Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
417688018 | Osteogenesis imperfecta, type IV A | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
673534011 | Osteogenesis imperfecta, type IV A (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4694694017 | Osteogenesis imperfecta type IV with normal teeth | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
837941000052114 | osteogenesis imperfecta, typ 4 A | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Osteogenesis imperfecta, type IV A (disorder) | Is a | Osteogenesis imperfecta with normal sclerae, dominant form | true | Inferred relationship | Some | ||
Osteogenesis imperfecta, type IV A (disorder) | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
Osteogenesis imperfecta, type IV A (disorder) | Finding site | Connective tissue structure | false | Inferred relationship | Some | ||
Osteogenesis imperfecta, type IV A (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Osteogenesis imperfecta, type IV A (disorder) | Finding site | Skeletal system structure | false | Inferred relationship | Some | 1 | |
Osteogenesis imperfecta, type IV A (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Osteogenesis imperfecta, type IV A (disorder) | Finding site | Connective tissue | false | Inferred relationship | Some | ||
Osteogenesis imperfecta, type IV A (disorder) | Associated morphology | kongenital dysplasi | false | Inferred relationship | Some | 1 | |
Osteogenesis imperfecta, type IV A (disorder) | Associated morphology | kongenital dysplasi | false | Inferred relationship | Some | 1 | |
Osteogenesis imperfecta, type IV A (disorder) | Finding site | Bone structure | false | Inferred relationship | Some | 1 | |
Osteogenesis imperfecta, type IV A (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Osteogenesis imperfecta, type IV A (disorder) | Finding site | Bone structure | false | Inferred relationship | Some | 2 | |
Osteogenesis imperfecta, type IV A (disorder) | Associated morphology | kongenital dysplasi | false | Inferred relationship | Some | 2 | |
Osteogenesis imperfecta, type IV A (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Osteogenesis imperfecta, type IV A (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Osteogenesis imperfecta, type IV A (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Osteogenesis imperfecta, type IV A (disorder) | Interprets | Bone formation | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets