Status: current, Primitive. Date: 31-Jan 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1463159012 | Congenital dystrophia brevicollis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
1483042010 | Congenital dystrophia brevicollis | en | Synonym | Active | Case insensitive | SNOMED CT core |
1493576014 | Nielsen's disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
1493577017 | Bonnevie-Ullrich and Klippel-Feil syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set