Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3310457019 | Hereditary geniospasm (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3310458012 | Hereditary geniospasm | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3311096010 | Familial trembling of chin | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3311180014 | Hereditary chin trembling | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary geniospasm | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary geniospasm | Is a | Movement disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary geniospasm | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary geniospasm | Is a | Facial nerve disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary geniospasm | Occurrence | Childhood | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hereditary geniospasm | Finding site | Facial nerve structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Hereditary geniospasm | Interprets | Movement | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR