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 |
| 3448833018 | Deletion of part of chromosome 12 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3448834012 | Deletion of part of chromosome 12 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3999971000052116 | deletion av del av kromosom 12 | 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 part of chromosome 12 (disorder) | Is a | Anomaly of chromosome pair 12 | true | Inferred relationship | Some | ||
| Deletion of part of chromosome 12 (disorder) | Is a | Deletion of part of autosome | true | Inferred relationship | Some | ||
| Deletion of part of chromosome 12 (disorder) | Associated morphology | Partial monosomy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Deletion of part of chromosome 12 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Deletion of part of chromosome 12 (disorder) | Finding site | Chromosome pair 12 | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| partiellt monosomi 12p-syndrom | Is a | False | Deletion of part of chromosome 12 (disorder) | Inferred relationship | Some | |
| Deletion of part of long arm of chromosome 12 (disorder) | Is a | True | Deletion of part of chromosome 12 (disorder) | Inferred relationship | Some | |
| Distal monosomy 12p | Is a | False | Deletion of part of chromosome 12 (disorder) | Inferred relationship | Some | |
| 12p12.1 microdeletion syndrome | Is a | False | Deletion of part of chromosome 12 (disorder) | Inferred relationship | Some | |
| Deletion of part of short arm of chromosome 12 (disorder) | Is a | True | Deletion of part of chromosome 12 (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR