Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3763721016 | Familial congenital controlateral synkinesia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763722011 | Hereditary congenital mirror movements | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763723018 | Isolated congenital mirror movements | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763724012 | Familial congenital mirror movements | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763725013 | Hereditary congenital controlateral synkinesia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763726014 | Isolated congenital controlateral synkinesia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763727017 | Familial congenital mirror movements (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763728010 | A rare genetic movement disorder with characteristics of involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body, which are present in various first-degree members of a family, persist beyond the first decade of life, and have no associated comorbidities. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial congenital mirror movements | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Familial congenital mirror movements | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Familial congenital mirror movements | Finding site | Structure of nervous system (body structure) | true | Inferred relationship | Some | 1 | |
| Familial congenital mirror movements | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Familial congenital mirror movements | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Familial congenital mirror movements | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial congenital mirror movements | Is a | Mirror movements | true | Inferred relationship | Some | ||
| Familial congenital mirror movements | Interprets | Movement | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR