Status: current, 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 |
153576011 | Congenital abnormal fusion of ulna | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
153577019 | Congenital fused ulna | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
836499015 | Congenital abnormal fusion of ulna (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1646861000005115 | Kongenit abnorm sammenvoksning af ulna | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Radioulnar synostosis | Is a | False | Congenital abnormal fusion of ulna | Inferred relationship | Some | |
Humeroulnar synostosis | Is a | True | Congenital abnormal fusion of ulna | Inferred relationship | Some | |
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. | Is a | False | Congenital abnormal fusion of ulna | Inferred relationship | Some | |
Congenital radioulnar synostosis | Is a | True | Congenital abnormal fusion of ulna | Inferred relationship | Some |
This concept is not in any reference sets