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 |
| 6802031000146114 | 'protein kinase cAMP-dependent type I regulatory subunit beta'-gerelateerde neurodegeneratieve dementie met intermediaire filamenten | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6802041000146118 | PRKAR1B-gerelateerde neurodegeneratieve dementie met intermediaire filamenten | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6802051000146115 | 'protein kinase cAMP-dependent type I regulatory subunit beta'-gerelateerde neurodegeneratieve dementie met intermediaire filamenten (aandoening) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 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 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Is a | Dementia | true | Inferred relationship | Some | ||
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Finding site | Brain structure | true | Inferred relationship | Some | 1 | |
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Is a | Degenerative disease of the central nervous system | false | Inferred relationship | Some | ||
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Associated morphology | degeneratie (afwijkende morfologie) | false | Inferred relationship | Some | 1 | |
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Interprets | Cognitive functions | true | Inferred relationship | Some | 2 | |
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | Is a | Degenerative brain disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR