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Familial colorectal cancer type X (disorder)
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.
Id1197359006
StatusPrimitive
Associated morphologyNeoplasm, malignant (primary)
Finding siteColon structure
ICD-10 complex map reference set
TargetC18.9
RuleTRUE
AdviceALWAYS C18.9 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
CorrelationSNOMED CT source code to target map code correlation not specified