Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4536636017 | Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4536637014 | Transient congenital hypothyroidism due to dual oxidase 2 mutation | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation | Is a | Congenital hypothyroidism | true | Inferred relationship | Some | ||
| Transient congenital hypothyroidism due to dual oxidase 2 mutation | Is a | Transient hypothyroidism | true | Inferred relationship | Some | ||
| Transient congenital hypothyroidism due to dual oxidase 2 mutation | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation | Due to | Chromosomal disorder | true | Inferred relationship | Some | 2 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation | Clinical course | Transitory | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR