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 |
| 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 |
| 892701000172113 | ataxie sporadique tardive d'étiologie indéterminée | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 921871000172115 | ataxie sporadique de l'adulte d'étiologie indéterminée | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Is a | Ataxia | false | Inferred relationship | Some | ||
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Is a | Idiopathic disease | true | Inferred relationship | Some | ||
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Is a | Late onset cerebellar ataxia | true | Inferred relationship | Some | ||
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Is a | Degenerative disorder | false | Inferred relationship | Some | ||
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Occurrence | Adulthood | true | Inferred relationship | Some | 1 | |
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Is a | Cerebellar ataxia | true | Inferred relationship | Some | ||
| Sporadic adult-onset ataxia of unknown etiology (disorder) | Is a | Cerebellar degeneration | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR