PhenoTips Enterprise Feature

Integrated Cancer Risk Assessment

Simplify your cancer risk assessment for breast and ovarian cancer, multiple genes, and non-cancer conditions to one click, launched within pedigrees.

Simplified workflow

One-click cancer risk assessment

Never enter the same information twice, compare GAIL, IBIS, PREMM5, and BOADICEA models with one click within pedigrees. Read about the specific cancers, mutations, and additional risk calculations available.

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Improved efficiency

Reclaim a day each week

Save 45 minutes per patient—7.5 hours a week—in administrative paperwork. Harness that reclaimed time for patient care instead.

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Data unification

Manage families together

Seeing members of the same family together has never been easier. Manage a family’s genetic information all in one place.

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Elevate your workflow

Our Cancer Risk Assessment tool calculates risk probability for multiple genes, Breast and Ovarian cancer, as well as non-cancer conditions, while integrating seamlessly into your existing workflow, simplifying and unifying cancer genetics.

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5 year, 10 year and lifetime risk calculations for breast and ovarian cancer

For breast cancer, GAIL, IBIS, and BOADICEA calculate lifetime risk, IBIS and BOADICEA calculate 10 year risk, and GAIL and BOADICEA calculate 5 year risk. For ovarian cancer, BOADICEA provides 5 year, 10 year, and lifetime risk calculations.

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Mutation probability for over 10 genes

The PREMM5 model for Lynch Syndrome calculates the probability of mutation for MLH1, MSH2, MSH5, MSH6, PMS2, and EPCAM genes, while BOADICEA provides the probability of mutation for CHEK2, ATM, BRCA1, BRCA2, and PALB2 genes.

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Additional non-cancer risk models

PhenoTips includes additional risk calculations such as an aortic root calculator for Marfan Syndrome, and will be updating the Cancer Risk Assessment tool to include risk calculations for Familial Hypercholesterolemia.

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Complete EHR integration

Eliminate all redundant data re-entry by integrating your complete Genomic Health Record with your EHR.

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Rapid preliminary triaging

When combined with Pre-Visit Patient Questionnaires, flag high-risk patients before their first appointment.

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Download reports

Save a timestamped PDF to your device complete with all calculations and model responses.

PhenoTips allows us to click a button and save anywhere from 15 to 30 minutes in extra work.

- Scott Weissman, MS, Cancer Service Lead Genetic Counselor, Genome Medical, San Francisco, CA, USA
Read the Case Study

See the Cancer Risk Assessment Tool in Action

Discover your cancer genetics workflow, simplified to one click within pedigrees.

Book a discovery call