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838276009: Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder)

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
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
3418251001000115 Guam-Parkinson-Demenz-Komplex de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5977261000241112 complexe de SLA (sclérose latérale amyotrophique), parkinsonisme et démence fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5977271000241116 complexe de sclérose latérale amyotrophique, parkinsonisme et démence fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5977281000241119 syndrome de Guam fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5977261000241112 complexe de SLA (sclérose latérale amyotrophique), parkinsonisme et démence fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5977271000241116 complexe de sclérose latérale amyotrophique, parkinsonisme et démence fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5977281000241119 syndrome de Guam fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3418251001000115 Guam-Parkinson-Demenz-Komplex de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Is a Dementia true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Is a Chronic organic mental disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Is a Amyotrophic lateral sclerosis true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Is a Parkinsonism true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Is a Degenerative disease of the central nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Is a Genetic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Finding site Structure of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Interprets Cognitive functions true Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Finding site Basal ganglion structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 6
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Has interpretation Slow true Inferred relationship Existential restriction modifier (core metadata concept) 6
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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