Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3438781019 | Family history of hemoglobinopathy E (situation) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 3438782014 | Family history of hemoglobinopathy E | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3438783016 | Family history of hemoglobin E disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3438784010 | Family history of haemoglobinopathy E | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3438785011 | Family history of haemoglobin E disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Family history of haemoglobinopathy E | Subject relationship context | Person in the family | true | Inferred relationship | Some | 1 | |
| Family history of haemoglobinopathy E | Is a | Family history of hereditary disease | true | Inferred relationship | Some | ||
| Family history of haemoglobinopathy E | Is a | Family history of haemoglobinopathy | true | Inferred relationship | Some | ||
| Family history of haemoglobinopathy E | Associated finding | Haemoglobin E disease | true | Inferred relationship | Some | 1 | |
| Family history of haemoglobinopathy E | Finding context | Known present | true | Inferred relationship | Some | 1 | |
| Family history of haemoglobinopathy E | Temporal context | Current or past | true | Inferred relationship | Some | 1 | |
| Family history of haemoglobinopathy E | Subject relationship context | Person in family of subject | false | Inferred relationship | Some | 1 | |
| Family history of haemoglobinopathy E | Is a | Family history of congenital disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Situation with explicit context foundation reference set
Problem/Diagnosis reference set
FHIR