Status: current, Defined. 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 | Case insensitive | SNOMED CT core |
| 3334046019 | Parkinsonism due to heredodegenerative disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Parkinsonism due to heredodegenerative disorder | Interprets | Movement | true | Inferred relationship | Some | 4 | |
| Parkinsonism due to heredodegenerative disorder | Has interpretation | Slow | true | Inferred relationship | Some | 4 | |
| Parkinsonism due to heredodegenerative disorder | Is a | Central nervous system complication | true | Inferred relationship | Some | ||
| Parkinsonism due to heredodegenerative disorder | Due to | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | 2 | |
| Parkinsonism due to heredodegenerative disorder | Is a | Secondary parkinsonism | true | Inferred relationship | Some | ||
| Parkinsonism due to heredodegenerative disorder | Finding site | Basal ganglion structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Parkinsonian pyramidal syndrome | Is a | True | Parkinsonism due to heredodegenerative disorder | Inferred relationship | Some | |
| Parkinsonism due to hereditary spastic paraplegia | Is a | True | Parkinsonism due to heredodegenerative disorder | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR