Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3727867012 | Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3727868019 | PRKAR1B-related neurodegenerative dementia with intermediate filaments | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3727869010 | Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3727870011 | A rare genetic neurodegenerative disease with characteristics of dementia and mild parkinsonism with poor levodopa response. Presenting clinical manifestations are memory problems, short attention span, disorientation, language impairment, rigidity, bradykinesia, postural instability and behavioural changes including apathy, anxiety and delusions. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3727871010 | A rare genetic neurodegenerative disease with characteristics of dementia and mild parkinsonism with poor levodopa response. Presenting clinical manifestations are memory problems, short attention span, disorientation, language impairment, rigidity, bradykinesia, postural instability and behavioral changes including apathy, anxiety and delusions. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
PRKAR1B-related neurodegenerative dementia with intermediate filaments | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
PRKAR1B-related neurodegenerative dementia with intermediate filaments | est un(e) (attribut) | démence | true | Inferred relationship | Some | ||
PRKAR1B-related neurodegenerative dementia with intermediate filaments | localisation d'une constatation (attribut) | structure de l'encéphale | true | Inferred relationship | Some | 1 | |
PRKAR1B-related neurodegenerative dementia with intermediate filaments | est un(e) (attribut) | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
PRKAR1B-related neurodegenerative dementia with intermediate filaments | est un(e) (attribut) | maladie dégénérative du système nerveux central | false | Inferred relationship | Some | ||
PRKAR1B-related neurodegenerative dementia with intermediate filaments | morphologie associée (attribut) | dégénérescence | false | Inferred relationship | Some | 1 | |
PRKAR1B-related neurodegenerative dementia with intermediate filaments | a pour interprétation (attribut) | altéré | true | Inferred relationship | Some | 2 | |
PRKAR1B-related neurodegenerative dementia with intermediate filaments | interprète (attribut) | fonctions cognitives | true | Inferred relationship | Some | 2 | |
PRKAR1B-related neurodegenerative dementia with intermediate filaments | est un(e) (attribut) | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
PRKAR1B-related neurodegenerative dementia with intermediate filaments | morphologie associée (attribut) | Degenerative abnormality | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets