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 |
3759925010 | Paternal uniparental disomy of chromosome X | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3759926011 | UPD(X)pat - paternal uniparental disomy of chromosome X | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3759927019 | Paternal uniparental disomy of chromosome X (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Paternal uniparental disomy of chromosome X | Is a | Anomaly of chromosome X | true | Inferred relationship | Existential restriction modifier | ||
Paternal uniparental disomy of chromosome X | Is a | Uniparental disomy of paternal origin | true | Inferred relationship | Existential restriction modifier | ||
Paternal uniparental disomy of chromosome X | Associated morphology | Alteration of chromosome structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Paternal uniparental disomy of chromosome X | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Paternal uniparental disomy of chromosome X | Finding site | Sex chromosome X | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets