Pedigree Integration
Integrate world-class pedigree, screening and genetic risk assessment tools.
Streamline access to family health history information for clinicians and patients by embedding into your existing clinical system or EHR.
Pedigree Functionality
Embed our comprehensive pedigree maker module that is licensed by top clinical genetics teams worldwide to assess their patients’ risk of hereditary diseases. No need to login to a separate system when you can utilize single sign-on (SSO) and embed this module as if it’s part of your system.
- Flexible licensing based on your specific needs
- Maintain control of patient data without it ever leaving your existing system
Embed forms to properly capture family health histories from patients.
Capturing family relationships is complex. FamGenix can provide this in as little as two screens and branded to your existing user interface.
- Gather necessary data to auto-generate pedigrees that meet the standards expected by genetics providers worldwide.
- Run multiple disease risk algorithms at once for cancer or cardio with a click of a button.
- Assess guidelines to properly refer the patient for additional services such as screenings or genetic counseling/testing.
Access our Risk Server to generate risk calculations for several diseases.
Integrate our risk assessment interface, or utilize our risk server to pass the data to us via an API call and get results you can absorb back into your system.
- Available risk models include:
- Tyrer-Cuzick v8 (IBIS)
- BOADICEA v6 (CanRisk)
- BayesMendel (BRCAPRO, MMRpro, PancPRO, MelaPRO)
- Gail
- Claus
- QRISK3 (Cardiovascular)
- Risk is calculated for 5 year, 10-year, and lifetime. Mutation probabilities are included for BRCA1, BRCA2, PALB2, ATM, CHEK2, P16, MLH1, MLH2, MLH6, and Pancreatic Gene.
- Alerts exist detailing if any required data is missing or if the model cannot be calculated for other reasons, so you can be confident your data inputs are sufficient.
Benefits of Integration
Efficiently Screen Patients
Identify high-risk individuals for hereditary diseases based on NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) or ACMG/NSGC Practice Guidelines.
Maintain Control of Patient Data
Embed our technology while retaining all patient data within your systems.
Save Time and Development Costs
License FamGenix at a fraction of the investment costs required to build your own tools.
Provide Proactive Early Detection
Increase patient satisfaction by empowering patients with knowledge about their health risks.
Increase Downstream Revenue
Provide additional services to patients and family members to manage hereditary disease risk.
Pedigree Experts
We have over 100 years combined experience in developing pedigree tools that are used worldwide by top clinical genetic teams.
Discover all of our integration options in depth.
Set up a demo, and let's chat about ways we can implement our pedigree tools in your environment or existing application.