Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3443236017 | Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3443237014 | Resistance to thyrotropin-releasing hormone syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3443238016 | TRH (thyrotropin-releasing hormone) resistance syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3443240014 | Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5403480018 | Resistance to thyrotropin-releasing hormone (TRH) syndrome is a type of central congenital hypothyroidism characterized by low levels of thyroid hormones due to insufficient release of thyroid-stimulating hormone (TSH) caused by pituitary resistance to TRH. It may or may not be observed from birth. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403481019 | Resistance to thyrotropin-releasing hormone (TRH) syndrome is a type of central congenital hypothyroidism characterised by low levels of thyroid hormones due to insufficient release of thyroid-stimulating hormone (TSH) caused by pituitary resistance to TRH. It may or may not be observed from birth. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) | Due to | Pituitary thyroid hormone resistance | true | Inferred relationship | Some | 1 | |
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) | Is a | Congenital central hypothyroidism (disorder) | true | Inferred relationship | Some | ||
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) | Finding site | Thyroid structure | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR