Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3499394011 | Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3499395012 | Exostosis, anetoderma, brachydactyly type E syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3633708016 | Exostosis, anetodermia, brachydactyly type E syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3499987016 | An association reported in a single kindred with characteristics of the variable presence of the following features: anetoderma (macular atrophy of the skin), multiple exostoses and brachydactyly type E. There have been no further descriptions in the literature since 1985. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Disorganized development of cartilaginous and fibrous components of the skeleton | true | Inferred relationship | Some | ||
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Connective tissue hereditary disorder (disorder) | true | Inferred relationship | Some | ||
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 2 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Finding site | Bone structure | false | Inferred relationship | Some | 2 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Finding site | Cartilage structure (body structure) | true | Inferred relationship | Some | 2 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Osteochondropathy | true | Inferred relationship | Some | ||
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 2 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Congenital anomaly of skeletal bone | true | Inferred relationship | Some | ||
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 3 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Associated morphology | Focal atrophy with macular pattern (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Congenital anomaly of skin | true | Inferred relationship | Some | ||
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) | Is a | Anetoderma | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets