Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3896344017 | Amyotrophic lateral sclerosis, parkinsonism, dementia of Guam syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3896345016 | Guam disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3896346015 | Lytico Bodig disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3896348019 | PDALS (parkinsonism, dementia, amyotrophic lateral sclerosis) complex | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3896351014 | Amyotrophic lateral sclerosis, parkinsonism, dementia complex | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3896352019 | Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5408862016 | A rare neurodegenerative disease characterized by extrapyramidal symptoms (rigidity, tremor, bradykinesia) and dementia, typically beginning in the fifth or sixth decade of life and progressing to a vegetative state with pelvicrural flexion contractures within few years. Oculomotor signs, olfactory dysfunction, and autonomic disturbances may also be observed. Neuropathological hallmarks are frontotemporally accentuated cerebral atrophy, as well as neurofibrillary tangles and neuronal loss in a characteristic distribution in cortical and subcortical regions. The disease is endemic to the Pacific Island of Guam. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5408863014 | A rare neurodegenerative disease characterised by extrapyramidal symptoms (rigidity, tremor, bradykinesia) and dementia, typically beginning in the fifth or sixth decade of life and progressing to a vegetative state with pelvicrural flexion contractures within few years. Oculomotor signs, olfactory dysfunction, and autonomic disturbances may also be observed. Neuropathological hallmarks are frontotemporally accentuated cerebral atrophy, as well as neurofibrillary tangles and neuronal loss in a characteristic distribution in cortical and subcortical regions. The disease is endemic to the Pacific Island of Guam. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Is a | Dementia | true | Inferred relationship | Some | ||
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Is a | Chronic organic mental disorder (disorder) | true | Inferred relationship | Some | ||
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Is a | Amyotrophic lateral sclerosis | true | Inferred relationship | Some | ||
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Is a | Parkinsonism | true | Inferred relationship | Some | ||
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Is a | Degenerative disease of the central nervous system | true | Inferred relationship | Some | ||
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Is a | Genetic disease | true | Inferred relationship | Some | ||
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Finding site | Structure of central nervous system (body structure) | true | Inferred relationship | Some | 1 | |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Interprets | Cognitive functions | true | Inferred relationship | Some | 2 | |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 3 | |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Finding site | Basal ganglion structure (body structure) | true | Inferred relationship | Some | 4 | |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Interprets | Movement | true | Inferred relationship | Some | 6 | |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex | Has interpretation | Slow | true | Inferred relationship | Some | 6 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)