Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3481956018 | Sporadic adult-onset ataxia of unknown etiology (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3481957010 | Sporadic adult-onset ataxia of unknown etiology | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3481958017 | Sporadic adult-onset ataxia of unknown aetiology | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3481959013 | Idiopathic late-onset cerebellar ataxia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3481960015 | Sporadic adult-onset ataxia of unknown origin | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
763571000241114 | ataxie sporadique tardive d'étiologie indéterminée (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
892701000172113 | ataxie sporadique tardive d'étiologie indéterminée | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
921871000172115 | ataxie sporadique de l'adulte d'étiologie indéterminée | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
3481961016 | Non-hereditary degenerative ataxia with characteristics of slowly progressive cerebellar syndrome (with ataxia of stance and gait, upper limb dysmetria and intention tremor, ataxic speech, and oculomotor abnormalities), presenting in adulthood (at around 50 years of age), that is not due to a known cause. Extracerebellar symptoms (e.g., decreased vibration sense and absent or decreased ankle reflexes), polyneuropathy and mild autonomic dysfunction may also be present. Mild cognitive impairment has also rarely been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Sporadic adult-onset ataxia of unknown etiology (disorder) | est un(e) (attribut) | Cerebellar degeneration | true | Inferred relationship | Some | ||
Sporadic adult-onset ataxia of unknown etiology (disorder) | est un(e) (attribut) | Ataxia | false | Inferred relationship | Some | ||
Sporadic adult-onset ataxia of unknown etiology (disorder) | est un(e) (attribut) | maladie idiopathique | true | Inferred relationship | Some | ||
Sporadic adult-onset ataxia of unknown etiology (disorder) | est un(e) (attribut) | Late onset cerebellar ataxia | true | Inferred relationship | Some | ||
Sporadic adult-onset ataxia of unknown etiology (disorder) | est un(e) (attribut) | affection dégénérative | false | Inferred relationship | Some | ||
Sporadic adult-onset ataxia of unknown etiology (disorder) | morphologie associée (attribut) | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Sporadic adult-onset ataxia of unknown etiology (disorder) | survenue (attribut) | Adulthood (qualifier value) | true | Inferred relationship | Some | 1 | |
Sporadic adult-onset ataxia of unknown etiology (disorder) | localisation d'une constatation (attribut) | structure cérébelleuse | true | Inferred relationship | Some | 1 | |
Sporadic adult-onset ataxia of unknown etiology (disorder) | est un(e) (attribut) | Cerebellar ataxia | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets