Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2007. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
345447015 | Congenital disorder of facial nerve | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
618363011 | Congenital disorder of facial nerve (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
76741000077114 | trouble congénital du nerf facial | 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 |
Congenital disorder of facial nerve | Is a | Facial nerve disorder | false | Inferred relationship | Some | ||
Congenital disorder of facial nerve | Is a | Congenital anomaly of head | false | Inferred relationship | Some | ||
Congenital disorder of facial nerve | Finding site | Facial nerve structure | false | Inferred relationship | Some | ||
Congenital disorder of facial nerve | Occurrence | Congenital | false | Inferred relationship | Some | ||
Congenital disorder of facial nerve | Is a | Congenital disease | true | Inferred relationship | Some | ||
Congenital disorder of facial nerve | Is a | Facial nerve disorder (disorder) | true | Inferred relationship | Some | ||
Congenital disorder of facial nerve | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital disorder of facial nerve | Finding site | Facial nerve structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital facial nerve palsy | Is a | True | Congenital disorder of facial nerve | Inferred relationship | Some | |
syndrome de Cayler | Is a | False | Congenital disorder of facial nerve | Inferred relationship | Some | |
A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). | Is a | False | Congenital disorder of facial nerve | Inferred relationship | Some | |
Facial hemiatrophy | Is a | False | Congenital disorder of facial nerve | Inferred relationship | Some |
This concept is not in any reference sets