Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3310457019 | Hereditary geniospasm (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3310458012 | Hereditary geniospasm | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3311096010 | Familial trembling of chin | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3311180014 | Hereditary chin trembling | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401669016 | A rare genetic tremor disorder characterized by recurrent episodes of involuntary tremor of the chin and lower lip due to isolated myoclonus of the mentalis muscle. Patients may represent more severe symptoms such as tongue biting and psychological distress. Even though neurological abnormalities are not associated, occasional involvement of sleep disorders and other facial muscles have been described. Sporadic cases were also reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401670015 | A rare genetic tremor disorder characterised by recurrent episodes of involuntary tremor of the chin and lower lip due to isolated myoclonus of the mentalis muscle. Patients may represent more severe symptoms such as tongue biting and psychological distress. Even though neurological abnormalities are not associated, occasional involvement of sleep disorders and other facial muscles have been described. Sporadic cases were also reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary geniospasm (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hereditary geniospasm (disorder) | Is a | Movement disorder | true | Inferred relationship | Some | ||
Hereditary geniospasm (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Hereditary geniospasm (disorder) | Is a | Facial nerve disorder (disorder) | true | Inferred relationship | Some | ||
Hereditary geniospasm (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
Hereditary geniospasm (disorder) | Finding site | Facial nerve structure | true | Inferred relationship | Some | 2 | |
Hereditary geniospasm (disorder) | Interprets | Movement | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)