Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3643234011 | Spastic ataxia with congenital miosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643235012 | Autosomal dominant spastic ataxia type 7 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643236013 | Spastic ataxia with congenital miosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3643237016 | A rare hereditary ataxia with characteristics of an apparently non-progressive or slowly progressive symmetrical ataxia of gait, pyramidal signs in the limbs, spasticity and hyperreflexia (especially in the lower limbs) together with dysarthria and impaired pupillary reaction to light, presenting as a fixed miosis. Nystagmus may also be present. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set