Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Oct 2025. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5483414018 | Neuronal ceroid lipofuscinosis type 7 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5483415017 | NCL7 - neuronal ceroid lipofuscinosis type 7 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5483416016 | Neuronal ceroid lipofuscinosis type 7 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5483417013 | A rare neuronal ceroid lipofuscinosis characterized by epilepsy with myoclonic, atonic, and bilateral tonic-clonic seizures, gait disturbance, and language difficulty/delay. Progressive motor and cognitive decline, personality disorders, myoclonus and visual loss are common clinical features become evident later in the disease progress. Age of onset is typically late-infantile, however few juvenile-onset patients are reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5483418015 | A rare neuronal ceroid lipofuscinosis characterised by epilepsy with myoclonic, atonic, and bilateral tonic-clonic seizures, gait disturbance, and language difficulty/delay. Progressive motor and cognitive decline, personality disorders, myoclonus and visual loss are common clinical features become evident later in the disease progress. Age of onset is typically late-infantile, however few juvenile-onset patients are reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Neuronal ceroid lipofuscinosis type 7 | Is a | Progressive myoclonic epilepsy | true | Inferred relationship | Some | ||
| Neuronal ceroid lipofuscinosis type 7 | Is a | Neuronal ceroid lipofuscinosis | true | Inferred relationship | Some | ||
| Neuronal ceroid lipofuscinosis type 7 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Neuronal ceroid lipofuscinosis type 7 | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 3 | |
| Neuronal ceroid lipofuscinosis type 7 | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Neuronal ceroid lipofuscinosis type 7 | Finding site | Brain structure | true | Inferred relationship | Some | 1 | |
| Neuronal ceroid lipofuscinosis type 7 | Associated morphology | Degenerative abnormality | 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)