familiair syndroom van papillair schildkliercarcinoom met renale papillaire neoplasie (aandoening) | | familiair syndroom van papillair schildkliercarcinoom met renale papillaire neoplasie | | fPTC/PRN
| | Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome | | An extremely rare inherited tumor syndrome within the familial nonmedullary thyroid cancer group. |
| DHD Diagnosis thesaurus reference set |
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | Target | C73 | Term | Maligne neoplasma van schildklier |
Target | D41.0 | Term | Neoplasma met onzeker of onbekend gedrag van nier |
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SNOMED CT to Orphanet simple map | 97290 |
SNOMED CT to ICD-10 extended map | Target | C73 | Rule | TRUE | Advice | ALWAYS C73 | MAPPED FOLLOWING WHO GUIDANCE | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE | Correlation | SNOMED CT source code to target map code correlation not specified |
Target | D41.0 | Rule | TRUE | Advice | ALWAYS D41.0 | MAPPED FOLLOWING SNOMED GUIDANCE | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE | Correlation | SNOMED CT source code to target map code correlation not specified |
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