Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4166865010 | Paternal uniparental disomy of chromosome 14 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4167334019 | Uniparental disomy of paternal origin of chromosome 14 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4167335018 | Uniparental disomy of paternal origin of chromosome 14 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Paternal uniparental disomy of chromosome 14 | Is a | Anomaly of chromosome pair 14 | true | Inferred relationship | Some | ||
| Paternal uniparental disomy of chromosome 14 | Is a | Uniparental disomy of paternal origin | true | Inferred relationship | Some | ||
| Paternal uniparental disomy of chromosome 14 | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Paternal uniparental disomy of chromosome 14 | Finding site | Chromosome pair 14 | true | Inferred relationship | Some | 1 | |
| Paternal uniparental disomy of chromosome 14 | Associated morphology | Alteration of chromosome structure | 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