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 |
3308133017 | The most frequent subtype of Joubert syndrome with manifestation of neurological features of Joubert Syndrome associated with retinal dystrophy. Prevalence is unknown. Age of onset and severity of retinal involvement are variable, ranging from congenital to progressive retinopathy with partial conservation of vision. To date, the most frequently mutated gene in this subtype is AHI1 (6q23.2), which accounts for about 20% of cases, following autosomal recessive inheritance. | 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 |
This concept is not in any reference sets