Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3701938013 | Paternal uniparental disomy of chromosome 6 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3701939017 | Paternal uniparental disomy of chromosome 6 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3701940015 | Paternal uniparental disomy of chromosome 6 is a uniparental disomy of paternal origin with characteristics of intrauterine growth retardation, transient neonatal diabetes mellitus, and macroglossia. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Paternal uniparental disomy of chromosome 6 | Finding site | Chromosome pair 6 | true | Inferred relationship | Some | 1 | |
| Paternal uniparental disomy of chromosome 6 | Associated morphology | Alteration of chromosome structure | true | Inferred relationship | Some | 1 | |
| Paternal uniparental disomy of chromosome 6 | Is a | Anomaly of chromosome pair 6 | true | Inferred relationship | Some | ||
| Paternal uniparental disomy of chromosome 6 | Is a | Uniparental disomy of paternal origin | true | Inferred relationship | Some | ||
| Paternal uniparental disomy of chromosome 6 | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR