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 |
3308138014 | Joubert syndrome with renal defect (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308139018 | Joubert syndrome with renal defect | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401442010 | Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with renal disease, in the absence of retinopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401443017 | Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with renal disease, in the absence of retinopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308138014 | Joubert syndrome with renal defect (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308139018 | Joubert syndrome with renal defect | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308140016 | A rare subtype of Joubert syndrome with manifestation of the neurological features of Joubert Syndrome associated with renal disease, in the absence of retinopathy. Prevalence is unknown. In most cases the renal disease manifests as juvenile nephronophthisis, with onset of clinical symptoms in the late first/early second decade of life, although in rare cases there may be infantile nephronophthisis, with onset in the first years of life. The most commonly mutated genes in this subtype are NPHP1 (2q13) and RPGRIP1L (16q12.2) with autosomal recessive inheritance. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401442010 | Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with renal disease, in the absence of retinopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401443017 | Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with renal disease, in the absence of retinopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3385941001000111 | Joubert-Syndrom mit Nierenstörung | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
948401000172117 | JS-R - Joubert syndrome with renal defect | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
961431000172110 | syndrome de Joubert avec atteinte rénale | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
948401000172117 | JS-R - Joubert syndrome with renal defect | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
961431000172110 | syndrome de Joubert avec atteinte rénale | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3385941001000111 | Joubert-Syndrom mit Nierenstörung | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)