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: C0865474
Disease: Parkinsonism or Parkinson's disease NOS
Parkinsonism or Parkinson's disease NOS 		1 0 1 1.00 0 0
CUI: C0865475
Disease: Idiopathic Parkinsonism or Parkinson's disease
Idiopathic Parkinsonism or Parkinson's disease 		1 0 1 1.00 0 0
CUI: C0865476
Disease: Primary Parkinsonism or Parkinson's disease
Primary Parkinsonism or Parkinson's disease 		1 0 1 1.00 0 0
CUI: C1854182
Disease: PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder)
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder) 		1 0 1 1.00 0 0
CUI: C0599458
Disease: glycosphingolipidoses
glycosphingolipidoses 		2 0 1 0.50 0 0
CUI: C0154536
Disease: Amphetamine or related acting sympathomimetic abuse
Amphetamine or related acting sympathomimetic abuse 		3 0 1 0.33 0 0
CUI: C1112261
Disease: Gaze palsy
Gaze palsy 		3 0 1 0.33 0 0
CUI: C0262424
Disease: CNS DEGENERATION
CNS DEGENERATION 		4 0 1 0.25 0 0
CUI: C1399358
Disease: Hemiparkinsonism
Hemiparkinsonism 		4 0 1 0.25 0 0
CUI: C1851958
Disease: Lewy Body Variant of Alzheimer Disease
Lewy Body Variant of Alzheimer Disease 		4 2 1 0.25 2 0.40
CUI: C1853445
Disease: PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET 		4 0 1 0.25 0 0
CUI: C4477086
Disease: Cotton wool plaques
Cotton wool plaques 		4 0 1 0.25 0 0
CUI: C1969363
Disease: Middle age onset
Middle age onset 		5 0 1 0.20 0 0
CUI: C0268250
Disease: Gaucher Disease, Type 2 (disorder)
Gaucher Disease, Type 2 (disorder) 		6 0 1 0.17 0 0
CUI: C1850442
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 5
CEROID LIPOFUSCINOSIS, NEURONAL, 5 		6 0 1 0.17 0 0
CUI: C0030508
Disease: Parasomnia
Parasomnia 		7 0 1 0.14 0 0
CUI: C0270733
Disease: Striatonigral Degeneration
Striatonigral Degeneration 		7 0 1 0.14 0 0
CUI: C0338473
Disease: Neuroaxonal Dystrophies
Neuroaxonal Dystrophies 		7 0 1 0.14 0 0
CUI: C1850100
Disease: PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder) 		7 6 1 0.14 1 1.0E-01
CUI: C0037019
Disease: Shy-Drager Syndrome
Shy-Drager Syndrome 		8 0 1 0.12 0 0
CUI: C0729555
Disease: Infection of digestive system
Infection of digestive system 		8 0 1 0.12 0 0
CUI: C1843792
Disease: FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED 		8 0 1 0.12 0 0
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease 		9 0 1 0.11 0 0
CUI: C0748903
Disease: spinal cord involvement
spinal cord involvement 		9 0 1 0.11 0 0
CUI: C1853833
Disease: Parkinson Disease 6, Autosomal Recessive Early-Onset
Parkinson Disease 6, Autosomal Recessive Early-Onset 		9 0 1 0.11 0 0