Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
345132017 | Benign hereditary chorea | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
618095015 | Benign hereditary chorea (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
946821000172113 | chorée bénigne familiale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
974451000172114 | chorée bénigne héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3452811001000111 | Chorea, benigne hereditäre | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Benign hereditary chorea | Is a | trouble présent principalement avec la chorée | false | Inferred relationship | Some | ||
Benign hereditary chorea | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | 1 | |
Benign hereditary chorea | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Benign hereditary chorea | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Benign hereditary chorea | Is a | Involuntary movement characterised by brief, unpredictable, irregular, non-stereotyped movements that flow randomly from one body part to another. | true | Inferred relationship | Some | ||
Benign hereditary chorea | Finding site | Structure of basal nucleus | true | Inferred relationship | Some | 1 | |
Benign hereditary chorea | Interprets | mouvement | false | Inferred relationship | Some | 3 | |
Benign hereditary chorea | Interprets | Movement observable | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A rare genetic hyperkinetic movement disorder characterized predominantly by chorea of variable severity, associated with bilateral striatal abnormalities on cerebral MRI. The disease is scarcely progressive, and cognitive performance is preserved in the majority of cases, although mild cognitive delay has also been reported. | Is a | True | Benign hereditary chorea | Inferred relationship | Some |
This concept is not in any reference sets