Status: current, Not sufficiently defined by necessary conditions definition status. Date: 01-Oct 2019. Module: SNOMED CT United Kingdom clinical extension module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1858221000000114 | Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT United Kingdom clinical extension module |
| 1858231000000111 | Antenatal screening combined ultrasound and blood test for Down's, Edwards' and Patau's syndromes done | en | Synonym | Active | Only initial character case insensitive | SNOMED CT United Kingdom clinical extension module |
| 1858281000000110 | Antenatal screening combined test for Down's, Edwards' and Patau's syndromes done | en | Synonym | Active | Only initial character case insensitive | SNOMED CT United Kingdom clinical extension module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Temporal context | Current or specified time | true | Inferred relationship | Existential restriction modifier | 1 | |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Associated procedure | Antenatal screening blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes (procedure) | true | Inferred relationship | Existential restriction modifier | 1 | |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Procedure context | Done | true | Inferred relationship | Existential restriction modifier | 1 | |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Subject relationship context | Subject of record | true | Inferred relationship | Existential restriction modifier | 1 | |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Temporal context | Current or specified time | true | Inferred relationship | Existential restriction modifier | 2 | |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Associated procedure | Antenatal screening blood test for Down, Edwards and Patau syndromes (procedure) | false | Inferred relationship | Existential restriction modifier | 1 | |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Subject relationship context | Subject of record | true | Inferred relationship | Existential restriction modifier | 2 | |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Is a | Procedure carried out on subject | true | Inferred relationship | Existential restriction modifier | ||
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Associated procedure | Ultrasound scan for fetal nuchal translucency | true | Inferred relationship | Existential restriction modifier | 2 | |
| Antenatal screening combined ultrasound and blood test for complete trisomy 21, complete trisomy 18 and complete trisomy 13 syndromes done (situation) | Procedure context | Done | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR