Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3705562016 | Progressive polyneuropathy with bilateral striatal necrosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3705563014 | Progressive polyneuropathy with bilateral striatal necrosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3705564015 | A rare genetic disorder of thiamine metabolism and transport with characteristics of the childhood-onset of recurrent episodes of flaccid paralysis and encephalopathy, associated with bilateral striatal necrosis and chronic progressive axonal polyneuropathy with proximal and distal muscle weakness, areflexia, contractures and foot deformities. Caused by homozygous mutation in the SLC25A19 gene on chromosome 17q25. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Lesion of brain | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Injury of superficial nerves of head AND/OR neck | false | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Injury of peripheral nerve | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Disorder of basal ganglia | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Polyneuropathy | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 3 | |
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Traumatic or nontraumatic brain injury | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Associated morphology | Necrosis | true | Inferred relationship | Some | 1 | |
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Chronic metabolic disorder | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Finding site | Corpus striatum structure | true | Inferred relationship | Some | 1 | |
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Metabolic encephalopathy | true | Inferred relationship | Some | ||
Progressive polyneuropathy with bilateral striatal necrosis | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Progressive polyneuropathy with bilateral striatal necrosis | Is a | Necrosis of anatomical site | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set