Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3757139016 | Parkinsonian pyramidal syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3757140019 | Pallidopyramidal syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3757141015 | Parkinsonian pyramidal syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3757142010 | A rare genetic neurological disorder with characteristics of the association of both parkinsonian (such as bradykinesia, rigidity and/or rest tremor) and pyramidal (such as increased reflexes, extensor plantar reflexes, pyramidal weakness or spasticity) manifestations, which vary according to the underlying associated disease (for example neurodegenerative disease, inborn errors of metabolism). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4352881000052119 | parkinsonismliknande pyramidalt syndrom | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Parkinsonian pyramidal syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Parkinsonian pyramidal syndrome (disorder) | Is a | Parkinsonism due to heredodegenerative disorder (disorder) | true | Inferred relationship | Some | ||
| Parkinsonian pyramidal syndrome (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Parkinsonian pyramidal syndrome (disorder) | Finding site | Basal ganglion structure (body structure) | true | Inferred relationship | Some | 1 | |
| Parkinsonian pyramidal syndrome (disorder) | Due to | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | 2 | |
| Parkinsonian pyramidal syndrome (disorder) | Interprets | Movement | true | Inferred relationship | Some | 4 | |
| Parkinsonian pyramidal syndrome (disorder) | Has interpretation | Slow | true | Inferred relationship | Some | 4 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR