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 |
| 5483354017 | Neuronal ceroid lipofuscinosis type 4 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5483355016 | Neuronal ceroid lipofuscinosis type 4 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5483356015 | NCL4 - neuronal ceroid lipofuscinosis type 4 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5483357012 | CLN4 disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5483358019 | A rare neuronal ceroid lipofuscinosis characterized by adult-onset (20-early 30 years) progressive generalized tonic-clonic and myoclonic seizures, speech deterioration, dementia and ataxia. Some patients may also exhibit Parkinsonism. Visual impairment is usually not present. This is the only ceroid lipofuscinosis form inherited dominantly. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5483359010 | A rare neuronal ceroid lipofuscinosis characterised by adult-onset (20-early 30 years) progressive generalised tonic-clonic and myoclonic seizures, speech deterioration, dementia and ataxia. Some patients may also exhibit Parkinsonism. Visual impairment is usually not present. This is the only ceroid lipofuscinosis form inherited dominantly. | 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 4 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Neuronal ceroid lipofuscinosis type 4 | Is a | Progressive myoclonic epilepsy | true | Inferred relationship | Some | ||
| Neuronal ceroid lipofuscinosis type 4 | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 4 | |
| Neuronal ceroid lipofuscinosis type 4 | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
| Neuronal ceroid lipofuscinosis type 4 | Occurrence | Adulthood | true | Inferred relationship | Some | 1 | |
| Neuronal ceroid lipofuscinosis type 4 | Finding site | Brain structure | true | Inferred relationship | Some | 1 | |
| Neuronal ceroid lipofuscinosis type 4 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Neuronal ceroid lipofuscinosis type 4 | Is a | Neuronal ceroid lipofuscinosis | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)