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 |
3308130019 | Joubert syndrome with ocular defect (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308131015 | Joubert syndrome with ocular defect | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308132010 | Joubert syndrome with retinopathy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401440019 | Joubert syndrome with ocular defect is, along with pure JS, the most frequent subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with retinal dystrophy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401441015 | Joubert syndrome with ocular defect is, along with pure JS, the most frequent subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with retinal dystrophy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Joubert syndrome with ocular defect (disorder) | Is a | Retinal disorder | true | Inferred relationship | Some | ||
Joubert syndrome with ocular defect (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Joubert syndrome with ocular defect (disorder) | Is a | Joubert syndrome (disorder) | true | Inferred relationship | Some | ||
Joubert syndrome with ocular defect (disorder) | Finding site | Retinal structure | true | Inferred relationship | Some | 2 | |
Joubert syndrome with ocular defect (disorder) | Associated morphology | Aplasia | false | Inferred relationship | Some | 2 | |
Joubert syndrome with ocular defect (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Joubert syndrome with ocular defect (disorder) | Finding site | Cerebellar vermis structure | false | Inferred relationship | Some | 2 | |
Joubert syndrome with ocular defect (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Joubert syndrome with ocular defect (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Some | 1 | |
Joubert syndrome with ocular defect (disorder) | Finding site | Cerebellar vermis structure | true | Inferred relationship | Some | 1 | |
Joubert syndrome with ocular defect (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)