Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3076152012 | Family history of single congenital anomaly | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3076184017 | Family history of single congenital anomaly (situation) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Family history of single congenital anomaly | Is a | Family history of development disorder | true | Inferred relationship | Some | ||
| Family history of single congenital anomaly | Subject relationship context | Person in the family | true | Inferred relationship | Some | 1 | |
| Family history of single congenital anomaly | Is a | Family history of congenital disease | true | Inferred relationship | Some | ||
| Family history of single congenital anomaly | Associated finding | Congenital anomaly | true | Inferred relationship | Some | 1 | |
| Family history of single congenital anomaly | Subject relationship context | Person in family of subject | false | Inferred relationship | Some | 1 | |
| Family history of single congenital anomaly | Temporal context | Current or past | true | Inferred relationship | Some | 1 | |
| Family history of single congenital anomaly | Finding context | Known present | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Situation with explicit context foundation reference set
Problem/Diagnosis reference set
FHIR