Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3322619019 | Aplasia of fibula and ectrodactyly syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3322620013 | Fibular aplasia and ectrodactyly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3322621012 | Familial ectrodactyly with fibular aplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3322622017 | Aplasia of fibula and ectrodactyly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3322623010 | This syndrome has characteristics of fibular aplasia and ectrodactyly. Less than 50 familial and sporadic cases have been reported in the literature. Shortening of the femur, a curved tibia, severe foot anomalies and pathologies of the hip, knee and ankle may also be present. The disorder is probably inherited as an autosomal dominant trait, with reduced penetrance, especially in females. | 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