10 4 7.5E-02 4 0.18
CUI: C3276036
Disease: High anterior hairline
High anterior hairline 		25 3 5 7.5E-02 1 5.6E-02
CUI: C0023221
Disease: Leg Length Inequality
Leg Length Inequality 		27 6 5 7.2E-02 3 0.16
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 24 7 7.2E-02 2 5.3E-02
CUI: C0017639
Disease: Gliosis
Gliosis 		102 0 10 7.2E-02 0 0
CUI: C0267071
Disease: Oropharyngeal Dysphagia
Oropharyngeal Dysphagia 		43 8 6 7.1E-02 1 4.3E-02
CUI: C0401146
Disease: Constipation - functional
Constipation - functional 		15 0 4 6.9E-02 0 0
CUI: C4021758
Disease: Delayed CNS myelination
Delayed CNS myelination 		21 4 4 6.2E-02 2 0.11
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		74 12 7 6.1E-02 2 7.7E-02