Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3311452015 | Peripheral resistance to thyroid hormone (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3311453013 | Peripheral resistance to thyroid hormone | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Peripheral resistance to thyroid hormone | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Peripheral resistance to thyroid hormone | Is a | Thyroid hormone responsiveness defect | true | Inferred relationship | Some | ||
| Peripheral resistance to thyroid hormone | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Peripheral resistance to thyroid hormone | Finding site | Thyroid structure | false | Inferred relationship | Some | ||
| Peripheral resistance to thyroid hormone | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Peripheral resistance to thyroid hormone | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital hypothyroidism due to peripheral resistance to thyroid hormone | Due to | True | Peripheral resistance to thyroid hormone | Inferred relationship | Some | 3 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR