Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4651001014 | Congenital hypothyroidism due to thyroid peroxidase mutation (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4651002019 | Congenital hypothyroidism due to thyroid peroxidase mutation | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hypothyroidism due to thyroid peroxidase mutation | Is a | Congenital hypothyroidism | true | Inferred relationship | Some | ||
| Congenital hypothyroidism due to thyroid peroxidase mutation | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital hypothyroidism due to thyroid peroxidase mutation | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR