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 |
| 3302194018 | Neurogenic arthrogryposis multiplex congenita (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302195017 | Neurogenic arthrogryposis multiplex congenita | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302201013 | A form of arthrogryposis multiplex congenital characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3302202018 | A form of arthrogryposis multiplex congenital characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Due to | Denervation atrophy of muscle | true | Inferred relationship | Some | 3 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Is a | Arthropathy associated with another disorder | false | Inferred relationship | Some | ||
| Neurogenic arthrogryposis multiplex congenita (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Neurogenic arthrogryposis multiplex congenita (disorder) | Is a | Arthrogryposis | false | Inferred relationship | Some | ||
| Neurogenic arthrogryposis multiplex congenita (disorder) | Is a | Hereditary disorder of musculoskeletal system | false | Inferred relationship | Some | ||
| Neurogenic arthrogryposis multiplex congenita (disorder) | Associated morphology | Contracture | false | Inferred relationship | Some | 2 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 2 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 1 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Interprets | Range of joint movement | false | Inferred relationship | Some | 2 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Finding site | Structure of joint region | true | Inferred relationship | Some | 1 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Has interpretation | Absent | false | Inferred relationship | Some | 2 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Is a | Joint movement absent | false | Inferred relationship | Some | ||
| Neurogenic arthrogryposis multiplex congenita (disorder) | Is a | Inherited arthrogryposis | true | Inferred relationship | Some | ||
| Neurogenic arthrogryposis multiplex congenita (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 4 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Interprets | Range of joint movement | true | Inferred relationship | Some | 4 | |
| Neurogenic arthrogryposis multiplex congenita (disorder) | Is a | Arthrogryposis multiplex congenita | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder) | Is a | True | Neurogenic arthrogryposis multiplex congenita (disorder) | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set
FHIR