Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 345784019 | Congenital apraxia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 618637013 | Congenital apraxia (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital apraxia | Finding site | Structure of musculoskeletal system | true | Inferred relationship | Some | 2 | |
| Congenital apraxia | Interprets | Nervous system function | false | Inferred relationship | Some | ||
| Congenital apraxia | Is a | Head finding | false | Inferred relationship | Some | ||
| Congenital apraxia | Is a | Finding of brain | true | Inferred relationship | Some | ||
| Congenital apraxia | Is a | Apraxia | true | Inferred relationship | Some | ||
| Congenital apraxia | Finding site | Structure of cerebrum | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Queensland allied health clinical finding reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set
FHIR