Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3700734011 | Crossed polysyndactyly (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3700735012 | Crossed polysyndactyly | en | Synonym | Active | Case insensitive | SNOMED CT core |
3700736013 | A rare genetic congenital limb malformation disorder with characteristics of unilateral or bilateral postaxial polydactyly in the hands and preaxial polydactyly in the feet, associated with bilateral cutaneous syndactyly of first, second and third toes. Cutaneous syndactyly in hands has also been reported in some patients. There have been no further descriptions in the literature since 1994. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Crossed polysyndactyly | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Crossed polysyndactyly | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Crossed polysyndactyly | Is a | Polysyndactyly | true | Inferred relationship | Some | ||
Crossed polysyndactyly | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Crossed polysyndactyly | Finding site | Digit structure | true | Inferred relationship | Some | 2 | |
Crossed polysyndactyly | Finding site | Digit structure | true | Inferred relationship | Some | 1 | |
Crossed polysyndactyly | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Crossed polysyndactyly | Associated morphology | Congenital abnormal fusion | true | Inferred relationship | Some | 2 | |
Crossed polysyndactyly | Associated morphology | Supernumerary 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
Problem/Diagnosis reference set