Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1229576012 | HSP - Hereditary spastic paraplegia | en | Synonym | Active | Case sensitive | SNOMED CT core |
2477033013 | Spastic congenital paraplegia | en | Synonym | Active | Case insensitive | SNOMED CT core |
66483014 | Hereditary spastic paraplegia | en | Synonym | Active | Case insensitive | SNOMED CT core |
66484015 | Strumpell-Lorrain disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
66485019 | Familial spastic paraplegia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
776456018 | Hereditary spastic paraplegia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set