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 |
3498441013 | Sillence syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3498442018 | Brachydactyly and distal symphalangism syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3498443011 | Brachydactyly and distal symphalangism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3499924013 | Syndrome that resembles type A1 brachydactyly (variable shortening of the middle phalanges of all digits) with associated symphalangism (producing a distal phalanx with the shape of a chess pawn). Scoliosis, clubfoot and tall stature are also characteristic. The syndrome has been described in one family with five affected individuals from three successive generations. Transmission appears to be autosomal dominant. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5564801000172113 | syndrome de brachydactylie et de symphalangisme distal | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
5564821000172118 | syndrome de Sillence | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
5564791000172112 | syndroom van brachydactylie en distaal symfalangisme | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
5564811000172111 | syndroom van Sillence | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Brachyphalangia | false | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Multiple malformation syndrome with limb defect as major feature | true | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Congenital anomaly of bone and joint | true | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Symphalangism | false | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Associated morphology | Abnormally short growth | true | Inferred relationship | Some | 2 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Finding site | Entire middle phalanx | true | Inferred relationship | Some | 2 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Associated morphology | Congenital ankylosis | false | Inferred relationship | Some | 2 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Finding site | Interphalangeal joint structure (body structure) | false | Inferred relationship | Some | 2 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Associated morphology | Abnormally short growth | false | Inferred relationship | Some | 3 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Finding site | Entire middle phalanx | false | Inferred relationship | Some | 3 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Distal interphalangeal joint symphalangism (disorder) | true | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Finding site | Structure of distal interphalangeal joint (body structure) | true | Inferred relationship | Some | 1 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Associated morphology | Ankylosis | true | Inferred relationship | Some | 1 | |
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Brachymesophalangia | true | Inferred relationship | Some | ||
Brachydactyly and distal symphalangism syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets