Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 143065010 | Achondroplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 143066011 | Chondrodystrophia fetalis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 143067019 | Achondroplastic dwarf | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 143068012 | Chondrodystrophia foetalis | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 143069016 | Osteosclerosis congenita | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 143070015 | Congenital osteosclerosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4436721000168112 | Chondrodystrophia foetalis | en | Synonym | Active | Case insensitive | SNOMED Clinical Terms Australian extension |
| 507012010 | Achondroplastic dwarfism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 828495014 | Achondroplasia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Short-limb skeletal dysplasia with severe combined immunodeficiency | Is a | False | Achondroplasia | Inferred relationship | Some | |
| Severe achondroplasia, developmental delay, acanthosis nigricans syndrome | Is a | True | Achondroplasia | Inferred relationship | Some | |
| Severe achondrolasia with developmental delay and acanthosis nigricans | Is a | False | Achondroplasia | Inferred relationship | Some | |
| Family history of achondroplasia | Associated finding | True | Achondroplasia | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set