Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Jun 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5068621019 | Hypothyroidism due to TSH receptor mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 5068622014 | Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 5068623016 | Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5068626012 | Hypothyroidism due to TSHR (thyroid stimulating hormone receptor) mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation | Is a | Autosomal hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation | Is a | Thyroid hormone responsiveness defect | true | Inferred relationship | Existential restriction modifier | ||
| Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation | Finding site | Thyroid structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR