Status: current, Defined. 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 | Case insensitive | SNOMED CT core |
| 3334076014 | Dementia due to chromosomal anomaly | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Dementia due to chromosomal anomaly | Interprets | Cognitive functions | true | Inferred relationship | Some | 1 | |
| Dementia due to chromosomal anomaly | Has interpretation | Impaired | true | Inferred relationship | Some | 1 | |
| Dementia due to chromosomal anomaly | Due to | Chromosomal disorder | true | Inferred relationship | Some | 2 | |
| Dementia due to chromosomal anomaly | Is a | Dementia associated with another disease | true | Inferred relationship | Some | ||
| Dementia due to chromosomal anomaly | Finding site | Brain structure | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Dementia due to fragile X syndrome | Is a | True | Dementia due to chromosomal anomaly | Inferred relationship | Some | |
| Dementia co-occurrent and due to Down syndrome | Is a | True | Dementia due to chromosomal anomaly | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Mental health disorder reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR