Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3442323013 | Polydactyly of biphalangeal thumb (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3442324019 | Polydactyly of biphalangeal thumb | en | Synonym | Active | Case insensitive | SNOMED CT core |
3442325018 | PPD1 - preaxial polydactyly type 1 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3442326017 | The most common form of preaxial polydactyly of fingers, a limb malformation syndrome, with characteristics of duplication of one or more skeletal components of a biphalangeal thumb. Hands are preferentially affected and the right hand is more commonly involved than the left. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Polydactyly of biphalangeal thumb | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Polydactyly of biphalangeal thumb | Is a | Radial polydactyly | true | Inferred relationship | Some | ||
Polydactyly of biphalangeal thumb | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Polydactyly of biphalangeal thumb | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Polydactyly of biphalangeal thumb | Is a | Polydactyly of thumb | false | Inferred relationship | Some | ||
Polydactyly of biphalangeal thumb | Associated morphology | Supernumerary structure | true | Inferred relationship | Some | 1 | |
Polydactyly of biphalangeal thumb | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Polydactyly of biphalangeal thumb | Finding site | Thumb 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