Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jun 2024. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4215751000146110 | Disorder of extensor tendon of hand (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4215761000146113 | Disorder of extensor tendon of hand | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4224261000146112 | Tendinopathy of extensor tendon of hand | 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 |
| Disorder of extensor tendon of hand (disorder) | Is a | Disorder of tendon of hand (disorder) | true | Inferred relationship | Some | ||
| Disorder of extensor tendon of hand (disorder) | Finding site | Structure of extensor tendon within hand | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Injury of extensor tendon of hand (disorder) | Is a | True | Disorder of extensor tendon of hand (disorder) | Inferred relationship | Some | |
| Inflammation of extensor tendon of hand (disorder) | Is a | True | Disorder of extensor tendon of hand (disorder) | Inferred relationship | Some | |
| A rare genetic congenital limb malformation with characteristics of bilateral anomalous attachment of the extensor tendons of the four ulnar fingers. Attachment occurs to the medial and lateral aspects of the middle phalanges leading to constant flexion in the mid phalangeal joints and inability to extend the fingers. There have been no further descriptions in the literature since 1980. | Is a | True | Disorder of extensor tendon of hand (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR