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 |
3755238016 | UPD(22)mat - maternal uniparental disomy of chromosome 22 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3755239012 | Maternal uniparental disomy of chromosome 22 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3755240014 | Maternal uniparental disomy of chromosome 22 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Maternal uniparental disomy of chromosome 22 | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Maternal uniparental disomy of chromosome 22 | Associated morphology | Alteration of chromosome structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Maternal uniparental disomy of chromosome 22 | Is a | Anomaly of chromosome pair 22 | true | Inferred relationship | Existential restriction modifier | ||
Maternal uniparental disomy of chromosome 22 | Is a | Uniparental disomy of maternal origin | true | Inferred relationship | Existential restriction modifier | ||
Maternal uniparental disomy of chromosome 22 | Finding site | Chromosome pair 22 | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets