Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 344267015 | Expressive aphasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 344268013 | Expressive dysphasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 617388018 | Expressive dysphasia (finding) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3475362018 | Non-fluent aphasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3475363011 | Non-fluent dysphasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1942861000005118 | Ekspressiv dysfasi | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Expressive dysphasia | Is a | Dysphasia | true | Inferred relationship | Some | ||
| Expressive dysphasia | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | ||
| Expressive dysphasia | Interprets | Nervous system function | false | Inferred relationship | Some | ||
| Expressive dysphasia | Interprets | Speech observable | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Broca's dysphasia | Is a | True | Expressive dysphasia | Inferred relationship | Some | |
| Efferent motor dysphasia | Is a | True | Expressive dysphasia | Inferred relationship | Some | |
| Ikke-flydende afasi | Is a | False | Expressive dysphasia | Inferred relationship | Some | |
| A rare genetic syndromic intellectual disability characterized by moderate to severe intellectual deficiency, language deficit (completely absent or significantly impaired speech), and distinctive facial dysmorphism (long face, straight eyebrows, and, less frequently, low-set ears and café-au-lait spots). Additional, variably observed features include motor delays, behavioral difficulties, and seizures. | Is a | True | Expressive dysphasia | Inferred relationship | Some |
This concept is not in any reference sets
FHIR