Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4651005017 | Congenital hypothyroidism due to thyroid deiodinase mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4651006016 | Congenital hypothyroidism due to thyroid deiodinase mutation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hypothyroidism due to thyroid deiodinase mutation | Is a | Congenital hypothyroidism | true | Inferred relationship | Existential restriction modifier | ||
| Congenital hypothyroidism due to thyroid deiodinase mutation | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital hypothyroidism due to thyroid deiodinase 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