Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3303556016 | Congenital absence of half of thyroid (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303557013 | Congenital absence of half of thyroid | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303558015 | Congenital hemiagenesis of thyroid | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303559011 | Thyroid hemiagenesis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5401063016 | Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401064010 | Thyroid hemiagenesis is a form of thyroid dysgenesis characterised by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital absence of half of thyroid (disorder) | Is a | Congenital absence of thyroid gland | true | Inferred relationship | Some | ||
| Congenital absence of half of thyroid (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Congenital absence of half of thyroid (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital absence of half of thyroid (disorder) | Finding site | Thyroid part | true | Inferred relationship | Some | 1 | |
| Congenital absence of half of thyroid (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Congenital absence of half of thyroid (disorder) | Associated morphology | Absence (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR