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 |
| 8687271000146116 | congenitale afwezigheid van helft van schildklier | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8687281000146119 | congenitale afwezigheid van helft van thyroïd | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8687291000146117 | congenitale afwezigheid van helft van glandula thyroidea | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8687301000146118 | congenitale afwezigheid van helft van schildklier (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3303560018 | 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. In symptomatic cases, clinical features and signs may include decreased activity and increased sleep, feeding difficulty, constipation and prolonged jaundice. Slow linear growth and developmental delay may also occur. Some familial cases have been reported suggesting genetic factors but to date none have been identified in humans. | 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 |
This concept is not in any reference sets
FHIR