| familiair niet-medullair schildkliercarcinoom (aandoening) | | familiair niet-medullair schildkliercarcinoom | | familiair NMTC
familiair non-medullair schildkliercarcinoom
| | Familial nonmedullary primary thyroid carcinoma | | FNMTC - familial nonmedullary thyroid carcinoma
| | 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. |
| | Id | 786038001 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | C73 | | Term | Maligne neoplasma van schildklier |
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| SNOMED CT to Orphanet simple map | 319487 |
| SNOMED CT to ICD-10 extended map | | Target | C73 | | Rule | TRUE | | Advice | ALWAYS C73 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE | | Correlation | SNOMED CT source code to target map code correlation not specified |
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