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 |
| 3301898016 | Distal arthrogryposis type 5 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301899012 | Distal arthrogryposis type 5 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301900019 | Arthrogryposis with oculomotor limitation and electroretinal anomaly | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301901015 | Distal arthrogryposis with ophthalmoplegia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3301902010 | Oculomelic amyoplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3313038016 | An inherited developmental defect syndrome characterized by multiple congenital contractures of limbs, without primary neurologic and/or muscle disease that affects limb function, and ocular anomalies (ptosis, external ophthalmoplegia and/or strabismus). Intelligence is normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3313039012 | An inherited developmental defect syndrome characterised by multiple congenital contractures of limbs, without primary neurologic and/or muscle disease that affects limb function, and ocular anomalies (ptosis, external ophthalmoplegia and/or strabismus). Intelligence is normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Distal arthrogryposis type 5 (disorder) | Is a | Distal arthrogryposis syndrome | true | Inferred relationship | Some | ||
| Distal arthrogryposis type 5 (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 5 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 5 (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 5 (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 2 | |
| Distal arthrogryposis type 5 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 5 (disorder) | Finding site | Structure of joint region | true | Inferred relationship | Some | 1 | |
| Distal arthrogryposis type 5 (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