Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3467197014 | Family history of multiple congenital anomalies (situation) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3467198016 | Family history of multiple congenital anomalies | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Family history of multiple congenital anomalies | Is a | Family history of development disorder | true | Inferred relationship | Some | ||
| Family history of multiple congenital anomalies | Subject relationship context | Person in the family | true | Inferred relationship | Some | 1 | |
| Family history of multiple congenital anomalies | Is a | Family history of congenital disease | true | Inferred relationship | Some | ||
| Family history of multiple congenital anomalies | Associated finding | Congenital malformation syndrome | true | Inferred relationship | Some | 1 | |
| Family history of multiple congenital anomalies | Finding context | Known present | true | Inferred relationship | Some | 1 | |
| Family history of multiple congenital anomalies | Temporal context | Current or past | true | Inferred relationship | Some | 1 | |
| Family history of multiple congenital anomalies | Subject relationship context | Person in family of subject | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Family history of achondroplasia | Is a | True | Family history of multiple congenital anomalies | Inferred relationship | Some | |
| Family history of Steinert myotonic dystrophy | Is a | False | Family history of multiple congenital anomalies | Inferred relationship | Some | |
| Family history of Prader-Willi syndrome | Is a | True | Family history of multiple congenital anomalies | Inferred relationship | Some | |
| Family history of fragile X syndrome | Is a | True | Family history of multiple congenital anomalies | Inferred relationship | Some | |
| Family history of Cowden syndrome | Is a | True | Family history of multiple congenital anomalies | Inferred relationship | Some |
Reference Sets
Situation with explicit context foundation reference set
Problem/Diagnosis reference set
FHIR