Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3334075013 | Dementia due to chromosomal anomaly (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3334076014 | Dementia due to chromosomal anomaly | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6733401000146110 | dementie door chromosoomafwijking | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6733411000146112 | dementie door chromosoomafwijking (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Dementia due to chromosomal anomaly (disorder) | Due to | Chromosomal disorder (disorder) | true | Inferred relationship | Some | 2 | |
| Dementia due to chromosomal anomaly (disorder) | Is a | Dementia associated with another disease (disorder) | true | Inferred relationship | Some | ||
| Dementia due to chromosomal anomaly (disorder) | Finding site | Brain structure | true | Inferred relationship | Some | 3 | |
| Dementia due to chromosomal anomaly (disorder) | Interprets | Cognitive functions | true | Inferred relationship | Some | 1 | |
| Dementia due to chromosomal anomaly (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Dementia with Down syndrome | Is a | True | Dementia due to chromosomal anomaly (disorder) | Inferred relationship | Some | |
| Dementia due to fragile X syndrome (disorder) | Is a | True | Dementia due to chromosomal anomaly (disorder) | Inferred relationship | Some | |
| Frontotemporal dementia due to TARDBP mutation | Is a | True | Dementia due to chromosomal anomaly (disorder) | Inferred relationship | Some | |
| Frontotemporal dementia due to VCP mutation (disorder) | Is a | True | Dementia due to chromosomal anomaly (disorder) | Inferred relationship | Some | |
| Frontotemporal dementia due to C9orf72 mutation (disorder) | Is a | True | Dementia due to chromosomal anomaly (disorder) | Inferred relationship | Some | |
| Frontotemporal dementia due to FUS mutation | Is a | True | Dementia due to chromosomal anomaly (disorder) | Inferred relationship | Some |
Reference Sets
FHIR