Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Parkinson Disease, Secondary Vascular
12 0 12 0.67 0 0
CUI: C0751415
Disease: Atherosclerotic Parkinsonism
Atherosclerotic Parkinsonism
12 0 12 0.67 0 0
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME
11 0 4 0.16 0 0
CUI: C0677050
Disease: Manganese Poisoning
Manganese Poisoning
16 0 4 0.13 0 0
CUI: C0037019
Disease: Shy-Drager Syndrome
Shy-Drager Syndrome
8 0 3 0.13 0 0
Parkinson Disease 6, Autosomal Recessive Early-Onset
9 0 3 0.12 0 0
Autosomal dominant late onset Parkinson disease
9 0 3 0.12 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome
28 0 5 0.12 0 0
Autosomal Dominant Juvenile Parkinson Disease
28 0 5 0.12 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental
28 0 5 0.12 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism
28 0 5 0.12 0 0
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease
11 0 3 0.12 0 0
CUI: C0003510
Disease: Aortitis Syndrome
Aortitis Syndrome
2 0 2 0.11 0 0
CUI: C0278015
Disease: Change in stool consistency
Change in stool consistency
2 0 2 0.11 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function
12 0 3 0.11 0 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction
12 0 3 0.11 0 0
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism
33 0 5 0.11 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism
34 3 5 0.11 1 0.33
CUI: C1112261
Disease: Gaze palsy
Gaze palsy
3 0 2 0.11 0 0
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis
14 0 3 0.10 0 0
CUI: C0030528
Disease: Paratyphoid Fever
Paratyphoid Fever
4 0 2 1.0E-01 0 0
CUI: C0353676
Disease: Organophosphorus Poisoning
Organophosphorus Poisoning
4 0 2 1.0E-01 0 0
CUI: C1399358
Disease: Hemiparkinsonism
Hemiparkinsonism
4 0 2 1.0E-01 0 0
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET
4 0 2 1.0E-01 0 0
CUI: C3494247
Disease: Organothiophosphonate Poisoning
Organothiophosphonate Poisoning
4 0 2 1.0E-01 0 0