Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | Reference Sets |
| 3467197014 | Family history of multiple congenital anomalies (situation) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
| 3467198016 | Family history of multiple congenital anomalies | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
| 4811911000052115 | familjeanamnes på multipla kongenitala anomalier | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) | Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Family history of multiple congenital anomalies (situation) | Is a | FH: Congenital anomaly | true | Inferred relationship | Some | ||
| Family history of multiple congenital anomalies (situation) | Associated finding | Congenital malformation syndrome (disorder) | true | Inferred relationship | Some | 1 | |
| Family history of multiple congenital anomalies (situation) | Finding context (attribute) | Known present (qualifier value) | true | Inferred relationship | Some | 1 | |
| Family history of multiple congenital anomalies (situation) | Temporal context (attribute) | Current or past (actual) (qualifier value) | true | Inferred relationship | Some | 1 | |
| Family history of multiple congenital anomalies (situation) | Subject relationship context (attribute) | Person in family of subject (person) | true | Inferred relationship | Some | 1 | |
| Family history of multiple congenital anomalies (situation) | Is a | Family history of development disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Family history of Steinert myotonic dystrophy (situation) | Is a | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some | |
| Family history of Prader-Willi syndrome | Is a | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some | |
| Family history of fragile X syndrome (situation) | Is a | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some | |
| Family history of Cowden syndrome (situation) | Is a | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some | |
| Family history of achondroplasia (situation) | Is a | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR