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 0.82 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 28 0.82 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 28 0.82 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 28 0.82 0 0
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism 		33 0 28 0.72 0 0
CUI: C0752105
Disease: Parkinsonism, Juvenile
Parkinsonism, Juvenile 		40 0 28 0.61 0 0
CUI: C1868675
Disease: PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE 		67 37 28 0.38 2 5.3E-02
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 10 0.22 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function 		12 0 7 0.18 0 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction 		12 0 7 0.18 0 0
CUI: C1843921
Disease: Postural instability
Postural instability 		60 0 14 0.17 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 8 0.17 0 0
CUI: C1112442
Disease: Female sexual dysfunction
Female sexual dysfunction 		22 0 8 0.17 0 0
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
Autosomal dominant late onset Parkinson disease 		9 5 6 0.16 1 0.14
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 9 0.16 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		57 5 12 0.15 1 0.14
CUI: C0085623
Disease: Akinesia
Akinesia 		43 3 10 0.15 1 0.20
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 6 0.14 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 27 10 0.14 2 7.1E-02
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 16 20 0.14 1 5.6E-02
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 32 10 0.13 2 6.1E-02
CUI: C0085637
Disease: Oculogyric crisis
Oculogyric crisis 		9 0 5 0.13 0 0
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		30 0 7 0.12 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		60 12 10 0.12 1 7.1E-02
CUI: C0013386
Disease: Dyskinesia, Drug-Induced
Dyskinesia, Drug-Induced 		32 0 7 0.12 0 0