Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
400926013 | Multiple enchondromata | en | Synonym | Active | Case insensitive | SNOMED CT core |
400927016 | Congenital enchondromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
400928014 | Ollier disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
400929018 | Dyschondroplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
400930011 | Ollier's disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
400931010 | Enchondromatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
660995016 | Enchondromatosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Metachondromatosis | Is a | True | Enchondromatosis | Inferred relationship | Some | |
Maffucci syndrome | Is a | True | Enchondromatosis | Inferred relationship | Some | |
Bone dysplasia Azouz type | Is a | False | Enchondromatosis | Inferred relationship | Some | |
Dysspondyloenchondromatosis | Is a | True | Enchondromatosis | Inferred relationship | Some | |
Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria | Is a | True | Enchondromatosis | Inferred relationship | Some | |
Cheirospondyloenchondromatosis | Is a | True | Enchondromatosis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set