Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3334075013 | Dementia due to chromosomal anomaly (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3334076014 | Dementia due to chromosomal anomaly | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Dementia due to chromosomal anomaly | Due to | Chromosomal disorder | true | Inferred relationship | Existential restriction modifier | 2 | |
| Dementia due to chromosomal anomaly | Is a | Dementia associated with another disease | true | Inferred relationship | Existential restriction modifier | ||
| Dementia due to chromosomal anomaly | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier | 3 | |
| Dementia due to chromosomal anomaly | Interprets | Cognitive functions | true | Inferred relationship | Existential restriction modifier | 1 | |
| Dementia due to chromosomal anomaly | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Dementia co-occurrent and due to Down syndrome | Is a | True | Dementia due to chromosomal anomaly | Inferred relationship | Existential restriction modifier | |
| Dementia due to fragile X syndrome | Is a | True | Dementia due to chromosomal anomaly | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR