Status: current, Defined. Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4589772018 | Duplication of part of short arm of chromosome 16 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4589774017 | Duplication of part of short arm of chromosome 16 | en | Synonym | Active | Case insensitive | SNOMED CT core |
4589775016 | Partial duplication of short arm of chromosome 16 | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Duplication of part of short arm of chromosome 16 | Is a | Partial trisomy of chromosome 16 | true | Inferred relationship | Some | ||
Duplication of part of short arm of chromosome 16 | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Duplication of part of short arm of chromosome 16 | Finding site | Short arm of chromosome | true | Inferred relationship | Some | 1 | |
Duplication of part of short arm of chromosome 16 | Associated morphology | Partial trisomy | true | Inferred relationship | Some | 1 | |
Duplication of part of short arm of chromosome 16 | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Duplication of part of short arm of chromosome 16 | Finding site | Chromosome pair 16 | true | Inferred relationship | Some | 2 | |
Duplication of part of short arm of chromosome 16 | Associated morphology | Partial trisomy | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Proximal 16p11.2 microduplication syndrome | Is a | True | Duplication of part of short arm of chromosome 16 | Inferred relationship | Some | |
16p13.11 microduplication syndrome | Is a | True | Duplication of part of short arm of chromosome 16 | Inferred relationship | Some | |
16p13.3 microduplication syndrome | Is a | True | Duplication of part of short arm of chromosome 16 | Inferred relationship | Some | |
16p11.2p12.2 microduplication syndrome | Is a | True | Duplication of part of short arm of chromosome 16 | Inferred relationship | Some |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set