Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2789776013 | Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2792566012 | Fibroblast growth factor receptor 3-related craniosynostosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2794177011 | Fibroblast growth factor receptor 3 (FGFR3) related craniosynostosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | est un(e) (attribut) | anomalie congénitale du crâne (trouble) | false | Inferred relationship | Some | ||
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | localisation d'une constatation (attribut) | Joint structure of suture of skull | true | Inferred relationship | Some | 1 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | est un(e) (attribut) | syndrome de craniosynostose (trouble) | true | Inferred relationship | Some | ||
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | morphologie associée (attribut) | Congenital premature fusion | false | Inferred relationship | Some | 1 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | localisation d'une constatation (attribut) | Structure of coronal suture of skull | false | Inferred relationship | Some | 1 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | localisation d'une constatation (attribut) | Structure of coronal suture of skull | false | Inferred relationship | Some | 1 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | morphologie associée (attribut) | Congenital premature fusion | true | Inferred relationship | Some | 1 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | est un(e) (attribut) | Congenital anomaly of bone and joint | false | Inferred relationship | Some | ||
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | est un(e) (attribut) | Cranial suture finding | false | Inferred relationship | Some | ||
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | est un(e) (attribut) | Disorder of skull (disorder) | false | Inferred relationship | Some | ||
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | est un(e) (attribut) | Disorder of bone development (disorder) | false | Inferred relationship | Some | ||
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | morphologie associée (attribut) | Congenital premature fusion | false | Inferred relationship | Some | 2 | |
| Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | localisation d'une constatation (attribut) | Joint structure of suture of skull | false | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Muenke syndrome | est un(e) (attribut) | True | Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | Inferred relationship | Some | |
| Crouzon syndrome with acanthosis nigricans (disorder) | est un(e) (attribut) | True | Fibroblast growth factor receptor 3-related craniosynostosis (disorder) | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR