PhenoTips Core
作成者: PhenoTips
PhenoTips Core Offering - A genomic health record improving workflows for clinical genetics.
PhenoTips is a unified, EHR-integrated Genomic Health Record designed to digitize medical genetics. By transforming unstructured clinical notes into structured data, it streamlines workflows for rare diseases and cancer genetics while unifying regional health systems.
Core Genomic Health Record
A centralized source of truth for genomic information, replacing fragmented tools with a searchable database of patient records. It stores machine-readable genes, diagnoses, and observations in one secure location.
- Unified database links individual patient records to shared family pedigrees for a holistic view.
- Standards-based approach utilizes Human Phenotype Ontology, OMIM, and Orphanet for gold-standard data coding.
- EHR integration offers full compatibility with existing hospital systems to streamline clinical workflows.
- Security and compliance measures ensure PhenoTips is fully GDPR, HIPAA, DSPT, and CE+ certified.
Pedigree Tool
Draw and manage complex family trees with a professional-grade pedigree editor designed for clinical genetics. This tool integrates directly with your patient records.
- Draw pedigrees quickly with an intuitive drag-and-drop interface or auto-generate them from patient intake forms.
- Record detailed clinical information for each family member, including cancer history and genetic test results.
- Export high-quality pedigree images for clinical reports or research publications.
Pre-Visit Patient Questionnaire
Digitize the patient intake process to save up to 30 minutes per appointment. Patients complete their history securely from home before they arrive.
- Automated pedigrees are created instantly when patients complete their family history, giving clinicians a head start.
- Targeted forms allow you to choose specialty-based questionnaires such as Cardiovascular, General Genetics, or Cancer.
- Multilingual support helps you reach a diverse patient population with multiple language options.
Cancer Genetics Solutions
Simplifies oncology workflows by unifying risk assessment and family history. It enables rapid triaging to identify high-risk patients before they enter the clinic.
- Efficiency gains allow clinicians to reclaim up to 7.5 hours a week by eliminating manual paperwork.
- Pedigree-embedded tools enable users to launch risk models like CanRisk and chemicals directly from the family tree.
- Comprehensive screening flags high-risk patients early using targeted digital intake forms.
Genomics for Health Systems
Connects EPRs, labs, and trusts into a single regional genomic record, preparing systems for scaling whole genome sequencing (WGS).
- System unity connects EPRs, laboratory hubs, and trusts into a single regional genomic record.
- Automated test requisition allows for the generation of pre-populated WGS test ordering forms with a single click.
AI-Powered Clinical Insights
Uses Natural Language Processing (NLP) to turn free-text referral notes into standardized clinical data.
- Concept recognition automatically suggests HPO terms from messy clinical notes using text mining.
- AI-ready formats transform patient information into data that is ready for advanced analysis and variant prioritization.
API & Developer Access
Unlock full programmatic control over your data to build custom integrations or research pipelines.
- RESTful infrastructure allows users to securely write and pull data using industry-standard protocols.
- Standardized data exchange leverages HL7v2 and FHIR standards for enterprise-level system connectivity.
