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Parkinson Disease (MONDO:0005180)

Open Trait in OLS
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A progressive degenerative disorder of the central nervous system characterized by loss of dopamine producing neurons in the substantia nigra and the presence of Lewy bodies in the substantia nigra and locus coeruleus. Signs and symptoms include tremor which is most pronounced during rest, muscle rigidity, slowing of the voluntary movements, a tendency to fall back, and a mask-like facial expression.

Overview
Category
nervous system disorder
Ontology ID
MONDO:0005180
Internal:6901
Synonyms
PD
Parkinson disease
Parkinson's disease
paralysis agitans
Mapped terms
DOID:14330
ICD10CM:G20
ICD10WHO:G20
ICD9:332
ICD9:332.0
MEDGEN:10590
MESH:D010300
NANDO:1200010
NCIT:C26845
OMIMPS:168600
Orphanet:319705
SCTID:49049000
UMLS:C0030567
birnlex:2098
icd11.foundation:296066191
Child terms
MONDO:0008199
MONDO:0009830
MONDO:0010796
MONDO:0013167
MONDO:0017279
MONDO:0957576

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PH77 Parkinson's disease

Clinical-Coded Phenotype

Disease or syndrome

Coding Systems:
ICD10 codes
Read codes v2
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CALIBER
Phenotype Library

Ontology terms:

Parkinson disease
Last updated 2021-10-06 Kuan V, Denaxas S, Gonzalez-Izquierdo A, …

PH2028 Parkinson's Disease (ICD10) V1.3

OpenCodelists Phenotype

Coding Systems:
ICD10 codes
Collections:
OpenCodelist
Phenotype Library
Last updated 2026-01-26 University of Bristol

PH2029 Parkinson's Disease (SNOMED-CT) V1.3

OpenCodelists Phenotype

Coding Systems:
SNOMED CT codes
Collections:
OpenCodelist
Phenotype Library
Last updated 2026-01-26 University of Bristol

PH3958 has_parkinsons

OpenCodelists Phenotype

Coding Systems:
SNOMED CT codes
Collections:
OpenCodelist
Phenotype Library
Last updated 2026-01-26 QCovid

PH3990 parkinsons

OpenCodelists Phenotype

Coding Systems:
Read codes v2
Collections:
OpenCodelist
Phenotype Library
Last updated 2026-01-26 QMUL Multimorbidity

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