Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3755234019 | Maternal uniparental disomy of chromosome 21 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3755235018 | Maternal uniparental disomy of chromosome 21 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3755236017 | UPD(21)mat - maternal uniparental disomy of chromosome 21 | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3755237014 | Maternal uniparental disomy of chromosome 21 is a uniparental disomy of maternal origin that does not seem to have an adverse impact on the phenotype of an individual. There is a possibility of homozygosity for a recessive disease mutation for which the mother is a carrier and specific phenotype depends on the inherited disorder. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Maternal uniparental disomy of chromosome 21 | Is a | Anomaly of chromosome pair 21 | true | Inferred relationship | Some | ||
| Maternal uniparental disomy of chromosome 21 | Finding site | Chromosome pair 21 | true | Inferred relationship | Some | 1 | |
| Maternal uniparental disomy of chromosome 21 | Is a | Uniparental disomy of maternal origin | true | Inferred relationship | Some | ||
| Maternal uniparental disomy of chromosome 21 | Associated morphology | Alteration of chromosome structure | true | Inferred relationship | Some | 1 | |
| Maternal uniparental disomy of chromosome 21 | 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