Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
788156014 | Thyroid hormone responsiveness defect (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
83919011 | Thyroid hormone responsiveness defect | en | Synonym | Active | Case insensitive | SNOMED CT core |
83920017 | Thyroid hormone unresponsiveness | en | Synonym | Active | Case insensitive | SNOMED CT core |
83922013 | Hypothyroidism due to thyroid insensitivity to TSH | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
83923015 | Congenital unresponsiveness to thyrotropin | en | Synonym | Active | Case insensitive | SNOMED CT core |
83928012 | Unresponsiveness of thyroid gland to thyrotropin | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Thyroid hormone responsiveness defect | Occurrence | Congenital | false | Inferred relationship | Some | ||
Thyroid hormone responsiveness defect | Is a | Inherited disorder of thyroid metabolism | true | Inferred relationship | Some | ||
Thyroid hormone responsiveness defect | Is a | Hypothyroidism | false | Inferred relationship | Some | ||
Thyroid hormone responsiveness defect | Is a | Congenital hypothyroidism | true | Inferred relationship | Some | ||
Thyroid hormone responsiveness defect | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Thyroid hormone responsiveness defect | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
Thyroid hormone responsiveness defect | Finding site | Entire endocrine gonad | false | Inferred relationship | Some | ||
Thyroid hormone responsiveness defect | Finding site | Thyroid structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Allan-Herndon-Dudley syndrome | Is a | True | Thyroid hormone responsiveness defect | Inferred relationship | Some | |
Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation | Is a | True | Thyroid hormone responsiveness defect | Inferred relationship | Some | |
Thyroid hormone resistance syndrome | Is a | True | Thyroid hormone responsiveness defect | Inferred relationship | Some | |
Familial non-autoimmune autosomal dominant hyperthyroidism | Due to | True | Thyroid hormone responsiveness defect | Inferred relationship | Some | 2 |
Peripheral resistance to thyroid hormone | Is a | True | Thyroid hormone responsiveness defect | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set