hereditair papillair niercelcarcinoom (aandoening) | | hereditair papillair niercelcarcinoom | | hereditair papillair NCC erfelijk papillair niercarcinoom
| | Hereditary papillary renal cell carcinoma | | A familial predisposition for developing bilateral and multifocal type 1 papillary renal carcinoma. Transmitted as an autosomal dominant trait with reduced penetrance, the syndrome is associated with germline mutations in the MET proto-oncogene (7q31). |
| Id | 715561008 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
SNOMED CT to Orphanet simple map | 47044 |
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 |
|
|