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: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 28 0.70 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 28 0.70 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 28 0.70 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 28 0.70 0 0
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism 		33 0 29 0.66 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		34 0 28 0.61 0 0
CUI: C1868675
Disease: PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE 		67 37 34 0.47 1 2.6E-02
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 11 0.22 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 0 16 0.21 0 0
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease 		11 0 8 0.19 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 11 0.18 0 0
CUI: C0085623
Disease: Akinesia
Akinesia 		43 0 12 0.17 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		57 0 14 0.17 0 0
CUI: C1843921
Disease: Postural instability
Postural instability 		60 0 14 0.16 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function 		12 0 7 0.16 0 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction 		12 0 7 0.16 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 8 0.15 0 0
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling 		28 0 9 0.15 0 0
CUI: C1112442
Disease: Female sexual dysfunction
Female sexual dysfunction 		22 0 8 0.15 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 0 22 0.15 0 0
CUI: C1851920
Disease: Dopa-Responsive Dystonia
Dopa-Responsive Dystonia 		28 0 8 0.13 0 0
CUI: C0013386
Disease: Dyskinesia, Drug-Induced
Dyskinesia, Drug-Induced 		32 0 8 0.12 0 0
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 6 0.12 0 0
CUI: C0085637
Disease: Oculogyric crisis
Oculogyric crisis 		9 0 5 0.11 0 0
CUI: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 0 5 0.11 0 0