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 |
| 3498318018 | Partial trisomy of chromosome 18 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3498319014 | Partial trisomy of chromosome 18 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3498320015 | Duplication of chromosome 18 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3999721000052118 | partiell trisomi av kromosom 18 | 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 |
| Partial trisomy of chromosome 18 (disorder) | Is a | Anomaly of chromosome pair 18 | true | Inferred relationship | Some | ||
| Partial trisomy of chromosome 18 (disorder) | Is a | Trisomy and partial trisomy of autosome | true | Inferred relationship | Some | ||
| Partial trisomy of chromosome 18 (disorder) | Associated morphology | Partial trisomy | true | Inferred relationship | Some | 1 | |
| Partial trisomy of chromosome 18 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Partial trisomy of chromosome 18 (disorder) | Finding site | Chromosome pair 18 | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 18p partial trisomy syndrome | Is a | True | Partial trisomy of chromosome 18 (disorder) | Inferred relationship | Some | |
| 18q partial trisomy syndrome | Is a | True | Partial trisomy of chromosome 18 (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR