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).
LHA-ID: 7Q0CEYUJ46-21 item is associated with this Model:
- https://apps.health-atlas.de/premm126/ (Website)
Human Disease: Hereditary breast ovarian cancer syndrome
Model type: Not specified
Model format: Not specified
Execution or visualisation environment: Not specified
Model image: No image specified
Created: 13th May 2019 at 14:12
Last updated: 27th Nov 2019 at 12:53
Last used: 24th May 2020 at 22:02