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Lynch syndrome 2

MONDO:0012249

An autosomal dominant hereditary neoplastic syndrome caused by pathogenic variants in the MLH1 mismatch repair gene. It is characterized by an increased risk of colorectal cancer in the absence of extensive polyposis, endometrial, ovarian, gastric, small intestinal, and urinary tract cancers, often occurring at younger ages.

Also known as: Hereditary non-polyposis colon cancer type 2, Hereditary nonpolyposis colorectal cancer type 2, Lynch 2 syndrome, MLH1-related Lynch syndrome, colorectal cancer, hereditary nonpolyposis, type 2, familial non-polyposis colon cancer type 2, COCA2, HNPCC2

2907 clinical trials for this condition and its sub-types, 3 tagged with Lynch syndrome 2 itself.

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