Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 178810015 | Refetoff syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 632762017 | Refetoff syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Refetoff syndrome | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Refetoff syndrome | Finding site | Thyroid structure | false | Inferred relationship | Some | ||
| Refetoff syndrome | Finding site | Entire endocrine gonad | false | Inferred relationship | Some | ||
| Refetoff syndrome | Is a | Inherited disorder of thyroid metabolism | false | Inferred relationship | Some | ||
| Refetoff syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Refetoff syndrome | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
| Refetoff syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Refetoff syndrome | Is a | Generalised thyroid hormone resistance | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR