Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3661199014 | Maternal uniparental disomy of chromosome 4 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3661200012 | Maternal uniparental disomy of chromosome 4 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3661201011 | Maternal uniparental disomy of chromosome 4 is an uniparental disomy of maternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only mother is a carrier. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4142301000052110 | maternell uniparental disomi i kromosom 4 | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Maternal uniparental disomy of chromosome 4 | Is a | Uniparental disomy of maternal origin (disorder) | true | Inferred relationship | Some | ||
| Maternal uniparental disomy of chromosome 4 | Associated morphology | Alteration of chromosome structure | true | Inferred relationship | Some | 1 | |
| Maternal uniparental disomy of chromosome 4 | Finding site | Chromosome pair 4 | true | Inferred relationship | Some | 1 | |
| Maternal uniparental disomy of chromosome 4 | Is a | Anomaly of chromosome pair 4 | true | Inferred relationship | Some | ||
| Maternal uniparental disomy of chromosome 4 | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR