Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3322637018 | Foix Chavany Marie syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3322638011 | Foix Chavany Marie syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3322639015 | Bilateral anterior opercular syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3322640018 | Facio-pharyngo-glosso-masticatory diplegia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3322641019 | Acortico-subcortical suprabulbar or pseudobulbar palsy of the lower cranial nerves, with characteristics of severe dysarthria and dysphagia associated with bilateral central facio-pharyngo-glosso-masticatory paralysis, with prominent automatic-voluntary dissociation in which involuntary movements of the affected muscles are preserved. Less than 150 cases have been described in the literature so far. Can occur at any age. Patients have severe speech disturbances and most are mute.Chewing and swallowing are severely impaired. Caused by developmental or acquired bilateral lesions of the anterior opercula. In children, it presents congenitally (bilateral opercular polymicrogyria) or as an acquired disorder due to encephalitis, epilepsy and neurodegenerative disorders. The syndrome is generally sporadic but some familial cases have been described. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Foix Chavany Marie syndrome | Is a | Multiple cranial nerve palsy | true | Inferred relationship | Some | ||
Foix Chavany Marie syndrome | Finding site | Cranial nerve structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set