Status: retired, Primitive. Date: 31-Jan 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 208373012 | Congenital dystrophia brevicollis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 208374018 | Bonnevie-Ullrich and Klippel-Feil syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 208375017 | Klippel-Feil and Turner syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 208376016 | Nielsen's disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 733732016 | Congenital dystrophia brevicollis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital dystrophia brevicollis | Is a | Autosomal hereditary disorder | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set
FHIR