Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5045351013 | Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
5045355016 | Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
5045356015 | Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
5045353011 | A rare mitochondrial disease with characteristics of a distinctive MRI pattern of cavitating leukodystrophy, predominantly in the posterior region of the cerebral hemispheres. The clinical picture varies widely between acute neurometabolic decompensation in infancy with loss of developmental milestones, seizures and pyramidal signs rapidly evolving into spastic tetraparesis, to subtle neurological symptoms presenting in adolescence. The disease course tends to stabilize over time in most patients and marked recovery of milestones may be observed. | en | Definition | Active | Case sensitive | SNOMED CT core |
5045354017 | A rare mitochondrial disease with characteristics of a distinctive MRI pattern of cavitating leucodystrophy, predominantly in the posterior region of the cerebral hemispheres. The clinical picture varies widely between acute neurometabolic decompensation in infancy with loss of developmental milestones, seizures and pyramidal signs rapidly evolving into spastic tetraparesis, to subtle neurological symptoms presenting in adolescence. The disease course tends to stabilise over time in most patients and marked recovery of milestones may be observed. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Is a | Leucodystrophy | true | Inferred relationship | Some | ||
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Is a | Mitochondrial cytopathy | true | Inferred relationship | Some | ||
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Is a | Peripheral neuropathy | true | Inferred relationship | Some | ||
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Clinical course | Non-progressive | true | Inferred relationship | Some | 3 | |
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 4 | |
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Finding site | Myelinated nerve fibre structure | true | Inferred relationship | Some | 1 | |
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Associated morphology | Myelin sheath alteration | true | Inferred relationship | Some | 1 | |
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Finding site | White matter structure of brain and spinal cord | true | Inferred relationship | Some | 2 | |
Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set