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: C0752105
Disease: Parkinsonism, Juvenile
Parkinsonism, Juvenile 		40 2 34 0.47 1 2.6E-02
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism 		33 0 30 0.43 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 28 0.42 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 28 0.42 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 28 0.42 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 28 0.42 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		34 3 28 0.38 2 5.3E-02
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 32 15 0.15 6 9.5E-02
CUI: C1843921
Disease: Postural instability
Postural instability 		60 0 16 0.14 0 0
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 11 0.14 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 12 0.14 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia 		133 16 24 0.14 1 1.9E-02
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 10 0.13 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		57 5 14 0.13 1 2.4E-02
CUI: C0085623
Disease: Akinesia
Akinesia 		43 3 12 0.12 1 2.6E-02
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease 		11 0 8 0.11 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function 		12 0 8 0.11 0 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction 		12 0 8 0.11 0 0
CUI: C1112442
Disease: Female sexual dysfunction
Female sexual dysfunction 		22 0 9 0.11 0 0
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		373 95 41 0.10 5 3.9E-02
CUI: C1853833
Disease: Parkinson Disease 6, Autosomal Recessive Early-Onset
Parkinson Disease 6, Autosomal Recessive Early-Onset 		9 25 7 0.10 1 1.6E-02
CUI: C0241700
Disease: Voice Fatigue
Voice Fatigue 		20 0 8 0.10 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		60 12 11 9.5E-02 1 2.1E-02
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 7 9.5E-02 0 0
CUI: C3805715
Disease: Short stepped shuffling gait
Short stepped shuffling gait 		16 0 7 9.2E-02 0 0