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).

LHA-ID: 7Q0CEYUJ46-2

1 item is associated with this Model:

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

Help
help Contributor and Creators

help Other creators

Kastrinos et al.
Activity

Views: 748

Created: 13th May 2019 at 14:12

Last updated: 27th Nov 2019 at 12:53

Last used: 24th May 2020 at 22:02

help Attributions

None

Related items

Powered by
(v.1.9.1)
Copyright © 2008 - 2019 The University of Manchester and HITS gGmbH
Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig