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 |
5403661011 | A rare genetic syndrome with limb malformations as a major feature characterized by brachydactyly and distal symphalangism, pes cavus, scoliosis, and normal stature. There have been no further descriptions in the literature since 1978. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403662016 | A rare genetic syndrome with limb malformations as a major feature characterised by brachydactyly and distal symphalangism, pes cavus, scoliosis, and normal stature. There have been no further descriptions in the literature since 1978. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
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
Component annotation with string value reference set (foundation metadata concept)