Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4168564014 | Agenesis of fibula | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4168565010 | Agenesis of fibula (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5997561000241115 | agénésie fibulaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5997571000241111 | agénésie de la fibula | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5997581000241113 | agénésie du péroné | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Agenesis of fibula | Is a | Congenital absence of fibula | false | Inferred relationship | Some | ||
Agenesis of fibula | Associated morphology | Agenesis (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Agenesis of fibula | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Agenesis of fibula | Finding site | Entire fibula | true | Inferred relationship | Some | 1 | |
Agenesis of fibula | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Agenesis of fibula | Is a | Aplasia of fibula | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital fibular deficiency type I | Is a | True | Agenesis of fibula | Inferred relationship | Some | |
Congenital fibular deficiency type II | Is a | True | Agenesis of fibula | Inferred relationship | Some | |
Congenital fibular deficiency type III | Is a | True | Agenesis of fibula | Inferred relationship | Some | |
Craniosynostosis fibular aplasia syndrome (disorder) | Is a | True | Agenesis of fibula | Inferred relationship | Some | |
Mesomelic dysplasia, Savarirayan type is characterized by severely hypoplastic and triangular-shaped tibiae, and absence of the fibulae. So far, two sporadic cases have been described. Moderate mesomelia of the upper limbs, proximal widening of the ulnas, pelvic anomalies and marked bilateral glenoid hypoplasia were also reported. | Is a | True | Agenesis of fibula | Inferred relationship | Some | |
Complete phocomelia of lower limb | Is a | True | Agenesis of fibula | Inferred relationship | Some |
Reference Sets