Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3423993012 | Facial onset sensory and motor neuronopathy syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3423994018 | Facial onset sensory and motor neuronopathy syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3423995017 | FOSMN syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3423996016 | FOSMN (facial onset sensory and motor neuronopathy) syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3423997013 | Facial onset sensory and motor neuronopathy is characterised initially by paraesthesia and numbness in the region of the trigeminal nerve distribution, which later progresses to involve the scalp, neck, upper trunk and upper limbs. Onset of motor manifestations occurs later with cramps, fasciculations, dysphagia, dysarthria, muscle weakness and atrophy. This syndrome has been described in four males and appears to be a slowly progressive neurodegenerative disease. | en | Definition | Active | Case sensitive | SNOMED CT core |
3423998015 | Facial onset sensory and motor neuronopathy is characterized initially by paresthesia and numbness in the region of the trigeminal nerve distribution, which later progresses to involve the scalp, neck, upper trunk and upper limbs. Onset of motor manifestations occurs later with cramps, fasciculations, dysphagia, dysarthria, muscle weakness and atrophy. This syndrome has been described in four males and appears to be a slowly progressive neurodegenerative disease. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Facial onset sensory and motor neuronopathy syndrome | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Facial onset sensory and motor neuronopathy syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Facial onset sensory and motor neuronopathy syndrome | Is a | Degenerative disease of the central nervous system | false | Inferred relationship | Some | ||
Facial onset sensory and motor neuronopathy syndrome | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Facial onset sensory and motor neuronopathy syndrome | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Facial onset sensory and motor neuronopathy syndrome | Finding site | Structure of central nervous system | 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
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set