Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 83919011 | Thyroid hormone responsiveness defect | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 83920017 | Thyroid hormone unresponsiveness | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 83921018 | Thyroid hormone resistance | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 83922013 | Hypothyroidism due to thyroid insensitivity to TSH | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 83923015 | Congenital unresponsiveness to thyrotropin | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 83924014 | Thyroid hormone resistance syndrome | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 83925010 | General resistance to thyrotropin | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 83926011 | TSH resistance | en | Synonym | Inactive | Entire term case sensitive | SNOMED CT core module |
| 83927019 | Resistance to thyroid stimulating hormone | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 83928012 | Unresponsiveness of thyroid gland to thyrotropin | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 83929016 | Resistance to thyrotropin | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 788156014 | Thyroid hormone responsiveness defect (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Thyroid hormone resistance syndrome | Is a | True | Thyroid hormone responsiveness defect | Inferred relationship | Existential restriction modifier | |
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Due to | True | Thyroid hormone responsiveness defect | Inferred relationship | Existential restriction modifier | 2 |
| Peripheral resistance to thyroid hormone | Is a | True | Thyroid hormone responsiveness defect | Inferred relationship | Existential restriction modifier | |
| Monocarboxylate transporter 8 deficiency | Is a | True | Thyroid hormone responsiveness defect | Inferred relationship | Existential restriction modifier | |
| Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation | Is a | True | Thyroid hormone responsiveness defect | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets