Status: retired, Primitive. Date: 31-Jul 2004. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
140678013 | Multiple exostoses syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
140679017 | Diaphyseal aclasis, external chondromatosis syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
506254014 | Diaphyseal aclasis | en | Synonym | Active | Case insensitive | SNOMED CT core |
506255010 | Osteochondromatosis syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
506256011 | Multiple cartilaginous exostoses | en | Synonym | Active | Case insensitive | SNOMED CT core |
506257019 | Hereditary deforming chondrodysplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
826783019 | Multiple exostoses syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Multiple exostoses syndrome | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Multiple exostoses syndrome | Is a | Disorganised development of cartilaginous and fibrous components of the skeleton | false | Inferred relationship | Some | ||
Multiple exostoses syndrome | Associated morphology | Dysplasia | false | Inferred relationship | Some | 1 | |
Multiple exostoses syndrome | Finding site | Skeletal system structure | false | Inferred relationship | Some | 1 | |
Multiple exostoses syndrome | Occurrence | Congenital | false | Inferred relationship | Some | ||
Multiple exostoses syndrome | Finding site | Bone structure | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian dialect reference set
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set