Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3424651015 | Polydactyly of index finger (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3424652010 | Polydactyly of index finger | en | Synonym | Active | Case insensitive | SNOMED CT core |
3424653017 | Preaxial polydactyly type 3 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3424654011 | PPD3- preaxial polydactyly type 3 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3424655012 | A limb malformation syndrome, where the thumb is replaced by one or two triphalangeal digits with dermatoglyphic pattern specific of the index finger. Two forms of PPD3 have been described, unilateral and bilateral. There have been no further descriptions in the literature since 1962. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Polydactyly of index finger | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Polydactyly of index finger | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Polydactyly of index finger | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Polydactyly of index finger | Is a | Polydactyly of fingers | true | Inferred relationship | Some | ||
Polydactyly of index finger | Associated morphology | Supernumerary structure | true | Inferred relationship | Some | 1 | |
Polydactyly of index finger | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Polydactyly of index finger | Finding site | Index 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
Problem/Diagnosis reference set