Status: current, Primitive. Date: 31-Jan 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3634089014 | Epigenetic disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3634090017 | Epigenetic disorder (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3777278011 | Changes in gene function that are mitotically and/or meiotically heritable and that do not entail a change in DNA sequence. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Epigenetic disorder | Is a | Disease | true | Inferred relationship | Some | ||
| Epigenetic disorder | Is a | Hereditary disease | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Imprinting error | Is a | True | Epigenetic disorder | Inferred relationship | Some |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR