Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3448853019 | Deletion of part of chromosome 19 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3448854013 | Deletion of part of chromosome 19 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deletion of part of chromosome 19 | Is a | Anomaly of chromosome pair 19 | true | Inferred relationship | Existential restriction modifier | ||
| Deletion of part of chromosome 19 | Is a | Deletion of part of autosome | true | Inferred relationship | Existential restriction modifier | ||
| Deletion of part of chromosome 19 | Associated morphology | Partial monosomy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Deletion of part of chromosome 19 | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Deletion of part of chromosome 19 | Finding site | Chromosome pair 19 | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 19p13.12 microdeletion syndrome | Is a | False | Deletion of part of chromosome 19 | Inferred relationship | Existential restriction modifier | |
| 19q13.11 microdeletion syndrome | Is a | False | Deletion of part of chromosome 19 | Inferred relationship | Existential restriction modifier | |
| Deletion of long arm of chromosome 19 | Is a | True | Deletion of part of chromosome 19 | Inferred relationship | Existential restriction modifier | |
| Deletion of short arm of chromosome 19 | Is a | True | Deletion of part of chromosome 19 | Inferred relationship | Existential restriction modifier | |
| 19p13.13 microdeletion syndrome | Is a | False | Deletion of part of chromosome 19 | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR