Link multiple family members to a single, LGBT-inclusive, standardized, and sharable pedigree. Capture complex family history, including consanguinity and detailed annotation, with a user-friendly pedigree drawing tool.
Leveraging the Human Phenotype Ontology (HPO), use predictive search, text-mining, or suggestions to easily capture high-quality clinical symptoms that can be exported directly to streamline test ordering.
Guide diagnosis with phenotype-based gene matching and disease suggestions. Or, use a simple search to record coded rare and common diseases leveraging Orphanet and OMIM.
Unify genomics with a single solution that makes your data searchable, sharable, standardized, and designed for the future.
Eliminate all redundant data re-entry by integrating your complete Genomic Health Record with your EHR software.Learn More
PhenoTips' Genomic Health Record is GDPR, DSPT, HIPAA, and CE+ certified and compliant.
Enter free-text referral or clinical notes and PhenoTips' will automatically run natural language processing to suggest Human Phenotype Ontology coded phenotypes.
Clinical measurements are automatically plotted as quantiles and growth curves, with abnormal values automatically recorded as Human Phenotype Ontology coded phenotypes.