Status: current, Defined. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1495220017 | Hereditary multiple exostosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2475975012 | Osteochondromatosis syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
2475976013 | Osteochondromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2475977016 | Diaphyseal aclasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
2475978014 | Multiple osteochondromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2475979018 | Multiple exostoses type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
378184019 | Multiple congenital exostosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
644882012 | Multiple congenital exostosis (disorder) | en | Fully specified name | Active | Case insensitive | 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
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set