Parkinson's Disease (SNOMED-CT) V1.3
Metadata
- Coding system
- SNOMED CT (UK Clinical Edition)
- Coding system release
- 36.2.0
- Organisation
- University of Bristol
- Codelist ID
- bristol/parkinsons-disease-snomed-ct-v13
- Version ID
- 7fc8a0df
- Number of codes included
- 32
About
Methodology
To identify Parkinson's disease, a code list was created by José Ignacio Cuitún Coronado (Senior Research Associate in Medical Statistics and Applied Health Data Science, University of Bristol) and reviewed by Elizabeth Coulthard (Professor of Cognitive Neurology, University of Bristol).
Step 1. We searched for the following key term: Parkinson
Step 2. We excluded irrelevant codes (e.g., codes indicating a prevalent diagnosis or where the diagnosis was unclear):
(A) Codes that identify a prevalent diagnosis:
- History of
(B) Codes that do not relate to the person:
- Family history
(C) Codes where the diagnosis is unclear:
- Assessment
- At risk
- Attendance
- Battery
- Tool
- Referral
- Invite / invitation
(D) Codes excluded upon review by the clinician:
- Society
- Committee
- Medication (partial exclusion)
- Substances (partial exclusion)
- Drugs (partial exclusion)
- Measure / measurement / test / scale questionnaire
- Amantidine hydrochloride [parkinsons]
- Bromocriptine [parkinsons]
- Cabergoline [parkinsons]
- Early onset parkinsonism and intellectual disability syndrome
- Restrictive lung disease due to Parkinson disease
- Unified Parkinsons disease rating scale score
No medication/drug/substance(s) were removed unless there was a clear example from the clinician.
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 101421000119107 | Dementia due to Parkinson's disease |
| 1156822001 | Autosomal recessive familial Parkinson disease |
| 1230308005 | Off-periods in Parkinson disease not responding to oral treatment |
| 1259080009 | Disorder of autonomic nervous system due to Parkinson disease |
| 154999006 | Parkinson's disease |
| 155000006 | Parkinson's disease |
| 15755701000119105 | Fluency disorder due to Parkinson disease |
| 192177005 | [X]Dementia in Parkinson's disease |
| 192825001 | Parkinson's disease |
| 194470003 | [X]Parkinsonism in diseases classified elsewhere |
| 230291001 | Juvenile Parkinson's disease |
| 265377002 | Symptomatic parkinsonism |
| 341551000000108 | Cerebral degeneration in Parkinson's disease |
| 368771000000107 | Cerebral degeneration in Parkinson's disease |
| 425390006 | Dementia associated with Parkinson's Disease |
| 438513002 | Cerebral degeneration due to Parkinson's disease |
| 477771000000108 | [X]Parkinsonism in diseases classified elsewhere |
| 479161000000109 | [X]Dementia in Parkinson's disease |
| 49049000 | Parkinson's disease |
| 51100001 | Hypokinetic parkinsonian dysphonia |
| 715345007 | Young onset Parkinson disease |
| 716107009 | Early onset parkinsonism and intellectual disability syndrome |
| 716662004 | Autosomal dominant late onset Parkinson disease |
| 718685006 | Orthostatic hypotension co-occurrent and due to Parkinson's disease |
| 719717006 | Psychosis co-occurrent and due to Parkinson's disease |
| 720466001 | Adult-onset dystonia parkinsonism |
| 722964001 | Atypical Parkinsonism |
| 722965000 | Parkinsonism due to heredodegenerative disorder |
| 724761004 | Sporadic Parkinson disease |
| 725146001 | Atypical juvenile parkinsonism |
| 725392005 | Autosomal dominant striatal neurodegeneration |
| 788911004 | Dissociative neurological symptom disorder co-occurrent with Parkinsonism |