Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3004433015 | Spinal dysraphism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3008898011 | Structural developmental anomalies of neurenteric canal (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3008993018 | Structural developmental anomalies of neuroenteric canal | en | Synonym (core metadata concept) | Inactive | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3009020016 | Structural developmental anomalies of neurenteric canal | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1995851000119115 | Spinal dysraphism (disorder) | en | Fully specified name | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Structural developmental anomalies of neurenteric canal (disorder) | Is a | Congenital malformation | true | Inferred relationship | Some | ||
| Structural developmental anomalies of neurenteric canal (disorder) | Is a | Disorder of embryonic structure (disorder) | true | Inferred relationship | Some | ||
| Structural developmental anomalies of neurenteric canal (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Structural developmental anomalies of neurenteric canal (disorder) | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 1 | |
| Structural developmental anomalies of neurenteric canal (disorder) | Finding site | Neurenteric canal | true | Inferred relationship | Some | 1 | |
| Structural developmental anomalies of neurenteric canal (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Structural developmental anomalies of neurenteric canal (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Primary tethered cord syndrome | Is a | True | Structural developmental anomalies of neurenteric canal (disorder) | Inferred relationship | Some | |
| Spina bifida aperta | Is a | True | Structural developmental anomalies of neurenteric canal (disorder) | Inferred relationship | Some | |
| Freeing of spinal tether | Has focus | True | Structural developmental anomalies of neurenteric canal (disorder) | Inferred relationship | Some | 2 |
| Repair of spinal dysraphism | Has focus | True | Structural developmental anomalies of neurenteric canal (disorder) | Inferred relationship | Some | 1 |
| Lipoma due to neurospinal dysraphism | Due to | True | Structural developmental anomalies of neurenteric canal (disorder) | Inferred relationship | Some | 2 |
| Dysraphism, cleft lip and palate, limb reduction defect syndrome | Is a | True | Structural developmental anomalies of neurenteric canal (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR