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 |
| 3464780015 | Deletion of part of short arm of chromosome 17 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3464781016 | Deletion of part of short arm of chromosome 17 | 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 |
| Deletion of part of short arm of chromosome 17 (disorder) | Is a | Deletion of part of chromosome 17 (disorder) | true | Inferred relationship | Some | ||
| Deletion of part of short arm of chromosome 17 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Deletion of part of short arm of chromosome 17 (disorder) | Finding site | Chromosome pair 17 | true | Inferred relationship | Some | 2 | |
| Deletion of part of short arm of chromosome 17 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
| Deletion of part of short arm of chromosome 17 (disorder) | Finding site | Chromosome pair 17 | true | Inferred relationship | Some | 3 | |
| Deletion of part of short arm of chromosome 17 (disorder) | Associated morphology | Partial monosomy (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
| Deletion of part of short arm of chromosome 17 (disorder) | Associated morphology | Deletion of short arm | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Distal 17p13.3 microdeletion syndrome | Is a | True | Deletion of part of short arm of chromosome 17 (disorder) | Inferred relationship | Some | |
| Distal 17p13.1 microdeletion syndrome (disorder) | Is a | True | Deletion of part of short arm of chromosome 17 (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR