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: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual 		39 5 11 0.15 1 5.0E-02
CUI: C0426980
Disease: Motor symptoms
Motor symptoms 		100 15 18 0.14 1 3.3E-02
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
Posterior cortical atrophy syndrome 		12 0 7 0.14 0 0
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		30 0 8 0.12 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 32 10 0.11 1 2.1E-02
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 6 0.11 0 0
CUI: C0751246
Disease: Illusions, Visual
Illusions, Visual 		5 0 5 0.11 0 0
CUI: C1961835
Disease: Gaucher Disease, Type 1
Gaucher Disease, Type 1 		48 124 9 0.11 1 7.2E-03
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		176 0 21 0.10 0 0
CUI: C0231779
Disease: Heel toe gait
Heel toe gait 		7 0 5 0.10 0 0
CUI: C0085632
Disease: Apathy
Apathy 		83 0 12 0.10 0 0
CUI: C0406191
Disease: Pseudofolliculitis
Pseudofolliculitis 		8 0 5 0.10 0 0
CUI: C0085623
Disease: Akinesia
Akinesia 		43 3 8 9.9E-02 1 5.6E-02
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 6 9.8E-02 0 0
CUI: C0233397
Disease: Psychological symptom
Psychological symptom 		33 0 7 9.7E-02 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		34 3 7 9.6E-02 1 5.6E-02
CUI: C0392678
Disease: Swallowing problem
Swallowing problem 		13 0 5 9.3E-02 0 0
CUI: C1955760
Disease: Idiopathic normal pressure hydrocephalus (INPH)
Idiopathic normal pressure hydrocephalus (INPH) 		25 0 6 9.2E-02 0 0
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		37 0 7 9.2E-02 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 16 15 9.1E-02 1 3.2E-02
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		122 79 14 9.1E-02 3 3.3E-02
CUI: C0282513
Disease: Primary Progressive Aphasia (disorder)
Primary Progressive Aphasia (disorder) 		51 0 8 9.0E-02 0 0
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		77 0 10 8.8E-02 0 0
CUI: C2220255
Disease: Motor disturbances
Motor disturbances 		16 0 5 8.8E-02 0 0
CUI: C0751783
Disease: Lafora Disease
Lafora Disease 		92 0 11 8.7E-02 0 0