Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303526013 | Syndactyly type 3 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3303527016 | Syndactyly type 3 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303528014 | Syndactyly of fingers 4 and 5 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303529018 | A rare congenital distal limb malformation with complete and bilateral syndactyly between the fourth and fifth fingers. In most cases, it is a soft tissue syndactyly, but occasionally the distal phalanges may be fused. The feet are not affected. Inherited in an autosomal dominant manner. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Syndactyly type 3 | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Syndactyly type 3 | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Syndactyly type 3 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Syndactyly type 3 | Is a | Syndactyly of fingers | true | Inferred relationship | Some | ||
Syndactyly type 3 | Associated morphology | Congenital abnormal fusion | true | Inferred relationship | Some | 1 | |
Syndactyly type 3 | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Syndactyly type 3 | Finding site | Finger structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set