Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3726032019 | Humero-radio-ulnar fusion | en | Synonym | Active | Case insensitive | SNOMED CT core |
3726035017 | Humero-radio-ulnar synostosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3726036016 | Humeroradioulnar synostosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3726037013 | Humeroradioulnar synostosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3726034018 | An extremely rare genetic congenital joint formation defect disorder with characteristics of unilateral or bilateral fusion of the humerus, radius and ulnar bones, leading to loss of elbow motion and in most, functional arm incapacity. It may appear as distal humeral bifurcation with absent elbow joint and shortened arm length on imaging. Hand abnormalities namely oligo-ectrosyndactyly may be associated. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set