Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2025. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5464060011 | Hereditary isolated MTC (medullary thyroid carcinoma) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5464061010 | Isolated familial MTC (medullary thyroid carcinoma) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5464062015 | Isolated familial medullary thyroid carcinoma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5464063013 | Hereditary isolated medullary thyroid carcinoma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5464064019 | Isolated familial medullary thyroid carcinoma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5464067014 | A rare thyroid tumor characterized by a malignant neoplasm derived from the calcitonin-secreting parafollicular C-cells of the thyroid and occurring familially, but not as a component of multiple endocrine neoplasia syndromes. The commonly multifocal, bilateral nodules are typically located at the junction of the upper and middle thirds of the thyroid lobes. Clinically, patients may present with diarrhea, flushing, or weight loss caused by excessive secretion of calcitonin by the tumor. In rare cases, the tumor can also cause Cushing syndrome due to ectopic corticotropin production. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5464068016 | A rare thyroid tumour characterised by a malignant neoplasm derived from the calcitonin-secreting parafollicular C-cells of the thyroid and occurring familially, but not as a component of multiple endocrine neoplasia syndromes. The commonly multifocal, bilateral nodules are typically located at the junction of the upper and middle thirds of the thyroid lobes. Clinically, patients may present with diarrhoea, flushing, or weight loss caused by excessive secretion of calcitonin by the tumour. In rare cases, the tumour can also cause Cushing syndrome due to ectopic corticotropin production. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Isolated familial medullary thyroid carcinoma | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Isolated familial medullary thyroid carcinoma | Is a | Medullary thyroid carcinoma | true | Inferred relationship | Some | ||
| Isolated familial medullary thyroid carcinoma | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Isolated familial medullary thyroid carcinoma | Is a | Hereditary cancer-predisposing syndrome | true | Inferred relationship | Some | ||
| Isolated familial medullary thyroid carcinoma | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
| Isolated familial medullary thyroid carcinoma | Associated morphology | Medullary thyroid carcinoma (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