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 |
| 3467197014 | Family history of multiple congenital anomalies (situation) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3467198016 | Family history of multiple congenital anomalies | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Family history of achondroplasia (situation) | est un(e) (attribut) | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some | |
| Family history of Steinert myotonic dystrophy (situation) | est un(e) (attribut) | False | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some | |
| Family history of Prader-Willi syndrome | est un(e) (attribut) | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some | |
| Family history of fragile X syndrome (situation) | est un(e) (attribut) | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some | |
| Family history of Cowden syndrome (situation) | est un(e) (attribut) | True | Family history of multiple congenital anomalies (situation) | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR