| familiair colorectaal carcinoom type X (aandoening) | | familiair colorectaal carcinoom type X | | familial colorectal cancer type X
FCCTX
|  | Dit is een vorm van kanker in je dikke darm of endeldarm. Je endeldarm is het laatste stuk van je darm, net voor je poepgat. Dit kan vaker voorkomen in je familie. | | Familial colorectal cancer type X | | FCCTX - familial colorectal cancer type X
| | A rare inherited cancer-predisposing syndrome characterized by the fulfilment of the Amsterdam criteria for hereditary nonpolyposis colorectal cancer (HNPCC) but without alterations, either somatic or germline, in the DNA mismatch repair (MMR) genes. |
| | Id | 1197359006 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | C18.9 | | Term | Maligne neoplasma van colon, niet gespecificeerd |
| Target | Z80.0 | | Term | Familie-anamnese met maligne neoplasma van spijsverteringsorganen |
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| SNOMED CT to ICD-10 extended map | | Target | C18.9 | | Rule | TRUE | | Advice | ALWAYS C18.9 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE | | Correlation | SNOMED CT source code to target map code correlation not specified |
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