Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3449522015 | X-linked hereditary spastic paraplegia (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
3449523013 | X-linked hereditary spastic paraplegia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
X-linked spastic paraplegia type 2 | Is a | True | X-linked hereditary spastic paraplegia | Inferred relationship | Existential restriction modifier | |
X-linked spastic paraplegia type 34 | Is a | False | X-linked hereditary spastic paraplegia | Inferred relationship | Existential restriction modifier | |
X-linked spastic paraplegia type 16 | Is a | False | X-linked hereditary spastic paraplegia | Inferred relationship | Existential restriction modifier | |
Monocarboxylate transporter 8 deficiency | Is a | True | X-linked hereditary spastic paraplegia | Inferred relationship | Existential restriction modifier | |
X-linked complex hereditary spastic paraplegia | Is a | True | X-linked hereditary spastic paraplegia | Inferred relationship | Existential restriction modifier | |
X-linked pure hereditary spastic paraplegia | Is a | True | X-linked hereditary spastic paraplegia | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets