Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer)
PREMM1,2 Model: Prediction Model for MLH1 and MSH2 Gene Mutations
The PREMM1,2 model is a clinical prediction rule designed to be used by healthcare professionals to estimate the probability that an individual carries a mutation in MLH1 or MSH2. Mutations in these genes are found in most patients with the Lynch syndrome. Learn more

