Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3701707019 | Genetic transient congenital hypothyroidism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3701708012 | Genetic transient congenital hypothyroidism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3701709016 | A rare thyroid disease with characteristics of a gene mutation induced, temporary deficiency of thyroid hormones at birth, which later reverts to normal with or without replacement therapy in the first few months or years of life. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Genetic transient congenital hypothyroidism | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
| Genetic transient congenital hypothyroidism | Is a | Congenital hypothyroidism | true | Inferred relationship | Some | ||
| Genetic transient congenital hypothyroidism | Is a | Transient hypothyroidism | true | Inferred relationship | Some | ||
| Genetic transient congenital hypothyroidism | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Genetic transient congenital hypothyroidism | Clinical course | Transitory | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR