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 |
| 3448853019 | Deletion of part of chromosome 19 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3448854013 | Deletion of part of chromosome 19 | 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 19 (disorder) | est un(e) (attribut) | Anomaly of chromosome pair 19 | true | Inferred relationship | Some | ||
| Deletion of part of chromosome 19 (disorder) | est un(e) (attribut) | Deletion of part of autosome | true | Inferred relationship | Some | ||
| Deletion of part of chromosome 19 (disorder) | morphologie associée (attribut) | Partial monosomy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Deletion of part of chromosome 19 (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Deletion of part of chromosome 19 (disorder) | localisation d'une constatation (attribut) | Chromosome pair 19 (cell structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 19p13.12 microdeletion syndrome (disorder) | est un(e) (attribut) | False | Deletion of part of chromosome 19 (disorder) | Inferred relationship | Some | |
| 19q13.11 microdeletion syndrome (disorder) | est un(e) (attribut) | False | Deletion of part of chromosome 19 (disorder) | Inferred relationship | Some | |
| Deletion of long arm of chromosome 19 (disorder) | est un(e) (attribut) | True | Deletion of part of chromosome 19 (disorder) | Inferred relationship | Some | |
| Deletion of short arm of chromosome 19 (disorder) | est un(e) (attribut) | True | Deletion of part of chromosome 19 (disorder) | Inferred relationship | Some | |
| 19p13.13 microdeletion syndrome (disorder) | est un(e) (attribut) | False | Deletion of part of chromosome 19 (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR