Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3334045015 | Parkinsonism due to heredodegenerative disorder (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3334046019 | Parkinsonism due to heredodegenerative disorder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Parkinsonism due to heredodegenerative disorder (disorder) | Due to | Hereditary degenerative disease of central nervous system (disorder) | true | Inferred relationship | Some | 2 | |
| Parkinsonism due to heredodegenerative disorder (disorder) | Is a | Secondary parkinsonism | true | Inferred relationship | Some | ||
| Parkinsonism due to heredodegenerative disorder (disorder) | Finding site | Basal ganglion structure (body structure) | true | Inferred relationship | Some | 1 | |
| Parkinsonism due to heredodegenerative disorder (disorder) | Interprets | Movement | true | Inferred relationship | Some | 4 | |
| Parkinsonism due to heredodegenerative disorder (disorder) | Has interpretation | Slow | true | Inferred relationship | Some | 4 | |
| Parkinsonism due to heredodegenerative disorder (disorder) | Is a | Central nervous system complication | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 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). | Is a | True | Parkinsonism due to heredodegenerative disorder (disorder) | Inferred relationship | Some | |
| Parkinsonism due to hereditary spastic paraplegia (disorder) | Is a | True | Parkinsonism due to heredodegenerative disorder (disorder) | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set
FHIR