Status: current, Not sufficiently defined by necessary conditions definition status. Date: 01-Jun 2019. Module: SNOMED CT United Kingdom clinical extension module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1624401000000116 | Childhood onset hereditary spastic paraplegia germline WGS (whole genome sequencing) targeting childhood onset hereditary spastic paraplegia panel | en | Synonym | Active | Only initial character case insensitive | SNOMED CT United Kingdom clinical extension module |
| 1624411000000119 | Germline whole genome sequencing targeting childhood onset hereditary spastic paraplegia panel for childhood onset hereditary spastic paraplegia (procedure) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT United Kingdom clinical extension module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Germline whole genome sequencing targeting childhood onset hereditary spastic paraplegia panel for childhood onset hereditary spastic paraplegia (procedure) | Is a | Germline whole genome sequencing targeting childhood onset hereditary spastic paraplegia panel (procedure) | true | Inferred relationship | Existential restriction modifier | ||
| Germline whole genome sequencing targeting childhood onset hereditary spastic paraplegia panel for childhood onset hereditary spastic paraplegia (procedure) | Method | Evaluation - action | false | Inferred relationship | Existential restriction modifier | ||
| Germline whole genome sequencing targeting childhood onset hereditary spastic paraplegia panel for childhood onset hereditary spastic paraplegia (procedure) | Method | Evaluation - action | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR