Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3301893013 | Distal arthrogryposis type 2B (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3301894019 | Distal arthrogryposis type 2B | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3301895018 | Sheldon-Hall syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3301896017 | Freeman-Sheldon syndrome variant | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3301897014 | Rare multiple congenital contracture syndrome characterized by contractures of distal joints of the limbs, triangular face, downslanting palpebral fissures, small mouth, and high arched palate. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3301964014 | Rare multiple congenital contracture syndrome characterised by contractures of distal joints of the limbs, triangular face, downslanting palpebral fissures, small mouth, and high arched palate. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3874661000052118 | Sheldon-Halls syndrom | sv | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Distal arthrogryposis type 2B (disorder) | Is a | Distal arthrogryposis syndrome | true | Inferred relationship | Some | ||
| Distal arthrogryposis type 2B (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 2B (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 2B (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 2B (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 2 | |
| Distal arthrogryposis type 2B (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 2B (disorder) | Finding site | Structure of joint region | true | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 2B (disorder) | Interprets | Range of joint movement | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR