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 |
| 1858861000000117 | National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant of unknown clinical significance (situation) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT United Kingdom clinical extension module |
| 1858871000000112 | NHS Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant of unknown clinical significance | en | Synonym | Active | Entire term case sensitive | SNOMED CT United Kingdom clinical extension module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant of unknown clinical significance (situation) | Subject relationship context | Subject of record | true | Inferred relationship | Existential restriction modifier | 1 | |
| National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant of unknown clinical significance (situation) | Temporal context | Current or specified time | true | Inferred relationship | Existential restriction modifier | 1 | |
| National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant of unknown clinical significance (situation) | Finding context | Probably present | true | Inferred relationship | Existential restriction modifier | 1 | |
| National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant of unknown clinical significance (situation) | Associated finding | Homozygous hemoglobinopathy | true | Inferred relationship | Existential restriction modifier | 1 | |
| National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant of unknown clinical significance (situation) | Is a | Possible clinical finding | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR