Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303372011 | Multiple epiphyseal dysplasia type 4 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3303373018 | Multiple epiphyseal dysplasia type 4 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303374012 | Autosomal recessive multiple epiphyseal dysplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303375013 | A multiple epiphyseal dysplasia with a late-childhood onset manifesting as joint pain involving hips, knees, wrists and fingers with occasional limitation of joint movements, deformity of hands, feet, and knees, scoliosis and slightly reduced adult height. Follows an autosomal recessive mode of transmission | en | Definition | Active | Case sensitive | 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
Problem/Diagnosis reference set