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 |
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