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 |
| 3448857018 | Deletion of short arm of chromosome 19 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3448858011 | Deletion of short arm of chromosome 19 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4000091000052119 | deletion av den korta armen på kromosom 19 | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deletion of short arm of chromosome 19 (disorder) | Is a | Deletion of part of chromosome 19 (disorder) | true | Inferred relationship | Some | ||
| Deletion of short arm of chromosome 19 (disorder) | Associated morphology | Deletion of short arm | true | Inferred relationship | Some | 2 | |
| Deletion of short arm of chromosome 19 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Deletion of short arm of chromosome 19 (disorder) | Finding site | Short arm of chromosome | false | Inferred relationship | Some | 2 | |
| Deletion of short arm of chromosome 19 (disorder) | Associated morphology | Partial monosomy (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
| Deletion of short arm of chromosome 19 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
| Deletion of short arm of chromosome 19 (disorder) | Finding site | Chromosome pair 19 | true | Inferred relationship | Some | 3 | |
| Deletion of short arm of chromosome 19 (disorder) | Finding site | Chromosome pair 19 | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 19p13.13 microdeletion syndrome (disorder) | Is a | True | Deletion of short arm of chromosome 19 (disorder) | Inferred relationship | Some | |
| Distal monosomy 19p13.3 (disorder) | Is a | True | Deletion of short arm of chromosome 19 (disorder) | Inferred relationship | Some | |
| 19p13.12 microdeletion syndrome (disorder) | Is a | True | Deletion of short arm of chromosome 19 (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR