Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4589774017 | Duplication of part of short arm of chromosome 16 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4589775016 | Partial duplication of short arm of chromosome 16 | 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 |
Duplication of part of short arm of chromosome 16 (disorder) | est un(e) (attribut) | Partial trisomy of chromosome 16 | true | Inferred relationship | Some | ||
Duplication of part of short arm of chromosome 16 (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
Duplication of part of short arm of chromosome 16 (disorder) | localisation d'une constatation (attribut) | Short arm of chromosome (cell structure) | true | Inferred relationship | Some | 1 | |
Duplication of part of short arm of chromosome 16 (disorder) | morphologie associée (attribut) | Partial trisomy | true | Inferred relationship | Some | 1 | |
Duplication of part of short arm of chromosome 16 (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 2 | |
Duplication of part of short arm of chromosome 16 (disorder) | localisation d'une constatation (attribut) | Chromosome pair 16 (cell structure) | true | Inferred relationship | Some | 2 | |
Duplication of part of short arm of chromosome 16 (disorder) | morphologie associée (attribut) | Partial trisomy | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Proximal 16p11.2 microduplication syndrome (disorder) | est un(e) (attribut) | True | Duplication of part of short arm of chromosome 16 (disorder) | Inferred relationship | Some | |
16p13.11 microduplication syndrome (disorder) | est un(e) (attribut) | True | Duplication of part of short arm of chromosome 16 (disorder) | Inferred relationship | Some | |
16p13.3 microduplication syndrome | est un(e) (attribut) | True | Duplication of part of short arm of chromosome 16 (disorder) | Inferred relationship | Some | |
syndrome de microduplication 16p11.2p12.2 | est un(e) (attribut) | True | Duplication of part of short arm of chromosome 16 (disorder) | Inferred relationship | Some |
This concept is not in any reference sets