Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
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 | SNOMED CT core module |
| 3443237014 | Resistance to thyrotropin-releasing hormone syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3443238016 | TRH (thyrotropin-releasing hormone) resistance syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3443240014 | Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | Due to | Pituitary thyroid hormone resistance | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier | ||
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | Is a | Congenital central hypothyroidism | true | Inferred relationship | Existential restriction modifier | ||
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | Finding site | Thyroid structure | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR