Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3307125015 | Autosomal dominant late onset Parkinson disease (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3307126019 | Autosomal dominant late onset Parkinson disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3307127011 | Hereditary late onset Parkinson disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5401350017 | Hereditary late-onset Parkinson disease (LOPD) is a form of Parkinson disease (PD), characterized by an age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia (LID). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401351018 | Hereditary late-onset Parkinson disease (LOPD) is a form of Parkinson disease (PD), characterised by an age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia (LID). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant late onset Parkinson disease (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant late onset Parkinson disease (disorder) | Is a | Parkinson's disease | true | Inferred relationship | Some | ||
Autosomal dominant late onset Parkinson disease (disorder) | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Autosomal dominant late onset Parkinson disease (disorder) | Finding site | Basal ganglion structure (body structure) | true | Inferred relationship | Some | 1 | |
Autosomal dominant late onset Parkinson disease (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal dominant late onset Parkinson disease (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Autosomal dominant late onset Parkinson disease (disorder) | Causative agent | Alpha-synuclein | false | Inferred relationship | Some | 1 | |
Autosomal dominant late onset Parkinson disease (disorder) | Interprets | Movement | true | Inferred relationship | Some | 3 | |
Autosomal dominant late onset Parkinson disease (disorder) | Has interpretation | Slow | true | Inferred relationship | Some | 3 | |
Autosomal dominant late onset Parkinson disease (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)