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 |
| 3302534011 | Lethal congenital contracture syndrome type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302535012 | Lethal congenital contracture syndrome type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302536013 | Herva disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3302537016 | Multiple contracture syndrome Finnish type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3302538014 | An autosomal recessive disorder that is the most severe, neonatally lethal form of arthrogryposis a disorder characterized by congenital nonprogressive joint contractures. The contractures can involve the upper or lower limbs and/or the vertebral column, leading to various degrees of flexion or extension limitations evident at birth. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3302539018 | An autosomal recessive disorder that is the most severe, neonatally lethal form of arthrogryposis a disorder characterised by congenital nonprogressive joint contractures. The contractures can involve the upper or lower limbs and/or the vertebral column, leading to various degrees of flexion or extension limitations evident at birth. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Lethal congenital contracture syndrome type 1 (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Lethal congenital contracture syndrome type 1 (disorder) | Is a | Arthrogryposis | false | Inferred relationship | Some | ||
| Lethal congenital contracture syndrome type 1 (disorder) | Is a | Hereditary disorder of musculoskeletal system | false | Inferred relationship | Some | ||
| Lethal congenital contracture syndrome type 1 (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 1 | |
| Lethal congenital contracture syndrome type 1 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Lethal congenital contracture syndrome type 1 (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 1 | |
| Lethal congenital contracture syndrome type 1 (disorder) | Is a | Inherited arthrogryposis | true | Inferred relationship | Some | ||
| Lethal congenital contracture syndrome type 1 (disorder) | Finding site | Structure of joint region | true | Inferred relationship | Some | 1 | |
| Lethal congenital contracture syndrome type 1 (disorder) | Interprets | Range of joint movement | true | Inferred relationship | Some | 2 | |
| Lethal congenital contracture syndrome type 1 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Lethal congenital contracture syndrome type 1 (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set
FHIR