PREMM1,2,6
Version 1

The PREMM1,2,6 has been developed as a pretest to decide whether patients suspected of having Lynch syndrome should be tested for germline mismatch repair gene mutations.
"PREMM1,2,6" is a logistic regression model. It calculates the risk of having a mutation in the mismatch repair genes MLH1, MSH2 and MSH6 (for single genes and overall) based on the personal and familial cancer history of the proband (colorectal, endometrial, and other Lynch syndrome related cancers).

Health Atlas ID: 7Q0CEYUJ46-2

1 item is associated with this Model:

Organism: Homo sapiens

Human Disease: Hereditary breast ovarian cancer syndrome

Model type: Not specified

Model format: R package

Execution or visualisation environment: Shiny

Model image: No image specified

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Views: 1283

Created: 13th May 2019 at 14:12

Last updated: 27th Nov 2019 at 12:53

Last used: 27th Jan 2021 at 13:47

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