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 |
| 3463894016 | Deletion of part of chromosome 21 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3463895015 | Deletion of part of chromosome 21 | 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 21 (disorder) | est un(e) (attribut) | anomalie du chromosome 21 | true | Inferred relationship | Some | ||
| Deletion of part of chromosome 21 (disorder) | est un(e) (attribut) | Deletion of part of autosome | true | Inferred relationship | Some | ||
| Deletion of part of chromosome 21 (disorder) | morphologie associée (attribut) | Partial monosomy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Deletion of part of chromosome 21 (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Deletion of part of chromosome 21 (disorder) | localisation d'une constatation (attribut) | Chromosome pair 21 (cell structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder) | est un(e) (attribut) | True | Deletion of part of chromosome 21 (disorder) | Inferred relationship | Some | |
| 21q22.11q22.12 microdeletion syndrome | est un(e) (attribut) | False | Deletion of part of chromosome 21 (disorder) | Inferred relationship | Some | |
| Distal deletion of chromosome 21 | est un(e) (attribut) | True | Deletion of part of chromosome 21 (disorder) | Inferred relationship | Some | |
| Proximal deletion of chromosome 21 (disorder) | est un(e) (attribut) | True | Deletion of part of chromosome 21 (disorder) | Inferred relationship | Some | |
| 21q partial monosomy syndrome | est un(e) (attribut) | True | Deletion of part of chromosome 21 (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR