| 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 hereditary nonpolyposis colon cancer defined in individuals meeting the Amsterdam criteria for Lynch syndrome, but lacking germline mutations in the mismatch repair genes. It is characterized by a later onset, preferential involvement of distal colon and rectum, lower risk of developing extracolonic cancer, a higher adenoma/carcinoma ratio, a higher differentiation of tumor cells, a more heterogeneous tumor architecture and an infiltrative growth pattern when compared to Lynch syndrome cases. |
| | 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 |
|
| 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 |
|
|
