Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2164905015 | Poland syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
63448017 | Poland anomaly | en | Synonym | Active | Case sensitive | SNOMED CT core |
63449013 | Poland anomalad | en | Synonym | Active | Case sensitive | SNOMED CT core |
63451012 | Unilateral defect of pectoralis muscle AND syndactyly of hand | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
773534012 | Poland anomaly (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3317334014 | Poland syndrome is marked by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand anomalies, including symbrachydactyly. Various anomalies of the breasts and nipples, and variable involvement of the hand and forearm (some patients having normal hands) have also been reported. The absence of other muscles around the shoulder girdle is a frequent feature. The syndrome is thought to be of vascular origin, for example a result of a disruption in the blood supply in the subclavian artery. Poland syndrome is most commonly a sporadic condition, but rare familial cases have been reported, compatible with an autosomal dominant mode of inheritance. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Craniofrontonasal dysplasia with Poland anomaly syndrome | Is a | True | Poland anomaly | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set