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: C0751831
Disease: Gait, Frontal
Gait, Frontal 		4 0 4 0.14 0 0
CUI: C0751832
Disease: Gait, Widebased
Gait, Widebased 		4 0 4 0.14 0 0
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual 		39 0 8 0.14 0 0
CUI: C4476759
Disease: Stooped posture
Stooped posture 		6 0 4 0.13 0 0
CUI: C1850100
Disease: PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder) 		7 0 4 0.13 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 0 18 0.13 0 0
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
Autosomal dominant late onset Parkinson disease 		9 0 4 0.12 0 0
CUI: C0401149
Disease: Chronic constipation
Chronic constipation 		47 0 8 0.12 0 0
CUI: C0241700
Disease: Voice Fatigue
Voice Fatigue 		20 0 5 0.12 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 0 8 0.11 0 0
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism 		33 0 6 0.11 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		34 0 6 0.11 0 0
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 4 0.11 0 0
CUI: C2931928
Disease: Mitochondrial cytopathy
Mitochondrial cytopathy 		4 0 3 0.10 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		60 0 8 1.0E-01 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls 		94 0 11 9.9E-02 0 0
CUI: C0085632
Disease: Apathy
Apathy 		83 0 10 9.9E-02 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 5 9.8E-02 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 5 9.8E-02 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 5 9.8E-02 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 5 9.8E-02 0 0
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		30 0 5 9.4E-02 0 0
CUI: C1868675
Disease: PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE 		67 0 8 9.2E-02 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 4 9.1E-02 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 0 6 8.8E-02 0 0