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- NCIT_C198604 IAO_0000115 "An autosomal dominant subtype of Parkinson disease, caused by mutation(s) in the SNCA gene, encoding alpha-synuclein. Mutation(s) in the SNCA gene are responsible for PARK1 and Lewy body dementia, and have overlapping phenotypes." @default.
- NCIT_C198604 NCIT_NHC0 "C198604" @default.
- NCIT_C198604 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C198604 NCIT_P108 "Parkinson Disease 4, Autosomal Dominant" @default.
- NCIT_C198604 NCIT_P322 "CTRP" @default.
- NCIT_C198604 NCIT_R100 NCIT_C12219 @default.
- NCIT_C198604 NCIT_R100 NCIT_C12438 @default.
- NCIT_C198604 NCIT_R100 NCIT_C12755 @default.
- NCIT_C198604 NCIT_R100 NCIT_C12919 @default.
- NCIT_C198604 NCIT_R100 NCIT_C13040 @default.
- NCIT_C198604 NCIT_R100 NCIT_C32221 @default.
- NCIT_C198604 NCIT_R176 NCIT_C16612 @default.
- NCIT_C198604 NCIT_R176 NCIT_C21295 @default.
- NCIT_C198604 NCIT_R176 NCIT_C28533 @default.
- NCIT_C198604 NCIT_R176 NCIT_C90101 @default.
- NCIT_C198604 normalizedInformationContent "100" @default.
- NCIT_C198604 referenceCount "1" @default.
- NCIT_C198604 hasExactSynonym "PARK4" @default.
- NCIT_C198604 hasExactSynonym "Parkinson Disease 4, Autosomal Dominant" @default.
- NCIT_C198604 inSubset NCIT_C165258 @default.
- NCIT_C198604 inSubset NCIT_C192842 @default.
- NCIT_C198604 type Class @default.
- NCIT_C198604 isDefinedBy ncit.owl @default.
- NCIT_C198604 label "Parkinson Disease 4, Autosomal Dominant" @default.
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