As genome-based testing and diagnosis become standard practice, prepare your health system to manage the wealth of genomic data with a single, intuitive solution.
Providing regional care is complex, and can vary from system to system. Let our experts guide you at each step and find the right solution for your unique challenges.
Book a demoDesigned for scaling genetics needs across regional health systems
Messy clinical notes read themselves
Concept Recognition
Focus on patient care instead of deciphering clinical notes. Standardized HPO terms are suggested from large chunks of free text for effortless symptom capture.
One click cancer risk assessment
Integrated Cancer Risk Assessment Tool
Streamline cancer risk assessments of Gail, IBIS, and other models into a simple click of a button, saving up to 30 minutes wasted with redundant family data re-entry.
Holistic, scalable care
Individual and Family Centric Data Capture
Trade your collection of genetics tools for a single solution that recognizes the importance of collecting and linking both patient and family level data.
Automate admin work
Custom Integrations
Never enter the same information twice. PhenoTips can integrate with your health systems’ electronic health record, variant prioritization tool, and more, for seamless communication between systems.
Increase efficiency by 50%
Patient Entered Data Draws Pedigrees
Save time during the first patient encounter. Increase efficiency by up to 50% by sending your patient a survey that auto-draws their pedigree.
Harness the power of computable data
Comprehensive Searchable Database
Grouping cohorts and searching your database should be simple. Search and filter for patients and families based on phenotypic presentation, diagnosis, genotype and more.
In addition to our health systems suite, all PhenoTips medical genetics solutions come equipped with the necessities of genomic medicine.
Over 95% of users agree PhenoTips is the best pedigree drawing software they’ve used.
More than simply listing symptoms, your standardized symptoms power your analysis.
Built-in diagnoses suggestions help you reach diagnosis sooner, even for rare diseases.
Read the Case StudyPhenoTips looks good and it’s just so easy to use. You really want something that people who are not IT savvy can pick up quickly, this is perfect, it’s so easy to pick up.
Receive an assessment from our experts to discover how PhenoTips can prepare your regional centre for the scaling of genomics.
Book a demo