Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3448831016 | Deletion of part of chromosome 11 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3448832011 | Deletion of part of chromosome 11 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deletion of part of chromosome 11 (disorder) | est un(e) (attribut) | Anomaly of chromosome pair 11 | true | Inferred relationship | Some | ||
| Deletion of part of chromosome 11 (disorder) | est un(e) (attribut) | Deletion of part of autosome | true | Inferred relationship | Some | ||
| Deletion of part of chromosome 11 (disorder) | morphologie associée (attribut) | Partial monosomy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Deletion of part of chromosome 11 (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Deletion of part of chromosome 11 (disorder) | localisation d'une constatation (attribut) | Chromosome pair 11 (cell structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 11p partial monosomy syndrome (disorder) | est un(e) (attribut) | True | Deletion of part of chromosome 11 (disorder) | Inferred relationship | Some | |
| 11q partial monosomy syndrome (disorder) | est un(e) (attribut) | True | Deletion of part of chromosome 11 (disorder) | Inferred relationship | Some | |
| Distal partial deletion of long arm of chromosome 11 (disorder) | est un(e) (attribut) | True | Deletion of part of chromosome 11 (disorder) | Inferred relationship | Some | |
| Oculootodental syndrome | est un(e) (attribut) | True | Deletion of part of chromosome 11 (disorder) | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR