Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4536637014 | Transient congenital hypothyroidism due to dual oxidase 2 mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4868931000172111 | passagère congenitale hypothyreoïdie door mutatie van 'dual oxidase 2'-gen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4868941000172116 | voorbijgaande congenitale hypothyroïdie door mutatie van DUOX-2 | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Is a | Congenital hypothyroidism | true | Inferred relationship | Some | ||
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Is a | Transient hypothyroidism | true | Inferred relationship | Some | ||
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Due to | Chromosomal disorder (disorder) | true | Inferred relationship | Some | 2 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Clinical course | Transitory | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set
FHIR