| 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 |
| DHD Diagnosis thesaurus reference set |
| 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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