Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4166863015 | Paternal uniparental disomy of chromosome 15 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4167336017 | Uniparental disomy of paternal origin of chromosome 15 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4167337014 | Uniparental disomy of paternal origin of chromosome 15 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Paternal uniparental disomy of chromosome 15 | Is a | Uniparental disomy of paternal origin | true | Inferred relationship | Some | ||
| Paternal uniparental disomy of chromosome 15 | Is a | Anomaly of chromosome pair 15 | true | Inferred relationship | Some | ||
| Paternal uniparental disomy of chromosome 15 | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Paternal uniparental disomy of chromosome 15 | Associated morphology | Alteration of chromosome structure | true | Inferred relationship | Some | 1 | |
| Paternal uniparental disomy of chromosome 15 | Finding site | Chromosome pair 15 | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR