Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
345081017 | Silver disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
3701800010 | Autosomal dominant spastic paraplegia type 17 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3701801014 | Autosomal dominant spastic paraplegia type 17 | en | Synonym | Active | Case insensitive | SNOMED CT core |
4674028016 | A complex hereditary spastic paraplegia with characteristics of progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. | 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