Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3311431011 | Recombinant chromosome 8 syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3311432016 | Recombinant chromosome 8 syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3311433014 | San Luis Valley syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3311434015 | Recombinant 8 syndrome, also known as San Luis Valley syndrome, is a complex chromosomal disorder that is due to a parental pericentric inversion of chromosome 8 with characteristics of major congenital heart anomalies, urogenital malformations, moderate to severe intellectual deficiency and mild craniofacial dysmorphism. The prevalence is unknown but the syndrome is rare. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Recombinant chromosome 8 syndrome (disorder) | est un(e) (attribut) | anomalie du chromosome 8 (trouble) | true | Inferred relationship | Some | ||
| Recombinant chromosome 8 syndrome (disorder) | morphologie associée (attribut) | Alteration of chromosome structure | true | Inferred relationship | Some | 1 | |
| Recombinant chromosome 8 syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Recombinant chromosome 8 syndrome (disorder) | localisation d'une constatation (attribut) | Chromosome pair 8 (cell structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR