Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 250097016 | FH: Congenital GIT anomaly | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| 541333015 | Family history: Congenital gastrointestinal tract anomaly (context-dependent category) | en | Fully specified name | Inactive | Only initial character case insensitive | SNOMED CT core module | 
| 2607189019 | Family history: Congenital gastrointestinal tract anomaly (situation) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module | 
| 2667860012 | Family history: Congenital gastrointestinal tract anomaly | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Family history of Cowden syndrome | Is a | True | Family history: Congenital gastrointestinal tract anomaly | Inferred relationship | Existential restriction modifier | 
This concept is not in any reference sets