Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3770076017 | Familial nonmedullary thyroid carcinoma | en | Synonym | Active | Case insensitive | SNOMED CT core |
3770077014 | Familial nonmedullary thyroid carcinoma (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3770078016 | FNMTC - familial nonmedullary thyroid carcinoma | en | Synonym | Active | Case sensitive | SNOMED CT core |
3770079012 | Familial non medullary thyroid carcinoma | en | Synonym | Active | Case insensitive | SNOMED CT core |
3770080010 | A rare hereditary nonmedullary thyroid carcinoma characterised by the presence of differentiated thyroid cancer of follicular cell origin in two or more first-degree relatives, in the absence of other familial tumour syndromes or radiation exposure. Frequent capsular invasion is observed. Biopsy reveals multicentric tumours with multiple adenomatous nodules with or without oxyphilia and follicular or papillary carcinoma histology. | en | Definition | Active | Case sensitive | SNOMED CT core |
3770081014 | A rare hereditary nonmedullary thyroid carcinoma characterized by the presence of differentiated thyroid cancer of follicular cell origin in two or more first-degree relatives, in the absence of other familial tumor syndromes or radiation exposure. Frequent capsular invasion is observed. Biopsy reveals multicentric tumors with multiple adenomatous nodules with or without oxyphilia and follicular or papillary carcinoma histology. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set