Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4166871016 | Proximal duplication of long arm of chromosome 17 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4166872011 | Proximal duplication of long arm of chromosome 17 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4051001000172118 | proximale duplicatie van lange arm van chromosoom 17 | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Proximal duplication of long arm of chromosome 17 (disorder) | Is a | 17q partial trisomy syndrome | true | Inferred relationship | Some | ||
| Proximal duplication of long arm of chromosome 17 (disorder) | Finding site | Long arm of chromosome | true | Inferred relationship | Some | 1 | |
| Proximal duplication of long arm of chromosome 17 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Proximal duplication of long arm of chromosome 17 (disorder) | Associated morphology | Partial trisomy | true | Inferred relationship | Some | 1 | |
| Proximal duplication of long arm of chromosome 17 (disorder) | Finding site | Chromosome pair 17 | true | Inferred relationship | Some | 2 | |
| Proximal duplication of long arm of chromosome 17 (disorder) | Associated morphology | Partial trisomy | true | Inferred relationship | Some | 2 | |
| Proximal duplication of long arm of chromosome 17 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR