Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4669928018 | Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4669929014 | Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
4669930016 | A rare genetic syndrome with limb malformations as a major feature with characteristics of preaxial polydactyly of the hands and feet with variable phenotypic expressivity in combination with hypertrichosis extending from the posterior hairline to the middle of the back. Reported limb malformations include triphalangeal thumbs, duplicated thumbs, preaxial extra ray and syndactyly between digits I and II in the hands, large or duplicated hallux and syndactyly between toes I and II in the feet. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Is a | Dysostosis | true | Inferred relationship | Some | ||
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Is a | Hypertrichosis | true | Inferred relationship | Some | ||
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Is a | Polydactyly | true | Inferred relationship | Some | ||
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Is a | Multiple malformation syndrome with limb defect as major feature | true | Inferred relationship | Some | ||
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Finding site | Bone structure of extremity | true | Inferred relationship | Some | 1 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Finding site | Digit structure | true | Inferred relationship | Some | 3 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Associated morphology | Supernumerary structure | true | Inferred relationship | Some | 3 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Finding site | Hair structure | true | Inferred relationship | Some | 2 | |
Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome | Associated morphology | Growth alteration | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set