Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
66483014 | Hereditary spastic paraplegia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
66484015 | Strumpell-Lorrain disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
66485019 | Familial spastic paraplegia syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
776456018 | Hereditary spastic paraplegia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
1229576012 | HSP - Hereditary spastic paraplegia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
2477033013 | Spastic congenital paraplegia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
This concept is not in any reference sets