Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jan 2025. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5428989018 | Parkinsonism with polyneuropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5428990010 | Parkinsonism with polyneuropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5428991014 | A rare parkinsonian syndrome due to neurodegenerative disease characterised by resting tremor (which may initially be asymmetric), rigidity, and bradykinesia. Polyneuropathy with neurogenic electromyography findings is present in the majority of the patients and reported in young age (early twenties) whereas parkinsonian symptoms are visible later in life (between 40 and 70 years of age). Additional clinical symptoms may include anxiety and depression. Mild diffuse muscular atrophy can also be detected in some patients. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5428992019 | A rare parkinsonian syndrome due to neurodegenerative disease characterized by resting tremor (which may initially be asymmetric), rigidity, and bradykinesia. Polyneuropathy with neurogenic electromyography findings is present in the majority of the patients and reported in young age (early twenties) whereas parkinsonian symptoms are visible later in life (between 40 and 70 years of age). Additional clinical symptoms may include anxiety and depression. Mild diffuse muscular atrophy can also be detected in some patients. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Parkinsonism with polyneuropathy (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Parkinsonism with polyneuropathy (disorder) | Is a | Mitochondrial cytopathy (disorder) | true | Inferred relationship | Some | ||
Parkinsonism with polyneuropathy (disorder) | Is a | Parkinsonism | true | Inferred relationship | Some | ||
Parkinsonism with polyneuropathy (disorder) | Is a | Polyneuropathy | true | Inferred relationship | Some | ||
Parkinsonism with polyneuropathy (disorder) | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 4 | |
Parkinsonism with polyneuropathy (disorder) | Interprets | Movement | true | Inferred relationship | Some | 2 | |
Parkinsonism with polyneuropathy (disorder) | Has interpretation | Slow | true | Inferred relationship | Some | 2 | |
Parkinsonism with polyneuropathy (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Parkinsonism with polyneuropathy (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Parkinsonism with polyneuropathy (disorder) | Is a | Cerebral degeneration (disorder) | true | Inferred relationship | Some | ||
Parkinsonism with polyneuropathy (disorder) | Finding site | Basal ganglion structure (body structure) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)