Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303486014 | Polydactyly of triphalangeal thumb (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3303487017 | Polydactyly of triphalangeal thumb | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401043011 | Polydactyly of a triphalangeal thumb or PPD2 is a form of preaxial polydactyly of fingers, a limb malformation syndrome, that is characterized by the presence of a usually opposable triphalangeal thumb with or without additional duplication of one or more skeletal components of the thumb. The thumb appearance can differ widely in shape (wedge to rectangular) or it can be deviated in the radio-ulnar plane (clinodactyly). PPD2 is also associated with systemic syndromes, including Holt-Oram syndrome and Fanconi anemia. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401044017 | Polydactyly of a triphalangeal thumb or PPD2 is a form of preaxial polydactyly of fingers, a limb malformation syndrome, that is characterised by the presence of a usually opposable triphalangeal thumb with or without additional duplication of one or more skeletal components of the thumb. The thumb appearance can differ widely in shape (wedge to rectangular) or it can be deviated in the radio-ulnar plane (clinodactyly). PPD2 is also associated with systemic syndromes, including Holt-Oram syndrome and Fanconi anaemia. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Polydactyly of triphalangeal thumb (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Polydactyly of triphalangeal thumb (disorder) | Is a | Triphalangeal thumb | true | Inferred relationship | Some | ||
Polydactyly of triphalangeal thumb (disorder) | Associated morphology | Supernumerary structure | false | Inferred relationship | Some | 2 | |
Polydactyly of triphalangeal thumb (disorder) | Finding site | Thumb structure | false | Inferred relationship | Some | 2 | |
Polydactyly of triphalangeal thumb (disorder) | Associated morphology | Supernumerary structure | false | Inferred relationship | Some | 3 | |
Polydactyly of triphalangeal thumb (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Polydactyly of triphalangeal thumb (disorder) | Finding site | Digit structure | false | Inferred relationship | Some | 3 | |
Polydactyly of triphalangeal thumb (disorder) | Associated morphology | Supernumerary structure | true | Inferred relationship | Some | 1 | |
Polydactyly of triphalangeal thumb (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Polydactyly of triphalangeal thumb (disorder) | Finding site | Thumb structure | false | Inferred relationship | Some | 1 | |
Polydactyly of triphalangeal thumb (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Polydactyly of triphalangeal thumb (disorder) | Finding site | Bone structure of phalanx of thumb | true | Inferred relationship | Some | 1 | |
Polydactyly of triphalangeal thumb (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Polydactyly of triphalangeal thumb (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Polydactyly of bilateral triphalangeal thumbs (disorder) | Is a | True | Polydactyly of triphalangeal thumb (disorder) | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)