PhenoTips is a proud partner of the NHS, helping trusts and regional alliances collaborate, engage patients, and offer consistent, accessible genomic care through a single, centralised Genomic Health Record.
PhenoTips' COO Dr. Pawel Buczkowicz presents the project making genomic expansion possible by equitably embedding and centralising genomics in the East Midlands and East of England region.
Designed for genomic mainstreaming, multidisciplinary team collaboration, and deep integrations.
Unite EHRs and streamline WGS test ordering
Avoid redundant data re-entry while uniting your health system. Your Genomic Health Record can integrate with any existing data management systems for seamless communication between systems, hospitals, labs, and trustsLearn More
Messy clinical notes read themselves
Focus on patient care instead of deciphering clinical notes. Standardized Human Phenotype Ontology (HPO) terms are suggested from large chunks of free text for effortless symptom capture.Learn More
Automate pedigree drawing
Patient Entered Data Draws Pedigrees
Improve patient engagement and save time during the first patient encounter by sending your patient a gender-inclusive digital family history questionnaire that automatically draws their pedigree.Learn More
One click cancer risk assessment
Pedigree-Embedded Risk Assessment Tool
Streamline cancer risk assessment by running four risk models simultaneously for any family member with a simple click of a button in pedigrees, saving time wasted on re-entering information already in other models and pedigrees.Learn More
Hollistic family care
Individual and Family Centric Data Capture
Build complex and inclusive pedigrees with a tool that understands the concept of family members, harnessing the latest standards to collect and link both patient and family level data.
Search, import, and export in bulk
Comprehensive Searchable Database
Harness the power of computable data to create cohorts and search your database. Search and filter for patients and families based on phenotypic presentation, diagnosis, genotype and much more.
All Genomic Health Records come equipped with the necessities of genomic medicine.
Build complex, standardized, and gender-inclusive pedigree charts with a user-friendly tool.
Easily store and capture rich clinical datasets with standard data models and HPO nomenclature.
Gene and diagnosis suggestions help you reach diagnosis sooner, even for rare diseases.
PhenoTips' Genomic Health Record is GDPR, DSPT, HIPAA, and CE+ certified and compliant.
PhenoTips 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.
The entire clinical genetics team, inherited cardiovascular team, and some other specialties such as Ophthalmology use PhenoTips on a daily basis. We save time as we no longer have to re-enter information for cancer risk calculations. It is easier to share and helps avoid unnecessary duplication of work. When requesting Whole exome/genome testing, we attach a printout from PhenoTips, rather than re-entering the data.