Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3662385016 | Paternal uniparental disomy of chromosome 21 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3662386015 | Paternal uniparental disomy of chromosome 21 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Paternal uniparental disomy of chromosome 21 | Finding site | Chromosome pair 21 | true | Inferred relationship | Existential restriction modifier | 1 | |
| Paternal uniparental disomy of chromosome 21 | Associated morphology | Alteration of chromosome structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Paternal uniparental disomy of chromosome 21 | Is a | Uniparental disomy of paternal origin | true | Inferred relationship | Existential restriction modifier | ||
| Paternal uniparental disomy of chromosome 21 | Is a | Anomaly of chromosome pair 21 | true | Inferred relationship | Existential restriction modifier | ||
| Paternal uniparental disomy of chromosome 21 | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR