| hereditair papillair niercelcarcinoom (aandoening) | | hereditair papillair niercelcarcinoom | | hereditair papillair NCC
erfelijk papillair niercarcinoom
| | Hereditary papillary renal cell carcinoma | | A rare familial renal cancer syndrome characterized by a predisposition for developing bilateral and multifocal classic type papillary renal cell carcinomas (formerly known as type 1 papillary renal cell carcinoma until the 2022 WHO classification of renal tumors). |
| | Id | 715561008 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| SNOMED CT to ICD-10 extended map | | Target | C64 | | Rule | TRUE | | Advice | ALWAYS C64 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE | | Correlation | SNOMED CT source code to target map code correlation not specified |
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