Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 153761017 | Congenital absence of thyroid gland | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 510169015 | Aplasia of thyroid with myxedema | en | Synonym | Inactive | Case insensitive | SNOMED CT core |
| 510170019 | Congenital thyroid aplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 510171015 | Aplasia of thyroid with myxoedema | en | Synonym | Inactive | Case insensitive | SNOMED CT core |
| 836614015 | Congenital absence of thyroid gland (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Thyroid hemiagenesis | Is a | True | Congenital absence of thyroid gland | Inferred relationship | Some | |
| Congenital hypothyroidism due to absence of thyroid gland | Due to | True | Congenital absence of thyroid gland | Inferred relationship | Some | 3 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set