| familiair colorectaal carcinoom type X (aandoening) | | familiair colorectaal carcinoom type X | | familial colorectal cancer type X
FCCTX
| | 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 |
| DHD Diagnosis thesaurus reference set |
| 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 Orphanet simple map | 440437 |
| 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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