| 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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